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

DYSPNOEA ( 2389 FDA reports)
PAIN ( 2110 FDA reports)
NAUSEA ( 2045 FDA reports)
DIZZINESS ( 1858 FDA reports)
FATIGUE ( 1820 FDA reports)
ASTHENIA ( 1684 FDA reports)
DIARRHOEA ( 1627 FDA reports)
HYPOTENSION ( 1493 FDA reports)
ANXIETY ( 1376 FDA reports)
VOMITING ( 1352 FDA reports)
OEDEMA PERIPHERAL ( 1337 FDA reports)
MYOCARDIAL INFARCTION ( 1324 FDA reports)
CHEST PAIN ( 1262 FDA reports)
FALL ( 1257 FDA reports)
ATRIAL FIBRILLATION ( 1247 FDA reports)
PNEUMONIA ( 1191 FDA reports)
ANAEMIA ( 1179 FDA reports)
HYPERTENSION ( 1164 FDA reports)
HEADACHE ( 1157 FDA reports)
RENAL FAILURE ( 1097 FDA reports)
DRUG INEFFECTIVE ( 1052 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1026 FDA reports)
PAIN IN EXTREMITY ( 988 FDA reports)
RENAL FAILURE ACUTE ( 959 FDA reports)
PYREXIA ( 953 FDA reports)
DEHYDRATION ( 936 FDA reports)
ARTHRALGIA ( 917 FDA reports)
BACK PAIN ( 912 FDA reports)
WEIGHT DECREASED ( 894 FDA reports)
DEPRESSION ( 881 FDA reports)
FLUSHING ( 881 FDA reports)
PRURITUS ( 869 FDA reports)
INJURY ( 858 FDA reports)
DEATH ( 850 FDA reports)
SYNCOPE ( 847 FDA reports)
BLOOD GLUCOSE INCREASED ( 820 FDA reports)
CEREBROVASCULAR ACCIDENT ( 811 FDA reports)
ABDOMINAL PAIN ( 806 FDA reports)
BRADYCARDIA ( 781 FDA reports)
MALAISE ( 781 FDA reports)
CONFUSIONAL STATE ( 723 FDA reports)
GAIT DISTURBANCE ( 700 FDA reports)
INSOMNIA ( 700 FDA reports)
BLOOD PRESSURE INCREASED ( 696 FDA reports)
PLEURAL EFFUSION ( 670 FDA reports)
URINARY TRACT INFECTION ( 664 FDA reports)
RASH ( 658 FDA reports)
COUGH ( 657 FDA reports)
DECREASED APPETITE ( 646 FDA reports)
DRUG INTERACTION ( 637 FDA reports)
CORONARY ARTERY DISEASE ( 628 FDA reports)
PARAESTHESIA ( 617 FDA reports)
HAEMOGLOBIN DECREASED ( 603 FDA reports)
EMOTIONAL DISTRESS ( 588 FDA reports)
SEPSIS ( 583 FDA reports)
LOSS OF CONSCIOUSNESS ( 578 FDA reports)
CONSTIPATION ( 575 FDA reports)
HYPOAESTHESIA ( 565 FDA reports)
SOMNOLENCE ( 563 FDA reports)
MYALGIA ( 558 FDA reports)
CARDIAC ARREST ( 553 FDA reports)
ERYTHEMA ( 545 FDA reports)
RESPIRATORY FAILURE ( 539 FDA reports)
MUSCLE SPASMS ( 537 FDA reports)
BLOOD CREATININE INCREASED ( 531 FDA reports)
PALPITATIONS ( 531 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 528 FDA reports)
THROMBOCYTOPENIA ( 520 FDA reports)
ABDOMINAL PAIN UPPER ( 503 FDA reports)
TACHYCARDIA ( 501 FDA reports)
HYPERHIDROSIS ( 498 FDA reports)
MUSCULAR WEAKNESS ( 487 FDA reports)
CONDITION AGGRAVATED ( 464 FDA reports)
HEART RATE INCREASED ( 462 FDA reports)
DYSPHAGIA ( 452 FDA reports)
RENAL IMPAIRMENT ( 452 FDA reports)
TREMOR ( 443 FDA reports)
WEIGHT INCREASED ( 427 FDA reports)
FEELING ABNORMAL ( 425 FDA reports)
CARDIAC FAILURE ( 419 FDA reports)
CONVULSION ( 418 FDA reports)
UNEVALUABLE EVENT ( 414 FDA reports)
ANHEDONIA ( 413 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 412 FDA reports)
PULMONARY EMBOLISM ( 412 FDA reports)
DEEP VEIN THROMBOSIS ( 409 FDA reports)
CARDIAC DISORDER ( 393 FDA reports)
CHILLS ( 392 FDA reports)
CHEST DISCOMFORT ( 385 FDA reports)
CONTUSION ( 385 FDA reports)
ANGINA PECTORIS ( 382 FDA reports)
DIABETES MELLITUS ( 382 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 380 FDA reports)
INFECTION ( 380 FDA reports)
BLOOD PRESSURE DECREASED ( 369 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 368 FDA reports)
CELLULITIS ( 357 FDA reports)
MULTI-ORGAN FAILURE ( 357 FDA reports)
OSTEONECROSIS OF JAW ( 356 FDA reports)
PULMONARY OEDEMA ( 352 FDA reports)
ARRHYTHMIA ( 347 FDA reports)
VISION BLURRED ( 344 FDA reports)
COMPLETED SUICIDE ( 336 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 333 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 332 FDA reports)
DYSPEPSIA ( 332 FDA reports)
BRONCHITIS ( 331 FDA reports)
HYPOKALAEMIA ( 327 FDA reports)
ABDOMINAL DISCOMFORT ( 326 FDA reports)
FEAR ( 326 FDA reports)
MENTAL STATUS CHANGES ( 325 FDA reports)
NEUROPATHY PERIPHERAL ( 324 FDA reports)
PLATELET COUNT DECREASED ( 323 FDA reports)
HYPERKALAEMIA ( 320 FDA reports)
MUSCULOSKELETAL PAIN ( 318 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 317 FDA reports)
OSTEOARTHRITIS ( 315 FDA reports)
STRESS ( 312 FDA reports)
HAEMORRHAGE ( 311 FDA reports)
BALANCE DISORDER ( 310 FDA reports)
FEELING HOT ( 308 FDA reports)
PANCYTOPENIA ( 308 FDA reports)
RECTAL HAEMORRHAGE ( 308 FDA reports)
ECONOMIC PROBLEM ( 301 FDA reports)
RENAL FAILURE CHRONIC ( 300 FDA reports)
ATELECTASIS ( 299 FDA reports)
MEMORY IMPAIRMENT ( 298 FDA reports)
MOBILITY DECREASED ( 297 FDA reports)
OEDEMA ( 293 FDA reports)
HYPONATRAEMIA ( 291 FDA reports)
CARDIOMEGALY ( 287 FDA reports)
MITRAL VALVE INCOMPETENCE ( 281 FDA reports)
RHABDOMYOLYSIS ( 276 FDA reports)
JOINT SWELLING ( 271 FDA reports)
HYPOGLYCAEMIA ( 269 FDA reports)
RENAL INJURY ( 269 FDA reports)
ARTHRITIS ( 265 FDA reports)
ABDOMINAL DISTENSION ( 263 FDA reports)
EPISTAXIS ( 260 FDA reports)
HEART RATE DECREASED ( 260 FDA reports)
HYPERGLYCAEMIA ( 258 FDA reports)
HEART RATE IRREGULAR ( 257 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 256 FDA reports)
DRY MOUTH ( 250 FDA reports)
HYPOXIA ( 249 FDA reports)
HAEMATOCRIT DECREASED ( 247 FDA reports)
SINUSITIS ( 246 FDA reports)
OVERDOSE ( 243 FDA reports)
LETHARGY ( 243 FDA reports)
HYPERSENSITIVITY ( 242 FDA reports)
HYPERLIPIDAEMIA ( 240 FDA reports)
BONE DISORDER ( 239 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 237 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 235 FDA reports)
SWELLING ( 234 FDA reports)
THROMBOSIS ( 234 FDA reports)
PAIN IN JAW ( 233 FDA reports)
PRODUCT QUALITY ISSUE ( 230 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 230 FDA reports)
GASTRITIS ( 230 FDA reports)
NECK PAIN ( 230 FDA reports)
AGITATION ( 227 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 227 FDA reports)
HAEMORRHOIDS ( 227 FDA reports)
DISORIENTATION ( 225 FDA reports)
DYSPNOEA EXERTIONAL ( 225 FDA reports)
BURNING SENSATION ( 224 FDA reports)
CORONARY ARTERY OCCLUSION ( 224 FDA reports)
OSTEOMYELITIS ( 224 FDA reports)
CHOLELITHIASIS ( 222 FDA reports)
DRUG DOSE OMISSION ( 221 FDA reports)
DYSURIA ( 218 FDA reports)
WHEEZING ( 216 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 215 FDA reports)
VENTRICULAR TACHYCARDIA ( 214 FDA reports)
BLOOD UREA INCREASED ( 214 FDA reports)
ALOPECIA ( 213 FDA reports)
VISUAL IMPAIRMENT ( 213 FDA reports)
HALLUCINATION ( 212 FDA reports)
CARDIO-RESPIRATORY ARREST ( 211 FDA reports)
BONE PAIN ( 209 FDA reports)
INCORRECT DOSE ADMINISTERED ( 209 FDA reports)
HAEMATURIA ( 208 FDA reports)
HEPATIC ENZYME INCREASED ( 208 FDA reports)
MYOCARDIAL ISCHAEMIA ( 208 FDA reports)
OFF LABEL USE ( 208 FDA reports)
PANCREATITIS ( 207 FDA reports)
DEFORMITY ( 205 FDA reports)
URTICARIA ( 204 FDA reports)
ARTERIOSCLEROSIS ( 203 FDA reports)
NEUTROPENIA ( 202 FDA reports)
TYPE 2 DIABETES MELLITUS ( 202 FDA reports)
OROPHARYNGEAL PAIN ( 200 FDA reports)
RENAL DISORDER ( 200 FDA reports)
MULTIPLE INJURIES ( 199 FDA reports)
UNRESPONSIVE TO STIMULI ( 196 FDA reports)
CYSTITIS ( 195 FDA reports)
DYSARTHRIA ( 195 FDA reports)
STAPHYLOCOCCAL INFECTION ( 193 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 192 FDA reports)
SKIN DISCOLOURATION ( 191 FDA reports)
AMNESIA ( 190 FDA reports)
CARDIOGENIC SHOCK ( 190 FDA reports)
BLOOD GLUCOSE DECREASED ( 185 FDA reports)
DRUG HYPERSENSITIVITY ( 185 FDA reports)
DYSGEUSIA ( 185 FDA reports)
SPINAL OSTEOARTHRITIS ( 183 FDA reports)
SUICIDAL IDEATION ( 183 FDA reports)
COLONIC POLYP ( 182 FDA reports)
CATARACT ( 181 FDA reports)
HOT FLUSH ( 181 FDA reports)
ABASIA ( 177 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 177 FDA reports)
VERTIGO ( 177 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 177 FDA reports)
POLLAKIURIA ( 176 FDA reports)
HIATUS HERNIA ( 176 FDA reports)
MUSCLE TWITCHING ( 175 FDA reports)
HAEMATOCHEZIA ( 174 FDA reports)
SWELLING FACE ( 174 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 174 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 172 FDA reports)
HYPOPHAGIA ( 172 FDA reports)
MULTIPLE MYELOMA ( 172 FDA reports)
INJECTION SITE PAIN ( 171 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 171 FDA reports)
RASH PRURITIC ( 171 FDA reports)
RIB FRACTURE ( 171 FDA reports)
DELIRIUM ( 169 FDA reports)
NASOPHARYNGITIS ( 169 FDA reports)
NERVOUSNESS ( 168 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 166 FDA reports)
PULMONARY HYPERTENSION ( 165 FDA reports)
ASTHMA ( 165 FDA reports)
HAEMOPTYSIS ( 165 FDA reports)
BLOOD SODIUM DECREASED ( 164 FDA reports)
RESPIRATORY ARREST ( 164 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 163 FDA reports)
METABOLIC ACIDOSIS ( 163 FDA reports)
SKIN HYPERTROPHY ( 162 FDA reports)
SPEECH DISORDER ( 161 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 161 FDA reports)
HAEMATOMA ( 161 FDA reports)
MEDICATION ERROR ( 161 FDA reports)
BLOOD POTASSIUM DECREASED ( 160 FDA reports)
LYMPHADENOPATHY ( 159 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 158 FDA reports)
SINUS TACHYCARDIA ( 158 FDA reports)
LUNG INFILTRATION ( 157 FDA reports)
PRESYNCOPE ( 156 FDA reports)
SINUS BRADYCARDIA ( 155 FDA reports)
DYSPHONIA ( 155 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 155 FDA reports)
ANGINA UNSTABLE ( 154 FDA reports)
LEUKOPENIA ( 154 FDA reports)
ORTHOSTATIC HYPOTENSION ( 154 FDA reports)
SKIN INDURATION ( 154 FDA reports)
SKIN ULCER ( 153 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 153 FDA reports)
DRUG TOXICITY ( 151 FDA reports)
RESPIRATORY DISTRESS ( 151 FDA reports)
PERICARDIAL EFFUSION ( 150 FDA reports)
CARDIOMYOPATHY ( 150 FDA reports)
DIVERTICULUM ( 150 FDA reports)
NEPHROLITHIASIS ( 150 FDA reports)
APLASIA PURE RED CELL ( 149 FDA reports)
DRY SKIN ( 149 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 149 FDA reports)
DRUG EFFECT DECREASED ( 148 FDA reports)
FLATULENCE ( 147 FDA reports)
FEBRILE NEUTROPENIA ( 146 FDA reports)
HIP FRACTURE ( 146 FDA reports)
HYPOTHYROIDISM ( 146 FDA reports)
SLEEP DISORDER ( 146 FDA reports)
OSTEONECROSIS ( 145 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 145 FDA reports)
DISEASE PROGRESSION ( 145 FDA reports)
HERPES ZOSTER ( 145 FDA reports)
NEOPLASM MALIGNANT ( 145 FDA reports)
IMPAIRED HEALING ( 143 FDA reports)
SWOLLEN TONGUE ( 143 FDA reports)
SEPTIC SHOCK ( 142 FDA reports)
SKIN EXFOLIATION ( 142 FDA reports)
BLOOD BILIRUBIN INCREASED ( 142 FDA reports)
METASTASES TO BONE ( 142 FDA reports)
GOUT ( 141 FDA reports)
HAEMODIALYSIS ( 141 FDA reports)
INFLUENZA LIKE ILLNESS ( 141 FDA reports)
OSTEOPOROSIS ( 141 FDA reports)
TOOTH EXTRACTION ( 141 FDA reports)
OXYGEN SATURATION DECREASED ( 140 FDA reports)
PSORIASIS ( 140 FDA reports)
SLEEP APNOEA SYNDROME ( 140 FDA reports)
ANOREXIA ( 140 FDA reports)
COAGULOPATHY ( 139 FDA reports)
FLUID RETENTION ( 139 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 139 FDA reports)
TREATMENT NONCOMPLIANCE ( 139 FDA reports)
SCAR ( 138 FDA reports)
GASTRIC ULCER ( 138 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 138 FDA reports)
BLISTER ( 137 FDA reports)
MENTAL DISORDER ( 137 FDA reports)
FIBROSIS ( 136 FDA reports)
HEPATIC FAILURE ( 136 FDA reports)
LEUKOCYTOSIS ( 136 FDA reports)
CORONARY ARTERY STENOSIS ( 135 FDA reports)
HYPOCALCAEMIA ( 135 FDA reports)
SKIN TIGHTNESS ( 135 FDA reports)
HAEMATEMESIS ( 134 FDA reports)
INFLUENZA ( 133 FDA reports)
URINARY INCONTINENCE ( 132 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 131 FDA reports)
ATRIAL FLUTTER ( 130 FDA reports)
MELAENA ( 130 FDA reports)
ASCITES ( 129 FDA reports)
HEAD INJURY ( 129 FDA reports)
COMA ( 128 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 128 FDA reports)
PALLOR ( 127 FDA reports)
PULMONARY CONGESTION ( 127 FDA reports)
URINARY RETENTION ( 127 FDA reports)
VISUAL ACUITY REDUCED ( 127 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 127 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 126 FDA reports)
BLOOD CALCIUM DECREASED ( 126 FDA reports)
CEREBRAL HAEMORRHAGE ( 126 FDA reports)
RENAL CYST ( 126 FDA reports)
SKIN BURNING SENSATION ( 126 FDA reports)
STOMATITIS ( 126 FDA reports)
VENTRICULAR FIBRILLATION ( 125 FDA reports)
GASTRITIS EROSIVE ( 125 FDA reports)
LEFT VENTRICULAR FAILURE ( 125 FDA reports)
OSTEOPENIA ( 124 FDA reports)
RIGHT VENTRICULAR FAILURE ( 124 FDA reports)
SURGERY ( 124 FDA reports)
POST PROCEDURAL COMPLICATION ( 123 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 123 FDA reports)
ANGIOEDEMA ( 123 FDA reports)
CEREBRAL INFARCTION ( 122 FDA reports)
HALLUCINATION, VISUAL ( 122 FDA reports)
SKIN LESION ( 122 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 121 FDA reports)
TINNITUS ( 121 FDA reports)
DIALYSIS ( 121 FDA reports)
VARICOSE VEIN ( 120 FDA reports)
EJECTION FRACTION DECREASED ( 119 FDA reports)
HEPATIC STEATOSIS ( 119 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 118 FDA reports)
FLUID OVERLOAD ( 117 FDA reports)
DYSKINESIA ( 116 FDA reports)
EMOTIONAL DISORDER ( 116 FDA reports)
SKIN DISORDER ( 116 FDA reports)
SUICIDE ATTEMPT ( 115 FDA reports)
CARDIAC MURMUR ( 114 FDA reports)
BLOOD POTASSIUM INCREASED ( 113 FDA reports)
ERECTILE DYSFUNCTION ( 113 FDA reports)
RHEUMATOID ARTHRITIS ( 113 FDA reports)
PROTHROMBIN TIME PROLONGED ( 112 FDA reports)
RESTLESSNESS ( 112 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 112 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 112 FDA reports)
OBESITY ( 112 FDA reports)
HEMIPARESIS ( 111 FDA reports)
MIGRAINE ( 111 FDA reports)
DENTAL CARIES ( 110 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 110 FDA reports)
SHOCK ( 110 FDA reports)
RASH ERYTHEMATOUS ( 108 FDA reports)
EMPHYSEMA ( 108 FDA reports)
GASTROINTESTINAL DISORDER ( 108 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 107 FDA reports)
INFLAMMATION ( 107 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 106 FDA reports)
PULMONARY FIBROSIS ( 106 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 105 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 104 FDA reports)
EAR PAIN ( 104 FDA reports)
EXPOSED BONE IN JAW ( 104 FDA reports)
FAECES DISCOLOURED ( 104 FDA reports)
ARTHROPATHY ( 103 FDA reports)
INJECTION SITE HAEMATOMA ( 103 FDA reports)
CIRCULATORY COLLAPSE ( 102 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 102 FDA reports)
INJECTION SITE ERYTHEMA ( 102 FDA reports)
PANIC ATTACK ( 102 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 102 FDA reports)
DISTURBANCE IN ATTENTION ( 101 FDA reports)
APHASIA ( 100 FDA reports)
COMPRESSION FRACTURE ( 100 FDA reports)
INTENTIONAL DRUG MISUSE ( 100 FDA reports)
OESOPHAGITIS ( 100 FDA reports)
REFRACTORY ANAEMIA ( 99 FDA reports)
ACUTE CORONARY SYNDROME ( 99 FDA reports)
AORTIC ANEURYSM ( 99 FDA reports)
ILL-DEFINED DISORDER ( 99 FDA reports)
NEURALGIA ( 99 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 98 FDA reports)
DEMENTIA ( 98 FDA reports)
FEELING COLD ( 98 FDA reports)
TOOTHACHE ( 98 FDA reports)
RASH GENERALISED ( 97 FDA reports)
COGNITIVE DISORDER ( 97 FDA reports)
INTESTINAL OBSTRUCTION ( 97 FDA reports)
LUNG DISORDER ( 97 FDA reports)
ACUTE RESPIRATORY FAILURE ( 96 FDA reports)
DECREASED INTEREST ( 96 FDA reports)
ENCEPHALOPATHY ( 96 FDA reports)
ANAL FISSURE ( 95 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 95 FDA reports)
DISCOMFORT ( 94 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 94 FDA reports)
JOINT STIFFNESS ( 94 FDA reports)
NASAL CONGESTION ( 94 FDA reports)
PNEUMONIA ASPIRATION ( 94 FDA reports)
EYE PAIN ( 93 FDA reports)
GASTROENTERITIS ( 93 FDA reports)
HYPOPNOEA ( 93 FDA reports)
MUSCLE TIGHTNESS ( 93 FDA reports)
NERVOUS SYSTEM DISORDER ( 93 FDA reports)
BLOOD ALBUMIN DECREASED ( 92 FDA reports)
MUCOSAL INFLAMMATION ( 92 FDA reports)
PANCREATITIS ACUTE ( 92 FDA reports)
THROAT IRRITATION ( 92 FDA reports)
ROAD TRAFFIC ACCIDENT ( 91 FDA reports)
CANDIDIASIS ( 91 FDA reports)
COORDINATION ABNORMAL ( 91 FDA reports)
CYANOSIS ( 91 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 91 FDA reports)
HYPOMAGNESAEMIA ( 91 FDA reports)
LOOSE TOOTH ( 91 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 91 FDA reports)
BONE LESION ( 90 FDA reports)
IRRITABILITY ( 90 FDA reports)
NIGHT SWEATS ( 90 FDA reports)
RHINORRHOEA ( 90 FDA reports)
TOOTH LOSS ( 90 FDA reports)
PRURITUS GENERALISED ( 89 FDA reports)
BLOOD URINE PRESENT ( 89 FDA reports)
DYSSTASIA ( 89 FDA reports)
INTENTIONAL OVERDOSE ( 89 FDA reports)
METASTASES TO LIVER ( 89 FDA reports)
ABNORMAL DREAMS ( 88 FDA reports)
AZOTAEMIA ( 88 FDA reports)
COLD SWEAT ( 88 FDA reports)
DIPLOPIA ( 88 FDA reports)
FEMUR FRACTURE ( 88 FDA reports)
ORAL PAIN ( 88 FDA reports)
PROTEINURIA ( 88 FDA reports)
VAGINAL ABSCESS ( 88 FDA reports)
PNEUMOTHORAX ( 87 FDA reports)
PROSTATE CANCER ( 87 FDA reports)
SINUS DISORDER ( 87 FDA reports)
TOOTH ABSCESS ( 87 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 86 FDA reports)
DISABILITY ( 86 FDA reports)
HYPERCALCAEMIA ( 86 FDA reports)
LUNG NEOPLASM ( 86 FDA reports)
BRONCHOSPASM ( 85 FDA reports)
RASH MACULAR ( 85 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 84 FDA reports)
CARDIOVASCULAR DISORDER ( 84 FDA reports)
FOOT FRACTURE ( 84 FDA reports)
GLAUCOMA ( 84 FDA reports)
HYPERCHOLESTEROLAEMIA ( 83 FDA reports)
HYPERTENSIVE CRISIS ( 83 FDA reports)
ILEUS ( 83 FDA reports)
