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

DYSPNOEA ( 3130 FDA reports)
NAUSEA ( 2880 FDA reports)
PAIN ( 2483 FDA reports)
ASTHENIA ( 2287 FDA reports)
DIARRHOEA ( 2229 FDA reports)
FATIGUE ( 2074 FDA reports)
VOMITING ( 2061 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2022 FDA reports)
PNEUMONIA ( 1995 FDA reports)
OEDEMA PERIPHERAL ( 1912 FDA reports)
ANAEMIA ( 1873 FDA reports)
ANXIETY ( 1839 FDA reports)
FALL ( 1780 FDA reports)
HYPOTENSION ( 1734 FDA reports)
DIZZINESS ( 1714 FDA reports)
PYREXIA ( 1630 FDA reports)
RENAL FAILURE ( 1564 FDA reports)
ATRIAL FIBRILLATION ( 1459 FDA reports)
RENAL FAILURE ACUTE ( 1458 FDA reports)
DEHYDRATION ( 1419 FDA reports)
HEADACHE ( 1394 FDA reports)
CHEST PAIN ( 1350 FDA reports)
BACK PAIN ( 1340 FDA reports)
HYPERTENSION ( 1277 FDA reports)
INJURY ( 1234 FDA reports)
PAIN IN EXTREMITY ( 1231 FDA reports)
ABDOMINAL PAIN ( 1206 FDA reports)
WEIGHT DECREASED ( 1205 FDA reports)
HYPOKALAEMIA ( 1170 FDA reports)
ARTHRALGIA ( 1156 FDA reports)
DEPRESSION ( 1150 FDA reports)
PLEURAL EFFUSION ( 1114 FDA reports)
DEATH ( 1112 FDA reports)
URINARY TRACT INFECTION ( 1100 FDA reports)
DRUG INEFFECTIVE ( 1057 FDA reports)
MYOCARDIAL INFARCTION ( 1016 FDA reports)
MALAISE ( 995 FDA reports)
SEPSIS ( 989 FDA reports)
CONFUSIONAL STATE ( 977 FDA reports)
COUGH ( 965 FDA reports)
THROMBOCYTOPENIA ( 957 FDA reports)
DECREASED APPETITE ( 952 FDA reports)
RESPIRATORY FAILURE ( 937 FDA reports)
CONSTIPATION ( 936 FDA reports)
BLOOD GLUCOSE INCREASED ( 875 FDA reports)
WEIGHT INCREASED ( 867 FDA reports)
INSOMNIA ( 860 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 824 FDA reports)
CEREBROVASCULAR ACCIDENT ( 819 FDA reports)
HAEMOGLOBIN DECREASED ( 799 FDA reports)
CARDIAC ARREST ( 763 FDA reports)
RASH ( 762 FDA reports)
CONDITION AGGRAVATED ( 755 FDA reports)
DEEP VEIN THROMBOSIS ( 716 FDA reports)
HYPOAESTHESIA ( 706 FDA reports)
EMOTIONAL DISTRESS ( 682 FDA reports)
SYNCOPE ( 680 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 679 FDA reports)
GAIT DISTURBANCE ( 676 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 675 FDA reports)
ECONOMIC PROBLEM ( 648 FDA reports)
ABDOMINAL PAIN UPPER ( 641 FDA reports)
PULMONARY EMBOLISM ( 639 FDA reports)
CARDIOMEGALY ( 635 FDA reports)
CORONARY ARTERY DISEASE ( 633 FDA reports)
CELLULITIS ( 632 FDA reports)
OSTEONECROSIS OF JAW ( 630 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 622 FDA reports)
SOMNOLENCE ( 615 FDA reports)
INFECTION ( 612 FDA reports)
OSTEOARTHRITIS ( 609 FDA reports)
BRADYCARDIA ( 603 FDA reports)
BRONCHITIS ( 600 FDA reports)
DRUG INTERACTION ( 599 FDA reports)
ATELECTASIS ( 598 FDA reports)
LOSS OF CONSCIOUSNESS ( 590 FDA reports)
HYPONATRAEMIA ( 589 FDA reports)
PRURITUS ( 584 FDA reports)
TACHYCARDIA ( 583 FDA reports)
BLOOD CREATININE INCREASED ( 582 FDA reports)
PANCYTOPENIA ( 580 FDA reports)
MUSCLE SPASMS ( 578 FDA reports)
CONVULSION ( 576 FDA reports)
DYSPHAGIA ( 567 FDA reports)
HYPERKALAEMIA ( 564 FDA reports)
CARDIAC FAILURE ( 561 FDA reports)
PARAESTHESIA ( 559 FDA reports)
OEDEMA ( 558 FDA reports)
PLATELET COUNT DECREASED ( 554 FDA reports)
NEUROPATHY PERIPHERAL ( 553 FDA reports)
NEUTROPENIA ( 552 FDA reports)
MITRAL VALVE INCOMPETENCE ( 546 FDA reports)
TREMOR ( 543 FDA reports)
PALPITATIONS ( 537 FDA reports)
MENTAL STATUS CHANGES ( 533 FDA reports)
MYALGIA ( 533 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 532 FDA reports)
MULTI-ORGAN FAILURE ( 531 FDA reports)
ERYTHEMA ( 530 FDA reports)
CHILLS ( 529 FDA reports)
DIABETES MELLITUS ( 527 FDA reports)
HYPERHIDROSIS ( 527 FDA reports)
PULMONARY OEDEMA ( 526 FDA reports)
RENAL IMPAIRMENT ( 520 FDA reports)
BLOOD PRESSURE INCREASED ( 519 FDA reports)
BONE DISORDER ( 518 FDA reports)
FEELING ABNORMAL ( 517 FDA reports)
MUSCULAR WEAKNESS ( 517 FDA reports)
HYPOXIA ( 516 FDA reports)
UNEVALUABLE EVENT ( 508 FDA reports)
CHEST DISCOMFORT ( 506 FDA reports)
PULMONARY HYPERTENSION ( 502 FDA reports)
ABDOMINAL DISTENSION ( 489 FDA reports)
BLOOD POTASSIUM DECREASED ( 484 FDA reports)
VISION BLURRED ( 481 FDA reports)
ANHEDONIA ( 480 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 471 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 470 FDA reports)
CONTUSION ( 460 FDA reports)
OSTEOMYELITIS ( 448 FDA reports)
HEART RATE INCREASED ( 446 FDA reports)
FEBRILE NEUTROPENIA ( 443 FDA reports)
PAIN IN JAW ( 442 FDA reports)
ARRHYTHMIA ( 436 FDA reports)
CHOLELITHIASIS ( 427 FDA reports)
MULTIPLE INJURIES ( 422 FDA reports)
ARTHRITIS ( 421 FDA reports)
HAEMORRHAGE ( 417 FDA reports)
SINUSITIS ( 417 FDA reports)
STRESS ( 410 FDA reports)
RENAL FAILURE CHRONIC ( 395 FDA reports)
CARDIAC DISORDER ( 385 FDA reports)
FLUSHING ( 384 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 383 FDA reports)
SEPTIC SHOCK ( 381 FDA reports)
SPINAL OSTEOARTHRITIS ( 381 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 380 FDA reports)
DYSPNOEA EXERTIONAL ( 375 FDA reports)
HYPERLIPIDAEMIA ( 367 FDA reports)
LETHARGY ( 365 FDA reports)
FEAR ( 363 FDA reports)
FLUID RETENTION ( 363 FDA reports)
RECTAL HAEMORRHAGE ( 363 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 363 FDA reports)
MEMORY IMPAIRMENT ( 362 FDA reports)
EPISTAXIS ( 359 FDA reports)
ASTHMA ( 357 FDA reports)
SWELLING ( 354 FDA reports)
ASCITES ( 352 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 351 FDA reports)
CARDIO-RESPIRATORY ARREST ( 350 FDA reports)
AMNESIA ( 348 FDA reports)
STAPHYLOCOCCAL INFECTION ( 346 FDA reports)
THROMBOSIS ( 345 FDA reports)
CARDIOMYOPATHY ( 344 FDA reports)
WHEEZING ( 342 FDA reports)
BALANCE DISORDER ( 340 FDA reports)
BLOOD PRESSURE DECREASED ( 339 FDA reports)
BONE PAIN ( 339 FDA reports)
HYPERGLYCAEMIA ( 339 FDA reports)
VENTRICULAR TACHYCARDIA ( 338 FDA reports)
VISUAL IMPAIRMENT ( 335 FDA reports)
MUSCULOSKELETAL PAIN ( 335 FDA reports)
DYSPEPSIA ( 334 FDA reports)
BLOOD UREA INCREASED ( 333 FDA reports)
LEUKOPENIA ( 330 FDA reports)
EJECTION FRACTION DECREASED ( 321 FDA reports)
UNRESPONSIVE TO STIMULI ( 321 FDA reports)
NECK PAIN ( 320 FDA reports)
HAEMATOCRIT DECREASED ( 319 FDA reports)
HYPERSENSITIVITY ( 319 FDA reports)
HAEMORRHOIDS ( 318 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 316 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 316 FDA reports)
FLUID OVERLOAD ( 315 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 313 FDA reports)
HYPOGLYCAEMIA ( 311 FDA reports)
ALOPECIA ( 306 FDA reports)
BLOOD BILIRUBIN INCREASED ( 305 FDA reports)
JOINT SWELLING ( 305 FDA reports)
DISEASE PROGRESSION ( 304 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 301 FDA reports)
ARTHROPATHY ( 300 FDA reports)
CATARACT ( 300 FDA reports)
HEPATIC FAILURE ( 300 FDA reports)
HEART RATE IRREGULAR ( 298 FDA reports)
LYMPHADENOPATHY ( 297 FDA reports)
RESPIRATORY DISTRESS ( 294 FDA reports)
OSTEONECROSIS ( 293 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 292 FDA reports)
ABDOMINAL DISCOMFORT ( 292 FDA reports)
IMPAIRED HEALING ( 292 FDA reports)
GASTRITIS ( 285 FDA reports)
OSTEOPENIA ( 285 FDA reports)
DENTAL CARIES ( 283 FDA reports)
HAEMATURIA ( 282 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 279 FDA reports)
PANCREATITIS ( 277 FDA reports)
SLEEP APNOEA SYNDROME ( 276 FDA reports)
COAGULOPATHY ( 276 FDA reports)
HIATUS HERNIA ( 276 FDA reports)
OVERDOSE ( 274 FDA reports)
ANGINA PECTORIS ( 272 FDA reports)
BLOOD GLUCOSE DECREASED ( 271 FDA reports)
SURGERY ( 269 FDA reports)
DYSARTHRIA ( 268 FDA reports)
HYPOTHYROIDISM ( 268 FDA reports)
ILL-DEFINED DISORDER ( 268 FDA reports)
AGITATION ( 267 FDA reports)
RHABDOMYOLYSIS ( 266 FDA reports)
LUNG INFILTRATION ( 265 FDA reports)
MALNUTRITION ( 264 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 263 FDA reports)
LEUKOCYTOSIS ( 262 FDA reports)
HALLUCINATION ( 261 FDA reports)
OXYGEN SATURATION DECREASED ( 260 FDA reports)
RENAL INJURY ( 260 FDA reports)
TOOTH EXTRACTION ( 260 FDA reports)
ARTERIOSCLEROSIS ( 258 FDA reports)
DRUG HYPERSENSITIVITY ( 256 FDA reports)
HERPES ZOSTER ( 256 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 255 FDA reports)
DIVERTICULUM ( 253 FDA reports)
METASTASES TO BONE ( 251 FDA reports)
DRY MOUTH ( 250 FDA reports)
RENAL CYST ( 247 FDA reports)
NEPHROLITHIASIS ( 246 FDA reports)
NEOPLASM MALIGNANT ( 242 FDA reports)
URINARY INCONTINENCE ( 242 FDA reports)
ANOREXIA ( 240 FDA reports)
MEDICATION ERROR ( 239 FDA reports)
CARDIAC MURMUR ( 238 FDA reports)
ENCEPHALOPATHY ( 237 FDA reports)
NERVOUSNESS ( 237 FDA reports)
PULMONARY CONGESTION ( 237 FDA reports)
TOOTHACHE ( 237 FDA reports)
VERTIGO ( 236 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 235 FDA reports)
HYPOPHAGIA ( 234 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 234 FDA reports)
SINUS TACHYCARDIA ( 234 FDA reports)
DYSURIA ( 231 FDA reports)
INFLUENZA LIKE ILLNESS ( 231 FDA reports)
MULTIPLE MYELOMA ( 231 FDA reports)
HYPOMAGNESAEMIA ( 230 FDA reports)
TYPE 2 DIABETES MELLITUS ( 230 FDA reports)
DISORIENTATION ( 225 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 225 FDA reports)
HAEMATOCHEZIA ( 225 FDA reports)
HAEMATOMA ( 225 FDA reports)
METABOLIC ACIDOSIS ( 225 FDA reports)
TREATMENT NONCOMPLIANCE ( 222 FDA reports)
OROPHARYNGEAL PAIN ( 221 FDA reports)
STOMATITIS ( 221 FDA reports)
GOUT ( 221 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 220 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 219 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 219 FDA reports)
PROTHROMBIN TIME PROLONGED ( 218 FDA reports)
HAEMOPTYSIS ( 217 FDA reports)
EXOSTOSIS ( 216 FDA reports)
DYSGEUSIA ( 214 FDA reports)
HIP FRACTURE ( 213 FDA reports)
OSTEOPOROSIS ( 213 FDA reports)
SLEEP DISORDER ( 213 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 212 FDA reports)
ABASIA ( 211 FDA reports)
MYOCARDIAL ISCHAEMIA ( 211 FDA reports)
OBESITY ( 211 FDA reports)
INFLAMMATION ( 210 FDA reports)
CARDIOGENIC SHOCK ( 208 FDA reports)
LUNG NEOPLASM ( 208 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 206 FDA reports)
PRODUCTIVE COUGH ( 206 FDA reports)
COMA ( 204 FDA reports)
DEFORMITY ( 203 FDA reports)
INCORRECT DOSE ADMINISTERED ( 203 FDA reports)
URINARY RETENTION ( 202 FDA reports)
VENTRICULAR FIBRILLATION ( 202 FDA reports)
SKIN ULCER ( 201 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 201 FDA reports)
GASTRIC ULCER ( 200 FDA reports)
PERICARDIAL EFFUSION ( 199 FDA reports)
DIPLOPIA ( 198 FDA reports)
LUNG DISORDER ( 198 FDA reports)
BLOOD POTASSIUM INCREASED ( 196 FDA reports)
DECREASED INTEREST ( 196 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 196 FDA reports)
URTICARIA ( 196 FDA reports)
EMPHYSEMA ( 195 FDA reports)
HEPATIC STEATOSIS ( 195 FDA reports)
INTERSTITIAL LUNG DISEASE ( 195 FDA reports)
COLITIS ( 194 FDA reports)
CANDIDIASIS ( 192 FDA reports)
BLOOD SODIUM DECREASED ( 191 FDA reports)
DELIRIUM ( 191 FDA reports)
ORTHOPNOEA ( 191 FDA reports)
RIB FRACTURE ( 191 FDA reports)
ORTHOSTATIC HYPOTENSION ( 190 FDA reports)
HEART RATE DECREASED ( 189 FDA reports)
ACUTE RESPIRATORY FAILURE ( 188 FDA reports)
HAEMATEMESIS ( 188 FDA reports)
BLISTER ( 186 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 186 FDA reports)
INJECTION SITE PAIN ( 186 FDA reports)
IRRITABILITY ( 186 FDA reports)
SWELLING FACE ( 184 FDA reports)
BURNING SENSATION ( 183 FDA reports)
MIGRAINE ( 182 FDA reports)
MENTAL DISORDER ( 181 FDA reports)
RENAL DISORDER ( 181 FDA reports)
SPEECH DISORDER ( 179 FDA reports)
HEPATIC ENZYME INCREASED ( 178 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 177 FDA reports)
DEMENTIA ( 176 FDA reports)
HOT FLUSH ( 176 FDA reports)
SPINAL COLUMN STENOSIS ( 176 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 175 FDA reports)
PRIMARY SEQUESTRUM ( 174 FDA reports)
VIRAL INFECTION ( 173 FDA reports)
ATRIAL FLUTTER ( 173 FDA reports)
EMOTIONAL DISORDER ( 172 FDA reports)
HYPOCALCAEMIA ( 172 FDA reports)
ELECTROLYTE IMBALANCE ( 171 FDA reports)
RESPIRATORY ARREST ( 171 FDA reports)
INFLUENZA ( 170 FDA reports)
MELAENA ( 170 FDA reports)
MUCOSAL INFLAMMATION ( 168 FDA reports)
PRESYNCOPE ( 168 FDA reports)
HYPOVOLAEMIA ( 167 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 165 FDA reports)
HYPERCHOLESTEROLAEMIA ( 165 FDA reports)
OFF LABEL USE ( 164 FDA reports)
PNEUMONIA ASPIRATION ( 164 FDA reports)
NASAL CONGESTION ( 163 FDA reports)
ROTATOR CUFF SYNDROME ( 163 FDA reports)
SCAR ( 163 FDA reports)
AORTIC VALVE INCOMPETENCE ( 163 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 163 FDA reports)
DISTURBANCE IN ATTENTION ( 162 FDA reports)
FEELING HOT ( 162 FDA reports)
MOUTH ULCERATION ( 162 FDA reports)
SPLENOMEGALY ( 162 FDA reports)
DIVERTICULITIS ( 161 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 160 FDA reports)
NASOPHARYNGITIS ( 159 FDA reports)
MOBILITY DECREASED ( 158 FDA reports)
BURSITIS ( 157 FDA reports)
HEPATOMEGALY ( 157 FDA reports)
IRON DEFICIENCY ANAEMIA ( 156 FDA reports)
JAUNDICE ( 156 FDA reports)
LIVER DISORDER ( 156 FDA reports)
ORAL PAIN ( 156 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 156 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 156 FDA reports)
ROAD TRAFFIC ACCIDENT ( 155 FDA reports)
SPINAL COMPRESSION FRACTURE ( 155 FDA reports)
DYSPHONIA ( 155 FDA reports)
DRUG DOSE OMISSION ( 154 FDA reports)
OESOPHAGITIS ( 154 FDA reports)
POLLAKIURIA ( 154 FDA reports)
RIGHT VENTRICULAR FAILURE ( 153 FDA reports)
SKIN DISCOLOURATION ( 153 FDA reports)
VISUAL ACUITY REDUCED ( 153 FDA reports)
FAILURE TO THRIVE ( 153 FDA reports)
DRUG TOXICITY ( 152 FDA reports)
FLATULENCE ( 152 FDA reports)
FUNGAL INFECTION ( 152 FDA reports)
APHASIA ( 151 FDA reports)
SINUS BRADYCARDIA ( 151 FDA reports)
TOOTH DISORDER ( 151 FDA reports)
GENERALISED OEDEMA ( 150 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 149 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 149 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 148 FDA reports)
BONE LESION ( 147 FDA reports)
BLOOD ALBUMIN DECREASED ( 146 FDA reports)
RHINORRHOEA ( 146 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 145 FDA reports)
COMPLETED SUICIDE ( 144 FDA reports)
CORONARY ARTERY OCCLUSION ( 144 FDA reports)
RASH PRURITIC ( 144 FDA reports)
PALLOR ( 143 FDA reports)
PNEUMONITIS ( 143 FDA reports)
TOOTH ABSCESS ( 143 FDA reports)
ABNORMAL BEHAVIOUR ( 143 FDA reports)
BLINDNESS ( 143 FDA reports)
DYSKINESIA ( 143 FDA reports)
PULMONARY FIBROSIS ( 142 FDA reports)
CEREBRAL HAEMORRHAGE ( 141 FDA reports)
GASTROINTESTINAL DISORDER ( 141 FDA reports)
AZOTAEMIA ( 140 FDA reports)
CEREBRAL INFARCTION ( 140 FDA reports)
SCOLIOSIS ( 140 FDA reports)
CYSTITIS ( 139 FDA reports)
FEMUR FRACTURE ( 139 FDA reports)
CAROTID ARTERY STENOSIS ( 138 FDA reports)
POST PROCEDURAL COMPLICATION ( 138 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 138 FDA reports)
RHEUMATOID ARTHRITIS ( 137 FDA reports)
STEVENS-JOHNSON SYNDROME ( 137 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 137 FDA reports)
GASTROENTERITIS ( 137 FDA reports)
HAEMODIALYSIS ( 137 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 136 FDA reports)
OSTEOSCLEROSIS ( 136 FDA reports)
PANIC ATTACK ( 136 FDA reports)
SUICIDAL IDEATION ( 136 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 136 FDA reports)
PURULENT DISCHARGE ( 134 FDA reports)
SHOCK ( 134 FDA reports)
LUMBAR SPINAL STENOSIS ( 134 FDA reports)
AORTIC STENOSIS ( 133 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 133 FDA reports)
CYANOSIS ( 133 FDA reports)
GINGIVAL BLEEDING ( 133 FDA reports)
GINGIVITIS ( 133 FDA reports)
HEPATIC CIRRHOSIS ( 133 FDA reports)
BLOOD CALCIUM DECREASED ( 132 FDA reports)
CARPAL TUNNEL SYNDROME ( 132 FDA reports)
HYPERSOMNIA ( 132 FDA reports)
MASS ( 132 FDA reports)
PANCREATITIS ACUTE ( 132 FDA reports)
PRODUCT QUALITY ISSUE ( 132 FDA reports)
SPONDYLOLISTHESIS ( 132 FDA reports)
RALES ( 131 FDA reports)
DECUBITUS ULCER ( 131 FDA reports)
CEREBRAL ATROPHY ( 130 FDA reports)
FACIAL PAIN ( 130 FDA reports)
FAECAL INCONTINENCE ( 130 FDA reports)
HEAD INJURY ( 130 FDA reports)
OSTEITIS ( 130 FDA reports)
PHYSICAL DISABILITY ( 129 FDA reports)
COMPRESSION FRACTURE ( 129 FDA reports)
FIBROMYALGIA ( 129 FDA reports)
ABNORMAL DREAMS ( 128 FDA reports)
DEVICE RELATED INFECTION ( 128 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 128 FDA reports)
HEMIPARESIS ( 128 FDA reports)
SKIN LESION ( 128 FDA reports)
TOOTH FRACTURE ( 128 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 127 FDA reports)
DRUG EFFECT DECREASED ( 127 FDA reports)
ILEUS ( 127 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 127 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 126 FDA reports)
BONE MARROW FAILURE ( 126 FDA reports)
FEELING COLD ( 126 FDA reports)
RESTLESSNESS ( 126 FDA reports)
NIGHT SWEATS ( 125 FDA reports)
TACHYPNOEA ( 125 FDA reports)
HYPERCALCAEMIA ( 125 FDA reports)
SINUS DISORDER ( 124 FDA reports)
SKIN DISORDER ( 123 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 123 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 123 FDA reports)
BREAST CANCER ( 122 FDA reports)
INTESTINAL OBSTRUCTION ( 122 FDA reports)
MENTAL IMPAIRMENT ( 122 FDA reports)
PNEUMOTHORAX ( 122 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 122 FDA reports)
TINNITUS ( 121 FDA reports)
TOOTH LOSS ( 121 FDA reports)
COLONIC POLYP ( 121 FDA reports)
DIALYSIS ( 121 FDA reports)
IRRITABLE BOWEL SYNDROME ( 121 FDA reports)
LABORATORY TEST ABNORMAL ( 121 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 120 FDA reports)
RASH ERYTHEMATOUS ( 119 FDA reports)
SYNOVIAL CYST ( 119 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 118 FDA reports)
DILATATION VENTRICULAR ( 118 FDA reports)
GROIN PAIN ( 118 FDA reports)
METASTASES TO LUNG ( 118 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 117 FDA reports)
EXCORIATION ( 117 FDA reports)
ESCHERICHIA INFECTION ( 116 FDA reports)
EYE PAIN ( 116 FDA reports)
JOINT INJURY ( 116 FDA reports)
MASTICATION DISORDER ( 116 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 115 FDA reports)
LOBAR PNEUMONIA ( 115 FDA reports)
NERVOUS SYSTEM DISORDER ( 115 FDA reports)
NEUTROPHIL COUNT DECREASED ( 115 FDA reports)
ADVERSE EVENT ( 114 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 114 FDA reports)
DISCOMFORT ( 114 FDA reports)
CHOLECYSTITIS ( 112 FDA reports)
DISABILITY ( 112 FDA reports)
EATING DISORDER ( 112 FDA reports)
LEFT ATRIAL DILATATION ( 112 FDA reports)
GLAUCOMA ( 111 FDA reports)
LACERATION ( 111 FDA reports)
MOOD ALTERED ( 110 FDA reports)
RENAL TUBULAR NECROSIS ( 110 FDA reports)
SKIN EXFOLIATION ( 110 FDA reports)
WOUND ( 110 FDA reports)
NEURALGIA ( 109 FDA reports)
OSTEOLYSIS ( 109 FDA reports)
ABSCESS ( 109 FDA reports)
CHRONIC SINUSITIS ( 109 FDA reports)
GALLBLADDER DISORDER ( 109 FDA reports)
ANGINA UNSTABLE ( 108 FDA reports)
COLD SWEAT ( 108 FDA reports)
ORAL CANDIDIASIS ( 108 FDA reports)
TENDERNESS ( 108 FDA reports)
PATHOLOGICAL FRACTURE ( 107 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 107 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 107 FDA reports)
DRY SKIN ( 107 FDA reports)
JAW FRACTURE ( 107 FDA reports)
DEAFNESS ( 106 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 105 FDA reports)
ORAL DISORDER ( 104 FDA reports)
RESPIRATORY DISORDER ( 104 FDA reports)
AGGRESSION ( 104 FDA reports)
BACTERAEMIA ( 104 FDA reports)
GINGIVAL PAIN ( 104 FDA reports)
CARDIOVASCULAR DISORDER ( 103 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 103 FDA reports)
LUNG INFECTION ( 103 FDA reports)
RADICULOPATHY ( 103 FDA reports)
RESTLESS LEGS SYNDROME ( 102 FDA reports)
DEPRESSED MOOD ( 102 FDA reports)
BREATH SOUNDS ABNORMAL ( 101 FDA reports)
HYPERBILIRUBINAEMIA ( 101 FDA reports)
HYPOALBUMINAEMIA ( 101 FDA reports)
INCONTINENCE ( 101 FDA reports)
BACK DISORDER ( 100 FDA reports)
CARDIAC VALVE DISEASE ( 100 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 99 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 99 FDA reports)
MULTIPLE SCLEROSIS ( 99 FDA reports)
THYROID DISORDER ( 99 FDA reports)
PLEURAL FIBROSIS ( 98 FDA reports)
RASH GENERALISED ( 98 FDA reports)
SICK SINUS SYNDROME ( 98 FDA reports)
