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

DYSPNOEA ( 2581 FDA reports)
PYREXIA ( 2390 FDA reports)
ANAEMIA ( 2380 FDA reports)
DIARRHOEA ( 2334 FDA reports)
RENAL FAILURE ACUTE ( 2308 FDA reports)
NAUSEA ( 2257 FDA reports)
RENAL FAILURE ( 2196 FDA reports)
FATIGUE ( 1934 FDA reports)
PNEUMONIA ( 1857 FDA reports)
ASTHENIA ( 1853 FDA reports)
PAIN ( 1799 FDA reports)
OEDEMA PERIPHERAL ( 1664 FDA reports)
DIZZINESS ( 1636 FDA reports)
HYPOTENSION ( 1607 FDA reports)
VOMITING ( 1589 FDA reports)
BLOOD CREATININE INCREASED ( 1346 FDA reports)
DEHYDRATION ( 1319 FDA reports)
DRUG INTERACTION ( 1316 FDA reports)
PLATELET COUNT DECREASED ( 1305 FDA reports)
FALL ( 1302 FDA reports)
THROMBOCYTOPENIA ( 1293 FDA reports)
HAEMOGLOBIN DECREASED ( 1260 FDA reports)
ATRIAL FIBRILLATION ( 1204 FDA reports)
MALAISE ( 1182 FDA reports)
RASH ( 1172 FDA reports)
SEPSIS ( 1142 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1117 FDA reports)
ANXIETY ( 1113 FDA reports)
PLEURAL EFFUSION ( 1104 FDA reports)
WEIGHT DECREASED ( 1070 FDA reports)
MYOCARDIAL INFARCTION ( 1046 FDA reports)
CHEST PAIN ( 1042 FDA reports)
HEADACHE ( 1033 FDA reports)
ARTHRALGIA ( 1020 FDA reports)
ABDOMINAL PAIN ( 1006 FDA reports)
HYPERTENSION ( 998 FDA reports)
BACK PAIN ( 987 FDA reports)
CONFUSIONAL STATE ( 987 FDA reports)
PAIN IN EXTREMITY ( 975 FDA reports)
CARDIAC FAILURE ( 974 FDA reports)
RENAL IMPAIRMENT ( 974 FDA reports)
PRURITUS ( 957 FDA reports)
FEBRILE NEUTROPENIA ( 956 FDA reports)
DEATH ( 936 FDA reports)
CONDITION AGGRAVATED ( 930 FDA reports)
DRUG INEFFECTIVE ( 917 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 894 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 866 FDA reports)
DECREASED APPETITE ( 864 FDA reports)
CONSTIPATION ( 854 FDA reports)
RESPIRATORY FAILURE ( 849 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 848 FDA reports)
NEUTROPENIA ( 845 FDA reports)
BLOOD GLUCOSE INCREASED ( 808 FDA reports)
DEPRESSION ( 801 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 801 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 789 FDA reports)
PANCYTOPENIA ( 787 FDA reports)
COUGH ( 786 FDA reports)
INJURY ( 771 FDA reports)
GOUT ( 770 FDA reports)
HYPERKALAEMIA ( 751 FDA reports)
SYNCOPE ( 702 FDA reports)
CEREBROVASCULAR ACCIDENT ( 670 FDA reports)
INFECTION ( 667 FDA reports)
BLOOD UREA INCREASED ( 656 FDA reports)
ERYTHEMA ( 656 FDA reports)
RHABDOMYOLYSIS ( 653 FDA reports)
RENAL FAILURE CHRONIC ( 650 FDA reports)
CARDIAC ARREST ( 650 FDA reports)
MYALGIA ( 636 FDA reports)
URINARY TRACT INFECTION ( 622 FDA reports)
LOSS OF CONSCIOUSNESS ( 610 FDA reports)
INSOMNIA ( 607 FDA reports)
GAIT DISTURBANCE ( 606 FDA reports)
MUSCULAR WEAKNESS ( 587 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 581 FDA reports)
BRADYCARDIA ( 580 FDA reports)
PARAESTHESIA ( 580 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 575 FDA reports)
MULTI-ORGAN FAILURE ( 573 FDA reports)
HYPOAESTHESIA ( 572 FDA reports)
HYPONATRAEMIA ( 570 FDA reports)
CORONARY ARTERY DISEASE ( 566 FDA reports)
HYPOKALAEMIA ( 550 FDA reports)
CELLULITIS ( 545 FDA reports)
FLUSHING ( 541 FDA reports)
CHILLS ( 526 FDA reports)
PULMONARY OEDEMA ( 518 FDA reports)
SOMNOLENCE ( 518 FDA reports)
INTERSTITIAL LUNG DISEASE ( 516 FDA reports)
WEIGHT INCREASED ( 512 FDA reports)
NEUROPATHY PERIPHERAL ( 505 FDA reports)
DISEASE PROGRESSION ( 498 FDA reports)
DIABETES MELLITUS ( 497 FDA reports)
DEEP VEIN THROMBOSIS ( 495 FDA reports)
RECTAL HAEMORRHAGE ( 483 FDA reports)
EMOTIONAL DISTRESS ( 476 FDA reports)
MUSCLE SPASMS ( 475 FDA reports)
OEDEMA ( 472 FDA reports)
STEVENS-JOHNSON SYNDROME ( 472 FDA reports)
BLOOD PRESSURE DECREASED ( 468 FDA reports)
TACHYCARDIA ( 465 FDA reports)
SEPTIC SHOCK ( 463 FDA reports)
EPISTAXIS ( 459 FDA reports)
HYPOGLYCAEMIA ( 459 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 458 FDA reports)
ABDOMINAL PAIN UPPER ( 455 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 454 FDA reports)
BLOOD BILIRUBIN INCREASED ( 450 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 450 FDA reports)
HYPERHIDROSIS ( 447 FDA reports)
PULMONARY EMBOLISM ( 446 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 445 FDA reports)
BLOOD PRESSURE INCREASED ( 444 FDA reports)
CARDIOMEGALY ( 444 FDA reports)
OSTEONECROSIS OF JAW ( 444 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 428 FDA reports)
LEUKOPENIA ( 424 FDA reports)
PALPITATIONS ( 422 FDA reports)
TREMOR ( 422 FDA reports)
MULTIPLE MYELOMA ( 421 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 417 FDA reports)
HAEMATOCRIT DECREASED ( 413 FDA reports)
CONVULSION ( 402 FDA reports)
VISION BLURRED ( 396 FDA reports)
NEUTROPHIL COUNT DECREASED ( 391 FDA reports)
HAEMORRHAGE ( 387 FDA reports)
DYSPHAGIA ( 386 FDA reports)
OSTEOMYELITIS ( 386 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 382 FDA reports)
ARRHYTHMIA ( 380 FDA reports)
HYPOXIA ( 379 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 379 FDA reports)
BRONCHITIS ( 376 FDA reports)
MENTAL STATUS CHANGES ( 376 FDA reports)
FEELING ABNORMAL ( 374 FDA reports)
HYPERURICAEMIA ( 371 FDA reports)
BONE DISORDER ( 367 FDA reports)
OSTEOARTHRITIS ( 366 FDA reports)
ANOREXIA ( 363 FDA reports)
ANGINA PECTORIS ( 360 FDA reports)
LIVER DISORDER ( 359 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 359 FDA reports)
HAEMATURIA ( 357 FDA reports)
STAPHYLOCOCCAL INFECTION ( 357 FDA reports)
TUMOUR LYSIS SYNDROME ( 353 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 349 FDA reports)
SINUSITIS ( 348 FDA reports)
SWELLING ( 343 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 341 FDA reports)
HERPES ZOSTER ( 339 FDA reports)
LYMPHADENOPATHY ( 339 FDA reports)
METABOLIC ACIDOSIS ( 337 FDA reports)
CONTUSION ( 336 FDA reports)
RENAL DISORDER ( 334 FDA reports)
HAEMORRHOIDS ( 331 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 330 FDA reports)
ATELECTASIS ( 329 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 326 FDA reports)
MITRAL VALVE INCOMPETENCE ( 326 FDA reports)
DYSPEPSIA ( 323 FDA reports)
BONE PAIN ( 321 FDA reports)
ANHEDONIA ( 320 FDA reports)
HAEMODIALYSIS ( 320 FDA reports)
CHEST DISCOMFORT ( 319 FDA reports)
HYPERGLYCAEMIA ( 318 FDA reports)
HEPATIC FAILURE ( 317 FDA reports)
OSTEONECROSIS ( 317 FDA reports)
HYPERSENSITIVITY ( 316 FDA reports)
ASCITES ( 311 FDA reports)
DIALYSIS ( 311 FDA reports)
SLEEP APNOEA SYNDROME ( 310 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 308 FDA reports)
STOMATITIS ( 305 FDA reports)
HYPERLIPIDAEMIA ( 296 FDA reports)
LUNG DISORDER ( 295 FDA reports)
JAUNDICE ( 293 FDA reports)
LEUKOCYTOSIS ( 290 FDA reports)
MUSCULOSKELETAL PAIN ( 289 FDA reports)
CARDIAC DISORDER ( 288 FDA reports)
CARDIO-RESPIRATORY ARREST ( 288 FDA reports)
HEPATIC ENZYME INCREASED ( 288 FDA reports)
PULMONARY HYPERTENSION ( 286 FDA reports)
UNEVALUABLE EVENT ( 284 FDA reports)
DISORIENTATION ( 282 FDA reports)
DYSPNOEA EXERTIONAL ( 282 FDA reports)
ABDOMINAL DISCOMFORT ( 281 FDA reports)
HEART RATE INCREASED ( 281 FDA reports)
LETHARGY ( 280 FDA reports)
NEOPLASM MALIGNANT ( 279 FDA reports)
OVERDOSE ( 279 FDA reports)
CHOLELITHIASIS ( 277 FDA reports)
ABDOMINAL DISTENSION ( 275 FDA reports)
BONE MARROW FAILURE ( 274 FDA reports)
BLOOD POTASSIUM INCREASED ( 273 FDA reports)
RESPIRATORY DISTRESS ( 269 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 267 FDA reports)
ARTHRITIS ( 259 FDA reports)
MYOCARDIAL ISCHAEMIA ( 259 FDA reports)
MELAENA ( 258 FDA reports)
SKIN EXFOLIATION ( 258 FDA reports)
THROMBOSIS ( 255 FDA reports)
HYPOTHYROIDISM ( 255 FDA reports)
NEPHROLITHIASIS ( 255 FDA reports)
ECONOMIC PROBLEM ( 254 FDA reports)
JOINT SWELLING ( 253 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 253 FDA reports)
DYSGEUSIA ( 252 FDA reports)
SPINAL OSTEOARTHRITIS ( 252 FDA reports)
VENTRICULAR TACHYCARDIA ( 252 FDA reports)
DRUG HYPERSENSITIVITY ( 251 FDA reports)
PANCREATITIS ( 250 FDA reports)
LUNG INFILTRATION ( 248 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 247 FDA reports)
DELIRIUM ( 245 FDA reports)
HALLUCINATION ( 244 FDA reports)
SKIN ULCER ( 244 FDA reports)
TOOTH EXTRACTION ( 244 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 243 FDA reports)
BLOOD URIC ACID INCREASED ( 241 FDA reports)
DYSURIA ( 241 FDA reports)
HEPATIC STEATOSIS ( 241 FDA reports)
URTICARIA ( 241 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 238 FDA reports)
GASTRITIS ( 238 FDA reports)
DRY MOUTH ( 235 FDA reports)
NECK PAIN ( 235 FDA reports)
HAEMATOCHEZIA ( 234 FDA reports)
MOBILITY DECREASED ( 234 FDA reports)
APLASIA PURE RED CELL ( 232 FDA reports)
URINARY RETENTION ( 232 FDA reports)
VERTIGO ( 230 FDA reports)
HAEMATEMESIS ( 230 FDA reports)
PAIN IN JAW ( 230 FDA reports)
PANCREATITIS ACUTE ( 229 FDA reports)
ORTHOSTATIC HYPOTENSION ( 228 FDA reports)
AGITATION ( 227 FDA reports)
BLOOD SODIUM DECREASED ( 227 FDA reports)
HAEMOPTYSIS ( 227 FDA reports)
ASTHMA ( 226 FDA reports)
DRUG ERUPTION ( 225 FDA reports)
IMPAIRED HEALING ( 224 FDA reports)
INFLAMMATION ( 224 FDA reports)
BLOOD POTASSIUM DECREASED ( 223 FDA reports)
CEREBRAL INFARCTION ( 223 FDA reports)
CARDIOMYOPATHY ( 221 FDA reports)
COLONIC POLYP ( 220 FDA reports)
EOSINOPHILIA ( 220 FDA reports)
DRUG TOXICITY ( 219 FDA reports)
OXYGEN SATURATION DECREASED ( 219 FDA reports)
FLUID OVERLOAD ( 218 FDA reports)
RASH GENERALISED ( 218 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 218 FDA reports)
SWELLING FACE ( 217 FDA reports)
COAGULOPATHY ( 217 FDA reports)
MEMORY IMPAIRMENT ( 216 FDA reports)
OSTEOPENIA ( 216 FDA reports)
SHOCK ( 215 FDA reports)
SPLENOMEGALY ( 215 FDA reports)
RASH ERYTHEMATOUS ( 214 FDA reports)
CATARACT ( 213 FDA reports)
FLUID RETENTION ( 213 FDA reports)
ABASIA ( 212 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 212 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 212 FDA reports)