INJECTION SITE HAEMORRHAGE ( 83 FDA reports)
LACTIC ACIDOSIS ( 83 FDA reports)
MOVEMENT DISORDER ( 83 FDA reports)
PHARYNGEAL OEDEMA ( 83 FDA reports)
SPINAL COLUMN STENOSIS ( 82 FDA reports)
ABNORMAL BEHAVIOUR ( 82 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 82 FDA reports)
DEAFNESS ( 82 FDA reports)
FAILURE TO THRIVE ( 82 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 82 FDA reports)
MOUTH ULCERATION ( 82 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 81 FDA reports)
CHROMATURIA ( 81 FDA reports)
JAUNDICE ( 81 FDA reports)
JAW FRACTURE ( 81 FDA reports)
ROTATOR CUFF SYNDROME ( 81 FDA reports)
PERIPHERAL COLDNESS ( 80 FDA reports)
PRODUCTIVE COUGH ( 80 FDA reports)
AORTIC STENOSIS ( 80 FDA reports)
EXTRASYSTOLES ( 80 FDA reports)
FAECAL INCONTINENCE ( 80 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 80 FDA reports)
HYPOVOLAEMIA ( 80 FDA reports)
LIP SWELLING ( 80 FDA reports)
AGGRESSION ( 79 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 79 FDA reports)
CARDIAC VALVE DISEASE ( 79 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 79 FDA reports)
MALNUTRITION ( 79 FDA reports)
MYELODYSPLASTIC SYNDROME ( 79 FDA reports)
RASH PAPULAR ( 79 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 79 FDA reports)
TRANSAMINASES INCREASED ( 79 FDA reports)
SUBDURAL HAEMATOMA ( 78 FDA reports)
ATRIOVENTRICULAR BLOCK ( 78 FDA reports)
CHOLECYSTITIS ( 77 FDA reports)
GRAND MAL CONVULSION ( 77 FDA reports)
HOSPITALISATION ( 77 FDA reports)
SUDDEN DEATH ( 77 FDA reports)
STENT PLACEMENT ( 76 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 76 FDA reports)
CEREBRAL ATROPHY ( 76 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 76 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 76 FDA reports)
INTERSTITIAL LUNG DISEASE ( 76 FDA reports)
JOINT CONTRACTURE ( 76 FDA reports)
METASTASES TO SPINE ( 76 FDA reports)
NEOPLASM PROGRESSION ( 76 FDA reports)
BLINDNESS ( 75 FDA reports)
CEREBRAL ISCHAEMIA ( 75 FDA reports)
FUNGAL INFECTION ( 75 FDA reports)
SKIN HYPERPIGMENTATION ( 75 FDA reports)
RETCHING ( 74 FDA reports)
BACTERAEMIA ( 74 FDA reports)
CLOSTRIDIAL INFECTION ( 74 FDA reports)
EATING DISORDER ( 74 FDA reports)
ELECTROLYTE IMBALANCE ( 74 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 73 FDA reports)
ANKLE FRACTURE ( 73 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 73 FDA reports)
CORONARY ARTERY BYPASS ( 73 FDA reports)
DECUBITUS ULCER ( 73 FDA reports)
DIVERTICULUM INTESTINAL ( 73 FDA reports)
LEFT ATRIAL DILATATION ( 73 FDA reports)
LIVER DISORDER ( 73 FDA reports)
NIGHTMARE ( 73 FDA reports)
ODYNOPHAGIA ( 73 FDA reports)
ORTHOPNOEA ( 73 FDA reports)
SCOLIOSIS ( 73 FDA reports)
RENAL TUBULAR NECROSIS ( 72 FDA reports)
ADVERSE EVENT ( 72 FDA reports)
DIABETIC KETOACIDOSIS ( 72 FDA reports)
DRUG INTOLERANCE ( 72 FDA reports)
LACERATION ( 72 FDA reports)
ANAPHYLACTIC REACTION ( 71 FDA reports)
ATAXIA ( 71 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 71 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 71 FDA reports)
FLANK PAIN ( 71 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 70 FDA reports)
DIVERTICULITIS ( 70 FDA reports)
DRY EYE ( 70 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 70 FDA reports)
LIMB INJURY ( 70 FDA reports)
PULMONARY MASS ( 70 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 70 FDA reports)
PERITONITIS ( 69 FDA reports)
TORSADE DE POINTES ( 69 FDA reports)
UROSEPSIS ( 69 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 69 FDA reports)
EYE SWELLING ( 69 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 69 FDA reports)
COLITIS ISCHAEMIC ( 68 FDA reports)
DIASTOLIC DYSFUNCTION ( 68 FDA reports)
ERUCTATION ( 68 FDA reports)
GALLBLADDER DISORDER ( 68 FDA reports)
HEPATIC CYST ( 68 FDA reports)
METASTASES TO LUNG ( 68 FDA reports)
SICK SINUS SYNDROME ( 68 FDA reports)
EXOSTOSIS ( 67 FDA reports)
GASTRIC DISORDER ( 67 FDA reports)
GROIN PAIN ( 67 FDA reports)
LOBAR PNEUMONIA ( 67 FDA reports)
LUNG NEOPLASM MALIGNANT ( 67 FDA reports)
DRUG LEVEL INCREASED ( 66 FDA reports)
GINGIVAL BLEEDING ( 66 FDA reports)
TROPONIN INCREASED ( 66 FDA reports)
ORAL DISORDER ( 65 FDA reports)
PRIMARY SEQUESTRUM ( 65 FDA reports)
TENDERNESS ( 65 FDA reports)
BACTERIAL INFECTION ( 65 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 65 FDA reports)
BODY TEMPERATURE INCREASED ( 65 FDA reports)
BREAST CANCER ( 65 FDA reports)
CAROTID ARTERY STENOSIS ( 65 FDA reports)
HEPATITIS ( 65 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 65 FDA reports)
ANGER ( 64 FDA reports)
BLINDNESS UNILATERAL ( 64 FDA reports)
CHOLECYSTITIS CHRONIC ( 64 FDA reports)
COLITIS ( 64 FDA reports)
FACIAL PAIN ( 64 FDA reports)
MIDDLE INSOMNIA ( 64 FDA reports)
PHYSICAL DISABILITY ( 64 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 64 FDA reports)
RESTLESS LEGS SYNDROME ( 64 FDA reports)
SPINAL COMPRESSION FRACTURE ( 64 FDA reports)
PATHOLOGICAL FRACTURE ( 63 FDA reports)
TARDIVE DYSKINESIA ( 63 FDA reports)
TENDONITIS ( 63 FDA reports)
TOOTH DISORDER ( 63 FDA reports)
ANURIA ( 63 FDA reports)
INTRACARDIAC THROMBUS ( 63 FDA reports)
LOCALISED INFECTION ( 63 FDA reports)
CYST ( 62 FDA reports)
ECCHYMOSIS ( 62 FDA reports)
PAIN OF SKIN ( 62 FDA reports)
RALES ( 62 FDA reports)
RESPIRATORY RATE INCREASED ( 62 FDA reports)
OSTEOLYSIS ( 61 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 61 FDA reports)
ULCER ( 61 FDA reports)
WOUND INFECTION ( 61 FDA reports)
CHOLECYSTECTOMY ( 61 FDA reports)
HYPOALBUMINAEMIA ( 61 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 61 FDA reports)
ACCIDENTAL OVERDOSE ( 60 FDA reports)
AGEUSIA ( 60 FDA reports)
AORTIC VALVE INCOMPETENCE ( 60 FDA reports)
GASTRIC HAEMORRHAGE ( 60 FDA reports)
GENERALISED OEDEMA ( 60 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 60 FDA reports)
ISCHAEMIA ( 60 FDA reports)
JOINT INJURY ( 60 FDA reports)
MASTICATION DISORDER ( 60 FDA reports)
MENTAL IMPAIRMENT ( 60 FDA reports)
WALKING AID USER ( 60 FDA reports)
PERIODONTAL DISEASE ( 59 FDA reports)
STEVENS-JOHNSON SYNDROME ( 59 FDA reports)
URINE OUTPUT DECREASED ( 59 FDA reports)
ABSCESS ( 59 FDA reports)
DEPRESSED MOOD ( 59 FDA reports)
ENTEROCOCCAL INFECTION ( 59 FDA reports)
HYDRONEPHROSIS ( 59 FDA reports)
HYPOACUSIS ( 59 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 58 FDA reports)
ISCHAEMIC STROKE ( 58 FDA reports)
MUSCLE ATROPHY ( 58 FDA reports)
ORAL CANDIDIASIS ( 58 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 58 FDA reports)
PULSE ABSENT ( 57 FDA reports)
VIRAL INFECTION ( 57 FDA reports)
CARDIAC PACEMAKER INSERTION ( 57 FDA reports)
DYSLIPIDAEMIA ( 57 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 57 FDA reports)
NEUTROPHIL COUNT DECREASED ( 57 FDA reports)
NOCTURIA ( 57 FDA reports)
BURSITIS ( 56 FDA reports)
HEPATIC CIRRHOSIS ( 56 FDA reports)
NO THERAPEUTIC RESPONSE ( 56 FDA reports)
TOOTH FRACTURE ( 56 FDA reports)
ONYCHOMYCOSIS ( 55 FDA reports)
POLYNEUROPATHY ( 55 FDA reports)
VAGINAL HAEMORRHAGE ( 55 FDA reports)
CARPAL TUNNEL SYNDROME ( 55 FDA reports)
DILATATION VENTRICULAR ( 55 FDA reports)
HAEMODYNAMIC INSTABILITY ( 55 FDA reports)
INFUSION RELATED REACTION ( 55 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 55 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 55 FDA reports)
MICTURITION URGENCY ( 55 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 54 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 54 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 54 FDA reports)
BODY HEIGHT DECREASED ( 54 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 54 FDA reports)
FACIAL BONES FRACTURE ( 54 FDA reports)
HYPERTENSIVE EMERGENCY ( 54 FDA reports)
JOINT EFFUSION ( 54 FDA reports)
RESPIRATORY TRACT INFECTION ( 54 FDA reports)
SENSORY DISTURBANCE ( 54 FDA reports)
RADICULOPATHY ( 53 FDA reports)
SKIN FIBROSIS ( 53 FDA reports)
ASPIRATION ( 53 FDA reports)
BASAL CELL CARCINOMA ( 53 FDA reports)
DEVICE RELATED INFECTION ( 53 FDA reports)
EYE DISORDER ( 53 FDA reports)
HYPERTHYROIDISM ( 53 FDA reports)
LUNG INFECTION ( 53 FDA reports)
MASS ( 53 FDA reports)
ABDOMINAL PAIN LOWER ( 52 FDA reports)
ADVERSE DRUG REACTION ( 52 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 52 FDA reports)
LABORATORY TEST ABNORMAL ( 52 FDA reports)
OCULAR HYPERAEMIA ( 52 FDA reports)
PNEUMONITIS ( 52 FDA reports)
SEDATION ( 52 FDA reports)
VENTRICULAR HYPERTROPHY ( 52 FDA reports)
PSYCHOTIC DISORDER ( 51 FDA reports)
RASH MACULO-PAPULAR ( 51 FDA reports)
THYROID DISORDER ( 51 FDA reports)
VENTRICULAR HYPOKINESIA ( 51 FDA reports)
BONE MARROW FAILURE ( 51 FDA reports)
DRUG ADMINISTRATION ERROR ( 51 FDA reports)
HAEMOLYTIC ANAEMIA ( 51 FDA reports)
CRYING ( 50 FDA reports)
DIABETIC NEUROPATHY ( 50 FDA reports)
EXCORIATION ( 50 FDA reports)
HEPATOTOXICITY ( 50 FDA reports)
HYPERSOMNIA ( 50 FDA reports)
KNEE ARTHROPLASTY ( 50 FDA reports)
LUMBAR SPINAL STENOSIS ( 50 FDA reports)
POISONING ( 50 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 50 FDA reports)
RESPIRATORY DISORDER ( 50 FDA reports)
ORAL INTAKE REDUCED ( 49 FDA reports)
PANCREATIC CARCINOMA ( 49 FDA reports)
PLASMACYTOMA ( 49 FDA reports)
PURPURA ( 49 FDA reports)
RHINITIS ALLERGIC ( 49 FDA reports)
SKIN PLAQUE ( 49 FDA reports)
SYNOVIAL CYST ( 49 FDA reports)
THROAT TIGHTNESS ( 49 FDA reports)
ACIDOSIS ( 49 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 49 FDA reports)
DERMATITIS ( 49 FDA reports)
EAR INFECTION ( 49 FDA reports)
FIBROMYALGIA ( 49 FDA reports)
FISTULA ( 49 FDA reports)
IRON DEFICIENCY ANAEMIA ( 49 FDA reports)
LOCAL SWELLING ( 49 FDA reports)
CHRONIC SINUSITIS ( 48 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 48 FDA reports)
ESCHERICHIA INFECTION ( 48 FDA reports)
EYE IRRITATION ( 48 FDA reports)
GINGIVAL PAIN ( 48 FDA reports)
IRRITABLE BOWEL SYNDROME ( 48 FDA reports)
JAW DISORDER ( 48 FDA reports)
KYPHOSIS ( 48 FDA reports)
OPEN WOUND ( 48 FDA reports)
UPPER LIMB FRACTURE ( 47 FDA reports)
BLOOD CHLORIDE DECREASED ( 47 FDA reports)
GANGRENE ( 47 FDA reports)
GOITRE ( 47 FDA reports)
HYPOAESTHESIA ORAL ( 47 FDA reports)
INTERMITTENT CLAUDICATION ( 47 FDA reports)
LIFE EXPECTANCY SHORTENED ( 47 FDA reports)
MULTIPLE DRUG OVERDOSE ( 47 FDA reports)
OCCULT BLOOD POSITIVE ( 47 FDA reports)
APNOEA ( 46 FDA reports)
BLOOD CALCIUM INCREASED ( 46 FDA reports)
DISEASE RECURRENCE ( 46 FDA reports)
GINGIVITIS ( 46 FDA reports)
GLOSSODYNIA ( 46 FDA reports)
MYOPATHY ( 46 FDA reports)
STOMACH DISCOMFORT ( 46 FDA reports)
TACHYARRHYTHMIA ( 46 FDA reports)
THINKING ABNORMAL ( 46 FDA reports)
ULCER HAEMORRHAGE ( 46 FDA reports)
OSTEITIS ( 45 FDA reports)
PHARYNGITIS ( 45 FDA reports)
POOR QUALITY SLEEP ( 45 FDA reports)
SCIATICA ( 45 FDA reports)
WITHDRAWAL SYNDROME ( 45 FDA reports)
DUODENAL ULCER ( 45 FDA reports)
EYE HAEMORRHAGE ( 45 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 45 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 45 FDA reports)
INJECTION SITE SWELLING ( 45 FDA reports)
MITRAL VALVE DISEASE ( 45 FDA reports)
MYOSITIS ( 45 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 44 FDA reports)
CATARACT OPERATION ( 44 FDA reports)
CONJUNCTIVITIS ( 44 FDA reports)
DRUG DEPENDENCE ( 44 FDA reports)
INJECTION SITE REACTION ( 44 FDA reports)
KIDNEY INFECTION ( 44 FDA reports)
LIMB DISCOMFORT ( 44 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 44 FDA reports)
ORGAN FAILURE ( 43 FDA reports)
OSTEOSCLEROSIS ( 43 FDA reports)
PREMATURE BABY ( 43 FDA reports)
TACHYPNOEA ( 43 FDA reports)
CHEST X-RAY ABNORMAL ( 43 FDA reports)
CHOLESTASIS ( 43 FDA reports)
HAND FRACTURE ( 43 FDA reports)
INCONTINENCE ( 43 FDA reports)
MACULAR DEGENERATION ( 43 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 43 FDA reports)
NON-CARDIAC CHEST PAIN ( 43 FDA reports)
BLOOD CULTURE POSITIVE ( 42 FDA reports)
BLOOD PRESSURE ABNORMAL ( 42 FDA reports)
BREATH SOUNDS ABNORMAL ( 42 FDA reports)
DIZZINESS POSTURAL ( 42 FDA reports)
ENDOCARDITIS ( 42 FDA reports)
GASTROENTERITIS VIRAL ( 42 FDA reports)
HAEMORRHAGIC STROKE ( 42 FDA reports)
HUMERUS FRACTURE ( 42 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 42 FDA reports)
MENISCUS LESION ( 42 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 42 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 42 FDA reports)
RENAL ATROPHY ( 42 FDA reports)
OLIGURIA ( 41 FDA reports)
PETECHIAE ( 41 FDA reports)
PLATELET COUNT INCREASED ( 41 FDA reports)
PYELONEPHRITIS ( 41 FDA reports)
THIRST ( 41 FDA reports)
ABSCESS JAW ( 41 FDA reports)
BONE NEOPLASM MALIGNANT ( 41 FDA reports)
CHOKING ( 41 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 41 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 41 FDA reports)
DIFFICULTY IN WALKING ( 41 FDA reports)
FACE OEDEMA ( 41 FDA reports)
MUSCLE DISORDER ( 41 FDA reports)
BRAIN OEDEMA ( 40 FDA reports)
COLON CANCER ( 40 FDA reports)
FEELING JITTERY ( 40 FDA reports)
HEART INJURY ( 40 FDA reports)
HIP ARTHROPLASTY ( 40 FDA reports)
HYPOPHOSPHATAEMIA ( 40 FDA reports)
LYMPHOMA ( 40 FDA reports)
MYOCLONUS ( 40 FDA reports)
SINUS HEADACHE ( 40 FDA reports)
SKIN NECROSIS ( 40 FDA reports)
TENDON RUPTURE ( 40 FDA reports)
PARALYSIS ( 39 FDA reports)
PARANOIA ( 39 FDA reports)
SEQUESTRECTOMY ( 39 FDA reports)
SKIN CANCER ( 39 FDA reports)
DELUSION ( 39 FDA reports)
HEARING IMPAIRED ( 39 FDA reports)
HEPATOMEGALY ( 39 FDA reports)
MEDICATION RESIDUE ( 39 FDA reports)
ANGIOPATHY ( 38 FDA reports)
AORTIC CALCIFICATION ( 38 FDA reports)
BREAST PAIN ( 38 FDA reports)
CATHETERISATION CARDIAC ( 38 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 38 FDA reports)
ESSENTIAL HYPERTENSION ( 38 FDA reports)
HEMIPLEGIA ( 38 FDA reports)
SEROTONIN SYNDROME ( 38 FDA reports)
SPLENOMEGALY ( 38 FDA reports)
THYROID NEOPLASM ( 38 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 37 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 37 FDA reports)
TRANSPLANT REJECTION ( 37 FDA reports)
WOUND ( 37 FDA reports)
ABDOMINAL TENDERNESS ( 37 FDA reports)
ANEURYSM ( 37 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 37 FDA reports)
BONE DENSITY DECREASED ( 37 FDA reports)
BRONCHOPNEUMONIA ( 37 FDA reports)
DEVICE MALFUNCTION ( 37 FDA reports)
ECZEMA ( 37 FDA reports)
GENERALISED ERYTHEMA ( 37 FDA reports)
HYPERPARATHYROIDISM ( 37 FDA reports)
JAW OPERATION ( 37 FDA reports)
LIPASE INCREASED ( 37 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 37 FDA reports)
MOTOR DYSFUNCTION ( 37 FDA reports)
ACCIDENTAL EXPOSURE ( 36 FDA reports)
ANGIONEUROTIC OEDEMA ( 36 FDA reports)
BLOOD COUNT ABNORMAL ( 36 FDA reports)
BODY TEMPERATURE DECREASED ( 36 FDA reports)
FAECALOMA ( 36 FDA reports)
HYDROCELE ( 36 FDA reports)
HYPOKINESIA ( 36 FDA reports)
HYPOTONIA ( 36 FDA reports)
INJECTION SITE PRURITUS ( 36 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 36 FDA reports)
PERIODONTITIS ( 36 FDA reports)
PERIPHERAL ISCHAEMIA ( 36 FDA reports)
RENAL ARTERY STENOSIS ( 36 FDA reports)
THROMBOSIS IN DEVICE ( 36 FDA reports)
VISUAL DISTURBANCE ( 36 FDA reports)
WRONG DRUG ADMINISTERED ( 36 FDA reports)
PARKINSON'S DISEASE ( 35 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 35 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 35 FDA reports)
UTERINE LEIOMYOMA ( 35 FDA reports)
VASCULITIS ( 35 FDA reports)
ACUTE HEPATIC FAILURE ( 35 FDA reports)
ACUTE PULMONARY OEDEMA ( 35 FDA reports)
BIPOLAR DISORDER ( 35 FDA reports)
BLADDER CANCER ( 35 FDA reports)
CARDIAC FLUTTER ( 35 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 35 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 35 FDA reports)
EMBOLIC STROKE ( 35 FDA reports)
EOSINOPHILIA ( 35 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 35 FDA reports)
HYPERTENSIVE HEART DISEASE ( 35 FDA reports)
INTESTINAL ISCHAEMIA ( 35 FDA reports)
INTESTINAL PERFORATION ( 35 FDA reports)
MENINGIOMA ( 35 FDA reports)
MOOD SWINGS ( 35 FDA reports)
BONE DEBRIDEMENT ( 34 FDA reports)
CERVICAL SPINAL STENOSIS ( 34 FDA reports)
CHOLECYSTITIS ACUTE ( 34 FDA reports)
CROHN'S DISEASE ( 34 FDA reports)
DEBRIDEMENT ( 34 FDA reports)
EYELID PTOSIS ( 34 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 34 FDA reports)
GINGIVAL SWELLING ( 34 FDA reports)
HAEMORRHAGIC ANAEMIA ( 34 FDA reports)
HYPERKERATOSIS ( 34 FDA reports)
HYPOAESTHESIA FACIAL ( 34 FDA reports)
INCREASED TENDENCY TO BRUISE ( 34 FDA reports)
LACRIMATION INCREASED ( 34 FDA reports)
LACUNAR INFARCTION ( 34 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 34 FDA reports)
MAJOR DEPRESSION ( 34 FDA reports)
MUSCULOSKELETAL DISORDER ( 34 FDA reports)
NEUROLOGICAL SYMPTOM ( 34 FDA reports)
NODAL RHYTHM ( 34 FDA reports)
OCULAR ICTERUS ( 34 FDA reports)
QUALITY OF LIFE DECREASED ( 34 FDA reports)
RHONCHI ( 34 FDA reports)
SEBORRHOEIC KERATOSIS ( 34 FDA reports)
SINUS CONGESTION ( 34 FDA reports)
SPINAL FRACTURE ( 34 FDA reports)
TYPE 1 DIABETES MELLITUS ( 34 FDA reports)
PERICARDITIS ( 33 FDA reports)
POLYURIA ( 33 FDA reports)
PROCEDURAL COMPLICATION ( 33 FDA reports)
PROTEIN URINE PRESENT ( 33 FDA reports)
SOCIAL PROBLEM ( 33 FDA reports)
SQUAMOUS CELL CARCINOMA ( 33 FDA reports)
SUDDEN CARDIAC DEATH ( 33 FDA reports)
TONGUE DISORDER ( 33 FDA reports)
VENOUS INSUFFICIENCY ( 33 FDA reports)
VENTRICULAR DYSFUNCTION ( 33 FDA reports)
ATRIAL TACHYCARDIA ( 33 FDA reports)
BLOOD MAGNESIUM DECREASED ( 33 FDA reports)