TORSADE DE POINTES ( 98 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 98 FDA reports)
DRY EYE ( 98 FDA reports)
INFUSION RELATED REACTION ( 98 FDA reports)
ECCHYMOSIS ( 97 FDA reports)
ENTEROCOCCAL INFECTION ( 97 FDA reports)
CLOSTRIDIAL INFECTION ( 96 FDA reports)
METASTASES TO LIVER ( 96 FDA reports)
MYOPATHY ( 96 FDA reports)
PROSTATE CANCER ( 96 FDA reports)
RHINITIS ALLERGIC ( 96 FDA reports)
URINE OUTPUT DECREASED ( 95 FDA reports)
WITHDRAWAL SYNDROME ( 95 FDA reports)
BLOOD CHLORIDE DECREASED ( 94 FDA reports)
FAECES DISCOLOURED ( 94 FDA reports)
FOOT FRACTURE ( 93 FDA reports)
SUBDURAL HAEMATOMA ( 93 FDA reports)
VENTRICULAR HYPOKINESIA ( 93 FDA reports)
RESPIRATORY RATE INCREASED ( 92 FDA reports)
ULCER ( 92 FDA reports)
EAR PAIN ( 92 FDA reports)
ECZEMA ( 92 FDA reports)
ERECTILE DYSFUNCTION ( 92 FDA reports)
HEPATITIS ( 92 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 91 FDA reports)
BACTERIAL INFECTION ( 91 FDA reports)
COLON CANCER ( 91 FDA reports)
LUNG NEOPLASM MALIGNANT ( 91 FDA reports)
PSORIASIS ( 91 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 91 FDA reports)
SOMNAMBULISM ( 91 FDA reports)
NEOPLASM PROGRESSION ( 90 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 90 FDA reports)
ASPIRATION ( 90 FDA reports)
JAW DISORDER ( 90 FDA reports)
LUNG CONSOLIDATION ( 90 FDA reports)
MUSCLE TIGHTNESS ( 90 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 90 FDA reports)
DIASTOLIC DYSFUNCTION ( 89 FDA reports)
GASTRIC DISORDER ( 89 FDA reports)
GRAND MAL CONVULSION ( 89 FDA reports)
INJECTION SITE ERYTHEMA ( 89 FDA reports)
ATRIOVENTRICULAR BLOCK ( 88 FDA reports)
CIRCULATORY COLLAPSE ( 88 FDA reports)
DRUG ADMINISTRATION ERROR ( 88 FDA reports)
PETECHIAE ( 88 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 88 FDA reports)
SWOLLEN TONGUE ( 88 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 87 FDA reports)
ANGER ( 87 FDA reports)
COGNITIVE DISORDER ( 86 FDA reports)
CROHN'S DISEASE ( 86 FDA reports)
CRYING ( 86 FDA reports)
DISEASE RECURRENCE ( 86 FDA reports)
DYSLIPIDAEMIA ( 86 FDA reports)
LOCALISED INFECTION ( 86 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 86 FDA reports)
ORAL INTAKE REDUCED ( 86 FDA reports)
POLYDIPSIA ( 86 FDA reports)
PROTEINURIA ( 86 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 86 FDA reports)
RETCHING ( 85 FDA reports)
WOUND INFECTION ( 85 FDA reports)
BLOOD MAGNESIUM DECREASED ( 85 FDA reports)
DRUG DEPENDENCE ( 85 FDA reports)
HYDRONEPHROSIS ( 85 FDA reports)
CHOLESTASIS ( 84 FDA reports)
DUODENAL ULCER ( 84 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 84 FDA reports)
DYSSTASIA ( 83 FDA reports)
GASTRITIS EROSIVE ( 83 FDA reports)
HALLUCINATION, AUDITORY ( 83 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 83 FDA reports)
SUDDEN DEATH ( 83 FDA reports)
PERITONITIS ( 82 FDA reports)
DIABETIC NEUROPATHY ( 82 FDA reports)
JOINT STIFFNESS ( 82 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 82 FDA reports)
BLOOD URINE PRESENT ( 81 FDA reports)
CARDIAC PACEMAKER INSERTION ( 81 FDA reports)
CHOLECYSTITIS CHRONIC ( 81 FDA reports)
DIVERTICULUM INTESTINAL ( 81 FDA reports)
HOSPITALISATION ( 81 FDA reports)
HYPERTHYROIDISM ( 81 FDA reports)
HYPOKINESIA ( 81 FDA reports)
INJECTION SITE HAEMATOMA ( 81 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 81 FDA reports)
KLEBSIELLA INFECTION ( 81 FDA reports)
LACTIC ACIDOSIS ( 81 FDA reports)
MITRAL VALVE CALCIFICATION ( 81 FDA reports)
MYELODYSPLASTIC SYNDROME ( 81 FDA reports)
NOCTURIA ( 81 FDA reports)
PULSE ABSENT ( 81 FDA reports)
SPINAL DISORDER ( 81 FDA reports)
VISUAL DISTURBANCE ( 81 FDA reports)
PERITONITIS BACTERIAL ( 80 FDA reports)
ADRENAL INSUFFICIENCY ( 80 FDA reports)
ANAPHYLACTIC REACTION ( 80 FDA reports)
CATHETERISATION CARDIAC ( 80 FDA reports)
CHOLECYSTITIS ACUTE ( 80 FDA reports)
CULTURE URINE POSITIVE ( 80 FDA reports)
HYPERNATRAEMIA ( 80 FDA reports)
INJECTION SITE HAEMORRHAGE ( 80 FDA reports)
ACCIDENTAL OVERDOSE ( 79 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 79 FDA reports)
HYPOPHOSPHATAEMIA ( 79 FDA reports)
PHARYNGITIS ( 79 FDA reports)
SKIN LACERATION ( 79 FDA reports)
TOBACCO USER ( 79 FDA reports)
PSEUDOMONAS INFECTION ( 78 FDA reports)
ATAXIA ( 78 FDA reports)
BODY TEMPERATURE INCREASED ( 78 FDA reports)
DRUG INTOLERANCE ( 78 FDA reports)
GINGIVAL DISORDER ( 78 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 78 FDA reports)
LOCAL SWELLING ( 78 FDA reports)
BEDRIDDEN ( 77 FDA reports)
THROAT IRRITATION ( 77 FDA reports)
VENTRICULAR HYPERTROPHY ( 77 FDA reports)
BRONCHOPNEUMONIA ( 76 FDA reports)
DEBRIDEMENT ( 76 FDA reports)
JOINT DISLOCATION ( 76 FDA reports)
LIMB INJURY ( 76 FDA reports)
CYTOLYTIC HEPATITIS ( 75 FDA reports)
ENDOTRACHEAL INTUBATION ( 75 FDA reports)
OCULAR HYPERAEMIA ( 75 FDA reports)
PHARYNGEAL OEDEMA ( 75 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 74 FDA reports)
ACUTE CORONARY SYNDROME ( 74 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 74 FDA reports)
ANKLE FRACTURE ( 74 FDA reports)
BONE DEBRIDEMENT ( 74 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 74 FDA reports)
FLANK PAIN ( 74 FDA reports)
MACULAR DEGENERATION ( 74 FDA reports)
AGRANULOCYTOSIS ( 73 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 73 FDA reports)
CORONARY ARTERY STENOSIS ( 73 FDA reports)
HYPOACUSIS ( 73 FDA reports)
INCREASED APPETITE ( 73 FDA reports)
INTESTINAL ISCHAEMIA ( 73 FDA reports)
JAW OPERATION ( 73 FDA reports)
MITRAL VALVE PROLAPSE ( 73 FDA reports)
PYELONEPHRITIS ( 73 FDA reports)
TENDONITIS ( 73 FDA reports)
TRANSAMINASES INCREASED ( 73 FDA reports)
UROSEPSIS ( 73 FDA reports)
NO THERAPEUTIC RESPONSE ( 72 FDA reports)
PERIODONTAL DISEASE ( 72 FDA reports)
PRURITUS GENERALISED ( 72 FDA reports)
TENSION ( 72 FDA reports)
TROPONIN INCREASED ( 72 FDA reports)
UPPER LIMB FRACTURE ( 72 FDA reports)
AORTIC ANEURYSM ( 72 FDA reports)
CHROMATURIA ( 72 FDA reports)
GINGIVAL SWELLING ( 72 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 72 FDA reports)
HEART VALVE INCOMPETENCE ( 72 FDA reports)
DILATATION ATRIAL ( 71 FDA reports)
LIFE EXPECTANCY SHORTENED ( 71 FDA reports)
LUMBAR RADICULOPATHY ( 71 FDA reports)
PURPURA ( 71 FDA reports)
NIGHTMARE ( 70 FDA reports)
RADIOTHERAPY ( 70 FDA reports)
RASH MACULO-PAPULAR ( 70 FDA reports)
TARDIVE DYSKINESIA ( 70 FDA reports)
CEREBRAL ISCHAEMIA ( 70 FDA reports)
HEPATIC LESION ( 70 FDA reports)
HYPOAESTHESIA ORAL ( 70 FDA reports)
JOINT EFFUSION ( 70 FDA reports)
MOVEMENT DISORDER ( 70 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 69 FDA reports)
DERMATITIS ( 69 FDA reports)
GOITRE ( 69 FDA reports)
KIDNEY INFECTION ( 69 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 69 FDA reports)
SLEEP TALKING ( 69 FDA reports)
ANGIOPATHY ( 68 FDA reports)
EXTRASYSTOLES ( 68 FDA reports)
FAMILY STRESS ( 68 FDA reports)
FRUSTRATION ( 68 FDA reports)
IMPAIRED WORK ABILITY ( 68 FDA reports)
ISCHAEMIA ( 68 FDA reports)
MENOPAUSE ( 68 FDA reports)
MENORRHAGIA ( 68 FDA reports)
ABDOMINAL TENDERNESS ( 67 FDA reports)
ACIDOSIS ( 67 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 67 FDA reports)
BREAST CANCER METASTATIC ( 67 FDA reports)
FACE OEDEMA ( 67 FDA reports)
HALLUCINATION, VISUAL ( 67 FDA reports)
PEPTIC ULCER ( 67 FDA reports)
ORAL CAVITY FISTULA ( 66 FDA reports)
PLATELET COUNT INCREASED ( 66 FDA reports)
PLEURITIC PAIN ( 66 FDA reports)
SKIN BURNING SENSATION ( 66 FDA reports)
SQUAMOUS CELL CARCINOMA ( 66 FDA reports)
ABORTION SPONTANEOUS ( 66 FDA reports)
ACUTE PULMONARY OEDEMA ( 66 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 66 FDA reports)
CERVICAL SPINAL STENOSIS ( 66 FDA reports)
CREPITATIONS ( 66 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 66 FDA reports)
HEARING IMPAIRED ( 66 FDA reports)
KNEE ARTHROPLASTY ( 66 FDA reports)
KYPHOSIS ( 66 FDA reports)
MUSCLE TWITCHING ( 66 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 65 FDA reports)
GANGRENE ( 65 FDA reports)
MYOCLONUS ( 65 FDA reports)
THYROID NEOPLASM ( 65 FDA reports)
NODULE ( 64 FDA reports)
ORAL INFECTION ( 64 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 64 FDA reports)
WALKING AID USER ( 64 FDA reports)
ABSCESS JAW ( 64 FDA reports)
ACTINOMYCOSIS ( 64 FDA reports)
BLOOD CALCIUM INCREASED ( 64 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 64 FDA reports)
CONJUNCTIVITIS ( 64 FDA reports)
CYST ( 64 FDA reports)
EXPOSED BONE IN JAW ( 64 FDA reports)
MENISCUS LESION ( 64 FDA reports)
MOUTH HAEMORRHAGE ( 64 FDA reports)
APNOEA ( 63 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 63 FDA reports)
LYMPHOEDEMA ( 63 FDA reports)
MUSCLE STRAIN ( 63 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 63 FDA reports)
VITREOUS FLOATERS ( 63 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 62 FDA reports)
POLYP ( 62 FDA reports)
SUICIDE ATTEMPT ( 62 FDA reports)
THIRST ( 62 FDA reports)
VAGINAL HAEMORRHAGE ( 62 FDA reports)
VASCULITIS ( 62 FDA reports)
ABDOMINAL HERNIA ( 62 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 62 FDA reports)
BASAL CELL CARCINOMA ( 62 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 62 FDA reports)
EYE DISORDER ( 62 FDA reports)
HAEMOLYSIS ( 62 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 62 FDA reports)
ANGIOEDEMA ( 61 FDA reports)
BED REST ( 61 FDA reports)
BLOOD CULTURE POSITIVE ( 61 FDA reports)
CATARACT OPERATION ( 61 FDA reports)
DEVICE MALFUNCTION ( 61 FDA reports)
SINUS CONGESTION ( 61 FDA reports)
SOCIAL PROBLEM ( 61 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 60 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 60 FDA reports)
CHEST X-RAY ABNORMAL ( 60 FDA reports)
EDENTULOUS ( 60 FDA reports)
HAEMODYNAMIC INSTABILITY ( 60 FDA reports)
HEPATIC CYST ( 60 FDA reports)
ISCHAEMIC STROKE ( 60 FDA reports)
LOWER LIMB FRACTURE ( 60 FDA reports)
ACCIDENTAL EXPOSURE ( 59 FDA reports)
CACHEXIA ( 59 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 59 FDA reports)
EXERCISE TOLERANCE DECREASED ( 59 FDA reports)
FIBROSIS ( 59 FDA reports)
FISTULA ( 59 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 59 FDA reports)
INTERMITTENT CLAUDICATION ( 59 FDA reports)
PLASMACYTOSIS ( 59 FDA reports)
PROCEDURAL COMPLICATION ( 59 FDA reports)
PROCEDURAL PAIN ( 59 FDA reports)
SCIATICA ( 59 FDA reports)
SENSORY DISTURBANCE ( 59 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 59 FDA reports)
VENTRICULAR DYSFUNCTION ( 59 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 58 FDA reports)
ONYCHOMYCOSIS ( 58 FDA reports)
PERIPHERAL ISCHAEMIA ( 58 FDA reports)
RASH MACULAR ( 58 FDA reports)
ADVERSE DRUG REACTION ( 58 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 58 FDA reports)
INTRACARDIAC THROMBUS ( 58 FDA reports)
ANURIA ( 57 FDA reports)
AORTIC VALVE DISEASE ( 57 FDA reports)
BODY HEIGHT DECREASED ( 57 FDA reports)
CEREBROVASCULAR DISORDER ( 57 FDA reports)
CONDUCTION DISORDER ( 57 FDA reports)
EAR INFECTION ( 57 FDA reports)
EYE SWELLING ( 57 FDA reports)
FIBULA FRACTURE ( 57 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 57 FDA reports)
LARYNGITIS ( 57 FDA reports)
PROCTALGIA ( 57 FDA reports)
PERIPHERAL COLDNESS ( 56 FDA reports)
TENDON DISORDER ( 56 FDA reports)
TONGUE INJURY ( 56 FDA reports)
WOUND DEHISCENCE ( 56 FDA reports)
ACTINIC KERATOSIS ( 56 FDA reports)
BILE DUCT STONE ( 56 FDA reports)
BLOOD DISORDER ( 56 FDA reports)
CARDIAC ENZYMES INCREASED ( 56 FDA reports)
COR PULMONALE ( 56 FDA reports)
EYE IRRITATION ( 56 FDA reports)
HEPATIC ENCEPHALOPATHY ( 56 FDA reports)
HYPERTHERMIA ( 56 FDA reports)
INCREASED TENDENCY TO BRUISE ( 56 FDA reports)
ENDODONTIC PROCEDURE ( 55 FDA reports)
ENURESIS ( 55 FDA reports)
HAEMANGIOMA ( 55 FDA reports)
PAROSMIA ( 55 FDA reports)
PROTEIN TOTAL DECREASED ( 55 FDA reports)
SPUTUM DISCOLOURED ( 55 FDA reports)
STENT PLACEMENT ( 55 FDA reports)
WOUND DRAINAGE ( 55 FDA reports)
SPINAL FRACTURE ( 54 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 54 FDA reports)
THROAT TIGHTNESS ( 54 FDA reports)
TOOTH INFECTION ( 54 FDA reports)
ACUTE PRERENAL FAILURE ( 54 FDA reports)
CHOLECYSTECTOMY ( 54 FDA reports)
COLITIS ISCHAEMIC ( 54 FDA reports)
FOOT DEFORMITY ( 54 FDA reports)
HEPATOTOXICITY ( 54 FDA reports)
INGROWING NAIL ( 54 FDA reports)
COORDINATION ABNORMAL ( 53 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 53 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 53 FDA reports)
HEPATIC CONGESTION ( 53 FDA reports)
INJECTION SITE IRRITATION ( 53 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 53 FDA reports)
JAUNDICE CHOLESTATIC ( 53 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 53 FDA reports)
PLASMACYTOMA ( 53 FDA reports)
STREPTOCOCCAL SEPSIS ( 53 FDA reports)
TONGUE ULCERATION ( 53 FDA reports)
VENOUS THROMBOSIS ( 53 FDA reports)
PLANTAR FASCIITIS ( 52 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 52 FDA reports)
TOXIC SKIN ERUPTION ( 52 FDA reports)
VITAMIN D DEFICIENCY ( 52 FDA reports)
WRIST FRACTURE ( 52 FDA reports)
INTENTIONAL DRUG MISUSE ( 52 FDA reports)
LACRIMATION INCREASED ( 52 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 52 FDA reports)
MECHANICAL VENTILATION ( 52 FDA reports)
BONE FRAGMENTATION ( 51 FDA reports)
BREAST MASS ( 51 FDA reports)
CARDIAC OPERATION ( 51 FDA reports)
DIFFICULTY IN WALKING ( 51 FDA reports)
DRUG ABUSE ( 51 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 51 FDA reports)
EOSINOPHILIA ( 51 FDA reports)
GASTROENTERITIS VIRAL ( 51 FDA reports)
GINGIVAL ULCERATION ( 51 FDA reports)
GRANULOMA ( 51 FDA reports)
MENSTRUAL DISORDER ( 51 FDA reports)
METABOLIC ENCEPHALOPATHY ( 51 FDA reports)
METASTASES TO SPINE ( 51 FDA reports)
MICTURITION URGENCY ( 51 FDA reports)
PULMONARY MASS ( 51 FDA reports)
RASH PAPULAR ( 51 FDA reports)
RECTOCELE ( 51 FDA reports)
RHONCHI ( 51 FDA reports)
STEM CELL TRANSPLANT ( 51 FDA reports)
VENOUS INSUFFICIENCY ( 51 FDA reports)
ODYNOPHAGIA ( 50 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 50 FDA reports)
RESPIRATORY TRACT CONGESTION ( 50 FDA reports)
THROMBOSIS IN DEVICE ( 50 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 50 FDA reports)
HYPERCAPNIA ( 50 FDA reports)
CAROTID BRUIT ( 49 FDA reports)
EROSIVE OESOPHAGITIS ( 49 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 49 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 49 FDA reports)
OEDEMA MOUTH ( 49 FDA reports)
PARKINSON'S DISEASE ( 49 FDA reports)
PSYCHOTIC DISORDER ( 49 FDA reports)
PLEURISY ( 48 FDA reports)
POLYURIA ( 48 FDA reports)
SEBORRHOEIC KERATOSIS ( 48 FDA reports)
SKIN CANCER ( 48 FDA reports)
ATRIAL TACHYCARDIA ( 48 FDA reports)
BLADDER CANCER ( 48 FDA reports)
BLINDNESS UNILATERAL ( 48 FDA reports)
BODY TEMPERATURE DECREASED ( 48 FDA reports)
BREAST PAIN ( 48 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 48 FDA reports)
DIABETIC KETOACIDOSIS ( 48 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 48 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 48 FDA reports)
LABILE BLOOD PRESSURE ( 48 FDA reports)
LYMPHOMA ( 48 FDA reports)
BLADDER DISORDER ( 47 FDA reports)
BRONCHIECTASIS ( 47 FDA reports)
BRUXISM ( 47 FDA reports)
FEELING JITTERY ( 47 FDA reports)
HAEMORRHAGIC ANAEMIA ( 47 FDA reports)
HYPERTENSIVE HEART DISEASE ( 47 FDA reports)
LIVER INJURY ( 47 FDA reports)
MEDICATION RESIDUE ( 47 FDA reports)
SINUS ARRHYTHMIA ( 47 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 47 FDA reports)
TIBIA FRACTURE ( 47 FDA reports)
OCCULT BLOOD POSITIVE ( 46 FDA reports)
RESPIRATORY TRACT INFECTION ( 46 FDA reports)
SKIN INDURATION ( 46 FDA reports)
SKIN TIGHTNESS ( 46 FDA reports)
SOFT TISSUE DISORDER ( 46 FDA reports)
STOMACH DISCOMFORT ( 46 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 46 FDA reports)
X-RAY ABNORMAL ( 46 FDA reports)
ABDOMINAL PAIN LOWER ( 46 FDA reports)
APHTHOUS STOMATITIS ( 46 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 46 FDA reports)
BONE OPERATION ( 46 FDA reports)
DECREASED ACTIVITY ( 46 FDA reports)
DIZZINESS POSTURAL ( 46 FDA reports)
DRY THROAT ( 46 FDA reports)
FACIAL PALSY ( 46 FDA reports)
GLOSSODYNIA ( 46 FDA reports)
LIPOMA ( 46 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 45 FDA reports)
ERUCTATION ( 45 FDA reports)
FACIAL BONES FRACTURE ( 45 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 45 FDA reports)
HEPATITIS C ( 45 FDA reports)
MITRAL VALVE DISEASE ( 45 FDA reports)
NEUTROPENIC SEPSIS ( 45 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 45 FDA reports)
OPEN REDUCTION OF FRACTURE ( 45 FDA reports)
PULMONARY HAEMORRHAGE ( 45 FDA reports)
TRANSPLANT REJECTION ( 45 FDA reports)
UMBILICAL HERNIA ( 45 FDA reports)
NERVE INJURY ( 44 FDA reports)
NEURODERMATITIS ( 44 FDA reports)
PNEUMONIA BACTERIAL ( 44 FDA reports)
POOR QUALITY SLEEP ( 44 FDA reports)
PROSTATOMEGALY ( 44 FDA reports)
SEDATION ( 44 FDA reports)
TRANSFUSION ( 44 FDA reports)
TRISMUS ( 44 FDA reports)
VARICOSE VEIN ( 44 FDA reports)
BONE DENSITY DECREASED ( 44 FDA reports)
BONE SWELLING ( 44 FDA reports)
CATHETER RELATED COMPLICATION ( 44 FDA reports)
GINGIVAL INFECTION ( 44 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 44 FDA reports)
ILEUS PARALYTIC ( 44 FDA reports)
LIMB DISCOMFORT ( 44 FDA reports)
LIPASE INCREASED ( 44 FDA reports)
LOOSE TOOTH ( 44 FDA reports)
MAJOR DEPRESSION ( 44 FDA reports)
METASTATIC NEOPLASM ( 44 FDA reports)
ADVERSE REACTION ( 43 FDA reports)
CYSTOCELE ( 43 FDA reports)
DEVICE FAILURE ( 43 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 43 FDA reports)
HERPES SIMPLEX ( 43 FDA reports)
MALIGNANT MELANOMA ( 43 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 43 FDA reports)
OESOPHAGEAL DISORDER ( 43 FDA reports)
PARAESTHESIA ORAL ( 43 FDA reports)
PITTING OEDEMA ( 43 FDA reports)
SEQUESTRECTOMY ( 43 FDA reports)
STRESS URINARY INCONTINENCE ( 43 FDA reports)
TUMOUR LYSIS SYNDROME ( 43 FDA reports)
ORAL HERPES ( 42 FDA reports)
RENAL ATROPHY ( 42 FDA reports)
SINOATRIAL BLOCK ( 42 FDA reports)
SUBCUTANEOUS NODULE ( 42 FDA reports)
TRACHEOBRONCHITIS ( 42 FDA reports)
URINE ODOUR ABNORMAL ( 42 FDA reports)
AREFLEXIA ( 42 FDA reports)
BLOOD PRESSURE ABNORMAL ( 42 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 42 FDA reports)
BONE MARROW TRANSPLANT ( 42 FDA reports)
BRAIN OEDEMA ( 42 FDA reports)
CHONDROMALACIA ( 42 FDA reports)
FRACTURE ( 42 FDA reports)
HUMERUS FRACTURE ( 42 FDA reports)
HYPERKERATOSIS ( 42 FDA reports)
HYPERPARATHYROIDISM ( 42 FDA reports)
ISCHAEMIC HEPATITIS ( 42 FDA reports)
JUGULAR VEIN DISTENSION ( 42 FDA reports)
LIP SWELLING ( 42 FDA reports)
MIDDLE INSOMNIA ( 42 FDA reports)
ABSCESS DRAINAGE ( 41 FDA reports)
BIPOLAR DISORDER ( 41 FDA reports)
BRONCHOSPASM ( 41 FDA reports)
CARDIAC OUTPUT DECREASED ( 41 FDA reports)
COSTOCHONDRITIS ( 41 FDA reports)
DENTAL OPERATION ( 41 FDA reports)
DENTURE WEARER ( 41 FDA reports)
EUPHORIC MOOD ( 41 FDA reports)
FACE INJURY ( 41 FDA reports)
GRAFT VERSUS HOST DISEASE ( 41 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 41 FDA reports)
METASTASES TO LYMPH NODES ( 41 FDA reports)
NEUTROPHIL COUNT INCREASED ( 41 FDA reports)
PARANOIA ( 41 FDA reports)
PORTAL HYPERTENSION ( 41 FDA reports)
PROTEIN URINE PRESENT ( 41 FDA reports)
RHINITIS ( 41 FDA reports)
VENOOCCLUSIVE DISEASE ( 41 FDA reports)
NECROSIS ( 40 FDA reports)
OESOPHAGEAL ULCER ( 40 FDA reports)
OTITIS MEDIA ( 40 FDA reports)
POLYNEUROPATHY ( 40 FDA reports)
RIGHT ATRIAL DILATATION ( 40 FDA reports)
SENSORY LOSS ( 40 FDA reports)
TENDON RUPTURE ( 40 FDA reports)
ACUTE HEPATIC FAILURE ( 40 FDA reports)
ANEURYSM ( 40 FDA reports)
CARDIAC FLUTTER ( 40 FDA reports)
DENTAL FISTULA ( 40 FDA reports)
DRUG LEVEL INCREASED ( 40 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 40 FDA reports)
KYPHOSCOLIOSIS ( 40 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 40 FDA reports)
MUSCLE INJURY ( 40 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 39 FDA reports)
ANAPHYLACTIC SHOCK ( 39 FDA reports)
BRADYARRHYTHMIA ( 39 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 39 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 39 FDA reports)
GASTRIC POLYPS ( 39 FDA reports)
GYNAECOMASTIA ( 39 FDA reports)
HAEMOLYTIC ANAEMIA ( 39 FDA reports)
HEART INJURY ( 39 FDA reports)