HEPATITIS ( 212 FDA reports)
DRY SKIN ( 211 FDA reports)
HAEMATOMA ( 211 FDA reports)
HYPERCALCAEMIA ( 211 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 211 FDA reports)
SKIN LESION ( 211 FDA reports)
RASH PRURITIC ( 209 FDA reports)
RENAL CYST ( 209 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 209 FDA reports)
BALANCE DISORDER ( 208 FDA reports)
MUCOSAL INFLAMMATION ( 208 FDA reports)
ENCEPHALOPATHY ( 207 FDA reports)
FEELING HOT ( 207 FDA reports)
PROTEINURIA ( 206 FDA reports)
AGRANULOCYTOSIS ( 205 FDA reports)
OROPHARYNGEAL PAIN ( 204 FDA reports)
DIVERTICULITIS ( 202 FDA reports)
PROTHROMBIN TIME PROLONGED ( 202 FDA reports)
PERICARDIAL EFFUSION ( 201 FDA reports)
COMA ( 201 FDA reports)
DEFORMITY ( 201 FDA reports)
AMNESIA ( 199 FDA reports)
ARTERIOSCLEROSIS ( 199 FDA reports)
CEREBRAL HAEMORRHAGE ( 199 FDA reports)
HYPOCALCAEMIA ( 197 FDA reports)
HYPOPHAGIA ( 197 FDA reports)
BLISTER ( 196 FDA reports)
RIGHT VENTRICULAR FAILURE ( 196 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 195 FDA reports)
DIVERTICULUM ( 192 FDA reports)
CHOLESTASIS ( 190 FDA reports)
DERMATITIS EXFOLIATIVE ( 190 FDA reports)
SKIN DISCOLOURATION ( 190 FDA reports)
NASOPHARYNGITIS ( 188 FDA reports)
PULMONARY CONGESTION ( 187 FDA reports)
RASH MACULO-PAPULAR ( 186 FDA reports)
TOXIC SKIN ERUPTION ( 186 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 186 FDA reports)
GASTRITIS EROSIVE ( 186 FDA reports)
WHEEZING ( 181 FDA reports)
UNRESPONSIVE TO STIMULI ( 180 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 180 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 179 FDA reports)
ALOPECIA ( 179 FDA reports)
HYPERBILIRUBINAEMIA ( 179 FDA reports)
GENERALISED OEDEMA ( 178 FDA reports)
DYSARTHRIA ( 177 FDA reports)
GASTRIC ULCER ( 176 FDA reports)
PURPURA ( 176 FDA reports)
PROSTATE CANCER ( 175 FDA reports)
SINUS TACHYCARDIA ( 175 FDA reports)
ARTHROPATHY ( 175 FDA reports)
OFF LABEL USE ( 173 FDA reports)
LACTIC ACIDOSIS ( 172 FDA reports)
CYSTITIS ( 171 FDA reports)
STRESS ( 171 FDA reports)
ROTATOR CUFF SYNDROME ( 169 FDA reports)
ERECTILE DYSFUNCTION ( 167 FDA reports)
RIB FRACTURE ( 166 FDA reports)
TREATMENT NONCOMPLIANCE ( 166 FDA reports)
BLOOD GLUCOSE DECREASED ( 165 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 165 FDA reports)
FEAR ( 165 FDA reports)
OSTEOPOROSIS ( 165 FDA reports)
MULTIPLE INJURIES ( 164 FDA reports)
PRODUCTIVE COUGH ( 163 FDA reports)
URINARY INCONTINENCE ( 163 FDA reports)
AZOTAEMIA ( 162 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 162 FDA reports)
LYMPHOMA ( 162 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 161 FDA reports)
HIATUS HERNIA ( 160 FDA reports)
HYPERCHOLESTEROLAEMIA ( 160 FDA reports)
ORAL PAIN ( 160 FDA reports)
PNEUMONITIS ( 160 FDA reports)
CARDIAC MURMUR ( 159 FDA reports)
ANURIA ( 157 FDA reports)
SUDDEN DEATH ( 157 FDA reports)
CORONARY ARTERY OCCLUSION ( 156 FDA reports)
ECZEMA ( 155 FDA reports)
HEPATOTOXICITY ( 155 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 154 FDA reports)
PNEUMONIA ASPIRATION ( 154 FDA reports)
BLOOD CALCIUM DECREASED ( 153 FDA reports)
HYPOALBUMINAEMIA ( 153 FDA reports)
LEFT VENTRICULAR FAILURE ( 153 FDA reports)
METASTASES TO BONE ( 153 FDA reports)
MYELODYSPLASTIC SYNDROME ( 153 FDA reports)
RENAL INJURY ( 152 FDA reports)
TENDERNESS ( 150 FDA reports)
FLATULENCE ( 150 FDA reports)
GASTROENTERITIS ( 150 FDA reports)
INFUSION RELATED REACTION ( 149 FDA reports)
BRONCHOPNEUMONIA ( 148 FDA reports)
DIVERTICULUM INTESTINAL ( 148 FDA reports)
PSORIASIS ( 148 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 148 FDA reports)
VISUAL ACUITY REDUCED ( 148 FDA reports)
RESTLESSNESS ( 147 FDA reports)
SINUS BRADYCARDIA ( 147 FDA reports)
EJECTION FRACTION DECREASED ( 147 FDA reports)
FAECES DISCOLOURED ( 147 FDA reports)
NEUTROPENIC SEPSIS ( 147 FDA reports)
MOUTH ULCERATION ( 146 FDA reports)
MUSCLE TWITCHING ( 146 FDA reports)
TOOTH DISORDER ( 146 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 145 FDA reports)
ENTEROCOCCAL INFECTION ( 145 FDA reports)
ACUTE RESPIRATORY FAILURE ( 144 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 144 FDA reports)
BURNING SENSATION ( 144 FDA reports)
FACE OEDEMA ( 143 FDA reports)
HEART RATE DECREASED ( 143 FDA reports)
TYPE 2 DIABETES MELLITUS ( 143 FDA reports)
SCAR ( 142 FDA reports)
SKIN INDURATION ( 142 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 142 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 142 FDA reports)
EAR PAIN ( 142 FDA reports)
PULMONARY FIBROSIS ( 141 FDA reports)
POLLAKIURIA ( 140 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 140 FDA reports)
HEAD INJURY ( 140 FDA reports)
HEART RATE IRREGULAR ( 140 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 140 FDA reports)
BONE LESION ( 138 FDA reports)
NASAL CONGESTION ( 138 FDA reports)
SPEECH DISORDER ( 137 FDA reports)
TINNITUS ( 136 FDA reports)
ANGINA UNSTABLE ( 136 FDA reports)
CYTOLYTIC HEPATITIS ( 135 FDA reports)
DYSPHONIA ( 135 FDA reports)
PALLOR ( 135 FDA reports)
SLEEP DISORDER ( 135 FDA reports)
TRANSAMINASES INCREASED ( 134 FDA reports)
AORTIC VALVE INCOMPETENCE ( 134 FDA reports)
BACTERIAL INFECTION ( 134 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 133 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 133 FDA reports)
BACTERAEMIA ( 132 FDA reports)
INFLUENZA LIKE ILLNESS ( 132 FDA reports)
PERITONITIS ( 132 FDA reports)
URINE OUTPUT DECREASED ( 132 FDA reports)
ILEUS ( 131 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 131 FDA reports)
COLITIS ( 130 FDA reports)
NERVOUSNESS ( 130 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 130 FDA reports)
RHEUMATOID ARTHRITIS ( 129 FDA reports)
HYPOVOLAEMIA ( 129 FDA reports)
NIGHT SWEATS ( 129 FDA reports)
HOT FLUSH ( 128 FDA reports)
ATRIAL FLUTTER ( 127 FDA reports)
BLOOD ALBUMIN DECREASED ( 127 FDA reports)
TOOTH ABSCESS ( 127 FDA reports)
VISUAL IMPAIRMENT ( 127 FDA reports)
RESPIRATORY ARREST ( 126 FDA reports)
BLOOD CULTURE POSITIVE ( 126 FDA reports)
ERYTHEMA MULTIFORME ( 126 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 125 FDA reports)
CORONARY ARTERY STENOSIS ( 125 FDA reports)
ECCHYMOSIS ( 125 FDA reports)
MYOPATHY ( 125 FDA reports)
RENAL TUBULAR NECROSIS ( 125 FDA reports)
VENTRICULAR FIBRILLATION ( 125 FDA reports)
RESPIRATORY DISORDER ( 124 FDA reports)
BURSITIS ( 124 FDA reports)
GOUTY ARTHRITIS ( 124 FDA reports)
JOINT STIFFNESS ( 124 FDA reports)
DEAFNESS ( 123 FDA reports)
NEOPLASM PROGRESSION ( 123 FDA reports)
TOOTH INFECTION ( 123 FDA reports)
VASCULITIS ( 122 FDA reports)
ANAL FISSURE ( 122 FDA reports)
CANDIDIASIS ( 122 FDA reports)
CIRCULATORY COLLAPSE ( 122 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 122 FDA reports)
EXOSTOSIS ( 122 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 121 FDA reports)
SKIN TIGHTNESS ( 121 FDA reports)
VARICOSE VEIN ( 121 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 120 FDA reports)
DISCOMFORT ( 120 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 119 FDA reports)
GASTROINTESTINAL DISORDER ( 119 FDA reports)
HYPOMAGNESAEMIA ( 119 FDA reports)
EOSINOPHIL COUNT INCREASED ( 118 FDA reports)
INCORRECT DOSE ADMINISTERED ( 118 FDA reports)
NERVOUS SYSTEM DISORDER ( 118 FDA reports)
OBESITY ( 118 FDA reports)
ROAD TRAFFIC ACCIDENT ( 118 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 117 FDA reports)
DERMATITIS ( 117 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 117 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 117 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 116 FDA reports)
SUBDURAL HAEMATOMA ( 116 FDA reports)
VENTRICULAR HYPERTROPHY ( 116 FDA reports)
PRESYNCOPE ( 115 FDA reports)
BODY TEMPERATURE INCREASED ( 115 FDA reports)
FUNGAL INFECTION ( 115 FDA reports)
INJECTION SITE PAIN ( 115 FDA reports)
LUNG NEOPLASM ( 115 FDA reports)
NOCTURIA ( 115 FDA reports)
LUNG INFECTION ( 114 FDA reports)
RASH MACULAR ( 113 FDA reports)
PULMONARY HAEMORRHAGE ( 112 FDA reports)
VIRAL INFECTION ( 112 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 112 FDA reports)
ILL-DEFINED DISORDER ( 112 FDA reports)
MEDICATION ERROR ( 112 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 111 FDA reports)
CYANOSIS ( 111 FDA reports)
NO THERAPEUTIC RESPONSE ( 111 FDA reports)
SKIN DISORDER ( 111 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 110 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 110 FDA reports)
ABSCESS ( 110 FDA reports)
AGGRESSION ( 110 FDA reports)
CARDIOGENIC SHOCK ( 110 FDA reports)
COMPRESSION FRACTURE ( 110 FDA reports)
DISTURBANCE IN ATTENTION ( 110 FDA reports)
GINGIVAL BLEEDING ( 109 FDA reports)
RHINORRHOEA ( 109 FDA reports)
SKIN HYPERTROPHY ( 108 FDA reports)
CONJUNCTIVITIS ( 108 FDA reports)
ANGIOEDEMA ( 107 FDA reports)
CHOLECYSTITIS ( 107 FDA reports)
COGNITIVE DISORDER ( 107 FDA reports)
DYSKINESIA ( 107 FDA reports)
PETECHIAE ( 107 FDA reports)
SPINAL COLUMN STENOSIS ( 107 FDA reports)
REFRACTORY ANAEMIA ( 106 FDA reports)
SINUS DISORDER ( 106 FDA reports)
MENTAL DISORDER ( 106 FDA reports)
INTESTINAL OBSTRUCTION ( 105 FDA reports)
AORTIC STENOSIS ( 104 FDA reports)
HYDRONEPHROSIS ( 104 FDA reports)
HYPOPNOEA ( 104 FDA reports)
OLIGURIA ( 104 FDA reports)
ORAL CANDIDIASIS ( 103 FDA reports)
RALES ( 103 FDA reports)
SURGERY ( 103 FDA reports)
HAEMOLYTIC ANAEMIA ( 102 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 102 FDA reports)
MIGRAINE ( 102 FDA reports)
OESOPHAGITIS ( 102 FDA reports)
ABNORMAL BEHAVIOUR ( 101 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 101 FDA reports)
FIBROSIS ( 101 FDA reports)
LACERATION ( 101 FDA reports)
TACHYPNOEA ( 101 FDA reports)
TOOTH LOSS ( 101 FDA reports)
PLATELET COUNT INCREASED ( 100 FDA reports)
RASH PAPULAR ( 100 FDA reports)
SUICIDAL IDEATION ( 100 FDA reports)
EYE SWELLING ( 100 FDA reports)
LUNG NEOPLASM MALIGNANT ( 100 FDA reports)