BREAST CANCER RECURRENT ( 33 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 33 FDA reports)
GYNAECOMASTIA ( 33 FDA reports)
MOOD ALTERED ( 33 FDA reports)
AGRANULOCYTOSIS ( 32 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 32 FDA reports)
CONDUCTION DISORDER ( 32 FDA reports)
DRUG DISPENSING ERROR ( 32 FDA reports)
DRUG PRESCRIBING ERROR ( 32 FDA reports)
ENDODONTIC PROCEDURE ( 32 FDA reports)
FOOT DEFORMITY ( 32 FDA reports)
GINGIVAL INFECTION ( 32 FDA reports)
HERNIA ( 32 FDA reports)
HYPERAESTHESIA ( 32 FDA reports)
NEPHRITIS INTERSTITIAL ( 32 FDA reports)
PHOTOPHOBIA ( 32 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 32 FDA reports)
SKIN IRRITATION ( 32 FDA reports)
SPINAL DISORDER ( 32 FDA reports)
WHEELCHAIR USER ( 32 FDA reports)
OSTEOMYELITIS ACUTE ( 31 FDA reports)
OVARIAN CYST ( 31 FDA reports)
PERSONALITY CHANGE ( 31 FDA reports)
SENSORY LOSS ( 31 FDA reports)
SOMNAMBULISM ( 31 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 31 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 31 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 31 FDA reports)
BONE LOSS ( 31 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 31 FDA reports)
ENDOTRACHEAL INTUBATION ( 31 FDA reports)
HEPATIC ENCEPHALOPATHY ( 31 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 31 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 31 FDA reports)
MELANOCYTIC NAEVUS ( 31 FDA reports)
MOUTH HAEMORRHAGE ( 31 FDA reports)
MULTIPLE SCLEROSIS ( 31 FDA reports)
OESOPHAGEAL PAIN ( 31 FDA reports)
ACTINIC KERATOSIS ( 30 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 30 FDA reports)
APHAGIA ( 30 FDA reports)
BLOOD CHLORIDE INCREASED ( 30 FDA reports)
CARDIAC TAMPONADE ( 30 FDA reports)
CAROTID ARTERY OCCLUSION ( 30 FDA reports)
DECREASED ACTIVITY ( 30 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 30 FDA reports)
DRUG ERUPTION ( 30 FDA reports)
EMBOLISM ( 30 FDA reports)
EPILEPSY ( 30 FDA reports)
EXTREMITY CONTRACTURE ( 30 FDA reports)
HAEMANGIOMA ( 30 FDA reports)
HALLUCINATION, AUDITORY ( 30 FDA reports)
HYPOTHERMIA ( 30 FDA reports)
MITRAL VALVE PROLAPSE ( 30 FDA reports)
NEUTROPENIC SEPSIS ( 30 FDA reports)
PLEURAL FIBROSIS ( 30 FDA reports)
PROCEDURAL PAIN ( 30 FDA reports)
SKIN WARM ( 30 FDA reports)
TIBIA FRACTURE ( 30 FDA reports)
TONGUE ULCERATION ( 30 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 30 FDA reports)
VASCULAR GRAFT ( 30 FDA reports)
VITAMIN B12 DEFICIENCY ( 30 FDA reports)
VITAMIN D DECREASED ( 30 FDA reports)
VITAMIN D DEFICIENCY ( 30 FDA reports)
WOUND SECRETION ( 30 FDA reports)
PROCTALGIA ( 29 FDA reports)
PROTEIN TOTAL DECREASED ( 29 FDA reports)
RETROPERITONEAL HAEMATOMA ( 29 FDA reports)
SKIN LACERATION ( 29 FDA reports)
TROPONIN I INCREASED ( 29 FDA reports)
URINE ANALYSIS ABNORMAL ( 29 FDA reports)
VASCULAR PSEUDOANEURYSM ( 29 FDA reports)
ACUTE SINUSITIS ( 29 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 29 FDA reports)
BLOOD CREATINE INCREASED ( 29 FDA reports)
BREAST MASS ( 29 FDA reports)
CEREBROVASCULAR DISORDER ( 29 FDA reports)
DILATATION ATRIAL ( 29 FDA reports)
FAMILY STRESS ( 29 FDA reports)
GINGIVAL RECESSION ( 29 FDA reports)
HEART RATE ABNORMAL ( 29 FDA reports)
HEART VALVE INCOMPETENCE ( 29 FDA reports)
IMPAIRED WORK ABILITY ( 29 FDA reports)
KLEBSIELLA INFECTION ( 29 FDA reports)
LYMPHOEDEMA ( 29 FDA reports)
METABOLIC ENCEPHALOPATHY ( 29 FDA reports)
METABOLIC SYNDROME ( 29 FDA reports)
NODULE ( 29 FDA reports)
CARDIAC ENZYMES INCREASED ( 28 FDA reports)
CHANGE OF BOWEL HABIT ( 28 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 28 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 28 FDA reports)
DERMAL CYST ( 28 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 28 FDA reports)
EROSIVE OESOPHAGITIS ( 28 FDA reports)
EYE INFECTION ( 28 FDA reports)
HEPATITIS ACUTE ( 28 FDA reports)
INADEQUATE ANALGESIA ( 28 FDA reports)
METABOLIC DISORDER ( 28 FDA reports)
METASTATIC NEOPLASM ( 28 FDA reports)
NO ADVERSE EVENT ( 28 FDA reports)
PEPTIC ULCER ( 28 FDA reports)
PERIPHERAL EMBOLISM ( 28 FDA reports)
SENSATION OF HEAVINESS ( 28 FDA reports)
VIITH NERVE PARALYSIS ( 28 FDA reports)
VISUAL FIELD DEFECT ( 28 FDA reports)
WOUND DEHISCENCE ( 28 FDA reports)
PARAESTHESIA ORAL ( 27 FDA reports)
PITTING OEDEMA ( 27 FDA reports)
PLEURITIC PAIN ( 27 FDA reports)
PURULENCE ( 27 FDA reports)
SPINAL CORD COMPRESSION ( 27 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 27 FDA reports)
TOBACCO USER ( 27 FDA reports)
TOOTH INFECTION ( 27 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 27 FDA reports)
WRIST FRACTURE ( 27 FDA reports)
ABDOMINAL HERNIA ( 27 FDA reports)
ANAPHYLACTIC SHOCK ( 27 FDA reports)
APPENDICITIS ( 27 FDA reports)
BLADDER DISORDER ( 27 FDA reports)
CORONARY ARTERY THROMBOSIS ( 27 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 27 FDA reports)
DERMATITIS ALLERGIC ( 27 FDA reports)
DRUG EFFECT INCREASED ( 27 FDA reports)
DUODENITIS ( 27 FDA reports)
FACET JOINT SYNDROME ( 27 FDA reports)
FACIAL PALSY ( 27 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 27 FDA reports)
HYPERVENTILATION ( 27 FDA reports)
IMMUNOSUPPRESSION ( 27 FDA reports)
INJECTION SITE MASS ( 27 FDA reports)
LIBIDO DECREASED ( 27 FDA reports)
LUNG CONSOLIDATION ( 27 FDA reports)
OEDEMA MOUTH ( 27 FDA reports)
ACNE ( 26 FDA reports)
ANORECTAL DISCOMFORT ( 26 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 26 FDA reports)
AREFLEXIA ( 26 FDA reports)
BACK DISORDER ( 26 FDA reports)
CREPITATIONS ( 26 FDA reports)
CULTURE URINE POSITIVE ( 26 FDA reports)
DENTAL FISTULA ( 26 FDA reports)
DIABETIC FOOT ( 26 FDA reports)
EYE PRURITUS ( 26 FDA reports)
EYELID OEDEMA ( 26 FDA reports)
FRACTURE ( 26 FDA reports)
FURUNCLE ( 26 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 26 FDA reports)
GRANULOCYTOPENIA ( 26 FDA reports)
HEPATIC NECROSIS ( 26 FDA reports)
HEPATITIS C ( 26 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 26 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 26 FDA reports)
NEPHROSCLEROSIS ( 26 FDA reports)
PERIORBITAL OEDEMA ( 26 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 26 FDA reports)
POLYP ( 26 FDA reports)
PSYCHIATRIC SYMPTOM ( 26 FDA reports)
PULMONARY THROMBOSIS ( 26 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 26 FDA reports)
RENAL CANCER ( 26 FDA reports)
RENAL TRANSPLANT ( 26 FDA reports)
RESPIRATORY TRACT CONGESTION ( 26 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 26 FDA reports)
SPONDYLOLISTHESIS ( 26 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 26 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 26 FDA reports)
THERAPY NON-RESPONDER ( 26 FDA reports)
THROMBOCYTOSIS ( 26 FDA reports)
VASCULAR CALCIFICATION ( 26 FDA reports)
VENTRICULAR ARRHYTHMIA ( 26 FDA reports)
PHOTOSENSITIVITY REACTION ( 25 FDA reports)
POLYDIPSIA ( 25 FDA reports)
PSEUDOMONAS INFECTION ( 25 FDA reports)
RADIUS FRACTURE ( 25 FDA reports)
RENAL PAIN ( 25 FDA reports)
SCAB ( 25 FDA reports)
SKIN HAEMORRHAGE ( 25 FDA reports)
SPUTUM DISCOLOURED ( 25 FDA reports)
URINE FLOW DECREASED ( 25 FDA reports)
APATHY ( 25 FDA reports)
APPLICATION SITE ERYTHEMA ( 25 FDA reports)
ARTERIAL DISORDER ( 25 FDA reports)
BEDRIDDEN ( 25 FDA reports)
BLINDNESS TRANSIENT ( 25 FDA reports)
BLOOD AMYLASE INCREASED ( 25 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 25 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 25 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 25 FDA reports)
CACHEXIA ( 25 FDA reports)
CAESAREAN SECTION ( 25 FDA reports)
CARDIAC FAILURE CHRONIC ( 25 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 25 FDA reports)
CARDIOPULMONARY FAILURE ( 25 FDA reports)
DEVICE OCCLUSION ( 25 FDA reports)
DRUG ABUSE ( 25 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 25 FDA reports)
EXERCISE TOLERANCE DECREASED ( 25 FDA reports)
FEMORAL NECK FRACTURE ( 25 FDA reports)
FLUID INTAKE REDUCED ( 25 FDA reports)
FORMICATION ( 25 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 25 FDA reports)
HAEMOLYSIS ( 25 FDA reports)
HEPATOCELLULAR DAMAGE ( 25 FDA reports)
HICCUPS ( 25 FDA reports)
INGUINAL HERNIA ( 25 FDA reports)
INJECTION SITE IRRITATION ( 25 FDA reports)
LUMBAR RADICULOPATHY ( 25 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 25 FDA reports)
MEDICAL DEVICE COMPLICATION ( 25 FDA reports)
NEPHROPATHY TOXIC ( 25 FDA reports)
NERVE INJURY ( 25 FDA reports)
ABSCESS ORAL ( 24 FDA reports)
APPARENT DEATH ( 24 FDA reports)
ASPERGILLOSIS ( 24 FDA reports)
AUTOIMMUNE HEPATITIS ( 24 FDA reports)
BRADYARRHYTHMIA ( 24 FDA reports)
CATHETER RELATED COMPLICATION ( 24 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
DERMATITIS EXFOLIATIVE ( 24 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 24 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 24 FDA reports)
ENTERITIS ( 24 FDA reports)
HAEMORRHAGIC DIATHESIS ( 24 FDA reports)
HAEMOTHORAX ( 24 FDA reports)
HYPERNATRAEMIA ( 24 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 24 FDA reports)
INTRACRANIAL ANEURYSM ( 24 FDA reports)
LARYNGEAL OEDEMA ( 24 FDA reports)
LIVER INJURY ( 24 FDA reports)
LOWER LIMB FRACTURE ( 24 FDA reports)
NEUTROPHIL COUNT INCREASED ( 24 FDA reports)
OESOPHAGEAL DISORDER ( 24 FDA reports)
OESOPHAGEAL STENOSIS ( 24 FDA reports)
PANCREATITIS CHRONIC ( 24 FDA reports)
PELVIC PAIN ( 24 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 24 FDA reports)
PULMONARY HAEMORRHAGE ( 24 FDA reports)
RETINAL HAEMORRHAGE ( 24 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 24 FDA reports)
SINUS ARRHYTHMIA ( 24 FDA reports)
SNEEZING ( 24 FDA reports)
TENDON DISORDER ( 24 FDA reports)
TESTICULAR PAIN ( 24 FDA reports)
ORAL DISCOMFORT ( 23 FDA reports)
ORCHITIS ( 23 FDA reports)
OTITIS MEDIA ( 23 FDA reports)
PERITONITIS BACTERIAL ( 23 FDA reports)
PROSTATOMEGALY ( 23 FDA reports)
RENAL ISCHAEMIA ( 23 FDA reports)
SKIN ATROPHY ( 23 FDA reports)
TUMOUR LYSIS SYNDROME ( 23 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 23 FDA reports)
X-RAY ABNORMAL ( 23 FDA reports)
XEROSIS ( 23 FDA reports)
YELLOW SKIN ( 23 FDA reports)
BLOOD URIC ACID INCREASED ( 23 FDA reports)
CARDIAC OPERATION ( 23 FDA reports)
CEREBRAL DISORDER ( 23 FDA reports)
DERMATITIS CONTACT ( 23 FDA reports)
DIABETIC NEPHROPATHY ( 23 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 23 FDA reports)
DRY THROAT ( 23 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 23 FDA reports)
EPIDIDYMITIS ( 23 FDA reports)
ERYSIPELAS ( 23 FDA reports)
HYPERBILIRUBINAEMIA ( 23 FDA reports)
HYPERCOAGULATION ( 23 FDA reports)
INFECTIOUS PERITONITIS ( 23 FDA reports)
INGROWING NAIL ( 23 FDA reports)
INITIAL INSOMNIA ( 23 FDA reports)
LARGE INTESTINAL ULCER ( 23 FDA reports)
MENINGITIS ( 23 FDA reports)
METASTASES TO LYMPH NODES ( 23 FDA reports)
MUSCLE CONTRACTURE ( 23 FDA reports)
NEPHROGENIC ANAEMIA ( 23 FDA reports)
NEUROGENIC BLADDER ( 23 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 23 FDA reports)
ACUTE PRERENAL FAILURE ( 22 FDA reports)
APPLICATION SITE PRURITUS ( 22 FDA reports)
ARTHROPOD BITE ( 22 FDA reports)
BK VIRUS INFECTION ( 22 FDA reports)
BLOOD IRON DECREASED ( 22 FDA reports)
BLOOD PH DECREASED ( 22 FDA reports)
BRONCHITIS CHRONIC ( 22 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 22 FDA reports)
CORONARY ANGIOPLASTY ( 22 FDA reports)
DIVERTICULAR PERFORATION ( 22 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 22 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 22 FDA reports)
ERYTHEMA MULTIFORME ( 22 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 22 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 22 FDA reports)
JOINT SPRAIN ( 22 FDA reports)
JUGULAR VEIN THROMBOSIS ( 22 FDA reports)
LEG AMPUTATION ( 22 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 22 FDA reports)
LOSS OF EMPLOYMENT ( 22 FDA reports)
LYMPHOPENIA ( 22 FDA reports)
MIOSIS ( 22 FDA reports)
NEURITIS ( 22 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 22 FDA reports)
NYSTAGMUS ( 22 FDA reports)
OCULAR HYPERTENSION ( 22 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 22 FDA reports)
ORAL HERPES ( 22 FDA reports)
OSTEORADIONECROSIS ( 22 FDA reports)
PROSTATITIS ( 22 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 22 FDA reports)
PURULENT DISCHARGE ( 22 FDA reports)
SENSATION OF FOREIGN BODY ( 22 FDA reports)
SERUM FERRITIN INCREASED ( 22 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 22 FDA reports)
WOUND DRAINAGE ( 22 FDA reports)
OVERWEIGHT ( 21 FDA reports)
PHLEBITIS ( 21 FDA reports)
PHOTOPSIA ( 21 FDA reports)
REFLUX OESOPHAGITIS ( 21 FDA reports)
RHINITIS ( 21 FDA reports)
STATUS EPILEPTICUS ( 21 FDA reports)
VITREOUS FLOATERS ( 21 FDA reports)
ABDOMINAL ABSCESS ( 21 FDA reports)
ANGIOPLASTY ( 21 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 21 FDA reports)
BLOOD DISORDER ( 21 FDA reports)
DIABETIC RETINOPATHY ( 21 FDA reports)
DYSAESTHESIA ( 21 FDA reports)
EXPIRED DRUG ADMINISTERED ( 21 FDA reports)
FULL BLOOD COUNT DECREASED ( 21 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 21 FDA reports)
HAIR GROWTH ABNORMAL ( 21 FDA reports)
HEPATIC LESION ( 21 FDA reports)
HUNGER ( 21 FDA reports)
IMPAIRED DRIVING ABILITY ( 21 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 21 FDA reports)
LARYNGITIS ( 21 FDA reports)
LEUKOENCEPHALOPATHY ( 21 FDA reports)
MALIGNANT HYPERTENSION ( 21 FDA reports)
METASTATIC PAIN ( 21 FDA reports)
MUSCLE STRAIN ( 21 FDA reports)
NASAL POLYPS ( 21 FDA reports)
NASAL SEPTUM DEVIATION ( 21 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 21 FDA reports)
ABSCESS LIMB ( 20 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 20 FDA reports)
ACTINOMYCOSIS ( 20 FDA reports)
AMMONIA INCREASED ( 20 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 20 FDA reports)
BARRETT'S OESOPHAGUS ( 20 FDA reports)
BENCE JONES PROTEINURIA ( 20 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 20 FDA reports)
BLOOD TEST ABNORMAL ( 20 FDA reports)
CARDIAC DEATH ( 20 FDA reports)
CARDIAC FAILURE ACUTE ( 20 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 20 FDA reports)
CUSHINGOID ( 20 FDA reports)
DEVICE FAILURE ( 20 FDA reports)
DROOLING ( 20 FDA reports)
DYSTONIA ( 20 FDA reports)
ESCHERICHIA SEPSIS ( 20 FDA reports)
FUNGAEMIA ( 20 FDA reports)
GASTRIC CANCER ( 20 FDA reports)
GASTROINTESTINAL PERFORATION ( 20 FDA reports)
GLOSSITIS ( 20 FDA reports)
HORDEOLUM ( 20 FDA reports)
IMPAIRED SELF-CARE ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 20 FDA reports)
KNEE OPERATION ( 20 FDA reports)
MACROCYTOSIS ( 20 FDA reports)
MECHANICAL VENTILATION ( 20 FDA reports)
MITRAL VALVE STENOSIS ( 20 FDA reports)
MONOCLONAL GAMMOPATHY ( 20 FDA reports)
MYOCARDITIS ( 20 FDA reports)
NECROTISING FASCIITIS ( 20 FDA reports)
NON-SMALL CELL LUNG CANCER ( 20 FDA reports)
ONYCHOMADESIS ( 20 FDA reports)
PERIARTHRITIS ( 20 FDA reports)
PERONEAL NERVE PALSY ( 20 FDA reports)
POST PROCEDURAL HAEMATOMA ( 20 FDA reports)
PROSTATE CANCER METASTATIC ( 20 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 20 FDA reports)
SCLERODERMA ( 20 FDA reports)
VENOUS THROMBOSIS ( 20 FDA reports)
OESOPHAGITIS ULCERATIVE ( 19 FDA reports)
OPERATIVE HAEMORRHAGE ( 19 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 19 FDA reports)
PIGMENTATION DISORDER ( 19 FDA reports)
PLANTAR FASCIITIS ( 19 FDA reports)
PNEUMONIA BACTERIAL ( 19 FDA reports)
POOR PERIPHERAL CIRCULATION ( 19 FDA reports)
PYURIA ( 19 FDA reports)
SCHIZOPHRENIA ( 19 FDA reports)
SELF-MEDICATION ( 19 FDA reports)
TESTICULAR SWELLING ( 19 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 19 FDA reports)
TONGUE INJURY ( 19 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 19 FDA reports)
TRISMUS ( 19 FDA reports)
TROPONIN T INCREASED ( 19 FDA reports)
URINARY HESITATION ( 19 FDA reports)
VASCULAR OCCLUSION ( 19 FDA reports)
WEIGHT FLUCTUATION ( 19 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 19 FDA reports)
ANASTOMOTIC LEAK ( 19 FDA reports)
AORTIC DILATATION ( 19 FDA reports)
APHONIA ( 19 FDA reports)
BACK INJURY ( 19 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 19 FDA reports)
BONE EROSION ( 19 FDA reports)
BRAIN DEATH ( 19 FDA reports)
BRAIN INJURY ( 19 FDA reports)
CHOLANGITIS ( 19 FDA reports)
CONCUSSION ( 19 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 19 FDA reports)
DIABETIC COMA ( 19 FDA reports)
EMPYEMA ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
FRACTURE NONUNION ( 19 FDA reports)
HEPATOCELLULAR INJURY ( 19 FDA reports)
HILAR LYMPHADENOPATHY ( 19 FDA reports)
HOMICIDAL IDEATION ( 19 FDA reports)
HYPERCAPNIA ( 19 FDA reports)
ILEUS PARALYTIC ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
LIGAMENT SPRAIN ( 19 FDA reports)
LIPOMA ( 19 FDA reports)
MALIGNANT MELANOMA ( 19 FDA reports)
MANIA ( 19 FDA reports)
METASTASIS ( 19 FDA reports)
NECROSIS ( 19 FDA reports)
ALCOHOL USE ( 18 FDA reports)
AORTIC VALVE DISEASE ( 18 FDA reports)
AORTIC VALVE STENOSIS ( 18 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 18 FDA reports)
ATRIAL SEPTAL DEFECT ( 18 FDA reports)
ATROPHY ( 18 FDA reports)
CALCULUS BLADDER ( 18 FDA reports)
CARDIAC ABLATION ( 18 FDA reports)
CARDIAC VALVE ABSCESS ( 18 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 18 FDA reports)
CERUMEN IMPACTION ( 18 FDA reports)
CYSTOCELE ( 18 FDA reports)
DRUG SCREEN POSITIVE ( 18 FDA reports)
EAR DISCOMFORT ( 18 FDA reports)
EARLY SATIETY ( 18 FDA reports)