HYPOTONIA ( 39 FDA reports)
HYPOVOLAEMIC SHOCK ( 39 FDA reports)
MICROCYTIC ANAEMIA ( 39 FDA reports)
PERFORMANCE STATUS DECREASED ( 39 FDA reports)
PYURIA ( 39 FDA reports)
STASIS DERMATITIS ( 39 FDA reports)
TEMPERATURE INTOLERANCE ( 39 FDA reports)
MYOSITIS ( 38 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 38 FDA reports)
PURULENCE ( 38 FDA reports)
SEROMA ( 38 FDA reports)
THINKING ABNORMAL ( 38 FDA reports)
UTERINE HAEMORRHAGE ( 38 FDA reports)
VIITH NERVE PARALYSIS ( 38 FDA reports)
ABSCESS NECK ( 38 FDA reports)
BRONCHITIS CHRONIC ( 38 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 38 FDA reports)
CORONARY ARTERY BYPASS ( 38 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 38 FDA reports)
HERNIA ( 38 FDA reports)
HIP ARTHROPLASTY ( 38 FDA reports)
HORMONE LEVEL ABNORMAL ( 38 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 38 FDA reports)
INJECTION SITE REACTION ( 38 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 38 FDA reports)
JOINT SPRAIN ( 38 FDA reports)
LOSS OF EMPLOYMENT ( 38 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 38 FDA reports)
LYMPHOPENIA ( 38 FDA reports)
MUSCLE ATROPHY ( 38 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 37 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 37 FDA reports)
BREAST CANCER FEMALE ( 37 FDA reports)
CHOKING ( 37 FDA reports)
DIABETIC RETINOPATHY ( 37 FDA reports)
ESCHERICHIA SEPSIS ( 37 FDA reports)
HEPATIC ENZYME ABNORMAL ( 37 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 37 FDA reports)
IMMUNOSUPPRESSION ( 37 FDA reports)
JOINT CREPITATION ( 37 FDA reports)
LICE INFESTATION ( 37 FDA reports)
MARROW HYPERPLASIA ( 37 FDA reports)
MOOD SWINGS ( 37 FDA reports)
ORAL DISCOMFORT ( 37 FDA reports)
PERONEAL NERVE PALSY ( 37 FDA reports)
PULMONARY GRANULOMA ( 37 FDA reports)
SKIN HYPERTROPHY ( 37 FDA reports)
NEUROPATHY ( 36 FDA reports)
PERIODONTITIS ( 36 FDA reports)
SKIN HYPERPIGMENTATION ( 36 FDA reports)
SKIN NECROSIS ( 36 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 36 FDA reports)
VARICES OESOPHAGEAL ( 36 FDA reports)
ADDISON'S DISEASE ( 36 FDA reports)
BLOOD CREATININE DECREASED ( 36 FDA reports)
CARDIOPULMONARY FAILURE ( 36 FDA reports)
CARDIOVERSION ( 36 FDA reports)
COLITIS ULCERATIVE ( 36 FDA reports)
COLLAPSE OF LUNG ( 36 FDA reports)
DRUG DISPENSING ERROR ( 36 FDA reports)
DRUG ERUPTION ( 36 FDA reports)
ESSENTIAL HYPERTENSION ( 36 FDA reports)
FIBRIN D DIMER INCREASED ( 36 FDA reports)
HAND FRACTURE ( 36 FDA reports)
HEART VALVE CALCIFICATION ( 36 FDA reports)
INTRACRANIAL ANEURYSM ( 36 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 36 FDA reports)
MUSCLE HAEMORRHAGE ( 36 FDA reports)
ABSCESS ORAL ( 35 FDA reports)
AORTIC VALVE SCLEROSIS ( 35 FDA reports)
ASPERGILLOSIS ( 35 FDA reports)
BILE DUCT OBSTRUCTION ( 35 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 35 FDA reports)
DERMATITIS EXFOLIATIVE ( 35 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 35 FDA reports)
GASTRIC HAEMORRHAGE ( 35 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 35 FDA reports)
GRANULOCYTOPENIA ( 35 FDA reports)
HILAR LYMPHADENOPATHY ( 35 FDA reports)
HYPOTHERMIA ( 35 FDA reports)
IMPAIRED DRIVING ABILITY ( 35 FDA reports)
MOTOR DYSFUNCTION ( 35 FDA reports)
NEPHROPATHY ( 35 FDA reports)
OLIGURIA ( 35 FDA reports)
OSTEORADIONECROSIS ( 35 FDA reports)
PERICARDITIS ( 35 FDA reports)
TONGUE DISORDER ( 35 FDA reports)
URINE FLOW DECREASED ( 35 FDA reports)
VENTRICULAR ARRHYTHMIA ( 35 FDA reports)
NEOPLASM ( 34 FDA reports)
PAROTITIS ( 34 FDA reports)
SPUTUM CULTURE POSITIVE ( 34 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 34 FDA reports)
VITAMIN B12 DEFICIENCY ( 34 FDA reports)
ANAEMIA POSTOPERATIVE ( 34 FDA reports)
APPLICATION SITE ERYTHEMA ( 34 FDA reports)
CARDIAC FAILURE CHRONIC ( 34 FDA reports)
CARDIAC TAMPONADE ( 34 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 34 FDA reports)
CATHETER RELATED INFECTION ( 34 FDA reports)
DEAFNESS NEUROSENSORY ( 34 FDA reports)
DYSTONIA ( 34 FDA reports)
EXTREMITY NECROSIS ( 34 FDA reports)
FAECALOMA ( 34 FDA reports)
HYPERTONIC BLADDER ( 34 FDA reports)
APHAGIA ( 33 FDA reports)
APLASTIC ANAEMIA ( 33 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 33 FDA reports)
BLOOD UREA DECREASED ( 33 FDA reports)
BLOOD URIC ACID INCREASED ( 33 FDA reports)
CERUMEN IMPACTION ( 33 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 33 FDA reports)
GASTROINTESTINAL PERFORATION ( 33 FDA reports)
INJECTION SITE PRURITUS ( 33 FDA reports)
MALABSORPTION ( 33 FDA reports)
MUSCLE DISORDER ( 33 FDA reports)
ORGAN FAILURE ( 33 FDA reports)
OVERWEIGHT ( 33 FDA reports)
PELVIC PAIN ( 33 FDA reports)
PULMONARY THROMBOSIS ( 33 FDA reports)
RADICULAR PAIN ( 33 FDA reports)
SKELETAL INJURY ( 33 FDA reports)
PELVIC FRACTURE ( 32 FDA reports)
PHLEBITIS ( 32 FDA reports)
QUALITY OF LIFE DECREASED ( 32 FDA reports)
RESPIRATORY ACIDOSIS ( 32 FDA reports)
SINUS HEADACHE ( 32 FDA reports)
SKIN ODOUR ABNORMAL ( 32 FDA reports)
STRESS FRACTURE ( 32 FDA reports)
SYNOVITIS ( 32 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 32 FDA reports)
WOUND SECRETION ( 32 FDA reports)
ANGIOPLASTY ( 32 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 32 FDA reports)
BLOOD CREATINE INCREASED ( 32 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 32 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 32 FDA reports)
BLOOD SODIUM INCREASED ( 32 FDA reports)
CHEILITIS ( 32 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 32 FDA reports)
EMBOLIC STROKE ( 32 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 32 FDA reports)
FUNGAEMIA ( 32 FDA reports)
INJECTION SITE EXTRAVASATION ( 32 FDA reports)
MANIA ( 32 FDA reports)
ANAEMIA MACROCYTIC ( 31 FDA reports)
AORTIC CALCIFICATION ( 31 FDA reports)
AORTIC VALVE STENOSIS ( 31 FDA reports)
APPLICATION SITE PRURITUS ( 31 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 31 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 31 FDA reports)
DELUSION ( 31 FDA reports)
EAR DISORDER ( 31 FDA reports)
GINGIVAL OEDEMA ( 31 FDA reports)
HYPERCOAGULATION ( 31 FDA reports)
HYPERTENSIVE CRISIS ( 31 FDA reports)
HYPOAESTHESIA FACIAL ( 31 FDA reports)
INGUINAL HERNIA ( 31 FDA reports)
INTENTIONAL OVERDOSE ( 31 FDA reports)
INTRAOCULAR LENS IMPLANT ( 31 FDA reports)
LARGE INTESTINE PERFORATION ( 31 FDA reports)
LEFT VENTRICULAR FAILURE ( 31 FDA reports)
LEG AMPUTATION ( 31 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 31 FDA reports)
OEDEMA MUCOSAL ( 31 FDA reports)
PNEUMONIA FUNGAL ( 31 FDA reports)
POOR PERIPHERAL CIRCULATION ( 31 FDA reports)
POSTURE ABNORMAL ( 31 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 31 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 31 FDA reports)
SENSATION OF FOREIGN BODY ( 31 FDA reports)
SKIN ATROPHY ( 31 FDA reports)
SKIN INFECTION ( 31 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 31 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 31 FDA reports)
OVARIAN CANCER ( 30 FDA reports)
PAIN OF SKIN ( 30 FDA reports)
PHOTOPHOBIA ( 30 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 30 FDA reports)
RETINAL HAEMORRHAGE ( 30 FDA reports)
SHOCK HAEMORRHAGIC ( 30 FDA reports)
STREPTOCOCCAL INFECTION ( 30 FDA reports)
SUDDEN CARDIAC DEATH ( 30 FDA reports)
THROMBOCYTOSIS ( 30 FDA reports)
TYPE 1 DIABETES MELLITUS ( 30 FDA reports)
WRONG DRUG ADMINISTERED ( 30 FDA reports)
ACUTE SINUSITIS ( 30 FDA reports)
BACK INJURY ( 30 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 30 FDA reports)
BLOOD COUNT ABNORMAL ( 30 FDA reports)
BONE NEOPLASM MALIGNANT ( 30 FDA reports)
BREAST CANCER RECURRENT ( 30 FDA reports)
COLECTOMY ( 30 FDA reports)
ENGRAFTMENT SYNDROME ( 30 FDA reports)
EPILEPSY ( 30 FDA reports)
FACET JOINT SYNDROME ( 30 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 30 FDA reports)
HEMIPLEGIA ( 30 FDA reports)
HEPATITIS ACUTE ( 30 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 30 FDA reports)
HYPERAESTHESIA ( 30 FDA reports)
HYPERURICAEMIA ( 30 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 30 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 30 FDA reports)
IRON DEFICIENCY ( 30 FDA reports)
LIGAMENT SPRAIN ( 30 FDA reports)
MEDICAL DEVICE COMPLICATION ( 30 FDA reports)
BIOPSY BONE ABNORMAL ( 29 FDA reports)
BREAST RECONSTRUCTION ( 29 FDA reports)
CLOSTRIDIUM COLITIS ( 29 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 29 FDA reports)
EYE HAEMORRHAGE ( 29 FDA reports)
EYE PRURITUS ( 29 FDA reports)
EYELID PTOSIS ( 29 FDA reports)
FANCONI SYNDROME ( 29 FDA reports)
FEMORAL NECK FRACTURE ( 29 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 29 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 29 FDA reports)
HUNGER ( 29 FDA reports)
HYSTERECTOMY ( 29 FDA reports)
MENINGIOMA ( 29 FDA reports)
MYDRIASIS ( 29 FDA reports)
MYELOMA RECURRENCE ( 29 FDA reports)
NERVE ROOT LESION ( 29 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 29 FDA reports)
OESOPHAGEAL STENOSIS ( 29 FDA reports)
PARALYSIS ( 29 FDA reports)
RENAL ARTERY STENOSIS ( 29 FDA reports)
RENAL CANCER ( 29 FDA reports)
RENAL INFARCT ( 29 FDA reports)
RENAL PAIN ( 29 FDA reports)
RESPIRATORY DEPRESSION ( 29 FDA reports)
TOBACCO ABUSE ( 29 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 29 FDA reports)
VAGINAL INFECTION ( 29 FDA reports)
VITAMIN D DECREASED ( 29 FDA reports)
NASAL SEPTUM DEVIATION ( 28 FDA reports)
NEPHROSCLEROSIS ( 28 FDA reports)
NERVE COMPRESSION ( 28 FDA reports)
NIKOLSKY'S SIGN ( 28 FDA reports)
NO ADVERSE EVENT ( 28 FDA reports)
NODAL ARRHYTHMIA ( 28 FDA reports)
NON-CARDIAC CHEST PAIN ( 28 FDA reports)
ORAL FIBROMA ( 28 FDA reports)
POSTOPERATIVE ILEUS ( 28 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 28 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 28 FDA reports)
PUPIL FIXED ( 28 FDA reports)
SKIN FIBROSIS ( 28 FDA reports)
TACHYARRHYTHMIA ( 28 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 28 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 28 FDA reports)
CARDIAC ANEURYSM ( 28 FDA reports)
CAROTID ARTERY OCCLUSION ( 28 FDA reports)
COLON ADENOMA ( 28 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 28 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 28 FDA reports)
INTESTINAL PERFORATION ( 28 FDA reports)
LACUNAR INFARCTION ( 28 FDA reports)
LARYNGEAL OEDEMA ( 28 FDA reports)
METABOLIC ALKALOSIS ( 28 FDA reports)
MULTIPLE FRACTURES ( 28 FDA reports)
ACCIDENT ( 27 FDA reports)
AMMONIA INCREASED ( 27 FDA reports)
BACTERIAL SEPSIS ( 27 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 27 FDA reports)
DYSAESTHESIA ( 27 FDA reports)
ERYTHEMA MULTIFORME ( 27 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 27 FDA reports)
GRIP STRENGTH DECREASED ( 27 FDA reports)
HEPATORENAL SYNDROME ( 27 FDA reports)
NARCOLEPSY ( 27 FDA reports)
ORAL DISCHARGE ( 27 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 27 FDA reports)
POLYCYTHAEMIA ( 27 FDA reports)
POST HERPETIC NEURALGIA ( 27 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 27 FDA reports)
RECTAL ABSCESS ( 27 FDA reports)
RETINOPATHY ( 27 FDA reports)
SENSATION OF HEAVINESS ( 27 FDA reports)
SINUS OPERATION ( 27 FDA reports)
SKIN IRRITATION ( 27 FDA reports)
THERMAL BURN ( 27 FDA reports)
THROMBOPHLEBITIS ( 27 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 27 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 27 FDA reports)
NEPHROPATHY TOXIC ( 26 FDA reports)
OPEN WOUND ( 26 FDA reports)
PIGMENTATION DISORDER ( 26 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 26 FDA reports)
RENAL MASS ( 26 FDA reports)
SERUM FERRITIN INCREASED ( 26 FDA reports)
SHOULDER PAIN ( 26 FDA reports)
SUBDURAL HAEMORRHAGE ( 26 FDA reports)
UTERINE LEIOMYOMA ( 26 FDA reports)
VISUAL FIELD DEFECT ( 26 FDA reports)
WALKING DISABILITY ( 26 FDA reports)
AORTIC VALVE CALCIFICATION ( 26 FDA reports)
APATHY ( 26 FDA reports)
BLOOD BICARBONATE DECREASED ( 26 FDA reports)
BLOOD PH DECREASED ( 26 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 26 FDA reports)
CARDIAC FAILURE ACUTE ( 26 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 26 FDA reports)
CATHETER SITE HAEMORRHAGE ( 26 FDA reports)
DERMAL CYST ( 26 FDA reports)
DUODENITIS ( 26 FDA reports)
DYSPNOEA EXACERBATED ( 26 FDA reports)
ENDOCARDITIS ( 26 FDA reports)
FEELING DRUNK ( 26 FDA reports)
FRACTURED SACRUM ( 26 FDA reports)
GALLBLADDER OPERATION ( 26 FDA reports)
HEPATIC MASS ( 26 FDA reports)
HEPATOSPLENOMEGALY ( 26 FDA reports)
HOMICIDAL IDEATION ( 26 FDA reports)
HYPERPHOSPHATAEMIA ( 26 FDA reports)
INADEQUATE ANALGESIA ( 26 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 26 FDA reports)
LABYRINTHITIS ( 26 FDA reports)
ADRENAL DISORDER ( 25 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 25 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 25 FDA reports)
BRAIN DEATH ( 25 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 25 FDA reports)
CERVICAL CORD COMPRESSION ( 25 FDA reports)
CHOLANGITIS ( 25 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 25 FDA reports)
DIABETIC NEPHROPATHY ( 25 FDA reports)
GINGIVAL ERYTHEMA ( 25 FDA reports)
HEPATOCELLULAR INJURY ( 25 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 25 FDA reports)
INJECTION SITE SWELLING ( 25 FDA reports)
LOCALISED OEDEMA ( 25 FDA reports)
LUNG ADENOCARCINOMA ( 25 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 25 FDA reports)
NEUROGENIC BLADDER ( 25 FDA reports)
OESOPHAGEAL SPASM ( 25 FDA reports)
OROPHARYNGEAL BLISTERING ( 25 FDA reports)
OVARIAN CYST ( 25 FDA reports)
PANCREATITIS CHRONIC ( 25 FDA reports)
PCO2 DECREASED ( 25 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 25 FDA reports)
QRS AXIS ABNORMAL ( 25 FDA reports)
SERRATIA BACTERAEMIA ( 25 FDA reports)
SKIN CANDIDA ( 25 FDA reports)
SNEEZING ( 25 FDA reports)
SPINAL CORD COMPRESSION ( 25 FDA reports)
SPINAL LAMINECTOMY ( 25 FDA reports)
STATUS EPILEPTICUS ( 25 FDA reports)
THERAPY NON-RESPONDER ( 25 FDA reports)
NEURITIS ( 24 FDA reports)
NODAL RHYTHM ( 24 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 24 FDA reports)
OCULAR ICTERUS ( 24 FDA reports)
PNEUMONIA VIRAL ( 24 FDA reports)
PROSTATE CANCER METASTATIC ( 24 FDA reports)
RADIUS FRACTURE ( 24 FDA reports)
SEPSIS SYNDROME ( 24 FDA reports)
SPLENIC INFARCTION ( 24 FDA reports)
SUBCUTANEOUS ABSCESS ( 24 FDA reports)
SYNOVIAL RUPTURE ( 24 FDA reports)
TENOSYNOVITIS ( 24 FDA reports)
URETERAL DISORDER ( 24 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 24 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 24 FDA reports)
ABDOMINAL ADHESIONS ( 24 FDA reports)
ADRENAL ADENOMA ( 24 FDA reports)
BLOOD CHLORIDE INCREASED ( 24 FDA reports)
BRONCHIAL SECRETION RETENTION ( 24 FDA reports)
CAECITIS ( 24 FDA reports)
FLAT AFFECT ( 24 FDA reports)
FURUNCLE ( 24 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 24 FDA reports)
HEART SOUNDS ABNORMAL ( 24 FDA reports)
HEPATIC FIBROSIS ( 24 FDA reports)
HEPATOJUGULAR REFLUX ( 24 FDA reports)
INFARCTION ( 24 FDA reports)
INITIAL INSOMNIA ( 24 FDA reports)
KIDNEY SMALL ( 24 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 24 FDA reports)
MULTIPLE DRUG OVERDOSE ( 24 FDA reports)
MUSCULOSKELETAL DISORDER ( 24 FDA reports)
AGEUSIA ( 23 FDA reports)
BONE EROSION ( 23 FDA reports)
BREAST TENDERNESS ( 23 FDA reports)
BUNDLE BRANCH BLOCK ( 23 FDA reports)
CALCINOSIS ( 23 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 23 FDA reports)
COMMUNICATION DISORDER ( 23 FDA reports)
EOSINOPHIL COUNT INCREASED ( 23 FDA reports)
GALLOP RHYTHM PRESENT ( 23 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 23 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 23 FDA reports)
HAEMOTHORAX ( 23 FDA reports)
HICCUPS ( 23 FDA reports)
HYPOPERFUSION ( 23 FDA reports)
INDURATION ( 23 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 23 FDA reports)
JUGULAR VEIN THROMBOSIS ( 23 FDA reports)
NEUROFIBROMA ( 23 FDA reports)
ONYCHALGIA ( 23 FDA reports)
PARONYCHIA ( 23 FDA reports)
PHOTOSENSITIVITY REACTION ( 23 FDA reports)
PROTEIN TOTAL INCREASED ( 23 FDA reports)
RESUSCITATION ( 23 FDA reports)
SENSITIVITY OF TEETH ( 23 FDA reports)
SKIN HAEMORRHAGE ( 23 FDA reports)
SYSTEMIC CANDIDA ( 23 FDA reports)
WOUND COMPLICATION ( 23 FDA reports)
NAIL DISORDER ( 22 FDA reports)
NASAL DRYNESS ( 22 FDA reports)
NICOTINE DEPENDENCE ( 22 FDA reports)
OESOPHAGEAL PAIN ( 22 FDA reports)
OTITIS MEDIA CHRONIC ( 22 FDA reports)
PANCREATIC DISORDER ( 22 FDA reports)
PERIPHERAL EMBOLISM ( 22 FDA reports)
PSYCHIATRIC SYMPTOM ( 22 FDA reports)
PULMONARY HILUM MASS ( 22 FDA reports)
RECTAL FISSURE ( 22 FDA reports)
SKIN WARM ( 22 FDA reports)
THYROID CYST ( 22 FDA reports)
UTERINE CANCER ( 22 FDA reports)
WHEELCHAIR USER ( 22 FDA reports)
WOUND HAEMORRHAGE ( 22 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 22 FDA reports)
AUTOIMMUNE HEPATITIS ( 22 FDA reports)
BARRETT'S OESOPHAGUS ( 22 FDA reports)
BLADDER DISCOMFORT ( 22 FDA reports)
BRAIN NEOPLASM ( 22 FDA reports)
CEREBELLAR ISCHAEMIA ( 22 FDA reports)
DERMATITIS BULLOUS ( 22 FDA reports)
DIABETIC COMA ( 22 FDA reports)
ENTEROCOLITIS ( 22 FDA reports)
EYE DISCHARGE ( 22 FDA reports)
FEAR OF DEATH ( 22 FDA reports)
FRACTURE NONUNION ( 22 FDA reports)
LICHENOID KERATOSIS ( 22 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 22 FDA reports)
ABNORMAL FAECES ( 21 FDA reports)
ABSCESS LIMB ( 21 FDA reports)
ALCOHOL ABUSE ( 21 FDA reports)
ALVEOLITIS ALLERGIC ( 21 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 21 FDA reports)
BLOOD IRON DECREASED ( 21 FDA reports)
BLOOD MAGNESIUM INCREASED ( 21 FDA reports)
BRAIN INJURY ( 21 FDA reports)
BREATH ODOUR ( 21 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 21 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 21 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 21 FDA reports)
DRUG PRESCRIBING ERROR ( 21 FDA reports)
DRUG SCREEN POSITIVE ( 21 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 21 FDA reports)
FISTULA REPAIR ( 21 FDA reports)
FLUID INTAKE REDUCED ( 21 FDA reports)
FUNGAL SKIN INFECTION ( 21 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 21 FDA reports)
HAIR GROWTH ABNORMAL ( 21 FDA reports)
HEART RATE ABNORMAL ( 21 FDA reports)
HEART TRANSPLANT ( 21 FDA reports)
HEPATIC NEOPLASM ( 21 FDA reports)
HEPATOCELLULAR DAMAGE ( 21 FDA reports)
INCOHERENT ( 21 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 21 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 21 FDA reports)
MALIGNANT HYPERTENSION ( 21 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 21 FDA reports)
METABOLIC SYNDROME ( 21 FDA reports)
MYASTHENIA GRAVIS ( 21 FDA reports)
MYOCARDITIS ( 21 FDA reports)
NAIL DYSTROPHY ( 21 FDA reports)
NEPHROTIC SYNDROME ( 21 FDA reports)
OCCIPITAL NEURALGIA ( 21 FDA reports)
ORAL SURGERY ( 21 FDA reports)
PUBIS FRACTURE ( 21 FDA reports)
PULMONARY VASCULAR DISORDER ( 21 FDA reports)
REFLUX OESOPHAGITIS ( 21 FDA reports)
URETERIC OBSTRUCTION ( 21 FDA reports)
VASODILATATION ( 21 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 21 FDA reports)
NON-SMALL CELL LUNG CANCER ( 20 FDA reports)
PNEUMONIA KLEBSIELLA ( 20 FDA reports)
PULSE ABNORMAL ( 20 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 20 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 20 FDA reports)
SERRATIA INFECTION ( 20 FDA reports)
SIALOADENITIS ( 20 FDA reports)
SNORING ( 20 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 20 FDA reports)
TOOTH EROSION ( 20 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 20 FDA reports)
VASCULAR CALCIFICATION ( 20 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 20 FDA reports)
ACUTE STRESS DISORDER ( 20 FDA reports)
ADENOCARCINOMA ( 20 FDA reports)
ADENOMYOSIS ( 20 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 20 FDA reports)
ANOXIC ENCEPHALOPATHY ( 20 FDA reports)
AORTIC DILATATION ( 20 FDA reports)
APHONIA ( 20 FDA reports)
APLASIA ( 20 FDA reports)
ARTHRITIS INFECTIVE ( 20 FDA reports)
ASPHYXIA ( 20 FDA reports)
AUTOIMMUNE DISORDER ( 20 FDA reports)
BIOPSY GINGIVAL ( 20 FDA reports)
BLEPHARITIS ( 20 FDA reports)
BONE MARROW OEDEMA ( 20 FDA reports)
BREAKTHROUGH PAIN ( 20 FDA reports)
BULLOUS LUNG DISEASE ( 20 FDA reports)