BASAL CELL CARCINOMA ( 99 FDA reports)
BONE DEBRIDEMENT ( 99 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 99 FDA reports)
CEREBRAL ATROPHY ( 99 FDA reports)
DRUG DOSE OMISSION ( 99 FDA reports)
POST PROCEDURAL COMPLICATION ( 99 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 98 FDA reports)
VAGINAL ABSCESS ( 98 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 97 FDA reports)
HEPATOMEGALY ( 97 FDA reports)
CAROTID ARTERY STENOSIS ( 96 FDA reports)
DISABILITY ( 96 FDA reports)
DISEASE RECURRENCE ( 96 FDA reports)
DRUG EFFECT DECREASED ( 96 FDA reports)
HYPOACUSIS ( 96 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 96 FDA reports)
HEPATIC CIRRHOSIS ( 95 FDA reports)
TOOTHACHE ( 94 FDA reports)
POLYNEUROPATHY ( 93 FDA reports)
PRIMARY SEQUESTRUM ( 93 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 93 FDA reports)
PRURITUS GENERALISED ( 92 FDA reports)
ACUTE PULMONARY OEDEMA ( 92 FDA reports)
GINGIVAL PAIN ( 92 FDA reports)
MALNUTRITION ( 92 FDA reports)
ORAL INTAKE REDUCED ( 92 FDA reports)
DENTAL CARIES ( 91 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 91 FDA reports)
HALLUCINATION, VISUAL ( 91 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 91 FDA reports)
LIPASE INCREASED ( 91 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 91 FDA reports)
RETCHING ( 91 FDA reports)
PRODUCT QUALITY ISSUE ( 90 FDA reports)
PROSTATOMEGALY ( 90 FDA reports)
TUMOUR FLARE ( 90 FDA reports)
DEMENTIA ( 90 FDA reports)
DIPLOPIA ( 90 FDA reports)
ENDODONTIC PROCEDURE ( 90 FDA reports)
ILEUS PARALYTIC ( 90 FDA reports)
DECREASED INTEREST ( 89 FDA reports)
ADVERSE EVENT ( 88 FDA reports)
ELECTROLYTE IMBALANCE ( 88 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 88 FDA reports)
HEMIPARESIS ( 88 FDA reports)
INFLUENZA ( 88 FDA reports)
IRRITABILITY ( 88 FDA reports)
LYMPHOPENIA ( 88 FDA reports)
MYOSITIS ( 88 FDA reports)
CARPAL TUNNEL SYNDROME ( 87 FDA reports)
DYSLIPIDAEMIA ( 87 FDA reports)
FEELING COLD ( 87 FDA reports)
GINGIVAL SWELLING ( 87 FDA reports)
ORTHOPNOEA ( 87 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 87 FDA reports)
BLINDNESS ( 86 FDA reports)
COMPLETED SUICIDE ( 86 FDA reports)
GLAUCOMA ( 86 FDA reports)
ANAPHYLACTIC REACTION ( 85 FDA reports)
GASTRIC DISORDER ( 85 FDA reports)
SKIN CANCER ( 85 FDA reports)
PHARYNGEAL OEDEMA ( 84 FDA reports)
RESPIRATORY TRACT INFECTION ( 84 FDA reports)
CARDIOVASCULAR DISORDER ( 84 FDA reports)
CLOSTRIDIAL INFECTION ( 84 FDA reports)
DRUG LEVEL INCREASED ( 84 FDA reports)
FISTULA ( 84 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 84 FDA reports)
HYPOTHERMIA ( 84 FDA reports)
ATAXIA ( 83 FDA reports)
OCULAR HYPERAEMIA ( 83 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 83 FDA reports)
ACIDOSIS ( 82 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 82 FDA reports)
LUMBAR SPINAL STENOSIS ( 82 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 81 FDA reports)
EMOTIONAL DISORDER ( 81 FDA reports)
EMPHYSEMA ( 81 FDA reports)
HEPATIC ENCEPHALOPATHY ( 81 FDA reports)
LABORATORY TEST ABNORMAL ( 81 FDA reports)
NEURALGIA ( 81 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 81 FDA reports)
SUICIDE ATTEMPT ( 81 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 80 FDA reports)
SWOLLEN TONGUE ( 80 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 80 FDA reports)
FEMUR FRACTURE ( 80 FDA reports)
LOOSE TOOTH ( 80 FDA reports)
APHASIA ( 79 FDA reports)
ATRIOVENTRICULAR BLOCK ( 79 FDA reports)
DEVICE RELATED INFECTION ( 79 FDA reports)
DUODENAL ULCER ( 79 FDA reports)
EXPOSED BONE IN JAW ( 79 FDA reports)
PURULENT DISCHARGE ( 79 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 79 FDA reports)
SCIATICA ( 78 FDA reports)
SPINAL COMPRESSION FRACTURE ( 78 FDA reports)
BLOOD CREATINE INCREASED ( 78 FDA reports)
CARDIAC FAILURE ACUTE ( 78 FDA reports)
DYSSTASIA ( 78 FDA reports)
HYPERTENSIVE CRISIS ( 78 FDA reports)
IRON DEFICIENCY ANAEMIA ( 78 FDA reports)
LUNG CONSOLIDATION ( 78 FDA reports)
NEPHROPATHY TOXIC ( 78 FDA reports)
CHROMATURIA ( 77 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 77 FDA reports)
DECUBITUS ULCER ( 77 FDA reports)
EYE PAIN ( 77 FDA reports)
GINGIVAL DISORDER ( 77 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 77 FDA reports)
HYPERNATRAEMIA ( 77 FDA reports)
LIP SWELLING ( 77 FDA reports)
ANAPHYLACTIC SHOCK ( 76 FDA reports)
EYE DISORDER ( 76 FDA reports)
HOSPITALISATION ( 76 FDA reports)
MYOCLONUS ( 76 FDA reports)
PROTEIN TOTAL DECREASED ( 76 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 76 FDA reports)
RESTLESS LEGS SYNDROME ( 76 FDA reports)
SKIN FIBROSIS ( 76 FDA reports)
ULCER ( 75 FDA reports)
EXCORIATION ( 75 FDA reports)
DIABETIC NEUROPATHY ( 74 FDA reports)
EATING DISORDER ( 74 FDA reports)
EYELID OEDEMA ( 74 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 74 FDA reports)
DIABETIC NEPHROPATHY ( 73 FDA reports)
GENERALISED ERYTHEMA ( 73 FDA reports)
HYPOPHOSPHATAEMIA ( 73 FDA reports)
APLASTIC ANAEMIA ( 72 FDA reports)
ATRIAL TACHYCARDIA ( 72 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 72 FDA reports)
DRUG INTOLERANCE ( 72 FDA reports)
FOOT FRACTURE ( 72 FDA reports)
HYPERTENSIVE HEART DISEASE ( 72 FDA reports)
OSTEOLYSIS ( 72 FDA reports)
PNEUMOTHORAX ( 72 FDA reports)
SICK SINUS SYNDROME ( 72 FDA reports)
SINUS CONGESTION ( 72 FDA reports)
ABSCESS DRAINAGE ( 71 FDA reports)
ACUTE HEPATIC FAILURE ( 71 FDA reports)
BLOOD URINE PRESENT ( 71 FDA reports)
LIVER INJURY ( 71 FDA reports)
BLOOD AMYLASE INCREASED ( 70 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 70 FDA reports)
GYNAECOMASTIA ( 70 FDA reports)
ISCHAEMIC STROKE ( 70 FDA reports)
NEPHROGENIC ANAEMIA ( 70 FDA reports)
NEPHROPATHY ( 70 FDA reports)
THERAPY NON-RESPONDER ( 70 FDA reports)
UROSEPSIS ( 70 FDA reports)
WOUND DEHISCENCE ( 70 FDA reports)
PARALYSIS ( 69 FDA reports)
PHARYNGITIS ( 69 FDA reports)
SKIN HYPERPIGMENTATION ( 69 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 69 FDA reports)
ASPERGILLOSIS ( 69 FDA reports)
BLADDER CANCER ( 69 FDA reports)
JOINT INJURY ( 69 FDA reports)
LARGE INTESTINE PERFORATION ( 69 FDA reports)
NEPHROTIC SYNDROME ( 69 FDA reports)
OSTEOSCLEROSIS ( 69 FDA reports)
FAILURE TO THRIVE ( 68 FDA reports)
GINGIVITIS ( 68 FDA reports)
INTESTINAL ISCHAEMIA ( 68 FDA reports)
JOINT EFFUSION ( 68 FDA reports)
SINOATRIAL BLOCK ( 68 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 68 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 68 FDA reports)
PERIORBITAL OEDEMA ( 67 FDA reports)
PERIPHERAL COLDNESS ( 67 FDA reports)
SOFT TISSUE INFLAMMATION ( 67 FDA reports)
TROPONIN INCREASED ( 67 FDA reports)
VISUAL DISTURBANCE ( 67 FDA reports)
BREATH SOUNDS ABNORMAL ( 67 FDA reports)
HAEMOLYSIS ( 67 FDA reports)
HERPES SIMPLEX ( 67 FDA reports)
JOINT CONTRACTURE ( 67 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 67 FDA reports)
AORTIC ANEURYSM ( 66 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 66 FDA reports)
FLUID INTAKE REDUCED ( 66 FDA reports)
GALLBLADDER DISORDER ( 66 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 66 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 66 FDA reports)
METASTASES TO LIVER ( 66 FDA reports)
ODYNOPHAGIA ( 66 FDA reports)
PATHOLOGICAL FRACTURE ( 66 FDA reports)
TENDON RUPTURE ( 66 FDA reports)
PHYSICAL DISABILITY ( 65 FDA reports)
SERUM FERRITIN INCREASED ( 65 FDA reports)
COLD SWEAT ( 65 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 65 FDA reports)
COORDINATION ABNORMAL ( 65 FDA reports)
ESCHERICHIA INFECTION ( 65 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 65 FDA reports)
MENTAL IMPAIRMENT ( 65 FDA reports)
NEUTROPHIL COUNT INCREASED ( 65 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 65 FDA reports)
ABSCESS JAW ( 64 FDA reports)
AORTIC DISSECTION ( 64 FDA reports)
BLOOD CHLORIDE DECREASED ( 64 FDA reports)
CATARACT OPERATION ( 64 FDA reports)
CHEST X-RAY ABNORMAL ( 64 FDA reports)
DILATATION VENTRICULAR ( 64 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 64 FDA reports)
GRAND MAL CONVULSION ( 64 FDA reports)
INJECTION SITE ERYTHEMA ( 64 FDA reports)
INTESTINAL PERFORATION ( 64 FDA reports)
PSEUDOMONAS INFECTION ( 64 FDA reports)
PANIC ATTACK ( 63 FDA reports)
PNEUMONIA FUNGAL ( 63 FDA reports)
STEM CELL TRANSPLANT ( 63 FDA reports)
WOUND ( 63 FDA reports)
ANGIOPATHY ( 63 FDA reports)
CEREBRAL ISCHAEMIA ( 63 FDA reports)
INCONTINENCE ( 63 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 63 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 62 FDA reports)
BLOOD MAGNESIUM DECREASED ( 62 FDA reports)
GASTRIC CANCER ( 62 FDA reports)
GINGIVAL ULCERATION ( 62 FDA reports)
LOCAL SWELLING ( 62 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 62 FDA reports)
RASH PUSTULAR ( 62 FDA reports)
PYELONEPHRITIS ( 61 FDA reports)
ABDOMINAL PAIN LOWER ( 61 FDA reports)
CARDIAC VALVE DISEASE ( 61 FDA reports)
DRY EYE ( 61 FDA reports)
EPILEPSY ( 61 FDA reports)
GANGRENE ( 61 FDA reports)
GINGIVAL INFECTION ( 61 FDA reports)
HYPERKERATOSIS ( 61 FDA reports)
HYPERSOMNIA ( 61 FDA reports)
KLEBSIELLA INFECTION ( 61 FDA reports)
LOBAR PNEUMONIA ( 61 FDA reports)
MUSCLE ATROPHY ( 61 FDA reports)
ORAL DISCOMFORT ( 61 FDA reports)
PAIN OF SKIN ( 61 FDA reports)
BREAST CANCER ( 60 FDA reports)
DERMATITIS BULLOUS ( 60 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 60 FDA reports)
IMPAIRED WORK ABILITY ( 60 FDA reports)
MACULAR DEGENERATION ( 60 FDA reports)
PANCREATIC CARCINOMA ( 60 FDA reports)
REFLUX OESOPHAGITIS ( 60 FDA reports)
SKIN BURNING SENSATION ( 60 FDA reports)
TENDONITIS ( 60 FDA reports)
QUALITY OF LIFE DECREASED ( 59 FDA reports)
SENSORY DISTURBANCE ( 59 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 59 FDA reports)
HEPATOSPLENOMEGALY ( 59 FDA reports)
HICCUPS ( 59 FDA reports)
JAW OPERATION ( 59 FDA reports)
ORAL HERPES ( 59 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 58 FDA reports)