EDENTULOUS ( 18 FDA reports)
ESCHERICHIA BACTERAEMIA ( 18 FDA reports)
FEAR OF DEATH ( 18 FDA reports)
HAEMOGLOBINURIA ( 18 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 18 FDA reports)
HYPERURICAEMIA ( 18 FDA reports)
INFARCTION ( 18 FDA reports)
ISCHAEMIC HEPATITIS ( 18 FDA reports)
LARGE INTESTINE PERFORATION ( 18 FDA reports)
LISTLESS ( 18 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 18 FDA reports)
MENIERE'S DISEASE ( 18 FDA reports)
MYELOPATHY ( 18 FDA reports)
NECK INJURY ( 18 FDA reports)
NEPHROPATHY ( 18 FDA reports)
NEPHROTIC SYNDROME ( 18 FDA reports)
PALATAL OEDEMA ( 18 FDA reports)
PARKINSONISM ( 18 FDA reports)
PELVIC FRACTURE ( 18 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 18 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 18 FDA reports)
QRS AXIS ABNORMAL ( 18 FDA reports)
RESPIRATORY ACIDOSIS ( 18 FDA reports)
RHEUMATOID NODULE ( 18 FDA reports)
SALIVARY HYPERSECRETION ( 18 FDA reports)
SCIATIC NERVE INJURY ( 18 FDA reports)
SMALL FOR DATES BABY ( 18 FDA reports)
THROMBOPHLEBITIS ( 18 FDA reports)
UVEITIS ( 18 FDA reports)
VEIN DISORDER ( 18 FDA reports)
PERICARDIAL HAEMORRHAGE ( 17 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 17 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 17 FDA reports)
RASH PUSTULAR ( 17 FDA reports)
SHOCK HAEMORRHAGIC ( 17 FDA reports)
SKIN SWELLING ( 17 FDA reports)
SNORING ( 17 FDA reports)
THERMAL BURN ( 17 FDA reports)
TOOTH INJURY ( 17 FDA reports)
TRIGEMINAL NEURALGIA ( 17 FDA reports)
VERTIGO POSITIONAL ( 17 FDA reports)
WOUND COMPLICATION ( 17 FDA reports)
APHTHOUS STOMATITIS ( 17 FDA reports)
BACTERIAL SEPSIS ( 17 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 17 FDA reports)
BRUXISM ( 17 FDA reports)
CAROTID ARTERY DISEASE ( 17 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 17 FDA reports)
GASTRIC POLYPS ( 17 FDA reports)
GINGIVAL DISORDER ( 17 FDA reports)
GRAFT DYSFUNCTION ( 17 FDA reports)
HYDROCEPHALUS ( 17 FDA reports)
INCOHERENT ( 17 FDA reports)
JUGULAR VEIN DISTENSION ( 17 FDA reports)
MENORRHAGIA ( 17 FDA reports)
MUSCLE HAEMORRHAGE ( 17 FDA reports)
MYOPIA ( 17 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 17 FDA reports)
ABNORMAL FAECES ( 16 FDA reports)
ANOXIC ENCEPHALOPATHY ( 16 FDA reports)
ANXIETY DISORDER ( 16 FDA reports)
AORTIC VALVE SCLEROSIS ( 16 FDA reports)
APPLICATION SITE RASH ( 16 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 16 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 16 FDA reports)
BONE DEFORMITY ( 16 FDA reports)
BRADYPHRENIA ( 16 FDA reports)
CARDIAC OUTPUT DECREASED ( 16 FDA reports)
CATHETER RELATED INFECTION ( 16 FDA reports)
CEREBRAL HAEMATOMA ( 16 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 16 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 16 FDA reports)
COLONOSCOPY ABNORMAL ( 16 FDA reports)
CYSTITIS HAEMORRHAGIC ( 16 FDA reports)
DEMYELINATION ( 16 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 16 FDA reports)
FACE INJURY ( 16 FDA reports)
HEPATORENAL SYNDROME ( 16 FDA reports)
HERPES SIMPLEX ( 16 FDA reports)
HYPERPLASIA ( 16 FDA reports)
INJECTION SITE RASH ( 16 FDA reports)
LIVEDO RETICULARIS ( 16 FDA reports)
MULTIPLE FRACTURES ( 16 FDA reports)
MUSCLE RIGIDITY ( 16 FDA reports)
MYDRIASIS ( 16 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 16 FDA reports)
PARAPLEGIA ( 16 FDA reports)
PEAU D'ORANGE ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
POLYMYALGIA RHEUMATICA ( 16 FDA reports)
PUPIL FIXED ( 16 FDA reports)
RESPIRATORY RATE DECREASED ( 16 FDA reports)
SECRETION DISCHARGE ( 16 FDA reports)
SENSATION OF PRESSURE ( 16 FDA reports)
SKIN WRINKLING ( 16 FDA reports)
SPLENIC INFARCTION ( 16 FDA reports)
SPUTUM CULTURE POSITIVE ( 16 FDA reports)
STREPTOCOCCAL INFECTION ( 16 FDA reports)
TERMINAL STATE ( 16 FDA reports)
THYROID CANCER ( 16 FDA reports)
TUBERCULOSIS ( 16 FDA reports)
UNDERDOSE ( 16 FDA reports)
URINARY TRACT OBSTRUCTION ( 16 FDA reports)
VERTEBROPLASTY ( 16 FDA reports)
VITREOUS DETACHMENT ( 16 FDA reports)
OPTIC ATROPHY ( 15 FDA reports)
ORAL INFECTION ( 15 FDA reports)
ORAL SURGERY ( 15 FDA reports)
PANCREATIC CYST ( 15 FDA reports)
PARESIS ( 15 FDA reports)
PATHOLOGICAL GAMBLING ( 15 FDA reports)
PRE-ECLAMPSIA ( 15 FDA reports)
PRODUCT ADHESION ISSUE ( 15 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 15 FDA reports)
RESPIRATORY ALKALOSIS ( 15 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 15 FDA reports)
RIGHT ATRIAL DILATATION ( 15 FDA reports)
SCRATCH ( 15 FDA reports)
SINUS ARREST ( 15 FDA reports)
SKIN FISSURES ( 15 FDA reports)
SOFT TISSUE DISORDER ( 15 FDA reports)
SUBDURAL HAEMORRHAGE ( 15 FDA reports)
TOXIC ENCEPHALOPATHY ( 15 FDA reports)
TOXIC SKIN ERUPTION ( 15 FDA reports)
TRANSFUSION ( 15 FDA reports)
TREATMENT FAILURE ( 15 FDA reports)
VASCULAR INSUFFICIENCY ( 15 FDA reports)
VENOUS OCCLUSION ( 15 FDA reports)
VOCAL CORD PARALYSIS ( 15 FDA reports)
ACUTE LEUKAEMIA ( 15 FDA reports)
ADENOCARCINOMA ( 15 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 15 FDA reports)
APPENDICITIS PERFORATED ( 15 FDA reports)
BILE DUCT OBSTRUCTION ( 15 FDA reports)
BONE MARROW OEDEMA ( 15 FDA reports)
BREAST TENDERNESS ( 15 FDA reports)
BUNION ( 15 FDA reports)
CHONDROPATHY ( 15 FDA reports)
COELIAC DISEASE ( 15 FDA reports)
COLLAPSE OF LUNG ( 15 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 15 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 15 FDA reports)
ENCEPHALITIS ( 15 FDA reports)
FEELING DRUNK ( 15 FDA reports)
FIBRIN D DIMER INCREASED ( 15 FDA reports)
FOREIGN BODY ( 15 FDA reports)
GRANULOMA ( 15 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 15 FDA reports)
HYPERREFLEXIA ( 15 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 15 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 15 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 15 FDA reports)
INCREASED APPETITE ( 15 FDA reports)
INTESTINAL MASS ( 15 FDA reports)
JOINT DISLOCATION ( 15 FDA reports)
LABILE BLOOD PRESSURE ( 15 FDA reports)
METASTASES TO ADRENALS ( 15 FDA reports)
NERVE COMPRESSION ( 15 FDA reports)
NEUROPATHY ( 15 FDA reports)
NODAL ARRHYTHMIA ( 15 FDA reports)
OESOPHAGEAL CARCINOMA ( 15 FDA reports)
ADRENAL NEOPLASM ( 14 FDA reports)
ANOSMIA ( 14 FDA reports)
ATHEROSCLEROSIS ( 14 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 14 FDA reports)
BILE DUCT STONE ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 14 FDA reports)
BLADDER OPERATION ( 14 FDA reports)
BLEPHARITIS ( 14 FDA reports)
BLEPHAROSPASM ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 14 FDA reports)
BLOOD SODIUM INCREASED ( 14 FDA reports)
BREAST CANCER FEMALE ( 14 FDA reports)
BRONCHIECTASIS ( 14 FDA reports)
CARDIAC VALVE VEGETATION ( 14 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 14 FDA reports)
CATHETER SITE HAEMORRHAGE ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
CLAVICLE FRACTURE ( 14 FDA reports)
COLON ADENOMA ( 14 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 14 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 14 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 14 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 14 FDA reports)
FIBULA FRACTURE ( 14 FDA reports)
FOOD POISONING ( 14 FDA reports)
FRUSTRATION ( 14 FDA reports)
GASTROINTESTINAL CARCINOMA ( 14 FDA reports)
GASTROINTESTINAL INFECTION ( 14 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 14 FDA reports)
GOUTY ARTHRITIS ( 14 FDA reports)
HAIR TEXTURE ABNORMAL ( 14 FDA reports)
HYPERTONIC BLADDER ( 14 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 14 FDA reports)
HYPOPERFUSION ( 14 FDA reports)
INJECTION SITE EXTRAVASATION ( 14 FDA reports)
INTESTINAL DILATATION ( 14 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 14 FDA reports)
LIPIDS INCREASED ( 14 FDA reports)
LOCALISED OEDEMA ( 14 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 14 FDA reports)
MENSTRUATION IRREGULAR ( 14 FDA reports)
MULTI-ORGAN DISORDER ( 14 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 14 FDA reports)
NASAL DISCOMFORT ( 14 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 14 FDA reports)
OESOPHAGEAL ULCER ( 14 FDA reports)
ORAL CAVITY FISTULA ( 14 FDA reports)
OTITIS EXTERNA ( 14 FDA reports)
PROSTATIC DISORDER ( 14 FDA reports)
PSORIATIC ARTHROPATHY ( 14 FDA reports)
RENAL COLIC ( 14 FDA reports)
RETINAL DETACHMENT ( 14 FDA reports)
SIALOADENITIS ( 14 FDA reports)
SKIN INJURY ( 14 FDA reports)
STRESS URINARY INCONTINENCE ( 14 FDA reports)
SYNOVITIS ( 14 FDA reports)
TOBACCO ABUSE ( 14 FDA reports)
TOE AMPUTATION ( 14 FDA reports)
TONGUE OEDEMA ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
VASCULAR GRAFT OCCLUSION ( 14 FDA reports)
VULVOVAGINAL DRYNESS ( 14 FDA reports)
OPTIC NEURITIS ( 13 FDA reports)
OROANTRAL FISTULA ( 13 FDA reports)
OROPHARYNGEAL BLISTERING ( 13 FDA reports)
OVARIAN CANCER ( 13 FDA reports)
PEMPHIGOID ( 13 FDA reports)
PO2 DECREASED ( 13 FDA reports)
POOR PERSONAL HYGIENE ( 13 FDA reports)
PREGNANCY ( 13 FDA reports)
PREMATURE LABOUR ( 13 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 13 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 13 FDA reports)
RESUSCITATION ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SEROMA ( 13 FDA reports)
SKIN HYPOPIGMENTATION ( 13 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 13 FDA reports)
SUFFOCATION FEELING ( 13 FDA reports)
SURGICAL PROCEDURE REPEATED ( 13 FDA reports)
UMBILICAL HERNIA ( 13 FDA reports)
URETERIC OBSTRUCTION ( 13 FDA reports)
URETHRAL STENOSIS ( 13 FDA reports)
VAGINAL INFECTION ( 13 FDA reports)
VASODILATATION ( 13 FDA reports)
VENA CAVA THROMBOSIS ( 13 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 13 FDA reports)
ABSCESS INTESTINAL ( 13 FDA reports)
ADENOMA BENIGN ( 13 FDA reports)
AKATHISIA ( 13 FDA reports)
ALCOHOLISM ( 13 FDA reports)
AORTIC DISORDER ( 13 FDA reports)
APPLICATION SITE IRRITATION ( 13 FDA reports)
ARTERIAL THROMBOSIS ( 13 FDA reports)
ARTHRITIS BACTERIAL ( 13 FDA reports)
ASPIRATION PLEURAL CAVITY ( 13 FDA reports)
BLADDER DISCOMFORT ( 13 FDA reports)
BLOOD BICARBONATE DECREASED ( 13 FDA reports)
BLOOD BLISTER ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 13 FDA reports)
CARDIOVERSION ( 13 FDA reports)
CEREBELLAR HAEMORRHAGE ( 13 FDA reports)
CHOKING SENSATION ( 13 FDA reports)
CHOLESTATIC LIVER INJURY ( 13 FDA reports)
DENTURE WEARER ( 13 FDA reports)
DYSTHYMIC DISORDER ( 13 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 13 FDA reports)
EPIGASTRIC DISCOMFORT ( 13 FDA reports)
EYE DISCHARGE ( 13 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 13 FDA reports)
GASTRODUODENITIS ( 13 FDA reports)
GASTROINTESTINAL NECROSIS ( 13 FDA reports)
GASTROINTESTINAL PAIN ( 13 FDA reports)
GINGIVAL EROSION ( 13 FDA reports)
GLOMERULONEPHRITIS ( 13 FDA reports)
HERNIA REPAIR ( 13 FDA reports)
HYPERMETROPIA ( 13 FDA reports)
HYPERTONIA ( 13 FDA reports)
IMMUNODEFICIENCY ( 13 FDA reports)
INJECTION SITE DISCOLOURATION ( 13 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 13 FDA reports)
INTRAOCULAR LENS IMPLANT ( 13 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 13 FDA reports)
MONOPLEGIA ( 13 FDA reports)
NECK MASS ( 13 FDA reports)
NERVE ROOT COMPRESSION ( 13 FDA reports)
ABSCESS DRAINAGE ( 12 FDA reports)
ABSCESS NECK ( 12 FDA reports)
ADRENAL INSUFFICIENCY ( 12 FDA reports)
AFFECT LABILITY ( 12 FDA reports)
ANAEMIA MACROCYTIC ( 12 FDA reports)
ANAL HAEMORRHAGE ( 12 FDA reports)
ARTERIAL HAEMORRHAGE ( 12 FDA reports)
ASTERIXIS ( 12 FDA reports)
BACTERIAL TEST POSITIVE ( 12 FDA reports)
BASEDOW'S DISEASE ( 12 FDA reports)
BLEEDING TIME PROLONGED ( 12 FDA reports)
BLOOD UREA DECREASED ( 12 FDA reports)
BREATH ODOUR ( 12 FDA reports)
BRUGADA SYNDROME ( 12 FDA reports)
BUNDLE BRANCH BLOCK ( 12 FDA reports)
CARBON DIOXIDE DECREASED ( 12 FDA reports)
CAROTID BRUIT ( 12 FDA reports)
CATHETER SITE HAEMATOMA ( 12 FDA reports)
COSTOCHONDRITIS ( 12 FDA reports)
DERMATITIS ACNEIFORM ( 12 FDA reports)
DERMATITIS BULLOUS ( 12 FDA reports)
DIABETIC COMPLICATION ( 12 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 12 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 12 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 12 FDA reports)
ENCEPHALOMALACIA ( 12 FDA reports)
EYE MOVEMENT DISORDER ( 12 FDA reports)
FACIAL PARESIS ( 12 FDA reports)
GASTRIC PERFORATION ( 12 FDA reports)
GASTRITIS ATROPHIC ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
HAEMARTHROSIS ( 12 FDA reports)
HAEMOGLOBIN ABNORMAL ( 12 FDA reports)
HALLUCINATIONS, MIXED ( 12 FDA reports)
HEPATIC MASS ( 12 FDA reports)
HYPERMAGNESAEMIA ( 12 FDA reports)
HYPERPHOSPHATAEMIA ( 12 FDA reports)
ILIAC ARTERY OCCLUSION ( 12 FDA reports)
IMMUNE SYSTEM DISORDER ( 12 FDA reports)
INJECTION SITE NODULE ( 12 FDA reports)
INJECTION SITE WARMTH ( 12 FDA reports)
INTENTIONAL SELF-INJURY ( 12 FDA reports)
INTESTINAL HAEMORRHAGE ( 12 FDA reports)
INTESTINAL ULCER ( 12 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 12 FDA reports)
LIVER TRANSPLANT ( 12 FDA reports)
LOWER EXTREMITY MASS ( 12 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 12 FDA reports)
MALLORY-WEISS SYNDROME ( 12 FDA reports)
MARROW HYPERPLASIA ( 12 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 12 FDA reports)
MITRAL VALVE CALCIFICATION ( 12 FDA reports)
NEUROTOXICITY ( 12 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 12 FDA reports)
NOSOCOMIAL INFECTION ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 12 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 12 FDA reports)
PANCREATIC ATROPHY ( 12 FDA reports)
PARONYCHIA ( 12 FDA reports)
PARTNER STRESS ( 12 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 12 FDA reports)
PELVIC HAEMATOMA ( 12 FDA reports)
PERIORBITAL HAEMATOMA ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
PLASMACYTOSIS ( 12 FDA reports)
POLYCYTHAEMIA ( 12 FDA reports)
POLYPECTOMY ( 12 FDA reports)
POST PROCEDURAL INFECTION ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
PROSTHESIS USER ( 12 FDA reports)
PROTHROMBIN TIME SHORTENED ( 12 FDA reports)
PULSE ABNORMAL ( 12 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 12 FDA reports)
PUPILS UNEQUAL ( 12 FDA reports)
PYELONEPHRITIS ACUTE ( 12 FDA reports)
RAYNAUD'S PHENOMENON ( 12 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 12 FDA reports)
RENAL MASS ( 12 FDA reports)
SCROTAL SWELLING ( 12 FDA reports)
SKELETAL INJURY ( 12 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
STENT OCCLUSION ( 12 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 12 FDA reports)
TEMPERATURE INTOLERANCE ( 12 FDA reports)
TINEA PEDIS ( 12 FDA reports)
TONGUE DISCOLOURATION ( 12 FDA reports)
TRANSPLANT FAILURE ( 12 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 12 FDA reports)
URINE ABNORMALITY ( 12 FDA reports)
ONYCHOCLASIS ( 11 FDA reports)
ORAL NEOPLASM BENIGN ( 11 FDA reports)
ORTHOSTATIC INTOLERANCE ( 11 FDA reports)
PANIC REACTION ( 11 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 11 FDA reports)
PERITONEAL DIALYSIS ( 11 FDA reports)
PERITONEAL HAEMORRHAGE ( 11 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 11 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 11 FDA reports)
POST HERPETIC NEURALGIA ( 11 FDA reports)
PULMONARY VASCULAR DISORDER ( 11 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 11 FDA reports)
ROSACEA ( 11 FDA reports)
SCAN ABNORMAL ( 11 FDA reports)
SERUM SICKNESS ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
SKIN REACTION ( 11 FDA reports)
SKIN TOXICITY ( 11 FDA reports)
SPLEEN DISORDER ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 11 FDA reports)
SUBCUTANEOUS ABSCESS ( 11 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 11 FDA reports)
TONGUE DRY ( 11 FDA reports)
TRAUMATIC HAEMATOMA ( 11 FDA reports)
TUBERCULIN TEST POSITIVE ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VESTIBULAR DISORDER ( 11 FDA reports)
VESTIBULAR NEURONITIS ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 11 FDA reports)
ADRENAL ADENOMA ( 11 FDA reports)
AMAUROSIS FUGAX ( 11 FDA reports)
ANION GAP INCREASED ( 11 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 11 FDA reports)
BIOPSY BONE ABNORMAL ( 11 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 11 FDA reports)
BLOOD CREATININE DECREASED ( 11 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 11 FDA reports)
CARDIAC FIBRILLATION ( 11 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 11 FDA reports)
CERVICAL CORD COMPRESSION ( 11 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 11 FDA reports)
CONTRAST MEDIA REACTION ( 11 FDA reports)
CORNEAL ABRASION ( 11 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 11 FDA reports)
DEPENDENCE ( 11 FDA reports)
DIABETIC GASTROPARESIS ( 11 FDA reports)
DROP ATTACKS ( 11 FDA reports)
DRUG ABUSER ( 11 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 11 FDA reports)
DUPUYTREN'S CONTRACTURE ( 11 FDA reports)
EJECTION FRACTION ABNORMAL ( 11 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 11 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 11 FDA reports)
EROSIVE DUODENITIS ( 11 FDA reports)
FLAT AFFECT ( 11 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 11 FDA reports)
GASTROENTERITIS RADIATION ( 11 FDA reports)
GLUCOSE URINE PRESENT ( 11 FDA reports)
HAEMATOMA INFECTION ( 11 FDA reports)
HEPATIC CALCIFICATION ( 11 FDA reports)