CAESAREAN SECTION ( 20 FDA reports)
CARBON DIOXIDE DECREASED ( 20 FDA reports)
CAROTID ARTERY DISEASE ( 20 FDA reports)
COCCYDYNIA ( 20 FDA reports)
DIVERTICULAR PERFORATION ( 20 FDA reports)
DRUG LEVEL DECREASED ( 20 FDA reports)
EARLY SATIETY ( 20 FDA reports)
FISTULA DISCHARGE ( 20 FDA reports)
FOREIGN BODY ( 20 FDA reports)
GASTROINTESTINAL NECROSIS ( 20 FDA reports)
HYPERVOLAEMIA ( 20 FDA reports)
IMMUNE SYSTEM DISORDER ( 20 FDA reports)
INJECTION SITE URTICARIA ( 20 FDA reports)
INTERVERTEBRAL DISCITIS ( 20 FDA reports)
INTESTINAL DILATATION ( 20 FDA reports)
INTESTINAL INFARCTION ( 20 FDA reports)
IRON OVERLOAD ( 20 FDA reports)
LIMB OPERATION ( 20 FDA reports)
LIP EROSION ( 20 FDA reports)
MEAN CELL VOLUME INCREASED ( 20 FDA reports)
METASTATIC PAIN ( 20 FDA reports)
MICTURITION FREQUENCY DECREASED ( 20 FDA reports)
ANGIONEUROTIC OEDEMA ( 19 FDA reports)
AORTIC ANEURYSM RUPTURE ( 19 FDA reports)
AORTIC THROMBOSIS ( 19 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 19 FDA reports)
ASBESTOSIS ( 19 FDA reports)
BARTHOLIN'S CYST ( 19 FDA reports)
BONE GIANT CELL TUMOUR ( 19 FDA reports)
BONE NEOPLASM ( 19 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 19 FDA reports)
BRONCHITIS ACUTE ( 19 FDA reports)
CATHETER SITE INFECTION ( 19 FDA reports)
CLAVICLE FRACTURE ( 19 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 19 FDA reports)
CYSTITIS NONINFECTIVE ( 19 FDA reports)
DENTAL PULP DISORDER ( 19 FDA reports)
DERMATITIS ACNEIFORM ( 19 FDA reports)
EMBOLISM ( 19 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 19 FDA reports)
ESCHERICHIA TEST POSITIVE ( 19 FDA reports)
EXERCISE LACK OF ( 19 FDA reports)
FOLLICULITIS ( 19 FDA reports)
FOOT OPERATION ( 19 FDA reports)
GALLBLADDER INJURY ( 19 FDA reports)
GASTROINTESTINAL PAIN ( 19 FDA reports)
GOUTY ARTHRITIS ( 19 FDA reports)
HAEMOGLOBINURIA ( 19 FDA reports)
HELICOBACTER INFECTION ( 19 FDA reports)
HIP SURGERY ( 19 FDA reports)
HYPERPHAGIA ( 19 FDA reports)
INJECTION SITE RASH ( 19 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 19 FDA reports)
LISTLESS ( 19 FDA reports)
MITRAL VALVE REPLACEMENT ( 19 FDA reports)
MULTIPLE ALLERGIES ( 19 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 19 FDA reports)
PANCREATIC CYST ( 19 FDA reports)
PATHOGEN RESISTANCE ( 19 FDA reports)
POISONING ( 19 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 19 FDA reports)
PRESBYOPIA ( 19 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 19 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 19 FDA reports)
SKIN PLAQUE ( 19 FDA reports)
SPLEEN DISORDER ( 19 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 19 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 19 FDA reports)
TREATMENT FAILURE ( 19 FDA reports)
URINE COLOUR ABNORMAL ( 19 FDA reports)
VASCULAR GRAFT ( 19 FDA reports)
VASCULAR GRAFT OCCLUSION ( 19 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 18 FDA reports)
NEUTROPENIC INFECTION ( 18 FDA reports)
NOCTURNAL DYSPNOEA ( 18 FDA reports)
OSTEOMYELITIS CHRONIC ( 18 FDA reports)
PORTAL VEIN THROMBOSIS ( 18 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 18 FDA reports)
RADIATION INJURY ( 18 FDA reports)
RADICAL MASTECTOMY ( 18 FDA reports)
RASH MORBILLIFORM ( 18 FDA reports)
SCAB ( 18 FDA reports)
SMOKER ( 18 FDA reports)
TEARFULNESS ( 18 FDA reports)
TERMINAL STATE ( 18 FDA reports)
TINEA PEDIS ( 18 FDA reports)
TOXIC ENCEPHALOPATHY ( 18 FDA reports)
TUBERCULOSIS ( 18 FDA reports)
UNDERDOSE ( 18 FDA reports)
URETHRAL OBSTRUCTION ( 18 FDA reports)
VENA CAVA THROMBOSIS ( 18 FDA reports)
ACCOMMODATION DISORDER ( 18 FDA reports)
ALCOHOL USE ( 18 FDA reports)
ANGIOFIBROMA ( 18 FDA reports)
APPENDICITIS ( 18 FDA reports)
ARTERIAL THROMBOSIS ( 18 FDA reports)
ASPIRATION PLEURAL CAVITY ( 18 FDA reports)
BILIARY TRACT DISORDER ( 18 FDA reports)
BLOOD AMYLASE INCREASED ( 18 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 18 FDA reports)
BONE GRAFT ( 18 FDA reports)
BONE MARROW DEPRESSION ( 18 FDA reports)
BREAST CYST ( 18 FDA reports)
CARDIAC FIBRILLATION ( 18 FDA reports)
CERVICAL MYELOPATHY ( 18 FDA reports)
COAGULATION TIME PROLONGED ( 18 FDA reports)
DEVICE RELATED SEPSIS ( 18 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 18 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 18 FDA reports)
EAR NEOPLASM ( 18 FDA reports)
EFFUSION ( 18 FDA reports)
EMPYEMA ( 18 FDA reports)
EXTREMITY CONTRACTURE ( 18 FDA reports)
FRACTURE DISPLACEMENT ( 18 FDA reports)
GENERALISED ERYTHEMA ( 18 FDA reports)
GLOSSITIS ( 18 FDA reports)
HALLUCINATIONS, MIXED ( 18 FDA reports)
HEPATITIS CHOLESTATIC ( 18 FDA reports)
HYPOVENTILATION ( 18 FDA reports)
KERATITIS ( 18 FDA reports)
LARGE INTESTINAL ULCER ( 18 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 18 FDA reports)
LIGAMENT RUPTURE ( 18 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 18 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 17 FDA reports)
ADRENAL MASS ( 17 FDA reports)
AFFECTIVE DISORDER ( 17 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 17 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 17 FDA reports)
ANXIETY DISORDER ( 17 FDA reports)
AORTIC DISORDER ( 17 FDA reports)
AORTIC DISSECTION ( 17 FDA reports)
APLASIA PURE RED CELL ( 17 FDA reports)
APPLICATION SITE RASH ( 17 FDA reports)
ARTHROPOD BITE ( 17 FDA reports)
BILIARY DYSKINESIA ( 17 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 17 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 17 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 17 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 17 FDA reports)
BRONCHIAL OBSTRUCTION ( 17 FDA reports)
CARDIOTOXICITY ( 17 FDA reports)
CEREBELLAR INFARCTION ( 17 FDA reports)
CHARLES BONNET SYNDROME ( 17 FDA reports)
CHOLECYSTITIS INFECTIVE ( 17 FDA reports)
CHRONIC FATIGUE SYNDROME ( 17 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 17 FDA reports)
COLON CANCER METASTATIC ( 17 FDA reports)
CONCUSSION ( 17 FDA reports)
CONNECTIVE TISSUE DISORDER ( 17 FDA reports)
DRUG ABUSER ( 17 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 17 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 17 FDA reports)
ENTEROVESICAL FISTULA ( 17 FDA reports)
EPIGASTRIC DISCOMFORT ( 17 FDA reports)
ERYSIPELAS ( 17 FDA reports)
EYE INFECTION ( 17 FDA reports)
EYE OEDEMA ( 17 FDA reports)
GINGIVAL EROSION ( 17 FDA reports)
HYPERREFLEXIA ( 17 FDA reports)
HYPOCOAGULABLE STATE ( 17 FDA reports)
INCISIONAL HERNIA ( 17 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 17 FDA reports)
INTESTINAL STENOSIS ( 17 FDA reports)
KLEBSIELLA TEST POSITIVE ( 17 FDA reports)
KNEE OPERATION ( 17 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 17 FDA reports)
MACROGLOSSIA ( 17 FDA reports)
MASTOIDITIS ( 17 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 17 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 17 FDA reports)
MONOPLEGIA ( 17 FDA reports)
NEOPLASM RECURRENCE ( 17 FDA reports)
OPPORTUNISTIC INFECTION ( 17 FDA reports)
PANCREATIC CARCINOMA ( 17 FDA reports)
PANIC REACTION ( 17 FDA reports)
PATELLA FRACTURE ( 17 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 17 FDA reports)
PERIORBITAL OEDEMA ( 17 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 17 FDA reports)
PERSONALITY CHANGE ( 17 FDA reports)
PHARYNGEAL DISORDER ( 17 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 17 FDA reports)
POLYMYALGIA RHEUMATICA ( 17 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 17 FDA reports)
PSORIATIC ARTHROPATHY ( 17 FDA reports)
RADICULITIS ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
SERUM SICKNESS ( 17 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 17 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 17 FDA reports)
SPINAL FUSION ACQUIRED ( 17 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 17 FDA reports)
THYROID CANCER ( 17 FDA reports)
TROPONIN I INCREASED ( 17 FDA reports)
ULCER HAEMORRHAGE ( 17 FDA reports)
UVEITIS ( 17 FDA reports)
WEIGHT FLUCTUATION ( 17 FDA reports)
NEPHRITIC SYNDROME ( 16 FDA reports)
NYSTAGMUS ( 16 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 16 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 16 FDA reports)
PATHOLOGICAL GAMBLING ( 16 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 16 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 16 FDA reports)
PHARYNGEAL ERYTHEMA ( 16 FDA reports)
PNEUMATOSIS INTESTINALIS ( 16 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 16 FDA reports)
POLYPECTOMY ( 16 FDA reports)
PROTEIN URINE ( 16 FDA reports)
PSEUDOMONAL SEPSIS ( 16 FDA reports)
RENAL CELL CARCINOMA ( 16 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 16 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 16 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 16 FDA reports)
SACROILIITIS ( 16 FDA reports)
SECRETION DISCHARGE ( 16 FDA reports)
SEROTONIN SYNDROME ( 16 FDA reports)
SKIN PAPILLOMA ( 16 FDA reports)
SKIN REACTION ( 16 FDA reports)
SPINAL DECOMPRESSION ( 16 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 16 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 16 FDA reports)
TRICUSPID VALVE DISEASE ( 16 FDA reports)
TUBERCULIN TEST POSITIVE ( 16 FDA reports)
URINE ANALYSIS ABNORMAL ( 16 FDA reports)
URINE OUTPUT INCREASED ( 16 FDA reports)
VASCULAR INSUFFICIENCY ( 16 FDA reports)
VENA CAVA FILTER INSERTION ( 16 FDA reports)
VENOUS OCCLUSION ( 16 FDA reports)
VENOUS STASIS ( 16 FDA reports)
VITREOUS HAEMORRHAGE ( 16 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 16 FDA reports)
ACNE ( 16 FDA reports)
ALVEOLOPLASTY ( 16 FDA reports)
ANISOCYTOSIS ( 16 FDA reports)
APPLICATION SITE IRRITATION ( 16 FDA reports)
APPLICATION SITE VESICLES ( 16 FDA reports)
BILIARY DILATATION ( 16 FDA reports)
BIOPSY BREAST ABNORMAL ( 16 FDA reports)
BLOOD LACTIC ACID INCREASED ( 16 FDA reports)
BLOOD PH INCREASED ( 16 FDA reports)
BLOOD TEST ABNORMAL ( 16 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 16 FDA reports)
BRAIN HERNIATION ( 16 FDA reports)
BREAST DISCHARGE ( 16 FDA reports)
CENTRAL OBESITY ( 16 FDA reports)
CHEMICAL POISONING ( 16 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 16 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 16 FDA reports)
CORONARY ANGIOPLASTY ( 16 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 16 FDA reports)
DERMATITIS CONTACT ( 16 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 16 FDA reports)
DRUG TOLERANCE ( 16 FDA reports)
ENDOMETRIAL CANCER ( 16 FDA reports)
EPICONDYLITIS ( 16 FDA reports)
EYELID OEDEMA ( 16 FDA reports)
FOOD INTOLERANCE ( 16 FDA reports)
GINGIVAL RECESSION ( 16 FDA reports)
HAEMOGLOBIN INCREASED ( 16 FDA reports)
HAEMORRHAGIC STROKE ( 16 FDA reports)
HEPATITIS FULMINANT ( 16 FDA reports)
HYDROCELE ( 16 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 16 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
JOINT CONTRACTURE ( 16 FDA reports)
JOINT LOCK ( 16 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 16 FDA reports)
LEUKAEMIA ( 16 FDA reports)
LOW TURNOVER OSTEOPATHY ( 16 FDA reports)
LUDWIG ANGINA ( 16 FDA reports)
LUNG HYPERINFLATION ( 16 FDA reports)
METABOLIC DISORDER ( 16 FDA reports)
METASTASIS ( 16 FDA reports)
MITRAL VALVE STENOSIS ( 16 FDA reports)
MUCOSAL HAEMORRHAGE ( 16 FDA reports)
ADENOMA BENIGN ( 15 FDA reports)
ADNEXA UTERI MASS ( 15 FDA reports)
APPARENT DEATH ( 15 FDA reports)
APPETITE DISORDER ( 15 FDA reports)
APPLICATION SITE PAIN ( 15 FDA reports)
ATROPHY ( 15 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 15 FDA reports)
BONE LOSS ( 15 FDA reports)
BRADYPHRENIA ( 15 FDA reports)
BRAIN SCAN ABNORMAL ( 15 FDA reports)
BREAST CALCIFICATIONS ( 15 FDA reports)
BREAST HAEMATOMA ( 15 FDA reports)
CHEMOTHERAPY ( 15 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 15 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 15 FDA reports)
COLON NEOPLASM ( 15 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 15 FDA reports)
CORNEAL OEDEMA ( 15 FDA reports)
CYSTITIS INTERSTITIAL ( 15 FDA reports)
CYSTOSCOPY ( 15 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 15 FDA reports)
GRAVITATIONAL OEDEMA ( 15 FDA reports)
GUILLAIN-BARRE SYNDROME ( 15 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 15 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 15 FDA reports)
HEPATITIS B ( 15 FDA reports)
HEPATITIS TOXIC ( 15 FDA reports)
HYDROPNEUMOTHORAX ( 15 FDA reports)
HYDROTHORAX ( 15 FDA reports)
HYPERCHLORAEMIA ( 15 FDA reports)
HYPERPLASIA ( 15 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 15 FDA reports)
HYPERVENTILATION ( 15 FDA reports)
IMMUNODEFICIENCY ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
INFECTED SKIN ULCER ( 15 FDA reports)
INJECTION SITE BRUISING ( 15 FDA reports)
INJECTION SITE MASS ( 15 FDA reports)
INTESTINAL ULCER ( 15 FDA reports)
LIBIDO DECREASED ( 15 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 15 FDA reports)
LIPIDS INCREASED ( 15 FDA reports)
LIVEDO RETICULARIS ( 15 FDA reports)
MASTECTOMY ( 15 FDA reports)
METASTASES TO ADRENALS ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 15 FDA reports)
OPTIC NEURITIS ( 15 FDA reports)
OSTEOMA ( 15 FDA reports)
PARTNER STRESS ( 15 FDA reports)
POST PROCEDURAL HAEMATOMA ( 15 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 15 FDA reports)
PSEUDODEMENTIA ( 15 FDA reports)
PULMONARY INFARCTION ( 15 FDA reports)
RAYNAUD'S PHENOMENON ( 15 FDA reports)
REGURGITATION ( 15 FDA reports)
RENAL TUBULAR ACIDOSIS ( 15 FDA reports)
RESPIRATORY RATE DECREASED ( 15 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 15 FDA reports)
SALIVARY HYPERSECRETION ( 15 FDA reports)
SEASONAL ALLERGY ( 15 FDA reports)
SHOULDER OPERATION ( 15 FDA reports)
SKIN FRAGILITY ( 15 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 15 FDA reports)
TRACHEOSTOMY ( 15 FDA reports)
ULCERATIVE KERATITIS ( 15 FDA reports)
NASAL DISORDER ( 14 FDA reports)
NEOPLASM SKIN ( 14 FDA reports)
NEUROLOGICAL SYMPTOM ( 14 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 14 FDA reports)
OXYGEN SUPPLEMENTATION ( 14 FDA reports)
PARAPARESIS ( 14 FDA reports)
PERIORBITAL HAEMATOMA ( 14 FDA reports)
PERITONEAL DIALYSIS ( 14 FDA reports)
PERNICIOUS ANAEMIA ( 14 FDA reports)
PERSONALITY DISORDER ( 14 FDA reports)
PLATELET COUNT ABNORMAL ( 14 FDA reports)
PO2 DECREASED ( 14 FDA reports)
PO2 INCREASED ( 14 FDA reports)
POLYCYSTIC OVARIES ( 14 FDA reports)
POSTNASAL DRIP ( 14 FDA reports)
PREGNANCY ( 14 FDA reports)
PREMATURE BABY ( 14 FDA reports)
PROTHROMBIN TIME SHORTENED ( 14 FDA reports)
RASH VESICULAR ( 14 FDA reports)
RECTAL POLYP ( 14 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
SALIVARY GLAND DISORDER ( 14 FDA reports)
SCHIZOPHRENIA ( 14 FDA reports)
SKIN TURGOR DECREASED ( 14 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 14 FDA reports)
SOFT TISSUE INFECTION ( 14 FDA reports)
SPONDYLITIS ( 14 FDA reports)
TOOTH INJURY ( 14 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 14 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VERTEBROPLASTY ( 14 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 14 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 14 FDA reports)
ABDOMINAL MASS ( 14 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 14 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 14 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 14 FDA reports)
ANIMAL BITE ( 14 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 14 FDA reports)
ASTERIXIS ( 14 FDA reports)
ATRIAL THROMBOSIS ( 14 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 14 FDA reports)
BLADDER SPASM ( 14 FDA reports)
BLOODY DISCHARGE ( 14 FDA reports)
BONE ABSCESS ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
BRAIN ABSCESS ( 14 FDA reports)
BREAST CANCER STAGE IV ( 14 FDA reports)
BREAST CELLULITIS ( 14 FDA reports)
CANDIDURIA ( 14 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 14 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
CENTRAL LINE INFECTION ( 14 FDA reports)
CHEST WALL OPERATION ( 14 FDA reports)
CHOKING SENSATION ( 14 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
CULTURE WOUND POSITIVE ( 14 FDA reports)
DIABETIC COMPLICATION ( 14 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 14 FDA reports)
EAR DISCOMFORT ( 14 FDA reports)
EAR HAEMORRHAGE ( 14 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 14 FDA reports)
ENCEPHALOMALACIA ( 14 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 14 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 14 FDA reports)
FIBROMA ( 14 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 14 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 14 FDA reports)
GASTROINTESTINAL INFECTION ( 14 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 14 FDA reports)
HAEMOPHILUS INFECTION ( 14 FDA reports)
HYDROURETER ( 14 FDA reports)
HYPOPROTEINAEMIA ( 14 FDA reports)
HYPOREFLEXIA ( 14 FDA reports)
ILIAC ARTERY STENOSIS ( 14 FDA reports)
INJECTION SITE NODULE ( 14 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 14 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 14 FDA reports)
KETOSIS ( 14 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 14 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 14 FDA reports)
MALLORY-WEISS SYNDROME ( 14 FDA reports)
MAXILLOFACIAL OPERATION ( 14 FDA reports)
MENSTRUATION IRREGULAR ( 14 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 14 FDA reports)
MUSCLE CRAMP ( 14 FDA reports)
ABDOMINAL ABSCESS ( 13 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
AORTIC VALVE REPLACEMENT ( 13 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 13 FDA reports)
ARTHRITIS BACTERIAL ( 13 FDA reports)
AXILLARY MASS ( 13 FDA reports)
BLADDER OPERATION ( 13 FDA reports)
BLINDNESS TRANSIENT ( 13 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 13 FDA reports)
BODY TINEA ( 13 FDA reports)
BREAST CANCER IN SITU ( 13 FDA reports)
CEREBRAL DISORDER ( 13 FDA reports)
CEREBRAL HAEMATOMA ( 13 FDA reports)
CIRRHOSIS ALCOHOLIC ( 13 FDA reports)
CONVERSION DISORDER ( 13 FDA reports)
CUSHINGOID ( 13 FDA reports)
DERMATITIS ALLERGIC ( 13 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 13 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 13 FDA reports)
EXPIRED DRUG ADMINISTERED ( 13 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 13 FDA reports)
FOOD AVERSION ( 13 FDA reports)
FULL BLOOD COUNT DECREASED ( 13 FDA reports)
GASTROENTERITIS RADIATION ( 13 FDA reports)
GLOMERULONEPHRITIS ( 13 FDA reports)
HAEMATOMA INFECTION ( 13 FDA reports)
HALO VISION ( 13 FDA reports)
HERNIA REPAIR ( 13 FDA reports)
HYPERMAGNESAEMIA ( 13 FDA reports)
HYPEROSMOLAR STATE ( 13 FDA reports)
HYPOCHLORAEMIA ( 13 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 13 FDA reports)
IMPAIRED SELF-CARE ( 13 FDA reports)
IMPLANT SITE INFECTION ( 13 FDA reports)
JOINT ARTHROPLASTY ( 13 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 13 FDA reports)
LEUKOENCEPHALOPATHY ( 13 FDA reports)
LUNG INJURY ( 13 FDA reports)
LYMPHOCYTOSIS ( 13 FDA reports)
MACROCYTOSIS ( 13 FDA reports)
MONOCYTE COUNT INCREASED ( 13 FDA reports)
MOUTH INJURY ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 13 FDA reports)
OTITIS EXTERNA ( 13 FDA reports)
OTITIS MEDIA ACUTE ( 13 FDA reports)
PANCREATIC MASS ( 13 FDA reports)
PANCREATIC NEOPLASM ( 13 FDA reports)
PARTIAL SEIZURES ( 13 FDA reports)
PCO2 INCREASED ( 13 FDA reports)
PHOTOPSIA ( 13 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 13 FDA reports)
POST-TRAUMATIC PAIN ( 13 FDA reports)
POSTMENOPAUSE ( 13 FDA reports)
PRESBYOESOPHAGUS ( 13 FDA reports)
PROTEUS INFECTION ( 13 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 13 FDA reports)
PSYCHOLOGICAL TRAUMA ( 13 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 13 FDA reports)
PULMONARY TOXICITY ( 13 FDA reports)
PULSE PRESSURE DECREASED ( 13 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 13 FDA reports)
PUPILS UNEQUAL ( 13 FDA reports)
RECTAL ULCER ( 13 FDA reports)
RENAL TUBULAR DISORDER ( 13 FDA reports)
SCLERODERMA ( 13 FDA reports)
SCOTOMA ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SELF-MEDICATION ( 13 FDA reports)
SINUS POLYP ( 13 FDA reports)
SINUSITIS FUNGAL ( 13 FDA reports)
SKIN GRAFT ( 13 FDA reports)