DILATATION ATRIAL ( 58 FDA reports)
FLANK PAIN ( 58 FDA reports)
GASTRIC HAEMORRHAGE ( 58 FDA reports)
HYPERTHERMIA ( 58 FDA reports)
INGUINAL HERNIA ( 58 FDA reports)
MOTOR DYSFUNCTION ( 58 FDA reports)
OPEN WOUND ( 58 FDA reports)
SKIN PAPILLOMA ( 58 FDA reports)
TENDON DISORDER ( 58 FDA reports)
TOOTH FRACTURE ( 58 FDA reports)
UMBILICAL HERNIA ( 58 FDA reports)
WOUND INFECTION ( 58 FDA reports)
SQUAMOUS CELL CARCINOMA ( 57 FDA reports)
ACUTE PRERENAL FAILURE ( 57 FDA reports)
ADVERSE DRUG REACTION ( 57 FDA reports)
BLOOD CALCIUM INCREASED ( 57 FDA reports)
CARDIAC PACEMAKER INSERTION ( 57 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 57 FDA reports)
HYPERPARATHYROIDISM ( 57 FDA reports)
LACUNAR INFARCTION ( 57 FDA reports)
ACUTE CORONARY SYNDROME ( 56 FDA reports)
HERNIA ( 56 FDA reports)
IRRITABLE BOWEL SYNDROME ( 56 FDA reports)
LACRIMATION INCREASED ( 56 FDA reports)
MASTICATION DISORDER ( 56 FDA reports)
MOUTH HAEMORRHAGE ( 56 FDA reports)
PSYCHOTIC DISORDER ( 56 FDA reports)
SCAB ( 56 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 56 FDA reports)
VENTRICULAR HYPOKINESIA ( 56 FDA reports)
PHOTOSENSITIVITY REACTION ( 55 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 55 FDA reports)
PROSTATITIS ( 55 FDA reports)
RADICULOPATHY ( 55 FDA reports)
RENAL ATROPHY ( 55 FDA reports)
RENAL CELL CARCINOMA ( 55 FDA reports)
SCOLIOSIS ( 55 FDA reports)
ACTINIC KERATOSIS ( 55 FDA reports)
AGEUSIA ( 55 FDA reports)
BRAIN OEDEMA ( 55 FDA reports)
COLON CANCER ( 55 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 55 FDA reports)
EAR INFECTION ( 55 FDA reports)
ENDOCARDITIS ( 55 FDA reports)
GINGIVAL RECESSION ( 55 FDA reports)
HEPATITIS CHOLESTATIC ( 55 FDA reports)
ORAL DISORDER ( 55 FDA reports)
CHOLECYSTITIS ACUTE ( 54 FDA reports)
DEPRESSED MOOD ( 54 FDA reports)
EXERCISE TOLERANCE DECREASED ( 54 FDA reports)
HAEMODYNAMIC INSTABILITY ( 54 FDA reports)
HEPATITIS ACUTE ( 54 FDA reports)
JAW FRACTURE ( 54 FDA reports)
RESPIRATORY RATE INCREASED ( 54 FDA reports)
PERIODONTITIS ( 53 FDA reports)
RHINITIS ALLERGIC ( 53 FDA reports)
THIRST ( 53 FDA reports)
VENOOCCLUSIVE DISEASE ( 53 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 53 FDA reports)
CATHETER RELATED INFECTION ( 53 FDA reports)
CREPITATIONS ( 53 FDA reports)
ISCHAEMIA ( 53 FDA reports)
MOVEMENT DISORDER ( 53 FDA reports)
HIP ARTHROPLASTY ( 52 FDA reports)
HYPERPHOSPHATAEMIA ( 52 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 52 FDA reports)
NEPHRITIS INTERSTITIAL ( 52 FDA reports)
OSTEITIS ( 52 FDA reports)
SKIN NECROSIS ( 52 FDA reports)
SUDDEN CARDIAC DEATH ( 52 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 52 FDA reports)
PNEUMONIA BACTERIAL ( 51 FDA reports)
PROTEIN URINE PRESENT ( 51 FDA reports)
SKIN REACTION ( 51 FDA reports)
CAPILLARY LEAK SYNDROME ( 51 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 51 FDA reports)
COLITIS ISCHAEMIC ( 51 FDA reports)
CULTURE URINE POSITIVE ( 51 FDA reports)
EYELID PTOSIS ( 51 FDA reports)
NEPHROSCLEROSIS ( 51 FDA reports)
APPENDICITIS ( 50 FDA reports)
BLINDNESS UNILATERAL ( 50 FDA reports)
ENTERITIS ( 50 FDA reports)
PITTING OEDEMA ( 50 FDA reports)
SKIN INFECTION ( 50 FDA reports)
PROCEDURAL COMPLICATION ( 49 FDA reports)
PULSE ABSENT ( 49 FDA reports)
VENOUS INSUFFICIENCY ( 49 FDA reports)
ACCIDENTAL OVERDOSE ( 49 FDA reports)
ANKLE FRACTURE ( 49 FDA reports)
ASPIRATION ( 49 FDA reports)
BARRETT'S OESOPHAGUS ( 49 FDA reports)
GRAFT VERSUS HOST DISEASE ( 49 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 49 FDA reports)
JAUNDICE CHOLESTATIC ( 49 FDA reports)
JAW DISORDER ( 49 FDA reports)
LEUKAEMIA ( 49 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 48 FDA reports)
BONE MARROW DEPRESSION ( 48 FDA reports)
CHEILITIS ( 48 FDA reports)
EXTRASYSTOLES ( 48 FDA reports)
FACIAL PALSY ( 48 FDA reports)
IRON DEFICIENCY ( 48 FDA reports)
LIMB INJURY ( 48 FDA reports)
METASTASES TO LYMPH NODES ( 48 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 48 FDA reports)
RENAL PAIN ( 48 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 48 FDA reports)
THROAT IRRITATION ( 48 FDA reports)
VISUAL FIELD DEFECT ( 48 FDA reports)
PERIODONTAL DISEASE ( 47 FDA reports)
PHLEBITIS ( 47 FDA reports)
SEBORRHOEIC DERMATITIS ( 47 FDA reports)
TACHYARRHYTHMIA ( 47 FDA reports)
VASCULAR CALCIFICATION ( 47 FDA reports)
X-RAY ABNORMAL ( 47 FDA reports)
B-CELL LYMPHOMA ( 47 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 47 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 47 FDA reports)
CARDIAC FAILURE CHRONIC ( 47 FDA reports)
CHOLECYSTECTOMY ( 47 FDA reports)
DIABETIC KETOACIDOSIS ( 47 FDA reports)
DRUG ADMINISTRATION ERROR ( 47 FDA reports)
GASTROENTERITIS VIRAL ( 47 FDA reports)
HIP FRACTURE ( 47 FDA reports)
METASTASIS ( 47 FDA reports)
MUSCLE TIGHTNESS ( 47 FDA reports)
NODULE ( 47 FDA reports)
AORTIC VALVE SCLEROSIS ( 46 FDA reports)
BLOOD BICARBONATE DECREASED ( 46 FDA reports)
DIFFICULTY IN WALKING ( 46 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 46 FDA reports)
RETINAL HAEMORRHAGE ( 46 FDA reports)
PARAESTHESIA ORAL ( 45 FDA reports)
PELVIC FRACTURE ( 45 FDA reports)
POOR QUALITY SLEEP ( 45 FDA reports)
SKIN FISSURES ( 45 FDA reports)
SKIN IRRITATION ( 45 FDA reports)
SPINAL FRACTURE ( 45 FDA reports)
TORSADE DE POINTES ( 45 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 45 FDA reports)
BODY TEMPERATURE DECREASED ( 45 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 45 FDA reports)
ERUCTATION ( 45 FDA reports)
FAECAL INCONTINENCE ( 45 FDA reports)
FOOT DEFORMITY ( 45 FDA reports)
HYPERTHYROIDISM ( 45 FDA reports)
METASTASES TO LUNG ( 45 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 44 FDA reports)
BONE OPERATION ( 44 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 44 FDA reports)
DEAFNESS NEUROSENSORY ( 44 FDA reports)
DIASTOLIC DYSFUNCTION ( 44 FDA reports)
HEPATIC CYST ( 44 FDA reports)
LIFE EXPECTANCY SHORTENED ( 44 FDA reports)
NECROSIS ( 44 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 44 FDA reports)
SPINAL DISORDER ( 44 FDA reports)
STOMACH DISCOMFORT ( 44 FDA reports)
WOUND SECRETION ( 44 FDA reports)
SKIN PLAQUE ( 43 FDA reports)
VENTRICULAR DYSFUNCTION ( 43 FDA reports)
ABSCESS LIMB ( 43 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 43 FDA reports)
BLOOD CHLORIDE INCREASED ( 43 FDA reports)
BLOOD SODIUM INCREASED ( 43 FDA reports)
CHRONIC SINUSITIS ( 43 FDA reports)
DIABETIC RETINOPATHY ( 43 FDA reports)
DIZZINESS POSTURAL ( 43 FDA reports)
ERYSIPELAS ( 43 FDA reports)
FIBRIN D DIMER INCREASED ( 43 FDA reports)
GOITRE ( 43 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 43 FDA reports)
LOCALISED INFECTION ( 43 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 43 FDA reports)
MANIA ( 43 FDA reports)
ABNORMAL DREAMS ( 42 FDA reports)
ANAEMIA MACROCYTIC ( 42 FDA reports)
CEREBROVASCULAR DISORDER ( 42 FDA reports)
CHOLECYSTITIS CHRONIC ( 42 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 42 FDA reports)
CYST ( 42 FDA reports)
DECREASED ACTIVITY ( 42 FDA reports)
DIVERTICULAR PERFORATION ( 42 FDA reports)
DRUG DEPENDENCE ( 42 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 42 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 42 FDA reports)
HEPATITIS TOXIC ( 42 FDA reports)
HUMERUS FRACTURE ( 42 FDA reports)
LEFT ATRIAL DILATATION ( 42 FDA reports)
OCCULT BLOOD POSITIVE ( 42 FDA reports)
OTITIS EXTERNA ( 42 FDA reports)
PARANOIA ( 42 FDA reports)
PCO2 DECREASED ( 42 FDA reports)
PERFORMANCE STATUS DECREASED ( 42 FDA reports)
PHOTOPHOBIA ( 42 FDA reports)
VITREOUS HAEMORRHAGE ( 42 FDA reports)
PROTEIN TOTAL INCREASED ( 41 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 41 FDA reports)
BEDRIDDEN ( 41 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 41 FDA reports)
BONE FRAGMENTATION ( 41 FDA reports)
COLITIS ULCERATIVE ( 41 FDA reports)
CROHN'S DISEASE ( 41 FDA reports)
GRANULOMA ( 41 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 41 FDA reports)
IMMUNODEFICIENCY ( 41 FDA reports)
MICTURITION URGENCY ( 41 FDA reports)
ANGER ( 40 FDA reports)
CLAVICLE FRACTURE ( 40 FDA reports)
DELUSION ( 40 FDA reports)
FEELING JITTERY ( 40 FDA reports)
FURUNCLE ( 40 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 40 FDA reports)
HYPOKINESIA ( 40 FDA reports)
INJECTION SITE HAEMORRHAGE ( 40 FDA reports)
JOINT DISLOCATION ( 40 FDA reports)
LIBIDO DECREASED ( 40 FDA reports)
MENISCUS LESION ( 40 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 40 FDA reports)
PEPTIC ULCER ( 40 FDA reports)
PERITONITIS BACTERIAL ( 40 FDA reports)
RASH MORBILLIFORM ( 40 FDA reports)
VITREOUS FLOATERS ( 40 FDA reports)
PERIPHERAL ISCHAEMIA ( 39 FDA reports)
PLEURISY ( 39 FDA reports)
PLEURITIC PAIN ( 39 FDA reports)
PULMONARY TOXICITY ( 39 FDA reports)
SHOCK HAEMORRHAGIC ( 39 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 39 FDA reports)
APNOEA ( 39 FDA reports)
AXONAL NEUROPATHY ( 39 FDA reports)
BLOOD PRESSURE ABNORMAL ( 39 FDA reports)
CARDIOPULMONARY FAILURE ( 39 FDA reports)
CRYING ( 39 FDA reports)
CYSTITIS HAEMORRHAGIC ( 39 FDA reports)
FRACTURE ( 39 FDA reports)
HYPOVOLAEMIC SHOCK ( 39 FDA reports)
INCREASED TENDENCY TO BRUISE ( 39 FDA reports)
NEUROTOXICITY ( 39 FDA reports)
NEUTROPENIC INFECTION ( 39 FDA reports)
ABDOMINAL TENDERNESS ( 38 FDA reports)
ALCOHOL USE ( 38 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 38 FDA reports)
GLOMERULONEPHRITIS ( 38 FDA reports)
GRANULOCYTOPENIA ( 38 FDA reports)
HAEMORRHAGIC DIATHESIS ( 38 FDA reports)
HYPOGLYCAEMIC COMA ( 38 FDA reports)
INJECTION SITE HAEMATOMA ( 38 FDA reports)
INTERMITTENT CLAUDICATION ( 38 FDA reports)
LYMPHOEDEMA ( 38 FDA reports)
MASS ( 38 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 38 FDA reports)
NIGHTMARE ( 38 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 38 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 38 FDA reports)