HEPATITIS CHOLESTATIC ( 11 FDA reports)
HEPATITIS TOXIC ( 11 FDA reports)
HYPERPHAGIA ( 11 FDA reports)
HYPOVENTILATION ( 11 FDA reports)
HYSTERECTOMY ( 11 FDA reports)
IMMOBILE ( 11 FDA reports)
INFECTED SKIN ULCER ( 11 FDA reports)
INFUSION SITE INFECTION ( 11 FDA reports)
LICHEN PLANUS ( 11 FDA reports)
LIVER ABSCESS ( 11 FDA reports)
LONG QT SYNDROME ( 11 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 11 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 11 FDA reports)
MUSCLE SPASTICITY ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
ABDOMINAL HAEMATOMA ( 10 FDA reports)
AFFECTIVE DISORDER ( 10 FDA reports)
ALCOHOL INTERACTION ( 10 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 10 FDA reports)
ANGIOMYOLIPOMA ( 10 FDA reports)
ANIMAL BITE ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
AORTIC VALVE REPLACEMENT ( 10 FDA reports)
APPLICATION SITE PAIN ( 10 FDA reports)
APPLICATION SITE VESICLES ( 10 FDA reports)
ARTERIAL STENOSIS ( 10 FDA reports)
ARTERIOSPASM CORONARY ( 10 FDA reports)
ATRIAL THROMBOSIS ( 10 FDA reports)
BLADDER OBSTRUCTION ( 10 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 10 FDA reports)
BLOOD IRON INCREASED ( 10 FDA reports)
BLOOD LACTIC ACID INCREASED ( 10 FDA reports)
BLOOD OSMOLARITY DECREASED ( 10 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 10 FDA reports)
BONE OPERATION ( 10 FDA reports)
BRAIN STEM INFARCTION ( 10 FDA reports)
BREAST ENLARGEMENT ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
CALCIPHYLAXIS ( 10 FDA reports)
CARDIAC ASTHMA ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
CARDIOTOXICITY ( 10 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 10 FDA reports)
CEREBRAL THROMBOSIS ( 10 FDA reports)
CERVIX CARCINOMA ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 10 FDA reports)
COMMUNICATION DISORDER ( 10 FDA reports)
CORONARY ARTERY RESTENOSIS ( 10 FDA reports)
CUBITAL TUNNEL SYNDROME ( 10 FDA reports)
DEFAECATION URGENCY ( 10 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 10 FDA reports)
DYSGRAPHIA ( 10 FDA reports)
EFFUSION ( 10 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
GALLBLADDER OPERATION ( 10 FDA reports)
GENITAL BURNING SENSATION ( 10 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 10 FDA reports)
HEAD DISCOMFORT ( 10 FDA reports)
HEART VALVE REPLACEMENT ( 10 FDA reports)
HEPATIC CONGESTION ( 10 FDA reports)
HYPOREFLEXIA ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INCORRECT STORAGE OF DRUG ( 10 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 10 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 10 FDA reports)
ISCHAEMIC ULCER ( 10 FDA reports)
JOINT WARMTH ( 10 FDA reports)
LACTOSE INTOLERANCE ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
LIPID METABOLISM DISORDER ( 10 FDA reports)
LUNG CANCER METASTATIC ( 10 FDA reports)
MACULAR OEDEMA ( 10 FDA reports)
MALABSORPTION ( 10 FDA reports)
MEAN CELL VOLUME DECREASED ( 10 FDA reports)
MICROCYTIC ANAEMIA ( 10 FDA reports)
MICTURITION DISORDER ( 10 FDA reports)
MIDDLE EAR EFFUSION ( 10 FDA reports)
MOUTH INJURY ( 10 FDA reports)
MUSCLE NECROSIS ( 10 FDA reports)
MUSCLE RUPTURE ( 10 FDA reports)
NAIL DISORDER ( 10 FDA reports)
NAIL DYSTROPHY ( 10 FDA reports)
NARCOTIC INTOXICATION ( 10 FDA reports)
NASAL DRYNESS ( 10 FDA reports)
NOCTURNAL DYSPNOEA ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 10 FDA reports)
OBSTRUCTIVE UROPATHY ( 10 FDA reports)
OLIGOHYDRAMNIOS ( 10 FDA reports)
ORAL FUNGAL INFECTION ( 10 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 10 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 10 FDA reports)
PCO2 DECREASED ( 10 FDA reports)
PERFORMANCE STATUS DECREASED ( 10 FDA reports)
PLATELET COUNT ABNORMAL ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
POOR VENOUS ACCESS ( 10 FDA reports)
PROTEIN TOTAL INCREASED ( 10 FDA reports)
PROTEUS INFECTION ( 10 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 10 FDA reports)
PSYCHOLOGICAL TRAUMA ( 10 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 10 FDA reports)
QUADRIPLEGIA ( 10 FDA reports)
RADICULITIS ( 10 FDA reports)
REGURGITATION ( 10 FDA reports)
RENAL TUBULAR ACIDOSIS ( 10 FDA reports)
RETINAL VEIN OCCLUSION ( 10 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 10 FDA reports)
SELF-INJURIOUS IDEATION ( 10 FDA reports)
SENSATION OF BLOOD FLOW ( 10 FDA reports)
SENSITIVITY OF TEETH ( 10 FDA reports)
SKIN INFECTION ( 10 FDA reports)
STRESS CARDIOMYOPATHY ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 10 FDA reports)
TELANGIECTASIA ( 10 FDA reports)
TENDON INJURY ( 10 FDA reports)
THYROID CYST ( 10 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 10 FDA reports)
TINEA CRURIS ( 10 FDA reports)
TOXIC NEUROPATHY ( 10 FDA reports)
TRAUMATIC BRAIN INJURY ( 10 FDA reports)
TRAUMATIC LUNG INJURY ( 10 FDA reports)
URINE OSMOLARITY DECREASED ( 10 FDA reports)
VASCULAR RUPTURE ( 10 FDA reports)
VENOUS THROMBOSIS LIMB ( 10 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
WOUND HAEMORRHAGE ( 10 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
OVARIAN ENLARGEMENT ( 9 FDA reports)
PAINFUL RESPIRATION ( 9 FDA reports)
PANCREATITIS RELAPSING ( 9 FDA reports)
PERICARDITIS CONSTRICTIVE ( 9 FDA reports)
PERITONEAL ADHESIONS ( 9 FDA reports)
PNEUMONIA FUNGAL ( 9 FDA reports)
PORTAL VEIN THROMBOSIS ( 9 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
RECTAL ABSCESS ( 9 FDA reports)
RECTAL PROLAPSE ( 9 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 9 FDA reports)
SACROILIITIS ( 9 FDA reports)
SEASONAL ALLERGY ( 9 FDA reports)
SHUNT OCCLUSION ( 9 FDA reports)
SKIN DESQUAMATION ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SOFT TISSUE INJURY ( 9 FDA reports)
SOPOR ( 9 FDA reports)
SPLENIC RUPTURE ( 9 FDA reports)
STEM CELL TRANSPLANT ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
THROAT CANCER ( 9 FDA reports)
TONGUE BITING ( 9 FDA reports)
TRANSFUSION REACTION ( 9 FDA reports)
TRIGGER FINGER ( 9 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
ABDOMINAL ADHESIONS ( 9 FDA reports)
ABDOMINAL RIGIDITY ( 9 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
ADNEXA UTERI CYST ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
ADVERSE REACTION ( 9 FDA reports)
ALCOHOL POISONING ( 9 FDA reports)
AMYLOIDOSIS ( 9 FDA reports)
APPENDICECTOMY ( 9 FDA reports)
APPETITE DISORDER ( 9 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
BIPOLAR I DISORDER ( 9 FDA reports)
BLOOD MAGNESIUM INCREASED ( 9 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 9 FDA reports)
BONE MARROW DEPRESSION ( 9 FDA reports)
BREAST CYST ( 9 FDA reports)
BREAST INFECTION ( 9 FDA reports)
BREAST OEDEMA ( 9 FDA reports)
BREAST PROSTHESIS USER ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CALCULUS URETERIC ( 9 FDA reports)
CANDIDURIA ( 9 FDA reports)
CARTILAGE INJURY ( 9 FDA reports)
CATHETER SITE INFECTION ( 9 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 9 FDA reports)
CERVICOBRACHIAL SYNDROME ( 9 FDA reports)
CHOREA ( 9 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 9 FDA reports)
COLON POLYPECTOMY ( 9 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 9 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 9 FDA reports)
CULTURE WOUND POSITIVE ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DEATH OF RELATIVE ( 9 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 9 FDA reports)
DISSOCIATION ( 9 FDA reports)
DRUG TOLERANCE ( 9 FDA reports)
DYSPHEMIA ( 9 FDA reports)
EAR DISORDER ( 9 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 9 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 9 FDA reports)
ENTERITIS INFECTIOUS ( 9 FDA reports)
ENURESIS ( 9 FDA reports)
EPIDERMOLYSIS ( 9 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
EYE INFLAMMATION ( 9 FDA reports)
EYE INJURY ( 9 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 9 FDA reports)
FINGER DEFORMITY ( 9 FDA reports)
FOETAL GROWTH RESTRICTION ( 9 FDA reports)
FOLLICULITIS ( 9 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 9 FDA reports)
GALLBLADDER INJURY ( 9 FDA reports)
GASTRINOMA ( 9 FDA reports)
GENERALISED ANXIETY DISORDER ( 9 FDA reports)
GENITAL HERPES ( 9 FDA reports)
GUILLAIN-BARRE SYNDROME ( 9 FDA reports)
HAEMOGLOBIN INCREASED ( 9 FDA reports)
HEART DISEASE CONGENITAL ( 9 FDA reports)
HEART SOUNDS ABNORMAL ( 9 FDA reports)
HEPATIC PAIN ( 9 FDA reports)
HERPES VIRUS INFECTION ( 9 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 9 FDA reports)
HYPERTRICHOSIS ( 9 FDA reports)
HYPOVOLAEMIC SHOCK ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 9 FDA reports)
INCISIONAL HERNIA ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INJECTION SITE URTICARIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 9 FDA reports)
INTERVERTEBRAL DISCITIS ( 9 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 9 FDA reports)
LEUKOCYTURIA ( 9 FDA reports)
LIGAMENT OPERATION ( 9 FDA reports)
LIP DISORDER ( 9 FDA reports)
LUMBAR SPINE FLATTENING ( 9 FDA reports)
MACULE ( 9 FDA reports)
METAPLASIA ( 9 FDA reports)
MICROANGIOPATHY ( 9 FDA reports)
MITRAL VALVE REPLACEMENT ( 9 FDA reports)
MONOPARESIS ( 9 FDA reports)
MUCOSAL DRYNESS ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 9 FDA reports)
NONSPECIFIC REACTION ( 9 FDA reports)
OBSTRUCTION GASTRIC ( 9 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 9 FDA reports)
OESOPHAGEAL SPASM ( 9 FDA reports)
ABDOMINAL INFECTION ( 8 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 8 FDA reports)
ACANTHOMA ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 8 FDA reports)
ACUTE ABDOMEN ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 8 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 8 FDA reports)
ANASTOMOTIC STENOSIS ( 8 FDA reports)
AORTIC ANEURYSM REPAIR ( 8 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 8 FDA reports)
ARTERIOVENOUS MALFORMATION ( 8 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 8 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 8 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 8 FDA reports)
BONE NEOPLASM ( 8 FDA reports)
BRAIN CONTUSION ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
BREAST CANCER IN SITU ( 8 FDA reports)
BREAST CANCER METASTATIC ( 8 FDA reports)
BRONCHIAL CARCINOMA ( 8 FDA reports)
CARDIAC HYPERTROPHY ( 8 FDA reports)
CARDIAC INFECTION ( 8 FDA reports)
CATHETER PLACEMENT ( 8 FDA reports)
CENTRAL LINE INFECTION ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 8 FDA reports)
CLAUSTROPHOBIA ( 8 FDA reports)
COLON CANCER RECURRENT ( 8 FDA reports)
COLONIC STENOSIS ( 8 FDA reports)
COR PULMONALE ( 8 FDA reports)
CULTURE POSITIVE ( 8 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 8 FDA reports)
DEVICE DISLOCATION ( 8 FDA reports)
DEVICE MISUSE ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIPLEGIA ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
EAR CONGESTION ( 8 FDA reports)
EJACULATION FAILURE ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
ENTEROCOCCAL SEPSIS ( 8 FDA reports)
EOSINOPHIL COUNT INCREASED ( 8 FDA reports)
ERB'S PALSY ( 8 FDA reports)
EXTERNAL EAR DISORDER ( 8 FDA reports)
FAECES HARD ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
FRACTURED SACRUM ( 8 FDA reports)
GALLOP RHYTHM PRESENT ( 8 FDA reports)
GINGIVAL ERYTHEMA ( 8 FDA reports)
GRIP STRENGTH DECREASED ( 8 FDA reports)
HAEMANGIOMA OF LIVER ( 8 FDA reports)
HAEMORRHAGE URINARY TRACT ( 8 FDA reports)
HAND DEFORMITY ( 8 FDA reports)
HELICOBACTER INFECTION ( 8 FDA reports)
HEPATORENAL FAILURE ( 8 FDA reports)
HEPATOSPLENOMEGALY ( 8 FDA reports)
HYPERVOLAEMIA ( 8 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 8 FDA reports)
INCISION SITE HAEMORRHAGE ( 8 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
INJECTION SITE SCAR ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 8 FDA reports)
INTRA-UTERINE DEATH ( 8 FDA reports)
IRON OVERLOAD ( 8 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 8 FDA reports)
JAUNDICE CHOLESTATIC ( 8 FDA reports)
KERATITIS ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LESION EXCISION ( 8 FDA reports)
LIP OEDEMA ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LOSS OF CONTROL OF LEGS ( 8 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
LYMPHADENECTOMY ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 8 FDA reports)
MEAN CELL VOLUME INCREASED ( 8 FDA reports)
MEDIASTINAL DISORDER ( 8 FDA reports)
MENOPAUSAL SYMPTOMS ( 8 FDA reports)
MITRAL VALVE REPAIR ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
MYCOSIS FUNGOIDES ( 8 FDA reports)
NAIL DISCOLOURATION ( 8 FDA reports)
NAIL HYPERTROPHY ( 8 FDA reports)
NASAL ULCER ( 8 FDA reports)
NEPHRITIS ( 8 FDA reports)
NODAL OSTEOARTHRITIS ( 8 FDA reports)
OBSTRUCTION ( 8 FDA reports)
OPEN REDUCTION OF FRACTURE ( 8 FDA reports)
OSTEOSARCOMA METASTATIC ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PANCREATIC MASS ( 8 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PENIS DISORDER ( 8 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 8 FDA reports)
PLEURAL DISORDER ( 8 FDA reports)
POLYMYOSITIS ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
PORTAL HYPERTENSION ( 8 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 8 FDA reports)
POTENTIATING DRUG INTERACTION ( 8 FDA reports)
PRODUCT TASTE ABNORMAL ( 8 FDA reports)
PSEUDODEMENTIA ( 8 FDA reports)
PSYCHOMOTOR RETARDATION ( 8 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 8 FDA reports)
PULMONARY GRANULOMA ( 8 FDA reports)
RADIATION OESOPHAGITIS ( 8 FDA reports)
RADIATION PNEUMONITIS ( 8 FDA reports)
RADIOTHERAPY ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RESORPTION BONE INCREASED ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 8 FDA reports)
RETINAL ARTERY OCCLUSION ( 8 FDA reports)
RETINAL TEAR ( 8 FDA reports)
SCOTOMA ( 8 FDA reports)
SKIN NODULE ( 8 FDA reports)
SMEAR CERVIX ABNORMAL ( 8 FDA reports)
SOMATISATION DISORDER ( 8 FDA reports)
SPINAL LAMINECTOMY ( 8 FDA reports)
STARING ( 8 FDA reports)
STRESS SYMPTOMS ( 8 FDA reports)
STUPOR ( 8 FDA reports)
SYNCOPE VASOVAGAL ( 8 FDA reports)
TEARFULNESS ( 8 FDA reports)
TEETH BRITTLE ( 8 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 8 FDA reports)
TETANY ( 8 FDA reports)
THORACOTOMY ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 8 FDA reports)
URINE KETONE BODY PRESENT ( 8 FDA reports)
UTERINE HAEMORRHAGE ( 8 FDA reports)
VASCULAR DEMENTIA ( 8 FDA reports)
VOCAL CORD DISORDER ( 8 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 8 FDA reports)
WEANING FAILURE ( 8 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 8 FDA reports)
WOUND TREATMENT ( 8 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
ORAL NEOPLASM ( 7 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
PALATAL DISORDER ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PAPILLOEDEMA ( 7 FDA reports)
PARATHYROID HAEMORRHAGE ( 7 FDA reports)
PEDAL PULSE DECREASED ( 7 FDA reports)
PENILE PAIN ( 7 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 7 FDA reports)
PNEUMONIA HAEMOPHILUS ( 7 FDA reports)
POISONING DELIBERATE ( 7 FDA reports)
POLYCYSTIC OVARIES ( 7 FDA reports)
POSITIVE ROMBERGISM ( 7 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 7 FDA reports)
POST PROCEDURAL PAIN ( 7 FDA reports)
POSTURE ABNORMAL ( 7 FDA reports)
PRESBYOPIA ( 7 FDA reports)
PRODUCT SIZE ISSUE ( 7 FDA reports)
PROSTATE INFECTION ( 7 FDA reports)
PROSTATIC CALCIFICATION ( 7 FDA reports)
PROSTATISM ( 7 FDA reports)
PSEUDOMONAL SEPSIS ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
RENAL INFARCT ( 7 FDA reports)
RENAL TUBULAR DISORDER ( 7 FDA reports)
RETINOPATHY ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
SCROTAL OEDEMA ( 7 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 7 FDA reports)
SEPSIS SYNDROME ( 7 FDA reports)
SINUS OPERATION ( 7 FDA reports)
SKIN MASS ( 7 FDA reports)
SLEEP TALKING ( 7 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
SOFT TISSUE INFLAMMATION ( 7 FDA reports)
SPIDER NAEVUS ( 7 FDA reports)
SPLENIC VEIN THROMBOSIS ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SUBMANDIBULAR MASS ( 7 FDA reports)
SUNBURN ( 7 FDA reports)
TALIPES ( 7 FDA reports)
TEMPORAL ARTERITIS ( 7 FDA reports)
THERAPY REGIMEN CHANGED ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
THYROIDITIS ( 7 FDA reports)
TONGUE COATED ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 7 FDA reports)
URETHRAL PAIN ( 7 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 7 FDA reports)
URINOMA ( 7 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
VERBAL ABUSE ( 7 FDA reports)
VICTIM OF SEXUAL ABUSE ( 7 FDA reports)
VIRAL LABYRINTHITIS ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
ADJUSTMENT DISORDER ( 7 FDA reports)
AIR EMBOLISM ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
ANAL ABSCESS ( 7 FDA reports)
ANASTOMOTIC FISTULA ( 7 FDA reports)
ANEURYSM RUPTURED ( 7 FDA reports)
ANION GAP DECREASED ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
AORTIC VALVE CALCIFICATION ( 7 FDA reports)
APLASTIC ANAEMIA ( 7 FDA reports)
BLADDER PAIN ( 7 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 7 FDA reports)
BLOOD VISCOSITY INCREASED ( 7 FDA reports)
BLOODY DISCHARGE ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BRAIN HERNIATION ( 7 FDA reports)
BRONCHITIS ACUTE ( 7 FDA reports)
BURN OESOPHAGEAL ( 7 FDA reports)