SMALL INTESTINAL PERFORATION ( 13 FDA reports)
SPINAL COLUMN INJURY ( 13 FDA reports)
SPINAL CORD DISORDER ( 13 FDA reports)
SPLENIC ABSCESS ( 13 FDA reports)
SUPERINFECTION ( 13 FDA reports)
TEMPORAL ARTERITIS ( 13 FDA reports)
THORACOTOMY ( 13 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 13 FDA reports)
TRANSFUSION REACTION ( 13 FDA reports)
TRIGGER FINGER ( 13 FDA reports)
URINARY HESITATION ( 13 FDA reports)
URINE ABNORMALITY ( 13 FDA reports)
VENOUS THROMBOSIS LIMB ( 13 FDA reports)
NECK MASS ( 12 FDA reports)
NEUROSIS ( 12 FDA reports)
NEUROTOXICITY ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 12 FDA reports)
OBSTRUCTION GASTRIC ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
ORAL FUNGAL INFECTION ( 12 FDA reports)
ORAL NEOPLASM ( 12 FDA reports)
PANIC DISORDER ( 12 FDA reports)
PARAPLEGIA ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
PAROTIDECTOMY ( 12 FDA reports)
PERICARDIAL DISEASE ( 12 FDA reports)
PLASTIC SURGERY ( 12 FDA reports)
POLYARTHRITIS ( 12 FDA reports)
POST PROCEDURAL INFECTION ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
PRESCRIBED OVERDOSE ( 12 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 12 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 12 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 12 FDA reports)
RENAL COLIC ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SCRATCH ( 12 FDA reports)
SKIN DEPIGMENTATION ( 12 FDA reports)
SPONDYLOLYSIS ( 12 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 12 FDA reports)
STEATORRHOEA ( 12 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 12 FDA reports)
TOE DEFORMITY ( 12 FDA reports)
TUMOUR NECROSIS ( 12 FDA reports)
URINARY TRACT OBSTRUCTION ( 12 FDA reports)
VASCULAR PURPURA ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
ACQUIRED PORPHYRIA ( 12 FDA reports)
ADRENOGENITAL SYNDROME ( 12 FDA reports)
ANAL FISSURE ( 12 FDA reports)
ARTERIAL DISORDER ( 12 FDA reports)
ARTERIOVENOUS FISTULA ( 12 FDA reports)
BENIGN TUMOUR EXCISION ( 12 FDA reports)
BIPOLAR I DISORDER ( 12 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 12 FDA reports)
BLOOD BICARBONATE INCREASED ( 12 FDA reports)
BLOOD BLISTER ( 12 FDA reports)
BONE SCAN ABNORMAL ( 12 FDA reports)
BREAST NEOPLASM ( 12 FDA reports)
CARBON DIOXIDE INCREASED ( 12 FDA reports)
CARDIORENAL SYNDROME ( 12 FDA reports)
CATATONIA ( 12 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 12 FDA reports)
CERVICAL DYSPLASIA ( 12 FDA reports)
CHANGE OF BOWEL HABIT ( 12 FDA reports)
CHEST INJURY ( 12 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 12 FDA reports)
CLAUSTROPHOBIA ( 12 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CORONARY ARTERY THROMBOSIS ( 12 FDA reports)
CORYNEBACTERIUM INFECTION ( 12 FDA reports)
DENTAL CARE ( 12 FDA reports)
DIABETIC GASTROPARESIS ( 12 FDA reports)
DISEASE COMPLICATION ( 12 FDA reports)
DYSPNOEA AT REST ( 12 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 12 FDA reports)
EMBOLISM VENOUS ( 12 FDA reports)
ENCEPHALITIS POST MEASLES ( 12 FDA reports)
ENTEROCOCCAL SEPSIS ( 12 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 12 FDA reports)
ESCHERICHIA BACTERAEMIA ( 12 FDA reports)
FEBRILE BONE MARROW APLASIA ( 12 FDA reports)
FEMORAL ARTERY OCCLUSION ( 12 FDA reports)
GASTRITIS ATROPHIC ( 12 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 12 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 12 FDA reports)
GENERALISED ANXIETY DISORDER ( 12 FDA reports)
GLIOSIS ( 12 FDA reports)
HAEMARTHROSIS ( 12 FDA reports)
HEART TRANSPLANT REJECTION ( 12 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 12 FDA reports)
INCISION SITE PAIN ( 12 FDA reports)
INTERTRIGO ( 12 FDA reports)
INTESTINAL HAEMORRHAGE ( 12 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 12 FDA reports)
IRON METABOLISM DISORDER ( 12 FDA reports)
JOINT PROSTHESIS USER ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
KLEBSIELLA BACTERAEMIA ( 12 FDA reports)
LIP HAEMORRHAGE ( 12 FDA reports)
LOWER EXTREMITY MASS ( 12 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 12 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 12 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 12 FDA reports)
METASTASES TO MENINGES ( 12 FDA reports)
MIOSIS ( 12 FDA reports)
MUCOSAL EROSION ( 12 FDA reports)
MUSCLE RIGIDITY ( 12 FDA reports)
ABDOMINAL RIGIDITY ( 11 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 11 FDA reports)
ACUTE LEUKAEMIA ( 11 FDA reports)
ACUTE PSYCHOSIS ( 11 FDA reports)
ADHESION ( 11 FDA reports)
ALVEOLITIS ( 11 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 11 FDA reports)
AORTIC BYPASS ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
ARTERIOSPASM CORONARY ( 11 FDA reports)
ARTERIOVENOUS MALFORMATION ( 11 FDA reports)
ATRIAL SEPTAL DEFECT ( 11 FDA reports)
BILE DUCT STENOSIS ( 11 FDA reports)
BLADDER NEOPLASM ( 11 FDA reports)
BREAST OPERATION ( 11 FDA reports)
CAPILLARY LEAK SYNDROME ( 11 FDA reports)
CATHETER SEPSIS ( 11 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 11 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 11 FDA reports)
CHOLANGITIS CHRONIC ( 11 FDA reports)
CHRONIC HEPATITIS ( 11 FDA reports)
CITROBACTER INFECTION ( 11 FDA reports)
COLON OPERATION ( 11 FDA reports)
COLONIC STENOSIS ( 11 FDA reports)
COLONOSCOPY ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 11 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 11 FDA reports)
CYSTITIS HAEMORRHAGIC ( 11 FDA reports)
DERMATITIS ATOPIC ( 11 FDA reports)
DIABETIC ULCER ( 11 FDA reports)
DISSOCIATION ( 11 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 11 FDA reports)
DYSPLASTIC NAEVUS ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 11 FDA reports)
ENTEROBACTER INFECTION ( 11 FDA reports)
ENTHESOPATHY ( 11 FDA reports)
FIBROUS HISTIOCYTOMA ( 11 FDA reports)
HAEMANGIOMA OF LIVER ( 11 FDA reports)
HAEMATOTOXICITY ( 11 FDA reports)
HAEMORRHOID OPERATION ( 11 FDA reports)
HEPATIC NECROSIS ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
HYPERTROPHY ( 11 FDA reports)
HYPOGLYCAEMIC COMA ( 11 FDA reports)
INJECTION SITE WARMTH ( 11 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 11 FDA reports)
KLEBSIELLA SEPSIS ( 11 FDA reports)
LABORATORY TEST INTERFERENCE ( 11 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 11 FDA reports)
LEUKAEMIA RECURRENT ( 11 FDA reports)
LOOSE BODY IN JOINT ( 11 FDA reports)
LUNG CANCER METASTATIC ( 11 FDA reports)
MEDIASTINITIS ( 11 FDA reports)
MELANOCYTIC NAEVUS ( 11 FDA reports)
METASTASES TO ABDOMINAL WALL ( 11 FDA reports)
METASTASES TO PLEURA ( 11 FDA reports)
MICROCYTOSIS ( 11 FDA reports)
MIGRAINE WITH AURA ( 11 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 11 FDA reports)
MUCOSAL DRYNESS ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 11 FDA reports)
MYELOPATHY ( 11 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 11 FDA reports)
NAIL OPERATION ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 11 FDA reports)
NEUROMYOPATHY ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
OESOPHAGITIS ULCERATIVE ( 11 FDA reports)
OPERATIVE HAEMORRHAGE ( 11 FDA reports)
ORGANISING PNEUMONIA ( 11 FDA reports)
PAIN EXACERBATED ( 11 FDA reports)
PANCREATIC INSUFFICIENCY ( 11 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 11 FDA reports)
PERICARDIAL HAEMORRHAGE ( 11 FDA reports)
PERITONEAL HAEMORRHAGE ( 11 FDA reports)
POLYSUBSTANCE ABUSE ( 11 FDA reports)
POOR DENTAL CONDITION ( 11 FDA reports)
POOR PERSONAL HYGIENE ( 11 FDA reports)
POSTOPERATIVE INFECTION ( 11 FDA reports)
PROCEDURAL NAUSEA ( 11 FDA reports)
PULMONARY AIR LEAKAGE ( 11 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 11 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
ROTATOR CUFF REPAIR ( 11 FDA reports)
SALPINGO-OOPHORECTOMY ( 11 FDA reports)
SEBORRHOEIC DERMATITIS ( 11 FDA reports)
SOFT TISSUE INFLAMMATION ( 11 FDA reports)
SPINAL FUSION SURGERY ( 11 FDA reports)
SPLENIC CALCIFICATION ( 11 FDA reports)
STARING ( 11 FDA reports)
SUBACUTE ENDOCARDITIS ( 11 FDA reports)
SURGICAL PROCEDURE REPEATED ( 11 FDA reports)
TRAUMATIC BRAIN INJURY ( 11 FDA reports)
URINARY TRACT DISORDER ( 11 FDA reports)
VITREOUS DETACHMENT ( 11 FDA reports)
VULVOVAGINAL DRYNESS ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 10 FDA reports)
NOSOCOMIAL INFECTION ( 10 FDA reports)
OESOPHAGEAL DILATATION ( 10 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 10 FDA reports)
OSTEITIS DEFORMANS ( 10 FDA reports)
OTORRHOEA ( 10 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 10 FDA reports)
PARAPSORIASIS ( 10 FDA reports)
PAROTID GLAND ENLARGEMENT ( 10 FDA reports)
PENILE INFECTION ( 10 FDA reports)
PERITONEAL ADHESIONS ( 10 FDA reports)
POOR VENOUS ACCESS ( 10 FDA reports)
POST PROCEDURAL PAIN ( 10 FDA reports)
PREMATURE LABOUR ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
RASH PUSTULAR ( 10 FDA reports)
RECURRENT CANCER ( 10 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 10 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 10 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 10 FDA reports)
SARCOIDOSIS ( 10 FDA reports)
SENSATION OF PRESSURE ( 10 FDA reports)
SERRATIA SEPSIS ( 10 FDA reports)
SINUS ARREST ( 10 FDA reports)
SKIN HYPOPIGMENTATION ( 10 FDA reports)
SKIN WRINKLING ( 10 FDA reports)
SPLENIC VEIN THROMBOSIS ( 10 FDA reports)
SPUTUM INCREASED ( 10 FDA reports)
STRESS INCONTINENCE ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SUBILEUS ( 10 FDA reports)
SUFFOCATION FEELING ( 10 FDA reports)
TESTICULAR PAIN ( 10 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 10 FDA reports)
TOE AMPUTATION ( 10 FDA reports)
TRIGEMINAL NEURALGIA ( 10 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
URGE INCONTINENCE ( 10 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 10 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 10 FDA reports)
WHITE BLOOD CELL COUNT ( 10 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 10 FDA reports)
ABDOMINAL SEPSIS ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
ALCOHOL POISONING ( 10 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 10 FDA reports)
BACTERIA URINE IDENTIFIED ( 10 FDA reports)
BACTERIAL TEST POSITIVE ( 10 FDA reports)
BENIGN GASTRIC NEOPLASM ( 10 FDA reports)
BILIARY COLIC ( 10 FDA reports)
BODY DYSMORPHIC DISORDER ( 10 FDA reports)
BREAST LUMP REMOVAL ( 10 FDA reports)
BREAST SWELLING ( 10 FDA reports)
BURNS SECOND DEGREE ( 10 FDA reports)
CANCER PAIN ( 10 FDA reports)
CARTILAGE INJURY ( 10 FDA reports)
CATARACT NUCLEAR ( 10 FDA reports)
CERVICOBRACHIAL SYNDROME ( 10 FDA reports)
COMMINUTED FRACTURE ( 10 FDA reports)
COMPLEX PARTIAL SEIZURES ( 10 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 10 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 10 FDA reports)
CUSHING'S SYNDROME ( 10 FDA reports)
CYSTOPEXY ( 10 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 10 FDA reports)
DEAFNESS UNILATERAL ( 10 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DERMATITIS PSORIASIFORM ( 10 FDA reports)
DEVICE BREAKAGE ( 10 FDA reports)
DEVICE DISLOCATION ( 10 FDA reports)
EAR CONGESTION ( 10 FDA reports)
EJECTION FRACTION ABNORMAL ( 10 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 10 FDA reports)
ENZYME ABNORMALITY ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
EPIDIDYMITIS ( 10 FDA reports)
EXANTHEM ( 10 FDA reports)
EXOPHTHALMOS ( 10 FDA reports)
EYE OPERATION ( 10 FDA reports)
EYELID DISORDER ( 10 FDA reports)
FACIAL PARESIS ( 10 FDA reports)
FOOD POISONING ( 10 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 10 FDA reports)
GENITAL HERPES ( 10 FDA reports)
HAEMORRHAGIC DIATHESIS ( 10 FDA reports)
HAND DEFORMITY ( 10 FDA reports)
HANGOVER ( 10 FDA reports)
HELICOBACTER GASTRITIS ( 10 FDA reports)
HEPATIC INFARCTION ( 10 FDA reports)
HODGKIN'S DISEASE ( 10 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 10 FDA reports)
INFERTILITY ( 10 FDA reports)
INGUINAL MASS ( 10 FDA reports)
INJECTION SITE INFECTION ( 10 FDA reports)
INJECTION SITE INFLAMMATION ( 10 FDA reports)
INJECTION SITE VESICLES ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 10 FDA reports)
KIDNEY ENLARGEMENT ( 10 FDA reports)
LIGAMENT DISORDER ( 10 FDA reports)
LIP BLISTER ( 10 FDA reports)
LITHOTRIPSY ( 10 FDA reports)
MACULOPATHY ( 10 FDA reports)
MAMMOPLASTY ( 10 FDA reports)
MENIERE'S DISEASE ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
MICROALBUMINURIA ( 10 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 10 FDA reports)
MUSCLE FATIGUE ( 10 FDA reports)
ABDOMINAL INFECTION ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 9 FDA reports)
AKATHISIA ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANASTOMOTIC LEAK ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
APRAXIA ( 9 FDA reports)
BENIGN BONE NEOPLASM ( 9 FDA reports)
BLADDER CATHETERISATION ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 9 FDA reports)
BRAIN OPERATION ( 9 FDA reports)
BREAST ENLARGEMENT ( 9 FDA reports)
BREAST HYPERPLASIA ( 9 FDA reports)
BRONCHOPLEURAL FISTULA ( 9 FDA reports)
CALCIUM DEFICIENCY ( 9 FDA reports)
CALCULUS BLADDER ( 9 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 9 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
CEREBELLAR ATROPHY ( 9 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 9 FDA reports)
CEREBRAL THROMBOSIS ( 9 FDA reports)
CHEST TUBE INSERTION ( 9 FDA reports)
CHRONIC HEPATIC FAILURE ( 9 FDA reports)
COLONIC OBSTRUCTION ( 9 FDA reports)
COMA HEPATIC ( 9 FDA reports)
COMA SCALE ABNORMAL ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 9 FDA reports)
CULTURE POSITIVE ( 9 FDA reports)
CULTURE STOOL POSITIVE ( 9 FDA reports)
DEFAECATION URGENCY ( 9 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 9 FDA reports)
DEVICE OCCLUSION ( 9 FDA reports)
DRUG-INDUCED LIVER INJURY ( 9 FDA reports)
DUODENAL STENOSIS ( 9 FDA reports)
EMPTY SELLA SYNDROME ( 9 FDA reports)
EXFOLIATIVE RASH ( 9 FDA reports)
GASTRIC INFECTION ( 9 FDA reports)
GLYCOSURIA ( 9 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 9 FDA reports)
HAEMORRHAGE URINARY TRACT ( 9 FDA reports)
HEART VALVE REPLACEMENT ( 9 FDA reports)
HEPATIC INFECTION FUNGAL ( 9 FDA reports)
HEPATIC VEIN OCCLUSION ( 9 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
HYPOPARATHYROIDISM ( 9 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 9 FDA reports)
IMMUNOGLOBULINS DECREASED ( 9 FDA reports)
INCISION SITE INFECTION ( 9 FDA reports)
INFECTIOUS PERITONITIS ( 9 FDA reports)
INFUSION SITE ERYTHEMA ( 9 FDA reports)
INNER EAR DISORDER ( 9 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 9 FDA reports)
IRITIS ( 9 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 9 FDA reports)
JOINT WARMTH ( 9 FDA reports)
LIP DISCOLOURATION ( 9 FDA reports)
LIP DRY ( 9 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 9 FDA reports)
MACULAR OEDEMA ( 9 FDA reports)
MASTITIS ( 9 FDA reports)
MEDIASTINAL SHIFT ( 9 FDA reports)
METAPLASIA ( 9 FDA reports)
METASTASES TO PERITONEUM ( 9 FDA reports)
MUCOSAL NECROSIS ( 9 FDA reports)
MUCOUS MEMBRANE DISORDER ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 9 FDA reports)
NEONATAL APNOEIC ATTACK ( 9 FDA reports)
PAINFUL RESPIRATION ( 9 FDA reports)
PEAU D'ORANGE ( 9 FDA reports)
PERICARDITIS CONSTRICTIVE ( 9 FDA reports)
PERTUSSIS ( 9 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 9 FDA reports)
QUADRIPARESIS ( 9 FDA reports)
RETINAL TEAR ( 9 FDA reports)
RETINITIS ( 9 FDA reports)
RHEUMATOID NODULE ( 9 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 9 FDA reports)
ROSACEA ( 9 FDA reports)
SCAPULA FRACTURE ( 9 FDA reports)
SEPTIC EMBOLUS ( 9 FDA reports)
SJOGREN'S SYNDROME ( 9 FDA reports)
SPONDYLOARTHROPATHY ( 9 FDA reports)
SYNCOPE VASOVAGAL ( 9 FDA reports)
TENDON INJURY ( 9 FDA reports)
TENOSYNOVITIS STENOSANS ( 9 FDA reports)
THERAPEUTIC PROCEDURE ( 9 FDA reports)
THROMBOCYTHAEMIA ( 9 FDA reports)
TONGUE DISCOLOURATION ( 9 FDA reports)
TONGUE NEOPLASM ( 9 FDA reports)
TUMOUR EXCISION ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
VASCULAR OCCLUSION ( 9 FDA reports)
VASCULAR PSEUDOANEURYSM ( 9 FDA reports)
VEIN DISORDER ( 9 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NASAL MUCOSAL DISORDER ( 8 FDA reports)
NEPHRECTOMY ( 8 FDA reports)
NOCARDIOSIS ( 8 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
ORTHOSTATIC INTOLERANCE ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 8 FDA reports)
PARACENTESIS ( 8 FDA reports)
PARAPROTEINAEMIA ( 8 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 8 FDA reports)
PHLEBOTHROMBOSIS ( 8 FDA reports)
PLASMAPHERESIS ( 8 FDA reports)
POLYMYOSITIS ( 8 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 8 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 8 FDA reports)
POST PROCEDURAL DISCHARGE ( 8 FDA reports)
POSTICTAL STATE ( 8 FDA reports)
POSTOPERATIVE FEVER ( 8 FDA reports)
PROCEDURAL HYPOTENSION ( 8 FDA reports)
PRODUCT TASTE ABNORMAL ( 8 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 8 FDA reports)
RADICULAR CYST ( 8 FDA reports)
RADICULITIS LUMBOSACRAL ( 8 FDA reports)
READING DISORDER ( 8 FDA reports)
RENAL HAEMORRHAGE ( 8 FDA reports)
RESIDUAL URINE ( 8 FDA reports)
RHINITIS SEASONAL ( 8 FDA reports)
SCHAMBERG'S DISEASE ( 8 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 8 FDA reports)
SCROTAL SWELLING ( 8 FDA reports)
SEBORRHOEA ( 8 FDA reports)
SHOULDER ARTHROPLASTY ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SPINAL DEFORMITY ( 8 FDA reports)
SPINAL HAEMANGIOMA ( 8 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 8 FDA reports)
STRESS ULCER ( 8 FDA reports)
STUPOR ( 8 FDA reports)
SUPRAPUBIC PAIN ( 8 FDA reports)
SYSTEMIC MYCOSIS ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 8 FDA reports)
THERAPY CESSATION ( 8 FDA reports)
TONGUE OEDEMA ( 8 FDA reports)
TRACHEITIS ( 8 FDA reports)
TRAUMATIC HAEMATOMA ( 8 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 8 FDA reports)
TUMOUR HAEMORRHAGE ( 8 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 8 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 8 FDA reports)
URINE KETONE BODY PRESENT ( 8 FDA reports)
VASCULAR BYPASS GRAFT ( 8 FDA reports)
VASCULAR DEMENTIA ( 8 FDA reports)
VITAMIN K DEFICIENCY ( 8 FDA reports)
VITH NERVE PARALYSIS ( 8 FDA reports)
VOMITING PROJECTILE ( 8 FDA reports)
ABSCESS INTESTINAL ( 8 FDA reports)
ACUTE ABDOMEN ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
ALLODYNIA ( 8 FDA reports)
AMPUTATION ( 8 FDA reports)
ANAESTHETIC COMPLICATION ( 8 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 8 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 8 FDA reports)
APALLIC SYNDROME ( 8 FDA reports)
APPLICATION SITE BURN ( 8 FDA reports)
ARTERIAL BYPASS OPERATION ( 8 FDA reports)
ATHEROSCLEROSIS ( 8 FDA reports)
AXONAL NEUROPATHY ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BACTERIAL DISEASE CARRIER ( 8 FDA reports)
BILIARY SEPSIS ( 8 FDA reports)
BLADDER OBSTRUCTION ( 8 FDA reports)
BLEPHAROSPASM ( 8 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 8 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BONE CANCER METASTATIC ( 8 FDA reports)
BONE MARROW DISORDER ( 8 FDA reports)
BRAIN STEM INFARCTION ( 8 FDA reports)
BUNION ( 8 FDA reports)
CARDIAC ASTHMA ( 8 FDA reports)
CARDIAC HYPERTROPHY ( 8 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 8 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 8 FDA reports)
CONTRAST MEDIA REACTION ( 8 FDA reports)
CORONARY ARTERY SURGERY ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DROOLING ( 8 FDA reports)
DRUG TOLERANCE INCREASED ( 8 FDA reports)
DYSPHEMIA ( 8 FDA reports)
ENDOMETRIOSIS ( 8 FDA reports)
ENDOPHTHALMITIS ( 8 FDA reports)
ENDOSCOPY ( 8 FDA reports)
ENERGY INCREASED ( 8 FDA reports)
ENTERITIS INFECTIOUS ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
EYE MOVEMENT DISORDER ( 8 FDA reports)
FACIAL WASTING ( 8 FDA reports)
FAECAL VOMITING ( 8 FDA reports)
FAT NECROSIS ( 8 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 8 FDA reports)
FUNGAL SEPSIS ( 8 FDA reports)
GASTRIC BYPASS ( 8 FDA reports)
GIANT CELL EPULIS ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
GLOBULINS INCREASED ( 8 FDA reports)