SKIN HAEMORRHAGE ( 38 FDA reports)
VENOUS THROMBOSIS ( 38 FDA reports)
VENTRICULAR ARRHYTHMIA ( 38 FDA reports)
PO2 DECREASED ( 37 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 37 FDA reports)
PURULENCE ( 37 FDA reports)
RENAL MASS ( 37 FDA reports)
RETINAL DETACHMENT ( 37 FDA reports)
SEBORRHOEIC KERATOSIS ( 37 FDA reports)
AFFECT LABILITY ( 37 FDA reports)
ANXIETY DISORDER ( 37 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 37 FDA reports)
BACTERIAL SEPSIS ( 37 FDA reports)
BREAST PAIN ( 37 FDA reports)
DERMATITIS ALLERGIC ( 37 FDA reports)
ENTEROCOLITIS ( 37 FDA reports)
FAECALOMA ( 37 FDA reports)
FEBRILE BONE MARROW APLASIA ( 37 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 37 FDA reports)
HALLUCINATION, AUDITORY ( 37 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 37 FDA reports)
HYPOPROTEINAEMIA ( 37 FDA reports)
INFARCTION ( 37 FDA reports)
INTENTIONAL DRUG MISUSE ( 37 FDA reports)
KYPHOSIS ( 37 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 36 FDA reports)
BRADYARRHYTHMIA ( 36 FDA reports)
BREAST MASS ( 36 FDA reports)
CATHETERISATION CARDIAC ( 36 FDA reports)
GASTROINTESTINAL NECROSIS ( 36 FDA reports)
HYPOTONIA ( 36 FDA reports)
LOWER LIMB FRACTURE ( 36 FDA reports)
MENINGITIS ( 36 FDA reports)
METASTASES TO SPINE ( 36 FDA reports)
MUSCLE HAEMORRHAGE ( 36 FDA reports)
OEDEMA MOUTH ( 36 FDA reports)
PARAPROTEINAEMIA ( 36 FDA reports)
PROTHROMBIN TIME SHORTENED ( 36 FDA reports)
PULPITIS DENTAL ( 36 FDA reports)
STENT PLACEMENT ( 36 FDA reports)
THROMBOCYTOSIS ( 36 FDA reports)
POLYURIA ( 35 FDA reports)
SCLERODERMA ( 35 FDA reports)
VITAMIN B12 DEFICIENCY ( 35 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 35 FDA reports)
ADRENAL INSUFFICIENCY ( 35 FDA reports)
ANGIONEUROTIC OEDEMA ( 35 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 35 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 35 FDA reports)
BRAIN INJURY ( 35 FDA reports)
BRONCHOSPASM ( 35 FDA reports)
CENTRAL LINE INFECTION ( 35 FDA reports)
CHOLANGITIS ( 35 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 35 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 35 FDA reports)
HEPATIC NECROSIS ( 35 FDA reports)
LUMBAR RADICULOPATHY ( 35 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 35 FDA reports)
MASTOIDITIS ( 35 FDA reports)
METABOLIC SYNDROME ( 35 FDA reports)
NEOPLASM ( 35 FDA reports)
OCULAR ICTERUS ( 35 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 34 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 34 FDA reports)
BONE EROSION ( 34 FDA reports)
BONE MARROW TRANSPLANT ( 34 FDA reports)
CALCULUS URETERIC ( 34 FDA reports)
CERUMEN IMPACTION ( 34 FDA reports)
CLOSTRIDIUM COLITIS ( 34 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 34 FDA reports)
CULTURE POSITIVE ( 34 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 34 FDA reports)
EYE LASER SURGERY ( 34 FDA reports)
HYPERPLASIA ( 34 FDA reports)
HYPOAESTHESIA ORAL ( 34 FDA reports)
MITRAL VALVE PROLAPSE ( 34 FDA reports)
QRS AXIS ABNORMAL ( 34 FDA reports)
RENAL OSTEODYSTROPHY ( 34 FDA reports)
VAGINAL HAEMORRHAGE ( 34 FDA reports)
PLEURAL FIBROSIS ( 33 FDA reports)
PRESBYOPIA ( 33 FDA reports)
PULMONARY MASS ( 33 FDA reports)
SEXUAL DYSFUNCTION ( 33 FDA reports)
SINUS ARRHYTHMIA ( 33 FDA reports)
THROMBOPHLEBITIS ( 33 FDA reports)
WEGENER'S GRANULOMATOSIS ( 33 FDA reports)
WOUND DRAINAGE ( 33 FDA reports)
ANEURYSM ( 33 FDA reports)
BACK DISORDER ( 33 FDA reports)
BLADDER OBSTRUCTION ( 33 FDA reports)
BLOOD TEST ABNORMAL ( 33 FDA reports)
CAECITIS ( 33 FDA reports)
CALCIPHYLAXIS ( 33 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 33 FDA reports)
EYE HAEMORRHAGE ( 33 FDA reports)
FULL BLOOD COUNT DECREASED ( 33 FDA reports)
HEPATITIS B ( 33 FDA reports)
HEPATOCELLULAR DAMAGE ( 33 FDA reports)
HYDROCEPHALUS ( 33 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 33 FDA reports)
IMMUNOSUPPRESSION ( 33 FDA reports)
LARGE INTESTINAL ULCER ( 33 FDA reports)
LICHENOID KERATOSIS ( 33 FDA reports)
MARROW HYPERPLASIA ( 33 FDA reports)
NODAL ARRHYTHMIA ( 33 FDA reports)
APHAGIA ( 32 FDA reports)
BLOOD IRON DECREASED ( 32 FDA reports)
BREAST TENDERNESS ( 32 FDA reports)
CACHEXIA ( 32 FDA reports)
CARDIAC TAMPONADE ( 32 FDA reports)
DEBRIDEMENT ( 32 FDA reports)
DUODENITIS ( 32 FDA reports)
EPIGASTRIC DISCOMFORT ( 32 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 32 FDA reports)
EYE PRURITUS ( 32 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 32 FDA reports)
GRIP STRENGTH DECREASED ( 32 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 32 FDA reports)
KNEE ARTHROPLASTY ( 32 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 32 FDA reports)
METASTATIC NEOPLASM ( 32 FDA reports)
ORAL INFECTION ( 32 FDA reports)
POOR DENTAL CONDITION ( 32 FDA reports)
SEQUESTRECTOMY ( 32 FDA reports)
SOPOR ( 32 FDA reports)
SPINAL LAMINECTOMY ( 32 FDA reports)
SPUTUM CULTURE POSITIVE ( 32 FDA reports)
STATUS EPILEPTICUS ( 32 FDA reports)
TUBERCULOSIS ( 32 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 32 FDA reports)
UTERINE LEIOMYOMA ( 32 FDA reports)
VITREOUS DETACHMENT ( 32 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 31 FDA reports)
TARDIVE DYSKINESIA ( 31 FDA reports)
THYROID DISORDER ( 31 FDA reports)
TYPE 1 DIABETES MELLITUS ( 31 FDA reports)
URINARY TRACT OBSTRUCTION ( 31 FDA reports)
URINE ODOUR ABNORMAL ( 31 FDA reports)
AORTIC CALCIFICATION ( 31 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 31 FDA reports)
BONE DENSITY DECREASED ( 31 FDA reports)
COLLAPSE OF LUNG ( 31 FDA reports)
DENTAL OPERATION ( 31 FDA reports)
EAR DISCOMFORT ( 31 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 31 FDA reports)
GLOSSODYNIA ( 31 FDA reports)
HAEMORRHAGIC ANAEMIA ( 31 FDA reports)
HEPATIC LESION ( 31 FDA reports)
HEPATOCELLULAR INJURY ( 31 FDA reports)
HODGKIN'S DISEASE ( 31 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 31 FDA reports)
INTENTIONAL OVERDOSE ( 31 FDA reports)
INTRACARDIAC THROMBUS ( 31 FDA reports)
KERATITIS ( 31 FDA reports)
METABOLIC ENCEPHALOPATHY ( 31 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 31 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 31 FDA reports)
NEUROPATHY ( 31 FDA reports)
NON-CARDIAC CHEST PAIN ( 31 FDA reports)
BLOOD COUNT ABNORMAL ( 30 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 30 FDA reports)
CAROTID ARTERY DISEASE ( 30 FDA reports)
COAGULATION TIME PROLONGED ( 30 FDA reports)
CORONARY ARTERY BYPASS ( 30 FDA reports)
DEMYELINATION ( 30 FDA reports)
DENTURE WEARER ( 30 FDA reports)
DERMAL CYST ( 30 FDA reports)
FACIAL PAIN ( 30 FDA reports)
HEARING IMPAIRED ( 30 FDA reports)
HEMIPLEGIA ( 30 FDA reports)
IMMUNE SYSTEM DISORDER ( 30 FDA reports)
JUGULAR VEIN DISTENSION ( 30 FDA reports)
KIDNEY INFECTION ( 30 FDA reports)
MALIGNANT MELANOMA ( 30 FDA reports)
MELANOCYTIC NAEVUS ( 30 FDA reports)
METABOLIC DISORDER ( 30 FDA reports)
MOUTH INJURY ( 30 FDA reports)
MUSCLE DISORDER ( 30 FDA reports)
MYDRIASIS ( 30 FDA reports)
MYOGLOBINURIA ( 30 FDA reports)
ONYCHOMYCOSIS ( 30 FDA reports)
ORAL CAVITY FISTULA ( 30 FDA reports)
PATHOGEN RESISTANCE ( 30 FDA reports)
PERSONALITY CHANGE ( 30 FDA reports)
PROCTALGIA ( 30 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 30 FDA reports)
VASCULAR GRAFT OCCLUSION ( 30 FDA reports)
PARKINSON'S DISEASE ( 29 FDA reports)
PERICARDITIS ( 29 FDA reports)
PLATELET DISORDER ( 29 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 29 FDA reports)
PULMONARY GRANULOMA ( 29 FDA reports)
RENAL ARTERY STENOSIS ( 29 FDA reports)
RENAL TUBULAR DISORDER ( 29 FDA reports)
STREPTOCOCCAL INFECTION ( 29 FDA reports)
STREPTOCOCCAL SEPSIS ( 29 FDA reports)
TOXIC ENCEPHALOPATHY ( 29 FDA reports)
UPPER LIMB FRACTURE ( 29 FDA reports)
VASCULAR PSEUDOANEURYSM ( 29 FDA reports)
ACCIDENTAL EXPOSURE ( 29 FDA reports)
AORTIC VALVE STENOSIS ( 29 FDA reports)
BLADDER CANCER RECURRENT ( 29 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 29 FDA reports)
BLOOD DISORDER ( 29 FDA reports)
BODY HEIGHT DECREASED ( 29 FDA reports)
CATHETER RELATED COMPLICATION ( 29 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 29 FDA reports)
DEVICE FAILURE ( 29 FDA reports)
DYSPLASTIC NAEVUS ( 29 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 29 FDA reports)
ESSENTIAL HYPERTENSION ( 29 FDA reports)
EYE IRRITATION ( 29 FDA reports)
GASTRODUODENITIS ( 29 FDA reports)
HERPES VIRUS INFECTION ( 29 FDA reports)
LIMB DISCOMFORT ( 29 FDA reports)
LIP EROSION ( 29 FDA reports)
ANAL HAEMORRHAGE ( 28 FDA reports)
APTYALISM ( 28 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 28 FDA reports)
EMBOLISM ( 28 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 28 FDA reports)
HAEMANGIOMA ( 28 FDA reports)
HEPATIC CONGESTION ( 28 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 28 FDA reports)
MICROCYTIC ANAEMIA ( 28 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 28 FDA reports)
NO ADVERSE EVENT ( 28 FDA reports)
OESOPHAGEAL ULCER ( 28 FDA reports)
OSTEOMYELITIS CHRONIC ( 28 FDA reports)
SENSORY LOSS ( 28 FDA reports)
SOFT TISSUE INFECTION ( 28 FDA reports)
SPUTUM DISCOLOURED ( 28 FDA reports)
SUBCUTANEOUS NODULE ( 28 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 28 FDA reports)
THROAT TIGHTNESS ( 28 FDA reports)
URINARY HESITATION ( 28 FDA reports)
VIITH NERVE PARALYSIS ( 28 FDA reports)
WALKING AID USER ( 28 FDA reports)
PROSTATE CANCER METASTATIC ( 27 FDA reports)
SEDATION ( 27 FDA reports)
SKIN EROSION ( 27 FDA reports)
SPONDYLOLISTHESIS ( 27 FDA reports)
SUBCUTANEOUS ABSCESS ( 27 FDA reports)
SUBILEUS ( 27 FDA reports)
SYNCOPE VASOVAGAL ( 27 FDA reports)
TRAUMATIC HAEMATOMA ( 27 FDA reports)
TRIGGER FINGER ( 27 FDA reports)
TROPONIN I INCREASED ( 27 FDA reports)
ARTERIAL STENOSIS ( 27 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 27 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 27 FDA reports)