CALCIUM METABOLISM DISORDER ( 7 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 7 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 7 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CEREBRAL MICROANGIOPATHY ( 7 FDA reports)
CHOLANGITIS SCLEROSING ( 7 FDA reports)
CHRONIC HEPATITIS ( 7 FDA reports)
CLOSTRIDIUM COLITIS ( 7 FDA reports)
COAGULATION TIME PROLONGED ( 7 FDA reports)
COAGULATION TIME SHORTENED ( 7 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 7 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CONVERSION DISORDER ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DEVICE ISSUE ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DIABETIC VASCULAR DISORDER ( 7 FDA reports)
DIAPHRAGMATIC HERNIA ( 7 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 7 FDA reports)
DRUG LEVEL DECREASED ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
DRY GANGRENE ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
EMBOLISM VENOUS ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENTEROCOLITIS ( 7 FDA reports)
EOSINOPHILIC PNEUMONIA ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
ESSENTIAL TREMOR ( 7 FDA reports)
EUPHORIC MOOD ( 7 FDA reports)
EYE ROLLING ( 7 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 7 FDA reports)
FEMORAL ARTERY ANEURYSM ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FOOD INTOLERANCE ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 7 FDA reports)
FUNGAL SEPSIS ( 7 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 7 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 7 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 7 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 7 FDA reports)
GLYCOSURIA ( 7 FDA reports)
GRAFT LOSS ( 7 FDA reports)
H1N1 INFLUENZA ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HAIR COLOUR CHANGES ( 7 FDA reports)
HEARING AID USER ( 7 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 7 FDA reports)
HEPATIC ENZYME ABNORMAL ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HEPATIC NEOPLASM ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HOSPICE CARE ( 7 FDA reports)
HYDROURETER ( 7 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 7 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 7 FDA reports)
HYPERTROPHY ( 7 FDA reports)
HYPOGLYCAEMIC COMA ( 7 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 7 FDA reports)
HYPOMANIA ( 7 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 7 FDA reports)
INFERTILITY ( 7 FDA reports)
INJECTION SITE BRUISING ( 7 FDA reports)
INJECTION SITE OEDEMA ( 7 FDA reports)
INJECTION SITE VESICLES ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
LIGAMENT RUPTURE ( 7 FDA reports)
LIP BLISTER ( 7 FDA reports)
LIVER TRANSPLANT REJECTION ( 7 FDA reports)
MADAROSIS ( 7 FDA reports)
MAMMOGRAM ABNORMAL ( 7 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 7 FDA reports)
MASTECTOMY ( 7 FDA reports)
MASTITIS ( 7 FDA reports)
MASTOIDITIS ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
METABOLIC ALKALOSIS ( 7 FDA reports)
MINERAL DEFICIENCY ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MUCOSAL HAEMORRHAGE ( 7 FDA reports)
MYELITIS TRANSVERSE ( 7 FDA reports)
MYOCARDIAL FIBROSIS ( 7 FDA reports)
NASAL DISORDER ( 7 FDA reports)
NEUROSENSORY HYPOACUSIS ( 7 FDA reports)
NIKOLSKY'S SIGN ( 7 FDA reports)
NODULE ON EXTREMITY ( 7 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 7 FDA reports)
ABDOMINAL NEOPLASM ( 6 FDA reports)
ABDOMINAL SEPSIS ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
ACROCHORDON ( 6 FDA reports)
ADENOCARCINOMA PANCREAS ( 6 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 6 FDA reports)
ADRENAL HAEMORRHAGE ( 6 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
ANAESTHETIC COMPLICATION ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ANOGENITAL WARTS ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 6 FDA reports)
AORTIC ANEURYSM RUPTURE ( 6 FDA reports)
AORTIC VALVE REPAIR ( 6 FDA reports)
APALLIC SYNDROME ( 6 FDA reports)
ARTERIAL BYPASS OPERATION ( 6 FDA reports)
ARTERIAL REPAIR ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
AURICULAR SWELLING ( 6 FDA reports)
BIFASCICULAR BLOCK ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BILIARY COLIC ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BIOPSY BONE MARROW ( 6 FDA reports)
BLAST CELL COUNT INCREASED ( 6 FDA reports)
BLOOD BICARBONATE INCREASED ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 6 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 6 FDA reports)
BLOOD URINE ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BREAST SWELLING ( 6 FDA reports)
BULLOUS LUNG DISEASE ( 6 FDA reports)
CARBON DIOXIDE ABNORMAL ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CARDIOPULMONARY BYPASS ( 6 FDA reports)
CENTRAL OBESITY ( 6 FDA reports)
CEREBELLAR ATROPHY ( 6 FDA reports)
CEREBROSCLEROSIS ( 6 FDA reports)
CERVICAL DYSPLASIA ( 6 FDA reports)
CHEST INJURY ( 6 FDA reports)
CHEST WALL MASS ( 6 FDA reports)
CHOLESTEROSIS ( 6 FDA reports)
CHROMATOPSIA ( 6 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 6 FDA reports)
CUTANEOUS VASCULITIS ( 6 FDA reports)
DELUSIONAL PERCEPTION ( 6 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 6 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 6 FDA reports)
DERMATITIS ATOPIC ( 6 FDA reports)
DEVICE BREAKAGE ( 6 FDA reports)
DEVICE LEAKAGE ( 6 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 6 FDA reports)
DISEASE COMPLICATION ( 6 FDA reports)
DISSOCIATIVE DISORDER ( 6 FDA reports)
DRUG CLEARANCE DECREASED ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
ELEVATED MOOD ( 6 FDA reports)
EMBOLISM ARTERIAL ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
ENTEROBACTER INFECTION ( 6 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 6 FDA reports)
EXERCISE LACK OF ( 6 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
EYELID DISORDER ( 6 FDA reports)
FACE LIFT ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FEEDING TUBE COMPLICATION ( 6 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 6 FDA reports)
FOOD AVERSION ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GENITAL SWELLING ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HAEMORRHOID OPERATION ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEAT RASH ( 6 FDA reports)
HELLP SYNDROME ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATIC CYST INFECTION ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
HISTOPLASMOSIS ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERSEXUALITY ( 6 FDA reports)
HYPOGONADISM ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
IATROGENIC INJURY ( 6 FDA reports)
ILEOSTOMY ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
IMPRISONMENT ( 6 FDA reports)
IMPULSE-CONTROL DISORDER ( 6 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTESTINAL STENOSIS ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
LIP EROSION ( 6 FDA reports)
LIP PAIN ( 6 FDA reports)
LOSS OF LIBIDO ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
LYMPHOCELE ( 6 FDA reports)
LYMPHOCYTOSIS ( 6 FDA reports)
MACROGLOSSIA ( 6 FDA reports)
MAGNESIUM DEFICIENCY ( 6 FDA reports)
METASTASES TO STOMACH ( 6 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 6 FDA reports)
MOUTH BREATHING ( 6 FDA reports)
MYOSCLEROSIS ( 6 FDA reports)
NASAL MUCOSAL DISORDER ( 6 FDA reports)
NEPHRECTOMY ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 6 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
ORAL PRURITUS ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
PACEMAKER COMPLICATION ( 6 FDA reports)
PAPULE ( 6 FDA reports)
PATHOGEN RESISTANCE ( 6 FDA reports)
PENILE INFECTION ( 6 FDA reports)
PENILE OEDEMA ( 6 FDA reports)
PERSONALITY DISORDER ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHAEOCHROMOCYTOMA ( 6 FDA reports)
PHARYNGEAL ABSCESS ( 6 FDA reports)
PNEUMONIA MYCOPLASMAL ( 6 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 6 FDA reports)
POSTOPERATIVE INFECTION ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 6 FDA reports)
PULMONARY RADIATION INJURY ( 6 FDA reports)
RADIATION SKIN INJURY ( 6 FDA reports)
RADICULAR PAIN ( 6 FDA reports)
RECTAL PROLAPSE REPAIR ( 6 FDA reports)
RECTAL TENESMUS ( 6 FDA reports)
RED BLOOD CELL ABNORMALITY ( 6 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RENAL CYST INFECTION ( 6 FDA reports)
RENAL NEOPLASM ( 6 FDA reports)
RENAL OSTEODYSTROPHY ( 6 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 6 FDA reports)
SARCOIDOSIS ( 6 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 6 FDA reports)
SCLERAL DISORDER ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SERRATIA INFECTION ( 6 FDA reports)
SHOULDER OPERATION ( 6 FDA reports)
SINOATRIAL BLOCK ( 6 FDA reports)
SKIN FRAGILITY ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
SKIN TURGOR DECREASED ( 6 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
SMALL INTESTINAL PERFORATION ( 6 FDA reports)
SPINAL FUSION SURGERY ( 6 FDA reports)
SPINAL PAIN ( 6 FDA reports)
SPLENIC HAEMORRHAGE ( 6 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 6 FDA reports)
STASIS DERMATITIS ( 6 FDA reports)
STEAL SYNDROME ( 6 FDA reports)
STENT REMOVAL ( 6 FDA reports)
SURGICAL FAILURE ( 6 FDA reports)
THERAPY CESSATION ( 6 FDA reports)
TOOTH DEPOSIT ( 6 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URETERAL NEOPLASM ( 6 FDA reports)
URGE INCONTINENCE ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
UTERINE MASS ( 6 FDA reports)
VAGINAL CANDIDIASIS ( 6 FDA reports)
VASCULAR BYPASS GRAFT ( 6 FDA reports)
VENOUS STASIS ( 6 FDA reports)
VENOUS STENOSIS ( 6 FDA reports)
VENTRICULAR FAILURE ( 6 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
OOPHORECTOMY ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 5 FDA reports)
OSTEOARTHROPATHY ( 5 FDA reports)
PALMAR ERYTHEMA ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PANCREATIC NEOPLASM ( 5 FDA reports)
PAPILLOMA VIRAL INFECTION ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARAPARESIS ( 5 FDA reports)
PARAPROTEINAEMIA ( 5 FDA reports)
PARATHYROID TUMOUR BENIGN ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 5 FDA reports)
PERFORATED ULCER ( 5 FDA reports)
PERINEAL PAIN ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
PICKWICKIAN SYNDROME ( 5 FDA reports)
PLEUROTHOTONUS ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 5 FDA reports)
PRESBYACUSIS ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROPIONIBACTERIUM INFECTION ( 5 FDA reports)
PROSTATIC ADENOMA ( 5 FDA reports)
PULMONARY ARTERY DILATATION ( 5 FDA reports)
PULMONARY CALCIFICATION ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
PURPURA SENILE ( 5 FDA reports)
RADIATION NEUROPATHY ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RECTAL FISSURE ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETICULOCYTE COUNT DECREASED ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
ROTATOR CUFF REPAIR ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 5 FDA reports)
SEMEN VOLUME DECREASED ( 5 FDA reports)
SERRATIA BACTERAEMIA ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SHOCK HYPOGLYCAEMIC ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SHUNT MALFUNCTION ( 5 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 5 FDA reports)
SINUS RHYTHM ( 5 FDA reports)
SKIN GRAFT ( 5 FDA reports)
SLEEP ATTACKS ( 5 FDA reports)
SPINAL DEFORMITY ( 5 FDA reports)
SPLENIC LESION ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
SUDDEN HEARING LOSS ( 5 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 5 FDA reports)
TARSAL TUNNEL SYNDROME ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TERMINAL DRIBBLING ( 5 FDA reports)
TERMINAL INSOMNIA ( 5 FDA reports)
TESTICULAR ATROPHY ( 5 FDA reports)
TESTICULAR MASS ( 5 FDA reports)
THYROTOXIC CRISIS ( 5 FDA reports)
TIC ( 5 FDA reports)
TONGUE BLISTERING ( 5 FDA reports)
TONGUE HAEMORRHAGE ( 5 FDA reports)
TOOTH AVULSION ( 5 FDA reports)
TUMOUR HAEMORRHAGE ( 5 FDA reports)
TUMOUR NECROSIS ( 5 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
URETHRAL HAEMORRHAGE ( 5 FDA reports)
URETHRAL OBSTRUCTION ( 5 FDA reports)
URETHRITIS ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
UTERINE FIBROSIS ( 5 FDA reports)
VASCULAR GRAFT COMPLICATION ( 5 FDA reports)
VESTIBULITIS ( 5 FDA reports)
VIRAL LOAD INCREASED ( 5 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 5 FDA reports)
WEIGHT ABNORMAL ( 5 FDA reports)
WHITE BLOOD CELL DISORDER ( 5 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 5 FDA reports)
ACCIDENT AT WORK ( 5 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 5 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
ADENOMYOSIS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
AMENORRHOEA ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 5 FDA reports)
ANAL PRURITUS ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 5 FDA reports)
AORTIC DISSECTION ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APPLICATION SITE BURN ( 5 FDA reports)
APPLICATION SITE URTICARIA ( 5 FDA reports)
ARACHNOID CYST ( 5 FDA reports)
ARTERIOVENOUS FISTULA ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
ASTROCYTOMA ( 5 FDA reports)
AURICULAR PERICHONDRITIS ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
B-CELL LYMPHOMA ( 5 FDA reports)
BENIGN BREAST NEOPLASM ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BLADDER NEOPLASM ( 5 FDA reports)
BLADDER PROLAPSE ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 5 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 5 FDA reports)
BLOOD PH INCREASED ( 5 FDA reports)
BLOOD PRESSURE ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BONE FISTULA ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BONE MARROW TOXICITY ( 5 FDA reports)
BONE SCAN ABNORMAL ( 5 FDA reports)
BOWEL SOUNDS ABNORMAL ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BRAIN STEM STROKE ( 5 FDA reports)
CALCULUS URINARY ( 5 FDA reports)
CANDIDA SEPSIS ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 5 FDA reports)
CATARACT NUCLEAR ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CERVICAL NEURITIS ( 5 FDA reports)
CHEST WALL ABSCESS ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
CIRRHOSIS ALCOHOLIC ( 5 FDA reports)
CITROBACTER INFECTION ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
COAGULATION TEST ABNORMAL ( 5 FDA reports)
COLOSTOMY ( 5 FDA reports)
COMA SCALE ABNORMAL ( 5 FDA reports)
COMPLEX PARTIAL SEIZURES ( 5 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 5 FDA reports)
COR PULMONALE CHRONIC ( 5 FDA reports)
CORONARY ARTERY ANEURYSM ( 5 FDA reports)
CORONARY ARTERY SURGERY ( 5 FDA reports)
CSF PROTEIN INCREASED ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
DISORDER OF ORBIT ( 5 FDA reports)
DISTRACTIBILITY ( 5 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 5 FDA reports)
DIZZINESS EXERTIONAL ( 5 FDA reports)
DRUG EFFECT PROLONGED ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 5 FDA reports)
EAR HAEMORRHAGE ( 5 FDA reports)
EATING DISORDER SYMPTOM ( 5 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 5 FDA reports)
ENDOCRINE DISORDER ( 5 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE LASER SURGERY ( 5 FDA reports)
EYEBALL RUPTURE ( 5 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 5 FDA reports)
FOLATE DEFICIENCY ( 5 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GALLBLADDER PERFORATION ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GILBERT'S SYNDROME ( 5 FDA reports)
GINGIVAL ABSCESS ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GLIOBLASTOMA ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 5 FDA reports)
GROWTH RETARDATION ( 5 FDA reports)
HAEMOGLOBIN ( 5 FDA reports)
HALO VISION ( 5 FDA reports)
HEAD AND NECK CANCER ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HERNIA HIATUS REPAIR ( 5 FDA reports)
HYPERCHLORHYDRIA ( 5 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPOGONADISM MALE ( 5 FDA reports)
ILIAC ARTERY STENOSIS ( 5 FDA reports)
IMPAIRED FASTING GLUCOSE ( 5 FDA reports)
INCISION SITE INFECTION ( 5 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 5 FDA reports)
INFLAMMATORY MARKER INCREASED ( 5 FDA reports)
INFUSION SITE PRURITUS ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE INFLAMMATION ( 5 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 5 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
KETOSIS ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LIGHT CHAIN DISEASE ( 5 FDA reports)
LISTERIA SEPSIS ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MASTOCYTOSIS ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 5 FDA reports)
MESENTERIC OCCLUSION ( 5 FDA reports)
METAMORPHOPSIA ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
METHAEMOGLOBINAEMIA ( 5 FDA reports)
MICTURITION FREQUENCY DECREASED ( 5 FDA reports)
MUSCLE INJURY ( 5 FDA reports)
MUSCLE SWELLING ( 5 FDA reports)
MYASTHENIA GRAVIS ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 5 FDA reports)
MYELOFIBROSIS ( 5 FDA reports)
NASAL SEPTUM PERFORATION ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
NIGHT BLINDNESS ( 5 FDA reports)
NOCARDIOSIS ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 5 FDA reports)
NORMAL NEWBORN ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACCIDENTAL NEEDLE STICK ( 4 FDA reports)