GLUCOSE URINE PRESENT ( 8 FDA reports)
HAEMORRHAGIC DISORDER ( 8 FDA reports)
HAIR TEXTURE ABNORMAL ( 8 FDA reports)
HERPES VIRUS INFECTION ( 8 FDA reports)
HOSTILITY ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
HYPOMANIA ( 8 FDA reports)
HYPOPNOEA ( 8 FDA reports)
IATROGENIC INJURY ( 8 FDA reports)
ILIAC ARTERY THROMBOSIS ( 8 FDA reports)
IMMOBILE ( 8 FDA reports)
INCISION SITE COMPLICATION ( 8 FDA reports)
INCISIONAL DRAINAGE ( 8 FDA reports)
INFUSION SITE INFECTION ( 8 FDA reports)
INFUSION SITE SWELLING ( 8 FDA reports)
INJECTION SITE DISCOLOURATION ( 8 FDA reports)
INJECTION SITE DISCOMFORT ( 8 FDA reports)
INJECTION SITE INDURATION ( 8 FDA reports)
INJURY CORNEAL ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 8 FDA reports)
LABILE HYPERTENSION ( 8 FDA reports)
LEUKOCYTURIA ( 8 FDA reports)
LIFE SUPPORT ( 8 FDA reports)
LIP ULCERATION ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
MENINGITIS ASEPTIC ( 8 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 8 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 8 FDA reports)
MUSCLE CONTRACTURE ( 8 FDA reports)
MUSCLE SPASTICITY ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACARODERMATITIS ( 7 FDA reports)
AFFECT LABILITY ( 7 FDA reports)
AKINESIA ( 7 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANDROGEN DEFICIENCY ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
APPENDIX DISORDER ( 7 FDA reports)
APPLICATION SITE REACTION ( 7 FDA reports)
ATROPHIC VULVOVAGINITIS ( 7 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 7 FDA reports)
AUTOIMMUNE THYROIDITIS ( 7 FDA reports)
BASEDOW'S DISEASE ( 7 FDA reports)
BIOPSY ENDOMETRIUM ( 7 FDA reports)
BK VIRUS INFECTION ( 7 FDA reports)
BLADDER PAIN ( 7 FDA reports)
BLADDER PROLAPSE ( 7 FDA reports)
BLEEDING TIME PROLONGED ( 7 FDA reports)
BLOOD OSMOLARITY INCREASED ( 7 FDA reports)
BLOOD SODIUM ABNORMAL ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 7 FDA reports)
BONE DENSITOMETRY ( 7 FDA reports)
BRAIN CONTUSION ( 7 FDA reports)
BREAST ABSCESS ( 7 FDA reports)
BRONCHIAL DISORDER ( 7 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 7 FDA reports)
CARCINOID SYNDROME ( 7 FDA reports)
CARCINOID TUMOUR ( 7 FDA reports)
CARDIAC SEPTAL DEFECT ( 7 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 7 FDA reports)
CARTILAGE ATROPHY ( 7 FDA reports)
CATHETER REMOVAL ( 7 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 7 FDA reports)
CHOLESTATIC LIVER INJURY ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 7 FDA reports)
COCCIDIOIDOMYCOSIS ( 7 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CRANIOCEREBRAL INJURY ( 7 FDA reports)
DELIRIUM TREMENS ( 7 FDA reports)
DENTAL PROSTHESIS USER ( 7 FDA reports)
DEVICE INEFFECTIVE ( 7 FDA reports)
DEVICE LEAKAGE ( 7 FDA reports)
DIAPHRAGMATIC HERNIA ( 7 FDA reports)
DRUG EFFECT INCREASED ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
DRUG TOLERANCE DECREASED ( 7 FDA reports)
DUODENAL PERFORATION ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
DYSMENORRHOEA ( 7 FDA reports)
EMBOLISM ARTERIAL ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
FEEDING TUBE COMPLICATION ( 7 FDA reports)
FEELING OF DESPAIR ( 7 FDA reports)
FUNGAL RASH ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTRIC PERFORATION ( 7 FDA reports)
GASTROINTESTINAL ULCER ( 7 FDA reports)
GENITAL EROSION ( 7 FDA reports)
GLIOBLASTOMA ( 7 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 7 FDA reports)
HAEMOCHROMATOSIS ( 7 FDA reports)
HEAD DISCOMFORT ( 7 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 7 FDA reports)
HOSPICE CARE ( 7 FDA reports)
HYPERKINESIA ( 7 FDA reports)
HYPERLACTACIDAEMIA ( 7 FDA reports)
HYPERTRICHOSIS ( 7 FDA reports)
HYPERVISCOSITY SYNDROME ( 7 FDA reports)
INJECTION SITE SCAB ( 7 FDA reports)
INTRACRANIAL HAEMATOMA ( 7 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 7 FDA reports)
LARYNGOSPASM ( 7 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 7 FDA reports)
LIP DISORDER ( 7 FDA reports)
LIVER TRANSPLANT REJECTION ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
LYMPHANGITIS ( 7 FDA reports)
LYMPHATIC OBSTRUCTION ( 7 FDA reports)
LYMPHOCELE ( 7 FDA reports)
LYMPHOCYTIC INFILTRATION ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 7 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 7 FDA reports)
MEDIASTINAL MASS ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
MENINGORRHAGIA ( 7 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 7 FDA reports)
METASTASES TO BONE MARROW ( 7 FDA reports)
METASTASES TO THORAX ( 7 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
MUSCLE RUPTURE ( 7 FDA reports)
MYOCARDIAL FIBROSIS ( 7 FDA reports)
NASAL OEDEMA ( 7 FDA reports)
NECK INJURY ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
NEUROENDOCRINE TUMOUR ( 7 FDA reports)
NEUTROPENIC COLITIS ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
NIPPLE PAIN ( 7 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 7 FDA reports)
OBSTRUCTIVE UROPATHY ( 7 FDA reports)
OCCULT BLOOD ( 7 FDA reports)
OCULAR HYPERTENSION ( 7 FDA reports)
OPTIC ATROPHY ( 7 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 7 FDA reports)
OTITIS EXTERNA FUNGAL ( 7 FDA reports)
OTOTOXICITY ( 7 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 7 FDA reports)
PACEMAKER COMPLICATION ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 7 FDA reports)
PANCREATITIS RELAPSING ( 7 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 7 FDA reports)
PELVIC FLUID COLLECTION ( 7 FDA reports)
PEMPHIGOID ( 7 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 7 FDA reports)
PETIT MAL EPILEPSY ( 7 FDA reports)
PLATELET AGGREGATION INCREASED ( 7 FDA reports)
PLEURAL HAEMORRHAGE ( 7 FDA reports)
PNEUMOMEDIASTINUM ( 7 FDA reports)
PNEUMONIA HAEMOPHILUS ( 7 FDA reports)
PNEUMOPERITONEUM ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
POST PROCEDURAL BILE LEAK ( 7 FDA reports)
PROCTITIS ( 7 FDA reports)
PROSTATITIS ( 7 FDA reports)
PROSTHESIS USER ( 7 FDA reports)
PSYCHOMOTOR RETARDATION ( 7 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 7 FDA reports)
RENAL LIPOMATOSIS ( 7 FDA reports)
RESPIRATORY ALKALOSIS ( 7 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 7 FDA reports)
RETINAL ARTERY OCCLUSION ( 7 FDA reports)
RETROPERITONEAL HAEMATOMA ( 7 FDA reports)
SARCOMA ( 7 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 7 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 7 FDA reports)
SELF-INJURIOUS IDEATION ( 7 FDA reports)
SERUM FERRITIN DECREASED ( 7 FDA reports)
SEXUAL DYSFUNCTION ( 7 FDA reports)
SKIN NODULE ( 7 FDA reports)
SKIN SWELLING ( 7 FDA reports)
SKULL FRACTURE ( 7 FDA reports)
SOMATOFORM DISORDER ( 7 FDA reports)
SOPOR ( 7 FDA reports)
SPLINT APPLICATION ( 7 FDA reports)
SPUTUM PURULENT ( 7 FDA reports)
SPUTUM RETENTION ( 7 FDA reports)
STENOTROPHOMONAS INFECTION ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
SYSTOLIC DYSFUNCTION ( 7 FDA reports)
T-CELL LYMPHOMA ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
THERAPY REGIMEN CHANGED ( 7 FDA reports)
THROMBECTOMY ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 7 FDA reports)
TRACHEAL HAEMORRHAGE ( 7 FDA reports)
TRANSPLANT FAILURE ( 7 FDA reports)
TRAUMATIC LIVER INJURY ( 7 FDA reports)
ULNA FRACTURE ( 7 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 7 FDA reports)
VENTRICULAR DYSKINESIA ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 7 FDA reports)
MYOPIA ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 6 FDA reports)
ONYCHOCLASIS ( 6 FDA reports)
OOPHORECTOMY ( 6 FDA reports)
OVARIAN CANCER RECURRENT ( 6 FDA reports)
OXYGEN SATURATION ABNORMAL ( 6 FDA reports)
PANCREATIC NECROSIS ( 6 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 6 FDA reports)
PANCREATIC PSEUDOCYST ( 6 FDA reports)
PAPILLOEDEMA ( 6 FDA reports)
PARANASAL SINUS DISCOMFORT ( 6 FDA reports)
PARATHYROID DISORDER ( 6 FDA reports)
PARATHYROID TUMOUR BENIGN ( 6 FDA reports)
PARESIS ( 6 FDA reports)
PEDAL PULSE DECREASED ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 6 FDA reports)
PERIANAL ABSCESS ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PLEURAL DECORTICATION ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
PNEUMONITIS CHEMICAL ( 6 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 6 FDA reports)
POST PROCEDURAL NAUSEA ( 6 FDA reports)
POST PROCEDURAL VOMITING ( 6 FDA reports)
POSTPARTUM DISORDER ( 6 FDA reports)
PULPITIS DENTAL ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RADIATION PNEUMONITIS ( 6 FDA reports)
RADICULITIS CERVICAL ( 6 FDA reports)
RECTAL PROLAPSE ( 6 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 6 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 6 FDA reports)
RENAL NEOPLASM ( 6 FDA reports)
RENAL TRANSPLANT ( 6 FDA reports)
RETINAL DEGENERATION ( 6 FDA reports)
RETINAL DISORDER ( 6 FDA reports)
RETINAL VASCULAR DISORDER ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
RHEUMATIC HEART DISEASE ( 6 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SALPINGITIS ( 6 FDA reports)
SHOCK HYPOGLYCAEMIC ( 6 FDA reports)
SIMPLE PARTIAL SEIZURES ( 6 FDA reports)
SKIN TOXICITY ( 6 FDA reports)
SLEEP ATTACKS ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
STILL'S DISEASE ADULT ONSET ( 6 FDA reports)
SUICIDAL BEHAVIOUR ( 6 FDA reports)
TIC ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TOOTH REPAIR ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TOXIC NODULAR GOITRE ( 6 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 6 FDA reports)
TUMOUR FLARE ( 6 FDA reports)
URETERIC DILATATION ( 6 FDA reports)
VASCULAR COMPRESSION ( 6 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 6 FDA reports)
VENTRICULAR FAILURE ( 6 FDA reports)
VERBAL ABUSE ( 6 FDA reports)
VITAMIN B12 DECREASED ( 6 FDA reports)
VITAMIN B12 INCREASED ( 6 FDA reports)
VOLVULUS ( 6 FDA reports)
WEIGHT ABNORMAL ( 6 FDA reports)
WEIGHT LOSS POOR ( 6 FDA reports)
XANTHOPSIA ( 6 FDA reports)
ABDOMINAL WALL ABSCESS ( 6 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 6 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 6 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
ADENOVIRUS INFECTION ( 6 FDA reports)
ADRENAL NEOPLASM ( 6 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 6 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 6 FDA reports)
ALCOHOLISM ( 6 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 6 FDA reports)
AMAUROSIS FUGAX ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANAL INFLAMMATION ( 6 FDA reports)
ANASTOMOTIC ULCER ( 6 FDA reports)
ANION GAP DECREASED ( 6 FDA reports)
ANION GAP INCREASED ( 6 FDA reports)
ANORECTAL DISCOMFORT ( 6 FDA reports)
ANTIBODY TEST POSITIVE ( 6 FDA reports)
APPENDICECTOMY ( 6 FDA reports)
ARACHNOIDITIS ( 6 FDA reports)
ARTERIAL RUPTURE ( 6 FDA reports)
ASCITES INFECTION ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
BACTERIA STOOL IDENTIFIED ( 6 FDA reports)
BASOPHIL COUNT INCREASED ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BILIARY CIRRHOSIS ( 6 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 6 FDA reports)
BLOOD CORTISOL DECREASED ( 6 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 6 FDA reports)
BLOOD FOLATE DECREASED ( 6 FDA reports)
BLOOD GLUCOSE ( 6 FDA reports)
BLOOD IRON INCREASED ( 6 FDA reports)
BLOOD OESTROGEN DECREASED ( 6 FDA reports)
BLOOD OSMOLARITY DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD URINE ( 6 FDA reports)
BONE FORMATION DECREASED ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BRAIN HYPOXIA ( 6 FDA reports)
BREAST DISORDER ( 6 FDA reports)
CALCIPHYLAXIS ( 6 FDA reports)
CARBON DIOXIDE ABNORMAL ( 6 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 6 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 6 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 6 FDA reports)
CELL DEATH ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 6 FDA reports)
CERVIX CARCINOMA ( 6 FDA reports)
CHOLESTEROSIS ( 6 FDA reports)
CHOREA ( 6 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 6 FDA reports)
COAGULATION TIME ABNORMAL ( 6 FDA reports)
COGWHEEL RIGIDITY ( 6 FDA reports)
COLONOSCOPY ABNORMAL ( 6 FDA reports)
COLORECTAL CANCER METASTATIC ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 6 FDA reports)
CRANIOTOMY ( 6 FDA reports)
CRYPTORCHISM ( 6 FDA reports)
CYSTITIS RADIATION ( 6 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DIABETES INSIPIDUS ( 6 FDA reports)
DIABETIC GASTROPATHY ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DRUG INTERACTION POTENTIATION ( 6 FDA reports)
DRUG RESISTANCE ( 6 FDA reports)
DRY GANGRENE ( 6 FDA reports)
DUODENAL POLYP ( 6 FDA reports)
DYSPAREUNIA ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 6 FDA reports)
ELECTROLYTE DEPLETION ( 6 FDA reports)
ENCEPHALITIS HERPES ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 6 FDA reports)
EXCESSIVE EYE BLINKING ( 6 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
FAECES HARD ( 6 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FOOD ALLERGY ( 6 FDA reports)
FOOD CRAVING ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
FRACTURE DELAYED UNION ( 6 FDA reports)
GALACTORRHOEA ( 6 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 6 FDA reports)
GASTRODUODENITIS ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GINGIVAL BLISTER ( 6 FDA reports)
GLOMERULOSCLEROSIS ( 6 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 6 FDA reports)
HAEMOGLOBIN ( 6 FDA reports)
HAEMOGLOBIN ABNORMAL ( 6 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEPATIC HAEMATOMA ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
HYPERTHERMIA MALIGNANT ( 6 FDA reports)
IMPLANT SITE THROMBOSIS ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 6 FDA reports)
INCISION SITE ERYTHEMA ( 6 FDA reports)
INCISION SITE HAEMATOMA ( 6 FDA reports)
INCISION SITE HAEMORRHAGE ( 6 FDA reports)
INCORRECT STORAGE OF DRUG ( 6 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INFUSION SITE PAIN ( 6 FDA reports)
INGUINAL HERNIA REPAIR ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTERCOSTAL RETRACTION ( 6 FDA reports)
INTERNAL HERNIA ( 6 FDA reports)
INTESTINAL MASS ( 6 FDA reports)
INTESTINAL POLYP ( 6 FDA reports)
INTRACRANIAL HYPOTENSION ( 6 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 6 FDA reports)
INTUBATION ( 6 FDA reports)
LAZINESS ( 6 FDA reports)
LENTIGO ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LOW BIRTH WEIGHT BABY ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYMPH GLAND INFECTION ( 6 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 6 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 6 FDA reports)
MACULAR HOLE ( 6 FDA reports)
MAMMOGRAM ABNORMAL ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
MONARTHRITIS ( 6 FDA reports)
MONOCYTOSIS ( 6 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 6 FDA reports)
MYELITIS TRANSVERSE ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 6 FDA reports)
ACCIDENTAL DEATH ( 5 FDA reports)
ACID BASE BALANCE ABNORMAL ( 5 FDA reports)
ACUTE LUNG INJURY ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANAL SPHINCTER ATONY ( 5 FDA reports)
ANGIOLIPOMA ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANOGENITAL WARTS ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
APPENDICITIS PERFORATED ( 5 FDA reports)
APPLICATION SITE DISCOLOURATION ( 5 FDA reports)
APTYALISM ( 5 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 5 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 5 FDA reports)
ARTHRODESIS ( 5 FDA reports)
ARTHROSCOPY ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 5 FDA reports)
BACTERIAL CULTURE POSITIVE ( 5 FDA reports)
BACTERIAL PYELONEPHRITIS ( 5 FDA reports)
BENIGN NEOPLASM ( 5 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 5 FDA reports)
BIOPSY ( 5 FDA reports)
BIOPSY BREAST ( 5 FDA reports)
BLADDER CYST ( 5 FDA reports)
BLADDER DISTENSION ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD KETONE BODY ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 5 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 5 FDA reports)
BLOOD UREA ABNORMAL ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BONE FISTULA ( 5 FDA reports)
BONE SARCOMA ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 5 FDA reports)
BREAST OEDEMA ( 5 FDA reports)
BRONCHOSTENOSIS ( 5 FDA reports)
BUNION OPERATION ( 5 FDA reports)
CARDIAC AMYLOIDOSIS ( 5 FDA reports)
CARDIAC DISCOMFORT ( 5 FDA reports)
CARDIAC PERFORATION ( 5 FDA reports)
CATHETER SITE PAIN ( 5 FDA reports)
CEREBRAL CALCIFICATION ( 5 FDA reports)
CERVIX CARCINOMA RECURRENT ( 5 FDA reports)
CHEST WALL MASS ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHOLANGITIS ACUTE ( 5 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 5 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 5 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 5 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CORONARY ARTERY REOCCLUSION ( 5 FDA reports)
CORRECTIVE LENS USER ( 5 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 5 FDA reports)
CUBITAL TUNNEL SYNDROME ( 5 FDA reports)
CYCLOTHYMIC DISORDER ( 5 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DENTAL NECROSIS ( 5 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DRUG DETOXIFICATION ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
ELECTRIC SHOCK ( 5 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 5 FDA reports)
ENDARTERECTOMY ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
ENTEROBACTER PNEUMONIA ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
EXTRADURAL ABSCESS ( 5 FDA reports)
EXTRADURAL HAEMATOMA ( 5 FDA reports)
EYEBALL RUPTURE ( 5 FDA reports)
EYELASH DISCOLOURATION ( 5 FDA reports)
FEAR OF DISEASE ( 5 FDA reports)
FINGER AMPUTATION ( 5 FDA reports)
FLUID IMBALANCE ( 5 FDA reports)
FOLATE DEFICIENCY ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
FUNGAL PERITONITIS ( 5 FDA reports)
GAMMOPATHY ( 5 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 5 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 5 FDA reports)
GRAFT COMPLICATION ( 5 FDA reports)
GRAFT INFECTION ( 5 FDA reports)
GRANULOCYTE COUNT INCREASED ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
GUTTATE PSORIASIS ( 5 FDA reports)
H1N1 INFLUENZA ( 5 FDA reports)
HAEMOBILIA ( 5 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 5 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 5 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HEMIANOPIA ( 5 FDA reports)
HEPATITIS C RNA INCREASED ( 5 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 5 FDA reports)
HYPERADRENALISM ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPOPROTHROMBINAEMIA ( 5 FDA reports)
HYPOVITAMINOSIS ( 5 FDA reports)
IMPAIRED FASTING GLUCOSE ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 5 FDA reports)
INFUSION SITE PRURITUS ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INSULIN RESISTANCE ( 5 FDA reports)
INTESTINAL RESECTION ( 5 FDA reports)
INTRASPINAL ABSCESS ( 5 FDA reports)
JOINT INJECTION ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
LACTOSE INTOLERANCE ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LESION EXCISION ( 5 FDA reports)
LEUKAEMIA PLASMACYTIC ( 5 FDA reports)
LEUKOPLAKIA ORAL ( 5 FDA reports)
LICHENIFICATION ( 5 FDA reports)
LIGHT CHAIN ANALYSIS ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LOCKED-IN SYNDROME ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
MESOTHELIOMA ( 5 FDA reports)
METASTASES TO OVARY ( 5 FDA reports)
METASTATIC LYMPHOMA ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MORTON'S NEUROMA ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NEUROBLASTOMA RECURRENT ( 5 FDA reports)
NEUROMA ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NIGHT BLINDNESS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
OBSTRUCTION ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
ONYCHOLYSIS ( 5 FDA reports)
OPTIC NERVE INJURY ( 5 FDA reports)
ORAL PRURITUS ( 5 FDA reports)
ORAL SOFT TISSUE DISORDER ( 5 FDA reports)
ORTHOSIS USER ( 5 FDA reports)
OS TRIGONUM SYNDROME ( 5 FDA reports)
OSTEOMALACIA ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PALATAL DISORDER ( 5 FDA reports)