CARDIAC ENZYMES INCREASED ( 27 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 27 FDA reports)
CORONARY ARTERY RESTENOSIS ( 27 FDA reports)
DRUG PRESCRIBING ERROR ( 27 FDA reports)
ESCHERICHIA SEPSIS ( 27 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 27 FDA reports)
FOLLICULITIS ( 27 FDA reports)
GASTRIC PERFORATION ( 27 FDA reports)
GASTRIC POLYPS ( 27 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 27 FDA reports)
IMPETIGO ( 27 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 27 FDA reports)
MIDDLE INSOMNIA ( 27 FDA reports)
MOOD ALTERED ( 27 FDA reports)
MUCOSAL ULCERATION ( 27 FDA reports)
MYOPIA ( 27 FDA reports)
OESOPHAGEAL PAIN ( 27 FDA reports)
ORAL SURGERY ( 27 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 26 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 26 FDA reports)
BLOOD UREA DECREASED ( 26 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 26 FDA reports)
COR PULMONALE ( 26 FDA reports)
CORONARY ARTERY THROMBOSIS ( 26 FDA reports)
DENTAL PROSTHESIS USER ( 26 FDA reports)
DRUG DISPENSING ERROR ( 26 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
ESCHERICHIA BACTERAEMIA ( 26 FDA reports)
FACIAL NEURALGIA ( 26 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 26 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 26 FDA reports)
INFECTIOUS PERITONITIS ( 26 FDA reports)
INJECTION SITE REACTION ( 26 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 26 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 26 FDA reports)
LYMPHADENITIS ( 26 FDA reports)
MEDICAL DEVICE COMPLICATION ( 26 FDA reports)
MEDICATION RESIDUE ( 26 FDA reports)
MUCOSAL EROSION ( 26 FDA reports)
NERVE INJURY ( 26 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 26 FDA reports)
PARONYCHIA ( 26 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 26 FDA reports)
PERITONEAL DIALYSIS ( 26 FDA reports)
PSYCHIATRIC SYMPTOM ( 26 FDA reports)
PULMONARY INFARCTION ( 26 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 26 FDA reports)
ROSACEA ( 26 FDA reports)
SCLERODACTYLIA ( 26 FDA reports)
SKIN TOXICITY ( 26 FDA reports)
TRANSPLANT FAILURE ( 26 FDA reports)
VENOUS OCCLUSION ( 26 FDA reports)
VIRAL PHARYNGITIS ( 26 FDA reports)
VITAMIN D DEFICIENCY ( 26 FDA reports)
POLYMYALGIA RHEUMATICA ( 25 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 25 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 25 FDA reports)
RASH VESICULAR ( 25 FDA reports)
RENAL CANCER ( 25 FDA reports)
SARCOIDOSIS ( 25 FDA reports)
SKIN LACERATION ( 25 FDA reports)
SKIN WARM ( 25 FDA reports)
SUBMANDIBULAR MASS ( 25 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 25 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 25 FDA reports)
VARICELLA ( 25 FDA reports)
ACUTE ABDOMEN ( 25 FDA reports)
APPENDICECTOMY ( 25 FDA reports)
ATROPHY ( 25 FDA reports)
AUTOIMMUNE DISORDER ( 25 FDA reports)
BLAST CELL COUNT INCREASED ( 25 FDA reports)
CARDIORENAL SYNDROME ( 25 FDA reports)
CATHETER SITE HAEMORRHAGE ( 25 FDA reports)
COLON ADENOMA ( 25 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 25 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 25 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 25 FDA reports)
FIBROMYALGIA ( 25 FDA reports)
GRANULOCYTE COUNT DECREASED ( 25 FDA reports)
GUILLAIN-BARRE SYNDROME ( 25 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 25 FDA reports)
HYPERPYREXIA ( 25 FDA reports)
HYPOREFLEXIA ( 25 FDA reports)
INTRAOCULAR LENS IMPLANT ( 25 FDA reports)
MEAN CELL VOLUME INCREASED ( 25 FDA reports)
MECHANICAL VENTILATION ( 25 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 25 FDA reports)
MUSCLE CONTRACTURE ( 25 FDA reports)
MUSCLE INJURY ( 25 FDA reports)
MUSCLE RUPTURE ( 25 FDA reports)
NEUTROPENIC COLITIS ( 25 FDA reports)
NIKOLSKY'S SIGN ( 25 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 25 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 25 FDA reports)
OVERWEIGHT ( 25 FDA reports)
ABDOMINAL ABSCESS ( 24 FDA reports)
ADRENAL NEOPLASM ( 24 FDA reports)
ALVEOLOPLASTY ( 24 FDA reports)
AMAUROSIS FUGAX ( 24 FDA reports)
ANORECTAL DISORDER ( 24 FDA reports)
APHONIA ( 24 FDA reports)
APLASIA ( 24 FDA reports)
ARTHRITIS BACTERIAL ( 24 FDA reports)
BLADDER CATHETERISATION ( 24 FDA reports)
BLADDER DISORDER ( 24 FDA reports)
BLEPHARITIS ( 24 FDA reports)
BLOOD CREATININE DECREASED ( 24 FDA reports)
BRONCHIECTASIS ( 24 FDA reports)
BUNDLE BRANCH BLOCK ( 24 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 24 FDA reports)
CEREBRAL HAEMATOMA ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 24 FDA reports)
ENDOTRACHEAL INTUBATION ( 24 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 24 FDA reports)
EROSIVE OESOPHAGITIS ( 24 FDA reports)
ERYTHEMA NODOSUM ( 24 FDA reports)
EYE OPERATION ( 24 FDA reports)
FRACTURED SACRUM ( 24 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 24 FDA reports)
GROIN PAIN ( 24 FDA reports)
HAEMARTHROSIS ( 24 FDA reports)
HAEMATOCRIT ABNORMAL ( 24 FDA reports)
HALLUCINATIONS, MIXED ( 24 FDA reports)
HEPATITIS FULMINANT ( 24 FDA reports)
HYPERMAGNESAEMIA ( 24 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 24 FDA reports)
INDURATION ( 24 FDA reports)
INTESTINAL HAEMORRHAGE ( 24 FDA reports)
JOINT SPRAIN ( 24 FDA reports)
LOGORRHOEA ( 24 FDA reports)
MAJOR DEPRESSION ( 24 FDA reports)
MALOCCLUSION ( 24 FDA reports)
MUCOUS MEMBRANE DISORDER ( 24 FDA reports)
MULTIPLE DRUG OVERDOSE ( 24 FDA reports)
MUSCULOSKELETAL DISORDER ( 24 FDA reports)
MYOCARDITIS ( 24 FDA reports)
NAIL DISORDER ( 24 FDA reports)
OSTEITIS DEFORMANS ( 24 FDA reports)
PLASMACYTOMA ( 24 FDA reports)
POLYARTHRITIS ( 24 FDA reports)
POLYDIPSIA ( 24 FDA reports)
RESPIRATORY ACIDOSIS ( 24 FDA reports)
RESPIRATORY DEPRESSION ( 24 FDA reports)
SOCIAL PROBLEM ( 24 FDA reports)
SYNOVIAL CYST ( 24 FDA reports)
THINKING ABNORMAL ( 24 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 24 FDA reports)
TOOTH INJURY ( 24 FDA reports)
WITHDRAWAL SYNDROME ( 24 FDA reports)
PATHOLOGICAL GAMBLING ( 23 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 23 FDA reports)
RADIOTHERAPY ( 23 FDA reports)
RENAL TRANSPLANT ( 23 FDA reports)
SENSATION OF FOREIGN BODY ( 23 FDA reports)
SEPSIS SYNDROME ( 23 FDA reports)
SEROTONIN SYNDROME ( 23 FDA reports)
SNORING ( 23 FDA reports)
T-CELL LYMPHOMA ( 23 FDA reports)
ULCER HAEMORRHAGE ( 23 FDA reports)
URINE ABNORMALITY ( 23 FDA reports)
URINE FLOW DECREASED ( 23 FDA reports)
UTERINE CANCER ( 23 FDA reports)
VASCULAR OCCLUSION ( 23 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 23 FDA reports)
AORTIC VALVE CALCIFICATION ( 23 FDA reports)
APATHY ( 23 FDA reports)
BACK INJURY ( 23 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 23 FDA reports)
BRAIN HERNIATION ( 23 FDA reports)
DEVICE MALFUNCTION ( 23 FDA reports)
ENTEROBACTER INFECTION ( 23 FDA reports)
EYE MOVEMENT DISORDER ( 23 FDA reports)
FEMORAL NECK FRACTURE ( 23 FDA reports)
GASTRITIS HAEMORRHAGIC ( 23 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 23 FDA reports)
HAEMOTHORAX ( 23 FDA reports)
HAND FRACTURE ( 23 FDA reports)
HYPERTONIC BLADDER ( 23 FDA reports)
IMMOBILE ( 23 FDA reports)
INCISIONAL DRAINAGE ( 23 FDA reports)
INGROWING NAIL ( 23 FDA reports)
LEUKOENCEPHALOPATHY ( 23 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 23 FDA reports)
MACULAR OEDEMA ( 23 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 23 FDA reports)
MULTIPLE SCLEROSIS ( 23 FDA reports)
MUSCLE RIGIDITY ( 23 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 22 FDA reports)
AMYLOIDOSIS ( 22 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 22 FDA reports)
BREAST CYST ( 22 FDA reports)
BRONCHITIS CHRONIC ( 22 FDA reports)
DERMATITIS CONTACT ( 22 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 22 FDA reports)
ENTEROCOCCAL SEPSIS ( 22 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 22 FDA reports)
EPIDIDYMITIS ( 22 FDA reports)
FEAR OF DEATH ( 22 FDA reports)
HAEMORRHAGIC STROKE ( 22 FDA reports)
IMPULSE-CONTROL DISORDER ( 22 FDA reports)
INJECTION SITE SWELLING ( 22 FDA reports)
LEG AMPUTATION ( 22 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 22 FDA reports)
MONOPARESIS ( 22 FDA reports)
MUSCLE STRAIN ( 22 FDA reports)
MYELOMA RECURRENCE ( 22 FDA reports)
PARAPARESIS ( 22 FDA reports)
PERIORBITAL HAEMATOMA ( 22 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 22 FDA reports)
PRURIGO ( 22 FDA reports)
PSORIATIC ARTHROPATHY ( 22 FDA reports)
RADIATION INJURY ( 22 FDA reports)
THYROID CANCER ( 22 FDA reports)
TONGUE DISCOLOURATION ( 22 FDA reports)
TRANSFUSION ( 22 FDA reports)
VASCULAR PURPURA ( 22 FDA reports)
VENOUS THROMBOSIS LIMB ( 22 FDA reports)
PERONEAL NERVE PALSY ( 21 FDA reports)
POLYP ( 21 FDA reports)
POST PROCEDURAL INFECTION ( 21 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 21 FDA reports)
SKIN SWELLING ( 21 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 21 FDA reports)
SMALL INTESTINE OPERATION ( 21 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 21 FDA reports)
THROMBOSIS IN DEVICE ( 21 FDA reports)
TOOTH IMPACTED ( 21 FDA reports)
ANOSMIA ( 21 FDA reports)
AORTIC DISORDER ( 21 FDA reports)
APHTHOUS STOMATITIS ( 21 FDA reports)
ARTHROPOD BITE ( 21 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 21 FDA reports)
BENIGN COLONIC NEOPLASM ( 21 FDA reports)
BILE DUCT OBSTRUCTION ( 21 FDA reports)
BLOOD PH DECREASED ( 21 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 21 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 21 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 21 FDA reports)
DRUG ABUSER ( 21 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 21 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 21 FDA reports)
EXANTHEM ( 21 FDA reports)
FACIAL BONES FRACTURE ( 21 FDA reports)
FUNGAEMIA ( 21 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 21 FDA reports)
HEART INJURY ( 21 FDA reports)