ACINETOBACTER INFECTION ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALBUMIN URINE PRESENT ( 4 FDA reports)
ALLODYNIA ( 4 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAL FISTULA ( 4 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INHIBITOR FOETOPATHY ( 4 FDA reports)
ANTICOAGULANT THERAPY ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APPLICATION SITE EXFOLIATION ( 4 FDA reports)
APPLICATION SITE PUSTULES ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ARTIFICIAL MENOPAUSE ( 4 FDA reports)
ASBESTOSIS ( 4 FDA reports)
ASPERGER'S DISORDER ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 4 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BILIARY CYST ( 4 FDA reports)
BITE ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLADDER HYPERTROPHY ( 4 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 4 FDA reports)
BLOOD ALCOHOL INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 4 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BRONCHIAL HAEMORRHAGE ( 4 FDA reports)
BRONCHIAL NEOPLASM ( 4 FDA reports)
CAECUM OPERATION ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 4 FDA reports)
CARCINOID TUMOUR ( 4 FDA reports)
CARDIAC STRESS TEST ( 4 FDA reports)
CARDIORENAL SYNDROME ( 4 FDA reports)
CATHETER SITE CELLULITIS ( 4 FDA reports)
CATHETER SITE DISCHARGE ( 4 FDA reports)
CATHETER SITE ERYTHEMA ( 4 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CD4/CD8 RATIO DECREASED ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
CHOROIDAL DETACHMENT ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COELIAC ARTERY STENOSIS ( 4 FDA reports)
COLECTOMY ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COLONIC OBSTRUCTION ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 4 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 4 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 4 FDA reports)
CORNEAL TRANSPLANT ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CRYOGLOBULINAEMIA ( 4 FDA reports)
CSF TEST ABNORMAL ( 4 FDA reports)
DEAFNESS TRANSITORY ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DELAYED SLEEP PHASE ( 4 FDA reports)
DENTAL DISCOMFORT ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DEVICE ADHESION ISSUE ( 4 FDA reports)
DEVICE INTERACTION ( 4 FDA reports)
DIABETIC FOOT INFECTION ( 4 FDA reports)
DIABETIC ULCER ( 4 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 4 FDA reports)
DISSEMINATED TUBERCULOSIS ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
EAR INJURY ( 4 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
ECTROPION ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 4 FDA reports)
ENDOMETRIAL CANCER ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EPICONDYLITIS ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EXTRAVASATION ( 4 FDA reports)
EYE INFECTION INTRAOCULAR ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FAT TISSUE INCREASED ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FEMORAL PULSE DECREASED ( 4 FDA reports)
FISTULA REPAIR ( 4 FDA reports)
FLASHBACK ( 4 FDA reports)
FOETAL HEART RATE DECREASED ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 4 FDA reports)
GINGIVAL ATROPHY ( 4 FDA reports)
GINGIVAL DISCOLOURATION ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HAEMOSTASIS ( 4 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEPATIC ARTERY OCCLUSION ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPERVIGILANCE ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
HYPOTONY OF EYE ( 4 FDA reports)
ILIAC ARTERY THROMBOSIS ( 4 FDA reports)
ILIUM FRACTURE ( 4 FDA reports)
IMPLANT SITE INDURATION ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INCORRECT PRODUCT STORAGE ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INFECTED CYST ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
IRITIS ( 4 FDA reports)
IVTH NERVE PARALYSIS ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
KIDNEY ENLARGEMENT ( 4 FDA reports)
KLEBSIELLA BACTERAEMIA ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LENS DISORDER ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LEUKAEMOID REACTION ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIFE SUPPORT ( 4 FDA reports)
LIGAMENT DISORDER ( 4 FDA reports)
LIGHT CHAIN ANALYSIS ( 4 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 4 FDA reports)
LIMB ASYMMETRY ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LINEAR IGA DISEASE ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LUNG HYPERINFLATION ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LUNG TRANSPLANT REJECTION ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MEDIASTINAL MASS ( 4 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 4 FDA reports)
MENINGORRHAGIA ( 4 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METASTASES TO SKIN ( 4 FDA reports)
METATARSALGIA ( 4 FDA reports)
MIXED LIVER INJURY ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MUCOSAL DISCOLOURATION ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTIPLE ALLERGIES ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 4 FDA reports)
MYELOMALACIA ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NASAL INFLAMMATION ( 4 FDA reports)
NEGATIVE THOUGHTS ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NEPHRITIS ALLERGIC ( 4 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OESOPHAGEAL INFECTION ( 4 FDA reports)
OESOPHAGEAL OEDEMA ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
OS TRIGONUM SYNDROME ( 4 FDA reports)
OSTEOMYELITIS CHRONIC ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
OTITIS MEDIA CHRONIC ( 4 FDA reports)
OVARIAN INFECTION ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PANCREATIC CALCIFICATION ( 4 FDA reports)
PANCREATIC DUCT DILATATION ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PAPILLOMA ( 4 FDA reports)
PARANASAL CYST ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 4 FDA reports)
PERIANAL ABSCESS ( 4 FDA reports)
PERINEPHRIC COLLECTION ( 4 FDA reports)
PERIPHERAL PULSE DECREASED ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL ABSCESS ( 4 FDA reports)
PERITONEAL DISORDER ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PHOBIA ( 4 FDA reports)
PHYSICAL ASSAULT ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PLASTIC SURGERY ( 4 FDA reports)
PLEURODESIS ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMOBILIA ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PRODUCT COLOUR ISSUE ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PROLONGED EXPIRATION ( 4 FDA reports)
PROTEIN URINE ABSENT ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PULMONARY HILUM MASS ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RENAL CYST RUPTURED ( 4 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
RETROPERITONEAL FIBROSIS ( 4 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
SCROTAL DISORDER ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SUSPICIOUSNESS ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 4 FDA reports)
TENSION ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THYROID CANCER METASTATIC ( 4 FDA reports)
THYROIDECTOMY ( 4 FDA reports)
THYROXINE FREE DECREASED ( 4 FDA reports)
THYROXINE FREE INCREASED ( 4 FDA reports)
TINEA INFECTION ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONIC CLONIC MOVEMENTS ( 4 FDA reports)
TONSILLAR DISORDER ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
TOOTH DISCOLOURATION ( 4 FDA reports)
TOOTH IMPACTED ( 4 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 4 FDA reports)
TRANSPLANT ABSCESS ( 4 FDA reports)
TRAUMATIC FRACTURE ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETEROSTOMY SITE DISCOMFORT ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VASCULAR ANOMALY ( 4 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VIRAL SINUSITIS ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
WEGENER'S GRANULOMATOSIS ( 4 FDA reports)
WEIGHT BEARING DIFFICULTY ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WHITE CLOT SYNDROME ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
ZYGOMYCOSIS ( 4 FDA reports)
ONYCHALGIA ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORGASM ABNORMAL ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
ORTHOSIS USER ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
OSTEITIS DEFORMANS ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PACEMAKER GENERATED RHYTHM ( 3 FDA reports)
PACHYMENINGITIS ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC ENLARGEMENT ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PAPILLARY MUSCLE DISORDER ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PERIDIVERTICULAR ABSCESS ( 3 FDA reports)
PERITONEAL HAEMATOMA ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PERTUSSIS ( 3 FDA reports)
PHAEOCHROMOCYTOMA MALIGNANT ( 3 FDA reports)
PHANTOM PAIN ( 3 FDA reports)
PHARYNGEAL ULCERATION ( 3 FDA reports)
PLASMAPHERESIS ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POOR DENTAL CONDITION ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTINFARCTION ANGINA ( 3 FDA reports)
POSTOPERATIVE ABSCESS ( 3 FDA reports)
POSTOPERATIVE THROMBOSIS ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 3 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATIC PAIN ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PSEUDOLYMPHOMA ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY SEPSIS ( 3 FDA reports)
PULSE PRESSURE INCREASED ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
RENAL CANCER METASTATIC ( 3 FDA reports)
RENAL NECROSIS ( 3 FDA reports)
RENAL SURGERY ( 3 FDA reports)
RENIN DECREASED ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RETINOIC ACID SYNDROME ( 3 FDA reports)
RHEUMATIC HEART DISEASE ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
ROTAVIRUS TEST POSITIVE ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SCLERODACTYLIA ( 3 FDA reports)
SCROTAL ABSCESS ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SEPSIS NEONATAL ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 3 FDA reports)
SINUS ANTROSTOMY ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SMALL INTESTINAL STENOSIS ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPERM COUNT DECREASED ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPONDYLITIC MYELOPATHY ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STENT MALFUNCTION ( 3 FDA reports)
STRESS ULCER ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUPERFICIAL INJURY OF EYE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 3 FDA reports)
SUPRANUCLEAR PALSY ( 3 FDA reports)
SUTURE RELATED COMPLICATION ( 3 FDA reports)
SYNOVECTOMY ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
SYSTEMIC SCLEROSIS ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
THROMBECTOMY ( 3 FDA reports)
THROMBIN TIME PROLONGED ( 3 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TONGUE HAEMATOMA ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOOTH MALFORMATION ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 3 FDA reports)
TOXIC NODULAR GOITRE ( 3 FDA reports)
TRACHEAL HAEMORRHAGE ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETERIC CANCER ( 3 FDA reports)
URETHRAL FISTULA ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINARY SEDIMENT ABNORMAL ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
UTERINE ENLARGEMENT ( 3 FDA reports)
VAGINITIS ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VASCULAR STENOSIS ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VITILIGO ( 3 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 3 FDA reports)
X-RAY ( 3 FDA reports)
ZINC DEFICIENCY ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
AMAUROSIS ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANAL PROLAPSE ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
AORTIC VALVE DISEASE MIXED ( 3 FDA reports)
APPENDICEAL ABSCESS ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
ARTERIAL CATHETERISATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BACTERIAL PYELONEPHRITIS ( 3 FDA reports)
BACTERIAL TOXAEMIA ( 3 FDA reports)
BASAL GANGLION DEGENERATION ( 3 FDA reports)
BASE EXCESS INCREASED ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 3 FDA reports)
BILE DUCT NECROSIS ( 3 FDA reports)
BILE DUCT STENT REMOVAL ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BIOPSY TONGUE ABNORMAL ( 3 FDA reports)
BLADDER ABLATION ( 3 FDA reports)
BLADDER DISTENSION ( 3 FDA reports)
BLADDER DYSFUNCTION ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN OPERATION ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST CELLULITIS ( 3 FDA reports)
BREAST DISORDER ( 3 FDA reports)
BREAST INDURATION ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARBUNCLE ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC AMYLOIDOSIS ( 3 FDA reports)
CARDIAC DISCOMFORT ( 3 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATARACT CORTICAL ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBROVASCULAR STENOSIS ( 3 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CHRONIC HEPATIC FAILURE ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 3 FDA reports)
COGNITIVE DETERIORATION ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON CANCER STAGE III ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 3 FDA reports)
COMPUTERISED TOMOGRAM ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORNEAL PIGMENTATION ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CROSS SENSITIVITY REACTION ( 3 FDA reports)
CYANOSIS CENTRAL ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS TEST ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DENTAL CARE ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DENTOFACIAL ANOMALY ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 3 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 3 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 3 FDA reports)
DNA ANTIBODY POSITIVE ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
EAR NEOPLASM MALIGNANT ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOMETRIAL DISORDER ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
ENLARGED CEREBRAL PERIVASCULAR SPACES ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXPLORATIVE LAPAROTOMY ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EYELID CYST ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FEMALE STERILISATION ( 3 FDA reports)
FEMORAL PULSE ABNORMAL ( 3 FDA reports)
FLUID IMBALANCE ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
FULL BLOOD COUNT INCREASED ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 3 FDA reports)
GASTROINTESTINAL FISTULA ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENITAL PAIN ( 3 FDA reports)
GINGIVAL BLISTER ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
GRANULOCYTES ABNORMAL ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
GROIN ABSCESS ( 3 FDA reports)
GUN SHOT WOUND ( 3 FDA reports)
HAEMANGIOMA OF SPLEEN ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEART VALVE STENOSIS ( 3 FDA reports)
HEAT OEDEMA ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERMETABOLISM ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPOALDOSTERONISM ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOSPADIAS ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
IDIOPATHIC URTICARIA ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INCISION SITE CELLULITIS ( 3 FDA reports)
INCISION SITE ERYTHEMA ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INHALATION THERAPY ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERCEPTED MEDICATION ERROR ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
INTRASPINAL ABSCESS ( 3 FDA reports)
JOINT FLUID DRAINAGE ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
KERATITIS BACTERIAL ( 3 FDA reports)
KERATOSIS OBTURANS ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 3 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 3 FDA reports)
LEUKAEMIA PLASMACYTIC ( 3 FDA reports)
LIDDLE'S SYNDROME ( 3 FDA reports)
LIP INJURY ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 3 FDA reports)
LIVIDITY ( 3 FDA reports)
LORDOSIS ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MECHANICAL ILEUS ( 3 FDA reports)
MEDIASTINUM NEOPLASM ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 3 FDA reports)
METASTASES TO BONE MARROW ( 3 FDA reports)
METASTASES TO NECK ( 3 FDA reports)
METASTASES TO PLEURA ( 3 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 3 FDA reports)
MITRAL VALVE DISEASE MIXED ( 3 FDA reports)
MOANING ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MUCKLE-WELLS SYNDROME ( 3 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MUSCLE FIBROSIS ( 3 FDA reports)
MYASTHENIC SYNDROME ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYODESOPSIA ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
NAIL GROWTH ABNORMAL ( 3 FDA reports)
NAIL INJURY ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEEDLE ISSUE ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 3 FDA reports)
NEUROPATHIC ARTHROPATHY ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL BRUIT ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACUTE CHEST SYNDROME ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADMINISTRATION RELATED REACTION ( 2 FDA reports)
ADRENALECTOMY ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALLERGIC COUGH ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMNIOCENTESIS ABNORMAL ( 2 FDA reports)