PARADOXICAL DRUG REACTION ( 5 FDA reports)
PERICARDIAL DRAINAGE ( 5 FDA reports)
PERINEPHRIC ABSCESS ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PLACENTAL DISORDER ( 5 FDA reports)
PNEUMONIA ESCHERICHIA ( 5 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 5 FDA reports)
POOR SUCKING REFLEX ( 5 FDA reports)
POST POLIO SYNDROME ( 5 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
POSTOPERATIVE ABSCESS ( 5 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
PROCEDURAL VOMITING ( 5 FDA reports)
PRODUCT PACKAGING ISSUE ( 5 FDA reports)
PROLONGED EXPIRATION ( 5 FDA reports)
PROPOFOL INFUSION SYNDROME ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PROSTATISM ( 5 FDA reports)
PROTEIN URINE ABSENT ( 5 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 5 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 5 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 5 FDA reports)
PSOAS ABSCESS ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
REACTIVE PSYCHOSIS ( 5 FDA reports)
RECTOCELE REPAIR ( 5 FDA reports)
REFLUX GASTRITIS ( 5 FDA reports)
REHABILITATION THERAPY ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETICULOCYTE COUNT DECREASED ( 5 FDA reports)
RETICULOCYTE COUNT INCREASED ( 5 FDA reports)
RETINOPATHY HYPERTENSIVE ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SCAN ABNORMAL ( 5 FDA reports)
SENILE DEMENTIA ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
SPLEEN CONGESTION ( 5 FDA reports)
SPLENIC LESION ( 5 FDA reports)
SPUTUM ABNORMAL ( 5 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 5 FDA reports)
STOMATITIS NECROTISING ( 5 FDA reports)
STOOL ANALYSIS ABNORMAL ( 5 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 5 FDA reports)
TEETH BRITTLE ( 5 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 5 FDA reports)
THORACOSTOMY ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
THYROIDECTOMY ( 5 FDA reports)
THYROIDITIS ( 5 FDA reports)
THYROXINE DECREASED ( 5 FDA reports)
THYROXINE FREE INCREASED ( 5 FDA reports)
TOE OPERATION ( 5 FDA reports)
TONGUE BITING ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 5 FDA reports)
UMBILICAL HERNIA REPAIR ( 5 FDA reports)
URETHRAL STENOSIS ( 5 FDA reports)
URINARY SEDIMENT ABNORMAL ( 5 FDA reports)
URINE CALCIUM INCREASED ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VASCULITIC RASH ( 5 FDA reports)
VASCULITIS NECROTISING ( 5 FDA reports)
VASOSPASM ( 5 FDA reports)
VENOUS STENOSIS ( 5 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 5 FDA reports)
VITAMIN B1 INCREASED ( 5 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WHITE BLOOD CELL DISORDER ( 5 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 5 FDA reports)
WOUND NECROSIS ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOSCLEROSIS ( 4 FDA reports)
NARCOTIC INTOXICATION ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NEOPLASM PROSTATE ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEUTROPHIL COUNT ( 4 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 4 FDA reports)
NIPPLE DISORDER ( 4 FDA reports)
NODAL OSTEOARTHRITIS ( 4 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OEDEMATOUS PANCREATITIS ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
ORAL LICHEN PLANUS ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
OSTEOSARCOMA METASTATIC ( 4 FDA reports)
OVARIAN ABSCESS ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PENILE ULCERATION ( 4 FDA reports)
PERICARDITIS LUPUS ( 4 FDA reports)
PERINEURIAL CYST ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PERITONEAL DISORDER ( 4 FDA reports)
PERITONEAL EFFUSION ( 4 FDA reports)
PERITONITIS SCLEROSING ( 4 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
PHLEBITIS SUPERFICIAL ( 4 FDA reports)
PILONIDAL CYST ( 4 FDA reports)
PIRIFORMIS SYNDROME ( 4 FDA reports)
PLEURODESIS ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PROCEDURAL SITE REACTION ( 4 FDA reports)
PRODUCT LABEL ISSUE ( 4 FDA reports)
PROSTATE CANCER RECURRENT ( 4 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 4 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 4 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 4 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL CANCER METASTATIC ( 4 FDA reports)
RENAL VESSEL DISORDER ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 4 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 4 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 4 FDA reports)
SEIZURE ANOXIC ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SERRATIA TEST POSITIVE ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SICKLE CELL TRAIT ( 4 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN CYST EXCISION ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
SOFT TISSUE MASS ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
STARVATION ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
TELANGIECTASIA ( 4 FDA reports)
TEMPORAL LOBE EPILEPSY ( 4 FDA reports)
TESTICULAR DISORDER ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
THROAT CANCER ( 4 FDA reports)
THYROID GLAND CANCER ( 4 FDA reports)
THYROID MASS ( 4 FDA reports)
TINEA INFECTION ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TORULOPSIS INFECTION ( 4 FDA reports)
TOXIC SHOCK SYNDROME ( 4 FDA reports)
TRACHEAL OBSTRUCTION ( 4 FDA reports)
TRICHIASIS ( 4 FDA reports)
TROPONIN T INCREASED ( 4 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
URETHRAL PAIN ( 4 FDA reports)
URETHRAL SPASM ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VEIN WALL HYPERTROPHY ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VIRAL LOAD INCREASED ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
VOCAL CORD POLYP ( 4 FDA reports)
VULVAR DYSPLASIA ( 4 FDA reports)
WEANING FAILURE ( 4 FDA reports)
WOUND TREATMENT ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 4 FDA reports)
ABNORMAL CLOTTING FACTOR ( 4 FDA reports)
ABSCESS SOFT TISSUE ( 4 FDA reports)
ACANTHOSIS NIGRICANS ( 4 FDA reports)
ACCELERATED HYPERTENSION ( 4 FDA reports)
ACCIDENTAL POISONING ( 4 FDA reports)
ACHLORHYDRIA ( 4 FDA reports)
ACNE PUSTULAR ( 4 FDA reports)
ADHESIOLYSIS ( 4 FDA reports)
ALDOLASE INCREASED ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ALLERGY TO CHEMICALS ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANGIODYSPLASIA ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 4 FDA reports)
APICAL GRANULOMA ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APPARENT LIFE THREATENING EVENT ( 4 FDA reports)
APPLICATION SITE DISCHARGE ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ATONIC SEIZURES ( 4 FDA reports)
AURA ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
AXILLARY VEIN THROMBOSIS ( 4 FDA reports)
BACILLUS INFECTION ( 4 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
BENIGN RENAL NEOPLASM ( 4 FDA reports)
BICYTOPENIA ( 4 FDA reports)
BILIARY NEOPLASM ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 4 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 4 FDA reports)
BLOOD HOMOCYSTEINE ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BLUE TOE SYNDROME ( 4 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
BONE INFECTION ( 4 FDA reports)
BOVINE TUBERCULOSIS ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BRAIN MIDLINE SHIFT ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BREAST DISORDER FEMALE ( 4 FDA reports)
BREAST FIBROSIS ( 4 FDA reports)
BREAST INFLAMMATION ( 4 FDA reports)
BREAST MICROCALCIFICATION ( 4 FDA reports)
BREAST NECROSIS ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BRONCHOPNEUMOPATHY ( 4 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CANDIDA TEST POSITIVE ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 4 FDA reports)
CARDIAC CIRRHOSIS ( 4 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 4 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 4 FDA reports)
CAROTID ARTERY ANEURYSM ( 4 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 4 FDA reports)
CAROTID ENDARTERECTOMY ( 4 FDA reports)
CATHETER SITE ERYTHEMA ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL HYPOPERFUSION ( 4 FDA reports)
CEREBRAL PALSY ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 4 FDA reports)
CHEYNE-STOKES RESPIRATION ( 4 FDA reports)
CHOLESTEROL GRANULOMA ( 4 FDA reports)
CHROMATOPSIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COGNITIVE DETERIORATION ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CRYOGLOBULINAEMIA ( 4 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
CUTANEOUS SARCOIDOSIS ( 4 FDA reports)
CUTANEOUS VASCULITIS ( 4 FDA reports)
DEATH OF RELATIVE ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DEVELOPMENTAL DELAY ( 4 FDA reports)
DEVICE DAMAGE ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIET REFUSAL ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DYSKINESIA OESOPHAGEAL ( 4 FDA reports)
ECTROPION ( 4 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 4 FDA reports)
ENDOCRINE DISORDER ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 4 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 4 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 4 FDA reports)
ENTEROBACTER SEPSIS ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
ERYTHROMELALGIA ( 4 FDA reports)
EX-TOBACCO USER ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
EYES SUNKEN ( 4 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FEELING GUILTY ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FOOT CRUSHING ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GAMBLING ( 4 FDA reports)
GANGLION ( 4 FDA reports)
GASTRIC VARICES ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 4 FDA reports)
GENITAL BURNING SENSATION ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GOUTY TOPHUS ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
GROWTH RETARDATION ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMATOCRIT ABNORMAL ( 4 FDA reports)
HAEMATOMA EVACUATION ( 4 FDA reports)
HEAT RASH ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC CANCER METASTATIC ( 4 FDA reports)
HEPATIC ENZYME DECREASED ( 4 FDA reports)
HEPATIC INFECTION ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATORENAL FAILURE ( 4 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERPROLACTINAEMIA ( 4 FDA reports)
ILIAC ARTERY OCCLUSION ( 4 FDA reports)
IMPLANT SITE EFFUSION ( 4 FDA reports)
IMPLANT SITE ERYTHEMA ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INFUSION SITE EXTRAVASATION ( 4 FDA reports)
INJECTION SITE OEDEMA ( 4 FDA reports)
INJECTION SITE PAPULE ( 4 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL FISTULA ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRIS ADHESIONS ( 4 FDA reports)
ISCHAEMIC ULCER ( 4 FDA reports)
JOINT INSTABILITY ( 4 FDA reports)
JOINT SURGERY ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LACRIMATION DECREASED ( 4 FDA reports)
LEPROSY ( 4 FDA reports)
LICHEN PLANUS ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LIMB DEFORMITY ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIP PAIN ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG LOBECTOMY ( 4 FDA reports)
LUNG TRANSPLANT ( 4 FDA reports)
LUPUS PNEUMONITIS ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MAMMARY DUCT ECTASIA ( 4 FDA reports)
MARITAL PROBLEM ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 4 FDA reports)
MECHANICAL ILEUS ( 4 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 4 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 4 FDA reports)
MENINGEAL DISORDER ( 4 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 4 FDA reports)
MITRAL VALVE SCLEROSIS ( 4 FDA reports)
MOANING ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MUSCLE ENZYME INCREASED ( 4 FDA reports)
MYCOBACTERIAL INFECTION ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
ABDOMINAL INJURY ( 3 FDA reports)
ABDOMINAL OPERATION ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACETABULUM FRACTURE ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE CHEST SYNDROME ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
ADRENAL CARCINOMA ( 3 FDA reports)
ADRENAL CORTEX NECROSIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALCOHOLIC ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ALLERGIC SINUSITIS ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANAPHYLACTOID SYNDROME OF PREGNANCY ( 3 FDA reports)
ANDROGENS DECREASED ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
ANHIDROSIS ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTICOAGULANT THERAPY ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
ANTITHROMBIN III DECREASED ( 3 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC BRUIT ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE SCAR ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
ARTERIAL STENT INSERTION ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 3 FDA reports)
ASPIRATION BREAST ( 3 FDA reports)
ATHERECTOMY ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BACTERIAL TOXAEMIA ( 3 FDA reports)
BASE EXCESS DECREASED ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 3 FDA reports)
BEZOAR ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BIOPSY HEART ABNORMAL ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 3 FDA reports)
BLADDER NECK OBSTRUCTION ( 3 FDA reports)
BLADDER TRABECULATION ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLASTOMYCOSIS ( 3 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID DECREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 3 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 3 FDA reports)
BONE FORMATION TEST ABNORMAL ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BREAST HAEMORRHAGE ( 3 FDA reports)
BREAST INDURATION ( 3 FDA reports)
BRONCHIAL HYPERACTIVITY ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARCINOID TUMOUR PULMONARY ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC MONITORING ( 3 FDA reports)
CARDIAC MYXOMA ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID ARTERY THROMBOSIS ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 3 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 3 FDA reports)
CEREBRAL FUNGAL INFECTION ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHOLANGITIS SCLEROSING ( 3 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 3 FDA reports)
CONJUNCTIVAL DISORDER ( 3 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CORYNEBACTERIUM SEPSIS ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CRYOTHERAPY ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CSF TEST ABNORMAL ( 3 FDA reports)
CUTIS LAXA ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DENTAL CLEANING ( 3 FDA reports)
DEVICE INTOLERANCE ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DEVICE STIMULATION ISSUE ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DISSOCIATIVE FUGUE ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 3 FDA reports)
DRESSLER'S SYNDROME ( 3 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DUODENOGASTRIC REFLUX ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ENCEPHALITIS VIRAL ( 3 FDA reports)
ENDOSCOPY ABNORMAL ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
ENTEROCELE ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EYE INFECTION INTRAOCULAR ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
FACIAL OPERATION ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 3 FDA reports)
GAIT DEVIATION ( 3 FDA reports)
GALLBLADDER ABSCESS ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTRIC PH DECREASED ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GENE MUTATION ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GRANULOMA SKIN ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOPHILUS SEPSIS ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HALLUCINATION, TACTILE ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEART AND LUNG TRANSPLANT ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HEPATITIS C POSITIVE ( 3 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 3 FDA reports)
HERPES DERMATITIS ( 3 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HYALOSIS ASTEROID ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERINSULINISM ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOPLASTIC ANAEMIA ( 3 FDA reports)
ICHTHYOSIS ACQUIRED ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
ILIAC VEIN OCCLUSION ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 3 FDA reports)
INFUSION SITE INDURATION ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE CELLULITIS ( 3 FDA reports)
INJECTION SITE EXFOLIATION ( 3 FDA reports)
INJECTION SITE PHLEBITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JOINT ADHESION ( 3 FDA reports)
KUSSMAUL RESPIRATION ( 3 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LARYNGEAL STENOSIS ( 3 FDA reports)
LDL/HDL RATIO DECREASED ( 3 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 3 FDA reports)
LERICHE SYNDROME ( 3 FDA reports)
LEUKOARAIOSIS ( 3 FDA reports)
LIGAMENT INJURY ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIPID METABOLISM DISORDER ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOCAL ANAESTHESIA ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MEDICAL DEVICE PAIN ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASES TO HEART ( 3 FDA reports)
METASTASES TO LARGE INTESTINE ( 3 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 3 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 3 FDA reports)
MIXED LIVER INJURY ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MUSCLE FIBROSIS ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYELOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MYOCARDIAL RUPTURE ( 3 FDA reports)
MYODESOPSIA ( 3 FDA reports)
MYOPATHY STEROID ( 3 FDA reports)
NAIL HYPERTROPHY ( 3 FDA reports)
NECROSIS ISCHAEMIC ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NERVE ROOT COMPRESSION ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OESOPHAGEAL IRRITATION ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 3 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 3 FDA reports)
OESTRADIOL DECREASED ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
OVARIAN ADENOMA ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
OXYGEN SATURATION ( 3 FDA reports)
PANCREAS TRANSPLANT ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PEPTIC ULCER PERFORATION ( 3 FDA reports)
PERFORMANCE FEAR ( 3 FDA reports)
PERIODONTAL OPERATION ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PERIPHERAL PULSE DECREASED ( 3 FDA reports)
PERIPHLEBITIS ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PERITONEAL ABSCESS ( 3 FDA reports)
PERITONEAL INFECTION ( 3 FDA reports)
PHAEOCHROMOCYTOMA ( 3 FDA reports)
PHANTOM PAIN ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PLASTIC SURGERY TO THE FACE ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PLEURAL CALCIFICATION ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PLEUROTHOTONUS ( 3 FDA reports)
PNEUMATOSIS ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONIA INFLUENZAL ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL CONSTIPATION ( 3 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 3 FDA reports)
POSTRENAL FAILURE ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PRODUCT CONTAMINATION ( 3 FDA reports)
PROSTATE INFECTION ( 3 FDA reports)
PROSTATIC OBSTRUCTION ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PSEUDO-BARTTER SYNDROME ( 3 FDA reports)
PSEUDOCYST ( 3 FDA reports)
PSEUDOMONAS BRONCHITIS ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
PUNCTURE SITE INFECTION ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
REACTION TO PRESERVATIVES ( 3 FDA reports)
RECTAL ADENOMA ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL ARTERY THROMBOSIS ( 3 FDA reports)
RENAL HAEMATOMA ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RESPIRATORY PARALYSIS ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RETICULOCYTOSIS ( 3 FDA reports)
RETINAL INFARCTION ( 3 FDA reports)
RETINAL SCAR ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETINOPATHY PROLIFERATIVE ( 3 FDA reports)
RETROPERITONEAL NEOPLASM ( 3 FDA reports)
SALIVARY GLAND CANCER ( 3 FDA reports)