HYPOVENTILATION ( 21 FDA reports)
IMMUNOGLOBULINS DECREASED ( 21 FDA reports)
INITIAL INSOMNIA ( 21 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 21 FDA reports)
LIPOMA ( 21 FDA reports)
NECROTISING FASCIITIS ( 21 FDA reports)
NERVE COMPRESSION ( 21 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 21 FDA reports)
ORAL MUCOSA EROSION ( 21 FDA reports)
AMYLASE INCREASED ( 20 FDA reports)
AORTIC DILATATION ( 20 FDA reports)
AORTIC VALVE DISEASE ( 20 FDA reports)
BLOOD PH INCREASED ( 20 FDA reports)
BRONCHIAL OBSTRUCTION ( 20 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 20 FDA reports)
DYSPNOEA AT REST ( 20 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 20 FDA reports)
EYE DISCHARGE ( 20 FDA reports)
FELTY'S SYNDROME ( 20 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 20 FDA reports)
HEART RATE ABNORMAL ( 20 FDA reports)
HEPATIC FIBROSIS ( 20 FDA reports)
HYPERVENTILATION ( 20 FDA reports)
HYPOPERFUSION ( 20 FDA reports)
INCISIONAL HERNIA ( 20 FDA reports)
KERATITIS HERPETIC ( 20 FDA reports)
LOCALISED OEDEMA ( 20 FDA reports)
MACROCYTOSIS ( 20 FDA reports)
MALLORY-WEISS SYNDROME ( 20 FDA reports)
MIOSIS ( 20 FDA reports)
NEUROGENIC BLADDER ( 20 FDA reports)
OESOPHAGEAL STENOSIS ( 20 FDA reports)
OPPORTUNISTIC INFECTION ( 20 FDA reports)
OTITIS MEDIA ( 20 FDA reports)
PANCREATIC DISORDER ( 20 FDA reports)
PEMPHIGOID ( 20 FDA reports)
PERITONEAL HAEMORRHAGE ( 20 FDA reports)
POOR VENOUS ACCESS ( 20 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 20 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 20 FDA reports)
RHINITIS ( 20 FDA reports)
SCRATCH ( 20 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 20 FDA reports)
SKIN HYPOPIGMENTATION ( 20 FDA reports)
SPINAL FUSION SURGERY ( 20 FDA reports)
SPINAL OPERATION ( 20 FDA reports)
SYSTEMIC CANDIDA ( 20 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 20 FDA reports)
TRIGEMINAL NEURALGIA ( 20 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 20 FDA reports)
VENA CAVA THROMBOSIS ( 20 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
PAPILLOEDEMA ( 19 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 19 FDA reports)
PORTAL HYPERTENSION ( 19 FDA reports)
RETINAL VEIN OCCLUSION ( 19 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 19 FDA reports)
SCROTAL SWELLING ( 19 FDA reports)
SHOULDER PAIN ( 19 FDA reports)
STENOTROPHOMONAS INFECTION ( 19 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 19 FDA reports)
TOE AMPUTATION ( 19 FDA reports)
TRANSPLANT REJECTION ( 19 FDA reports)
VASCULAR GRAFT ( 19 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 19 FDA reports)
WRONG DRUG ADMINISTERED ( 19 FDA reports)
ABDOMINAL HERNIA ( 19 FDA reports)
ACCIDENT ( 19 FDA reports)
ACINETOBACTER INFECTION ( 19 FDA reports)
ACNE ( 19 FDA reports)
ACTINOMYCOSIS ( 19 FDA reports)
AFFECTIVE DISORDER ( 19 FDA reports)
ALCOHOLISM ( 19 FDA reports)
ALVEOLITIS ( 19 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 19 FDA reports)
AORTIC ANEURYSM RUPTURE ( 19 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 19 FDA reports)
BONE NEOPLASM ( 19 FDA reports)
CAESAREAN SECTION ( 19 FDA reports)
CARDIOTOXICITY ( 19 FDA reports)
CONDUCTION DISORDER ( 19 FDA reports)
COR PULMONALE CHRONIC ( 19 FDA reports)
CULTURE WOUND POSITIVE ( 19 FDA reports)
DIABETIC FOOT ( 19 FDA reports)
DUODENAL ULCER PERFORATION ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
FASCIITIS ( 19 FDA reports)
HYPERAESTHESIA ( 19 FDA reports)
HYPERAMYLASAEMIA ( 19 FDA reports)
HYPERREFLEXIA ( 19 FDA reports)
HYPOCHLORAEMIA ( 19 FDA reports)
HYPOCOAGULABLE STATE ( 19 FDA reports)
INTERVERTEBRAL DISCITIS ( 19 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 19 FDA reports)
LABILE BLOOD PRESSURE ( 19 FDA reports)
LARYNGITIS ( 19 FDA reports)
LIMB OPERATION ( 19 FDA reports)
MALABSORPTION ( 19 FDA reports)
MANTLE CELL LYMPHOMA ( 19 FDA reports)
MONOCLONAL GAMMOPATHY ( 19 FDA reports)
MYELOFIBROSIS ( 19 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 19 FDA reports)
PANCREATITIS CHRONIC ( 19 FDA reports)
PANCREATITIS NECROTISING ( 19 FDA reports)
BIPOLAR DISORDER ( 18 FDA reports)
BLOOD MAGNESIUM INCREASED ( 18 FDA reports)
BONE NEOPLASM MALIGNANT ( 18 FDA reports)
COMPARTMENT SYNDROME ( 18 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 18 FDA reports)
DRUG RESISTANCE ( 18 FDA reports)
DYSAESTHESIA ( 18 FDA reports)
DYSPHASIA ( 18 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 18 FDA reports)
FAMILY STRESS ( 18 FDA reports)
GASTROINTESTINAL INFECTION ( 18 FDA reports)
GLOMERULOSCLEROSIS ( 18 FDA reports)
HAEMORRHAGE URINARY TRACT ( 18 FDA reports)
HEPATITIS C ( 18 FDA reports)
HEPATOJUGULAR REFLUX ( 18 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 18 FDA reports)
HYPERCREATININAEMIA ( 18 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 18 FDA reports)
HYPERTONIA ( 18 FDA reports)
IMPULSIVE BEHAVIOUR ( 18 FDA reports)
LARYNGITIS VIRAL ( 18 FDA reports)
LUNG HYPERINFLATION ( 18 FDA reports)
LYMPHOCYTOSIS ( 18 FDA reports)
MACULOPATHY ( 18 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 18 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 18 FDA reports)
NASAL ULCER ( 18 FDA reports)
NOCTURNAL DYSPNOEA ( 18 FDA reports)
OPEN ANGLE GLAUCOMA ( 18 FDA reports)
PEAU D'ORANGE ( 18 FDA reports)
PELVIC PAIN ( 18 FDA reports)
PLASMACYTOSIS ( 18 FDA reports)
PRESCRIBED OVERDOSE ( 18 FDA reports)
PROCEDURAL PAIN ( 18 FDA reports)
RADICULITIS LUMBOSACRAL ( 18 FDA reports)
RECTAL CANCER ( 18 FDA reports)
SCOTOMA ( 18 FDA reports)
SENSATION OF HEAVINESS ( 18 FDA reports)
SPLENIC INFARCTION ( 18 FDA reports)
STRESS FRACTURE ( 18 FDA reports)
STRIDOR ( 18 FDA reports)
TONSILLITIS ( 18 FDA reports)
TRANSFUSION REACTION ( 18 FDA reports)
VARICES OESOPHAGEAL ( 18 FDA reports)
PIGMENTATION DISORDER ( 17 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 17 FDA reports)
POOR PERIPHERAL CIRCULATION ( 17 FDA reports)
POST HERPETIC NEURALGIA ( 17 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 17 FDA reports)
RADIAL NERVE PALSY ( 17 FDA reports)
RAYNAUD'S PHENOMENON ( 17 FDA reports)
RECURRENT CANCER ( 17 FDA reports)
RENAL TUBULAR ACIDOSIS ( 17 FDA reports)
SKIN ATROPHY ( 17 FDA reports)
SPINAL HAEMANGIOMA ( 17 FDA reports)
STASIS DERMATITIS ( 17 FDA reports)
SUBDURAL HAEMORRHAGE ( 17 FDA reports)
THROMBOCYTHAEMIA ( 17 FDA reports)
TONGUE DISORDER ( 17 FDA reports)
UNDERDOSE ( 17 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 17 FDA reports)
URETHRAL STENOSIS ( 17 FDA reports)
URINARY TRACT DISORDER ( 17 FDA reports)
VOLVULUS ( 17 FDA reports)
WOUND HAEMORRHAGE ( 17 FDA reports)
WRIST FRACTURE ( 17 FDA reports)
ABNORMAL FAECES ( 17 FDA reports)
ADRENAL MASS ( 17 FDA reports)
ANGIOPLASTY ( 17 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 17 FDA reports)
BILE DUCT CANCER ( 17 FDA reports)
BILE DUCT STONE ( 17 FDA reports)
BIOPSY BONE MARROW ( 17 FDA reports)
BK VIRUS INFECTION ( 17 FDA reports)
BLOOD BICARBONATE INCREASED ( 17 FDA reports)
BREAKTHROUGH PAIN ( 17 FDA reports)
BREAST CANCER FEMALE ( 17 FDA reports)
BRONCHIAL DISORDER ( 17 FDA reports)
BRONCHITIS ACUTE ( 17 FDA reports)
CARBUNCLE ( 17 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 17 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 17 FDA reports)
CEREBELLAR INFARCTION ( 17 FDA reports)
CHOLECYSTITIS INFECTIVE ( 17 FDA reports)
CORONARY ANGIOPLASTY ( 17 FDA reports)
EAR DISORDER ( 17 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 17 FDA reports)
ENCEPHALITIS HERPES ( 17 FDA reports)
ENCEPHALOMALACIA ( 17 FDA reports)
EPISCLERITIS ( 17 FDA reports)
EXTREMITY CONTRACTURE ( 17 FDA reports)
FORMICATION ( 17 FDA reports)
GASTROINTESTINAL PERFORATION ( 17 FDA reports)
HAEMATOCRIT INCREASED ( 17 FDA reports)
HAEMATOSPERMIA ( 17 FDA reports)
HEART VALVE INCOMPETENCE ( 17 FDA reports)
HYPERCOAGULATION ( 17 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 17 FDA reports)
MACULAR HOLE ( 17 FDA reports)
MALIGNANT HYPERTENSION ( 17 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 17 FDA reports)
MITRAL VALVE CALCIFICATION ( 17 FDA reports)
MONOCYTE COUNT INCREASED ( 17 FDA reports)
ORGAN FAILURE ( 17 FDA reports)
ABSCESS INTESTINAL ( 16 FDA reports)
ACROCHORDON ( 16 FDA reports)
ADENOCARCINOMA ( 16 FDA reports)
ALVEOLITIS ALLERGIC ( 16 FDA reports)
APPETITE DISORDER ( 16 FDA reports)
APPLICATION SITE ERYTHEMA ( 16 FDA reports)
ASTHENOPIA ( 16 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 16 FDA reports)
BLADDER MASS ( 16 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 16 FDA reports)
BRAIN NEOPLASM ( 16 FDA reports)
CARDIAC FLUTTER ( 16 FDA reports)
CATHETER SEPSIS ( 16 FDA reports)
CEREBELLAR HAEMORRHAGE ( 16 FDA reports)
CHOKING ( 16 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 16 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
COLONOSCOPY ABNORMAL ( 16 FDA reports)
CORYNEBACTERIUM INFECTION ( 16 FDA reports)
CYTOKINE RELEASE SYNDROME ( 16 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 16 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 16 FDA reports)
DIABETIC COMA ( 16 FDA reports)
DRUG ABUSE ( 16 FDA reports)
ENANTHEMA ( 16 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 16 FDA reports)
FACE INJURY ( 16 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 16 FDA reports)
FINGER DEFORMITY ( 16 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 16 FDA reports)
GOUTY TOPHUS ( 16 FDA reports)
HAEMOGLOBIN INCREASED ( 16 FDA reports)
HELICOBACTER GASTRITIS ( 16 FDA reports)
HEPATIC ENZYME ABNORMAL ( 16 FDA reports)
HYDROCELE ( 16 FDA reports)
HYPERCAPNIA ( 16 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 16 FDA reports)
INCOHERENT ( 16 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
INJECTION SITE RASH ( 16 FDA reports)
LACTOSE INTOLERANCE ( 16 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 16 FDA reports)