AMNIOTIC CAVITY INFECTION ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANOSOGNOSIA ( 2 FDA reports)
ANTERIOR CHAMBER FLARE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTICHOLINERGIC SYNDROME ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
AORTIC ELONGATION ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE DISCHARGE ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE INFECTION ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ASPIRATION JOINT ABNORMAL ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
ATRIAL PRESSURE INCREASED ( 2 FDA reports)
AURA ( 2 FDA reports)
AUTOANTIBODY POSITIVE ( 2 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 2 FDA reports)
AVERSION ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BED REST ( 2 FDA reports)
BENIGN OVARIAN TUMOUR ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY THYROID GLAND ABNORMAL ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD IRON ( 2 FDA reports)
BLOOD IRON ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ( 2 FDA reports)
BLOOD UREA ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOODY AIRWAY DISCHARGE ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE FISSURE ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIAC SARCOIDOSIS ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CAROTID ARTERY STENT INSERTION ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHYLOTHORAX ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COAGULATION TIME ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL THINNING ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRYOFIBRINOGENAEMIA ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYSTOPEXY ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOKINE RELEASE SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEATH OF FRIEND ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DENGUE FEVER ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC ENTEROPATHY ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISSECTING CORONARY ARTERY ANEURYSM ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DUODENAL OBSTRUCTION ( 2 FDA reports)
DUODENAL STENOSIS ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPLASTIC NAEVUS ( 2 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EAR NEOPLASM ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
EMPYEMA DRAINAGE ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROBACTER PNEUMONIA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EOSINOPHIL CATIONIC PROTEIN INCREASED ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERYTHROPSIA ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FACTOR V INHIBITION ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FASCIECTOMY ( 2 FDA reports)
FAT REDISTRIBUTION ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMORAL BRUIT ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FIBROSIS TENDINOUS ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLSTONE ILEUS ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROOESOPHAGITIS ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOPERFUSION ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HAEMORRHAGIC ASCITES ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEART AND LUNG TRANSPLANT ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HEMIPLEGIC MIGRAINE ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B POSITIVE ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HOMOCYSTINAEMIA ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOPHYSITIS ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYSTEROSCOPY ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
IIIRD NERVE PARESIS ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFECTIVE SPONDYLITIS ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE INDURATION ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE DESQUAMATION ( 2 FDA reports)
INJECTION SITE EXFOLIATION ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRAOCULAR MELANOMA ( 2 FDA reports)
IRIS ADHESIONS ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
KYPHOSCOLIOSIS ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOOSE ASSOCIATIONS ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULAR ISCHAEMIA ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MEGAKARYOCYTES DECREASED ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO MUSCLE ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MORGANELLA TEST POSITIVE ( 2 FDA reports)
MORNING GLORY SYNDROME ( 2 FDA reports)
MUCOSA VESICLE ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 2 FDA reports)
MUSCLE REATTACHMENT ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL PSORIASIS ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEONATAL ANURIA ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEURILEMMOMA MALIGNANT ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NITRITE URINE ABSENT ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 2 FDA reports)
NORMAL TENSION GLAUCOMA ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 2 FDA reports)
OESOPHAGITIS CHEMICAL ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORAL PAPILLOMA ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OROPHARYNGITIS FUNGAL ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PATIENT ISOLATION ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERINEPHRIC EFFUSION ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 2 FDA reports)
PERIPROSTHETIC FRACTURE ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PINEOCYTOMA ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURISY VIRAL ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYARTERITIS NODOSA ( 2 FDA reports)
POLYCYSTIC LIVER DISEASE ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 2 FDA reports)
PULMONARY ARTERY ANEURYSM ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY BULLA ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL HYPERTENSION ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RETINAL ANEURYSM ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RETINOPATHY OF PREMATURITY ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SACRALISATION ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALPINGO-OOPHORITIS ( 2 FDA reports)
SARCOMA METASTATIC ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SINUS PERFORATION ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN GRAFT INFECTION ( 2 FDA reports)
SLEEP-RELATED EATING DISORDER ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SMALL INTESTINE GANGRENE ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 2 FDA reports)
SPINAL CORD PARALYSIS ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TABLET ISSUE ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THROMBIN TIME SHORTENED ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROID OPERATION ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TROPONIN I ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URAEMIC ENCEPHALOPATHY ( 2 FDA reports)
URAEMIC GASTROPATHY ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO ABNORMAL ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE HYPOTONUS ( 2 FDA reports)
VARICOCELE ( 2 FDA reports)
VARICOPHLEBITIS ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR STENT INSERTION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICLE RUPTURE ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBRAL WEDGING ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VESSEL PUNCTURE SITE PRURITUS ( 2 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VITAMIN B12 ABNORMAL ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VOCAL CORD PARESIS ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VOLVULUS OF SMALL BOWEL ( 2 FDA reports)
VON WILLEBRAND'S FACTOR ACTIVITY INCREASED ( 2 FDA reports)
VON WILLEBRAND'S FACTOR ANTIGEN INCREASED ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WHITE BLOOD CELLS STOOL ( 2 FDA reports)
OESOPHAGEAL STENT INSERTION ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGECTOMY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC DISCS BLURRED ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORBITAL CYST ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOMYELITIS FUNGAL ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERCONFIDENCE ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER SYNDROME ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PAPILLA OF VATER STENOSIS ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARASPINAL ABSCESS ( 1 FDA reports)
PARASYSTOLE ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARATHYROID TUMOUR MALIGNANT ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC EXENTERATION ( 1 FDA reports)
PELVIC FLOOR REPAIR ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERICARDITIS URAEMIC ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PRIMARY HYPOGONADISM ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTOSCOPY ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOANGINA ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PTERYGIUM ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RABIES ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADIATION PERICARDITIS ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RADIOTHERAPY TO THROAT ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY GLAND OPERATION ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAN LYMPH NODES ( 1 FDA reports)
SCHISTOSOMIASIS ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCROTAL OPERATION ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC NECROSIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHUNT BLOOD FLOW EXCESSIVE ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN WOUND ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERM COUNT ZERO ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPINOCEREBELLAR ATAXIA ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBACUTE HEPATIC FAILURE ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBGALEAL HAEMATOMA ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THERMOHYPOAESTHESIA ( 1 FDA reports)
THORACIC CAVITY DRAINAGE TEST ABNORMAL ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC SPINE FLATTENING ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBIN TIME ABNORMAL ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID CANCER STAGE II ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROID PAIN ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXIN BINDING GLOBULIN ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE CANCER METASTATIC ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH DELAMINATION ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSMYOCARDIAL REVASCULARISATION ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
TREPONEMA TEST POSITIVE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE DECREASED ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN T ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL NECROSIS ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC DIVERSION OPERATION ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL CARUNCLE ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URINARY ANASTOMOTIC LEAK ( 1 FDA reports)
URINARY BLADDER ABSCESS ( 1 FDA reports)
URINARY BLADDER EXCISION ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM ABNORMAL ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROSTOMY COMPLICATION ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VALVULOPLASTY CARDIAC ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN B1 DECREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD LIPOINJECTION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WALL NEOPLASM ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABSCESS STERILE ( 1 FDA reports)
ACALCULIA ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCESSORY CARDIAC PATHWAY ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED PORPHYRIA ( 1 FDA reports)
ACRODERMATITIS ENTEROPATHICA ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE POST ASTHMATIC AMYOTROPHY ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADENOVIRAL UPPER RESPIRATORY INFECTION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE ABSENT ( 1 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL POLYP ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIOGRAM RETINA ABNORMAL ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANKLE ARTHROPLASTY ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIACETYLCHOLINE RECEPTOR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL CATHETERISATION ABNORMAL ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOGRAM RENAL ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTERITIS CORONARY ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTIFICIAL HEART DEVICE USER ( 1 FDA reports)
ARTIFICIAL URINARY SPHINCTER IMPLANT ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AUTOANTIBODY TEST ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE CULTURE POSITIVE ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLADDER CATHETER REPLACEMENT ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD COPPER ABNORMAL ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URINE ABSENT ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BOTULISM ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSA CALCIFICATION ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C1 ESTERASE INHIBITOR DECREASED ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC PACEMAKER EVALUATION ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT CONGENITAL ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHOLANGIOGRAM ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLEDOCHOENTEROSTOMY ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROPLASTY ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHORDOMA ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD EXPOSURE INJURY ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 INCREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 1 FDA reports)
CONGENITAL NAEVUS ( 1 FDA reports)
CONGENITAL NAIL DISORDER ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
CONJUNCTIVAL ABRASION ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COPPER DEFICIENCY ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL IMPLANT ( 1 FDA reports)
CORNEAL INFECTION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY BYPASS THROMBOSIS ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE INFECTION ( 1 FDA reports)
CRANIECTOMY ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CSF SHUNT OPERATION ( 1 FDA reports)
CUTANEOUS ANTHRAX ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTOSARCOMA PHYLLODES ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELUSION OF REPLACEMENT ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIGITAL ULCER ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF STERNUM ( 1 FDA reports)
DISTRIBUTIVE SHOCK ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULITIS MECKEL'S ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCRINE PANCREATIC DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXERCISE TEST ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FOSTER-KENNEDY SYNDROME ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FREE HAEMOGLOBIN PRESENT ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS HYPERTROPHIC ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS PARACOLON BACILLUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROSTOMY FAILURE ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL CYST ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMORRHAGE NEONATAL ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CANCER STAGE IV ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B ANTIBODY ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE CALCIFICATION ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERNAL HERNIA ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
IVTH NERVE PARESIS ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATECTOMY ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE III ( 1 FDA reports)
LARYNGEAL CANCER STAGE IV ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
LEUKAEMIA MONOCYTIC ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOERYTHROBLASTOSIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER GRAFT LOSS ( 1 FDA reports)
LOEFFLER'S SYNDROME ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF BLADDER SENSATION ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MANTLE CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDIASTINAL OPERATION ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENISCUS OPERATION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC NEOPLASM ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTASES TO THYROID ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILIA ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MUCOCUTANEOUS ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
MYXOEDEMA COMA ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEUROBORRELIOSIS ( 1 FDA reports)
NEUROCYSTICERCOSIS ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE II ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NONINFECTIOUS PERITONITIS ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCUPATIONAL THERAPY ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)