SALPINGECTOMY ( 3 FDA reports)
SCROTAL DISORDER ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SEBACEOUS CYST EXCISION ( 3 FDA reports)
SEBACEOUS HYPERPLASIA ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SMALL INTESTINE OPERATION ( 3 FDA reports)
SOFT TISSUE NECROSIS ( 3 FDA reports)
SOMATISATION DISORDER ( 3 FDA reports)
SPEECH REHABILITATION ( 3 FDA reports)
SPINAL CORD INJURY CERVICAL ( 3 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 3 FDA reports)
SPIROMETRY ABNORMAL ( 3 FDA reports)
SPLENIC HAEMATOMA ( 3 FDA reports)
SPLENIC NECROSIS ( 3 FDA reports)
SPONDYLITIC MYELOPATHY ( 3 FDA reports)
SPONTANEOUS HAEMATOMA ( 3 FDA reports)
STEROID THERAPY ( 3 FDA reports)
STOMACH MASS ( 3 FDA reports)
SUBMANDIBULAR MASS ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SURGICAL STAPLING ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
SUTURE INSERTION ( 3 FDA reports)
SYSTEMIC SCLEROSIS ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
TETANY ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBIN TIME PROLONGED ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID CANCER METASTATIC ( 3 FDA reports)
THYROTOXIC CRISIS ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 3 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TUMOUR PAIN ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 3 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URETHRITIS ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 3 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINITIS ( 3 FDA reports)
VAGINITIS ATROPHIC ( 3 FDA reports)
VASCULAR GRAFT COMPLICATION ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 3 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
VIRAL CARDIOMYOPATHY ( 3 FDA reports)
VIRAL RHINITIS ( 3 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 3 FDA reports)
WANDERING PACEMAKER ( 3 FDA reports)
WHITE CLOT SYNDROME ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
WOUND EVISCERATION ( 3 FDA reports)
WOUND INFECTION BACTERIAL ( 3 FDA reports)
X-RAY LIMB ABNORMAL ( 3 FDA reports)
YAWNING ( 3 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NAIL AVULSION ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NAIL TOXICITY ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASAL TURBINATE ABNORMALITY ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NELSON'S SYNDROME ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OEDEMA NEONATAL ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
OMENTUM NEOPLASM ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARANASAL CYST ( 2 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PARATHYROID TUMOUR ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERICARDIAL FIBROSIS ( 2 FDA reports)
PERICARDITIS RHEUMATIC ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERITONEAL HAEMATOMA ( 2 FDA reports)
PERIUMBILICAL ABSCESS ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHOTOCOAGULATION ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLASMA CELLS PRESENT ( 2 FDA reports)
PLATELET DESTRUCTION INCREASED ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 2 FDA reports)
POST-TRAUMATIC HEADACHE ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE CONSTIPATION ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 2 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT BARCODE ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROTEUS TEST POSITIVE ( 2 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PULMONARY PNEUMATOCELE ( 2 FDA reports)
PULMONARY VALVE REPLACEMENT ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PYELECTASIA ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYOMETRA ( 2 FDA reports)
PYONEPHROSIS ( 2 FDA reports)
PYOPNEUMOTHORAX ( 2 FDA reports)
RADIATION NEUROPATHY ( 2 FDA reports)
RADICULITIS BRACHIAL ( 2 FDA reports)
RADIOTHERAPY TO BRAIN ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL LYMPHOCELE ( 2 FDA reports)
RENAL SCAN ABNORMAL ( 2 FDA reports)
RENIN DECREASED ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY FATIGUE ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY SIGHS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINOPATHY OF PREMATURITY ( 2 FDA reports)
RETINOSCHISIS ( 2 FDA reports)
RETROGRADE EJACULATION ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RIB EXCISION ( 2 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALIVARY GLAND OPERATION ( 2 FDA reports)
SALMONELLA BACTERAEMIA ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SARCOMA OF SKIN ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SECONDARY SYPHILIS ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SOCIAL FEAR ( 2 FDA reports)
SOLAR ELASTOSIS ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINAL CORD INJURY THORACIC ( 2 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 2 FDA reports)
STENT MALFUNCTION ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STERNAL INJURY ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMATITIS HAEMORRHAGIC ( 2 FDA reports)
STOMATOCOCCAL INFECTION ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUCROSE INTOLERANCE ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
TESTICULAR CYST ( 2 FDA reports)
THALASSAEMIA BETA ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THROMBOEMBOLECTOMY ( 2 FDA reports)
THYROID OPERATION ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH IMPACTED ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TOXICOLOGIC TEST ( 2 FDA reports)
TRACHEAL CANCER ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRICHORRHEXIS ( 2 FDA reports)
TRICUSPID VALVE REPAIR ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TUMOUR RUPTURE ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINE POTASSIUM INCREASED ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE NEOPLASM ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICOCELE ( 2 FDA reports)
VASCULAR CAUTERISATION ( 2 FDA reports)
VASCULAR HEADACHE ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN C DEFICIENCY ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VOCAL CORD PARESIS ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVAL HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WEIGHT CONTROL ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
XEROPHTHALMIA ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACINETOBACTER BACTERAEMIA ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 2 FDA reports)
ACQUIRED PHIMOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANAL POLYP ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANALGESIC THERAPY ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANASTOMOTIC FISTULA ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANDROGENETIC ALOPECIA ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTIDEPRESSANT DRUG CLEARANCE DECREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTOGRAM ABNORMAL ( 2 FDA reports)
APHAKIA ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARCUS LIPOIDES ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARTERIAL FIBROSIS ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHROFIBROSIS ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASPIRATION JOINT ABNORMAL ( 2 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AURICULAR PERICHONDRITIS ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 2 FDA reports)
BACTERIAL FOOD POISONING ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BASAL GANGLIA INFARCTION ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BETA 2 MICROGLOBULIN DECREASED ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BIOPSY PANCREAS ABNORMAL ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD GLUCAGON ABNORMAL ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ( 2 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW GRANULOMA ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
BRONCHOSCOPY ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BRUCELLOSIS ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
CALCIFICATION OF MUSCLE ( 2 FDA reports)
CALCIUM IONISED ABNORMAL ( 2 FDA reports)
CALCIUM IONISED INCREASED ( 2 FDA reports)
CALCIUM METABOLISM DISORDER ( 2 FDA reports)
CANDIDA OSTEOMYELITIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC REHABILITATION THERAPY ( 2 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 2 FDA reports)
CATHETER CULTURE POSITIVE ( 2 FDA reports)
CAUTERY TO NOSE ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CD4/CD8 RATIO INCREASED ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CHEMICAL BURN OF SKIN ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLELITHOTOMY ( 2 FDA reports)
CHONDRECTOMY ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHONDROPLASTY ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 2 FDA reports)
COMPLEMENT FACTOR DECREASED ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL NAEVUS ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
COR PULMONALE CHRONIC ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORONA VIRUS INFECTION ( 2 FDA reports)
CORONARY BYPASS THROMBOSIS ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 2 FDA reports)
DEATH OF COMPANION ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEHYDROEPIANDROSTERONE TEST ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DEVICE BATTERY ISSUE ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DEVICE PACING ISSUE ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG THERAPY ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 2 FDA reports)
ECHOCARDIOGRAM ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELLIPTOCYTOSIS ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENDOCARDIAL DISEASE ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROBIASIS ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
EPIPHYSEAL DISORDER ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE DEGENERATIVE DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FAILURE TO CAPTURE ( 2 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FREE HAEMOGLOBIN PRESENT ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL ENDOCARDITIS ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
FUSOBACTERIUM INFECTION ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GAMMA RADIATION THERAPY TO PROSTATE ( 2 FDA reports)
GARDNERELLA INFECTION ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRITIS ALCOHOLIC ( 2 FDA reports)
GASTRO-INTESTINAL FISTULA ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 2 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 2 FDA reports)
GASTROSTOMY FAILURE ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENDER IDENTITY DISORDER ( 2 FDA reports)
GENITAL CANDIDIASIS ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEARING AID USER ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 2 FDA reports)
HEPATIC ARTERY ANEURYSM ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC VEIN DILATATION ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS D ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATITIS INFECTIOUS ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HEPATOBLASTOMA ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HIV TEST POSITIVE ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYPERADRENOCORTICISM ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPERMETABOLISM ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILIUM FRACTURE ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTED SEBACEOUS CYST ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE NERVE DAMAGE ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRIDOCELE ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
ISCHAEMIC LIMB PAIN ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT IRRIGATION ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LATENT SYPHILIS ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LEUKAEMIC INFILTRATION ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LEUKODYSTROPHY ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LOOSE ASSOCIATIONS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LUMBAR PUNCTURE ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPH NODE CANCER METASTATIC ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MASTOID ABSCESS ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 2 FDA reports)
MEDIASTINAL FIBROSIS ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
METASTASES TO THYROID ( 2 FDA reports)
MICROVASCULAR ANGINA ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MILK-ALKALI SYNDROME ( 2 FDA reports)
MINERAL DEFICIENCY ( 2 FDA reports)
MITRAL VALVE DISEASE MIXED ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUELLER'S MIXED TUMOUR ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYELOCYTE PRESENT ( 2 FDA reports)
ABDOMINAL EXPLORATION ( 1 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCESSORY NAVICULAR SYNDROME ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTINIC ELASTOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADRENAL CORTEX ATROPHY ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALPHA-2 MACROGLOBULIN INCREASED ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTERIOR CHAMBER FLARE ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATYPICAL FIBROXANTHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIAL TEST NEGATIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARIATRIC GASTRIC BALLOON INSERTION ( 1 FDA reports)
BARTHOLIN'S ABSCESS ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE CULTURE POSITIVE ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TEMPERATURE NORMAL ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOSCOPY NORMAL ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIUM PHOSPHATE PRODUCT INCREASED ( 1 FDA reports)
CALCULUS PROSTATIC ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON DIOXIDE ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC TELEMETRY ABNORMAL ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CAROTID PULSE INCREASED ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CARTILAGE DEVELOPMENT DISORDER ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS PASTEURELLA ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL DYSGENESIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBRAL SALT-WASTING SYNDROME ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CEREBROSPINAL FISTULA ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVIX OPERATION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHLAMYDIA IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOLESTATIC PRURITUS ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOT RETRACTION TIME SHORTENED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORTISOL FREE URINE DECREASED ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIECTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT ( 1 FDA reports)
CULTURE URINE NEGATIVE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEHYDROEPIANDROSTERONE DECREASED ( 1 FDA reports)
DELAYED ENGRAFTMENT ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE ALARM ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC BULLOSIS ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPEDESIS ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIURETIC THERAPY ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRAIN OF CEREBRAL SUBDURAL SPACE ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EATON-LAMBERT SYNDROME ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECTOPIC ACTH SYNDROME ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EISENMENGER'S SYNDROME ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIC COLITIS ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTRINSIC ILIAC VEIN COMPRESSION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYELASH THICKENING ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FAMILIAL PERIODIC PARALYSIS ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUCHS' SYNDROME ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OCCULT BLOOD POSITIVE ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENETIC COUNSELLING ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS MALE ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GITELMAN'S SYNDROME ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
HAEMATINURIA ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HEREDITARY CEREBRAL DEGENERATION ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOTHYROIDISM POSTOPERATIVE ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTED INSECT BITE ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PUSTULE ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE JOINT REDNESS ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSPIRATORY CAPACITY ABNORMAL ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
IVTH NERVE PARESIS ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
K-RAS GENE MUTATION ( 1 FDA reports)
KERATITIS VIRAL ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KWASHIORKOR ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEFT VENTRICULAR HEAVE ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LISTERIA ENCEPHALITIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LONG QT SYNDROME CONGENITAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGIOMA MALIGNANT ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL ENZYME DEFICIENCY ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYELOBLAST COUNT INCREASED ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NATURAL KILLER CELL COUNT DECREASED ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL LESION EXCISION ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGECTOMY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONYCHOMALACIA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHOPEDIC EXAMINATION ABNORMAL ( 1 FDA reports)
ORTNER'S SYNDROME ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOSARCOMA RECURRENT ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCOAST'S TUMOUR ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS ISLET CELL TRANSPLANT ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PINEAL GLAND CYST ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
PO2 ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POEMS SYNDROME ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYSTIC LIVER DISEASE ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOCHOLINESTERASE DEFICIENCY ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION EXPOSURE ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RATHKE'S CLEFT CYST ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL NUCLEATED MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL FUNCTION TEST ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL SALT-WASTING SYNDROME ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID FACTOR DECREASED ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALT CRAVING ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN BRAIN ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL IRRITATION ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHUNT BLOOD FLOW EXCESSIVE ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STROKE IN EVOLUTION ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TETRALOGY OF FALLOT REPAIR ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID ATROPHY ( 1 FDA reports)
THYROIDITIS ACUTE ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRISOMY 13 ( 1 FDA reports)
TRISOMY 8 ( 1 FDA reports)
TRUANCY ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETERIC DIVERSION OPERATION ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE ANALYSIS ( 1 FDA reports)
URINE ARSENIC INCREASED ( 1 FDA reports)
URINE CHLORIDE DECREASED ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VACCINATION FAILURE ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR DISSECTION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULOGRAM ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VERTIGO LABYRINTHINE ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIITH NERVE INJURY ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITAMIN K INCREASED ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)