LIPODYSTROPHY ACQUIRED ( 16 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 16 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 16 FDA reports)
MONONEURITIS ( 16 FDA reports)
MUSCLE CRAMP ( 16 FDA reports)
NASAL DISCOMFORT ( 16 FDA reports)
NASAL DRYNESS ( 16 FDA reports)
NYSTAGMUS ( 16 FDA reports)
OXYGEN SUPPLEMENTATION ( 16 FDA reports)
PAROTID GLAND ENLARGEMENT ( 16 FDA reports)
PLEURAL DISORDER ( 16 FDA reports)
PREMATURE BABY ( 16 FDA reports)
RECTAL POLYP ( 16 FDA reports)
RESUSCITATION ( 16 FDA reports)
RETINAL ARTERY OCCLUSION ( 16 FDA reports)
RETROPERITONEAL HAEMATOMA ( 16 FDA reports)
SCROTAL OEDEMA ( 16 FDA reports)
SEASONAL ALLERGY ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 16 FDA reports)
SPLENIC CYST ( 16 FDA reports)
SPLENIC GRANULOMA ( 16 FDA reports)
TONGUE BITING ( 16 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 16 FDA reports)
TRISMUS ( 16 FDA reports)
UTERINE ENLARGEMENT ( 16 FDA reports)
VASODILATATION ( 16 FDA reports)
WOUND COMPLICATION ( 16 FDA reports)
YELLOW SKIN ( 16 FDA reports)
PAROSMIA ( 15 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 15 FDA reports)
PERSONALITY DISORDER ( 15 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 15 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 15 FDA reports)
PROCEDURAL HYPOTENSION ( 15 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 15 FDA reports)
PSEUDOMONAL SEPSIS ( 15 FDA reports)
RADIUS FRACTURE ( 15 FDA reports)
RESPIRATORY TRACT CONGESTION ( 15 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 15 FDA reports)
SINUS HEADACHE ( 15 FDA reports)
SKIN CANDIDA ( 15 FDA reports)
SOFT TISSUE MASS ( 15 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 15 FDA reports)
STUPOR ( 15 FDA reports)
TEMPORAL ARTERITIS ( 15 FDA reports)
TENDON PAIN ( 15 FDA reports)
TONGUE ULCERATION ( 15 FDA reports)
TOXIC SHOCK SYNDROME ( 15 FDA reports)
TREATMENT FAILURE ( 15 FDA reports)
UMBILICAL HERNIA REPAIR ( 15 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 15 FDA reports)
ACTINIC ELASTOSIS ( 15 FDA reports)
ACUTE LEUKAEMIA ( 15 FDA reports)
ALCOHOLIC LIVER DISEASE ( 15 FDA reports)
AMMONIA INCREASED ( 15 FDA reports)
APPARENT DEATH ( 15 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 15 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 15 FDA reports)
ATHEROSCLEROSIS ( 15 FDA reports)
BICYTOPENIA ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLOOD BLISTER ( 15 FDA reports)
BONE MARROW DISORDER ( 15 FDA reports)
CARDIAC OPERATION ( 15 FDA reports)
CATHETER PLACEMENT ( 15 FDA reports)
CATHETER SITE INFECTION ( 15 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 15 FDA reports)
CEREBRAL DISORDER ( 15 FDA reports)
COMA HEPATIC ( 15 FDA reports)
COMMUNICATION DISORDER ( 15 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 15 FDA reports)
CSF PROTEIN INCREASED ( 15 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 15 FDA reports)
DYSLALIA ( 15 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 15 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 15 FDA reports)
EYE INFECTION ( 15 FDA reports)
FOLATE DEFICIENCY ( 15 FDA reports)
GINGIVAL ERYTHEMA ( 15 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 15 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 15 FDA reports)
HYPERMETROPIA ( 15 FDA reports)
HYPOPROTHROMBINAEMIA ( 15 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 15 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 15 FDA reports)
IRITIS ( 15 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 15 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 15 FDA reports)
MENINGIOMA ( 15 FDA reports)
MICROANGIOPATHY ( 15 FDA reports)
MITRAL VALVE DISEASE ( 15 FDA reports)
MOOD SWINGS ( 15 FDA reports)
MYELITIS TRANSVERSE ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER ( 15 FDA reports)
ABSCESS NECK ( 14 FDA reports)
ADENOMA BENIGN ( 14 FDA reports)
ALCOHOL POISONING ( 14 FDA reports)
BACILLUS INFECTION ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLEEDING TIME PROLONGED ( 14 FDA reports)
BLOOD CREATININE ABNORMAL ( 14 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 14 FDA reports)
BRONCHIAL CARCINOMA ( 14 FDA reports)
CALCINOSIS ( 14 FDA reports)
CARDIAC HYPERTROPHY ( 14 FDA reports)
CERVICAL SPINAL STENOSIS ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 14 FDA reports)
CUSHINGOID ( 14 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 14 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 14 FDA reports)
DISEASE COMPLICATION ( 14 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 14 FDA reports)
DRY THROAT ( 14 FDA reports)
ECHOCARDIOGRAM ( 14 FDA reports)
ELECTROLYTE DEPLETION ( 14 FDA reports)
ENTEROBACTER SEPSIS ( 14 FDA reports)
EROSIVE DUODENITIS ( 14 FDA reports)
FACET JOINT SYNDROME ( 14 FDA reports)
GASTROINTESTINAL CARCINOMA ( 14 FDA reports)
GASTROINTESTINAL PAIN ( 14 FDA reports)
HEAD DISCOMFORT ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 14 FDA reports)
HYPERPHAGIA ( 14 FDA reports)
ILLUSION ( 14 FDA reports)
INADEQUATE ANALGESIA ( 14 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 14 FDA reports)
INCREASED APPETITE ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 14 FDA reports)
INTESTINAL INFARCTION ( 14 FDA reports)
KERATOACANTHOMA ( 14 FDA reports)
LIGAMENT RUPTURE ( 14 FDA reports)
LIGHT CHAIN DISEASE ( 14 FDA reports)
LIP OEDEMA ( 14 FDA reports)
LIVEDO RETICULARIS ( 14 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 14 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 14 FDA reports)
MULTI-ORGAN DISORDER ( 14 FDA reports)
MYASTHENIA GRAVIS ( 14 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 14 FDA reports)
NEUROLOGICAL SYMPTOM ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 14 FDA reports)
OESOPHAGEAL SPASM ( 14 FDA reports)
ORGANISING PNEUMONIA ( 14 FDA reports)
PARTNER STRESS ( 14 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 14 FDA reports)
PERIRECTAL ABSCESS ( 14 FDA reports)
PNEUMONIA KLEBSIELLA ( 14 FDA reports)
PO2 INCREASED ( 14 FDA reports)
POLYTRAUMATISM ( 14 FDA reports)
PULMONARY MYCOSIS ( 14 FDA reports)
PUPIL FIXED ( 14 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 14 FDA reports)
RENAL NEOPLASM ( 14 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 14 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 14 FDA reports)
RHONCHI ( 14 FDA reports)
SALIVARY HYPERSECRETION ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SCAN BONE MARROW ABNORMAL ( 14 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 14 FDA reports)
SINUS POLYP ( 14 FDA reports)
SOFT TISSUE DISORDER ( 14 FDA reports)
SPLENIC HAEMORRHAGE ( 14 FDA reports)
SUPERINFECTION ( 14 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 14 FDA reports)
TOOTH DISCOLOURATION ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
PATELLA FRACTURE ( 13 FDA reports)
PELVIC MASS ( 13 FDA reports)
PERICARDIAL HAEMORRHAGE ( 13 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 13 FDA reports)
PHOTOPSIA ( 13 FDA reports)
PINGUECULA ( 13 FDA reports)
PULMONARY SEPSIS ( 13 FDA reports)
PULMONARY TUBERCULOSIS ( 13 FDA reports)
RECTAL ABSCESS ( 13 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 13 FDA reports)
RENAL ANEURYSM ( 13 FDA reports)
REPERFUSION ARRHYTHMIA ( 13 FDA reports)
RETINOPATHY ( 13 FDA reports)
RHINALGIA ( 13 FDA reports)
SCHIZOPHRENIA ( 13 FDA reports)
SECRETION DISCHARGE ( 13 FDA reports)
SKIN DESQUAMATION ( 13 FDA reports)
SKIN NODULE ( 13 FDA reports)
SOFT TISSUE INJURY ( 13 FDA reports)
SOMNAMBULISM ( 13 FDA reports)
SPONDYLITIS ( 13 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 13 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 13 FDA reports)
TEMPERATURE INTOLERANCE ( 13 FDA reports)
THYROID MASS ( 13 FDA reports)
TUMOUR NECROSIS ( 13 FDA reports)
URETHRAL OBSTRUCTION ( 13 FDA reports)
URGE INCONTINENCE ( 13 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 13 FDA reports)
ANAL FISTULA ( 13 FDA reports)
ASPIRATION JOINT ( 13 FDA reports)
AUTOIMMUNE HEPATITIS ( 13 FDA reports)
BACTERIA STOOL IDENTIFIED ( 13 FDA reports)
BACTERIAL TEST POSITIVE ( 13 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 13 FDA reports)
BLOOD ALBUMIN INCREASED ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 13 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 13 FDA reports)
BLOOD URIC ACID DECREASED ( 13 FDA reports)
BONE LESION EXCISION ( 13 FDA reports)
BONE MARROW TOXICITY ( 13 FDA reports)
BRAIN STEM INFARCTION ( 13 FDA reports)
CALCIUM METABOLISM DISORDER ( 13 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 13 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 13 FDA reports)
CERVICOBRACHIAL SYNDROME ( 13 FDA reports)
CHEYNE-STOKES RESPIRATION ( 13 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 13 FDA reports)
CLONUS ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 13 FDA reports)
DEAFNESS UNILATERAL ( 13 FDA reports)
DISSEMINATED TUBERCULOSIS ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
EARLY SATIETY ( 13 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 13 FDA reports)
EMPYEMA ( 13 FDA reports)
GAZE PALSY ( 13 FDA reports)
H1N1 INFLUENZA ( 13 FDA reports)
HAEMATOTOXICITY ( 13 FDA reports)
HAND DEFORMITY ( 13 FDA reports)
HELICOBACTER INFECTION ( 13 FDA reports)
HERNIA REPAIR ( 13 FDA reports)
HIP SURGERY ( 13 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 13 FDA reports)
HUNGER ( 13 FDA reports)
HYPERLACTACIDAEMIA ( 13 FDA reports)
HYPERVOLAEMIA ( 13 FDA reports)
IMPAIRED DRIVING ABILITY ( 13 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 13 FDA reports)
INJECTION SITE IRRITATION ( 13 FDA reports)
LEUKAEMIA PLASMACYTIC ( 13 FDA reports)
LEUKAEMIA RECURRENT ( 13 FDA reports)
MAMMOGRAM ( 13 FDA reports)
MENINGITIS BACTERIAL ( 13 FDA reports)
NASAL POLYPS ( 13 FDA reports)
NEPHRITIS ( 13 FDA reports)
ONYCHALGIA ( 13 FDA reports)
OPTIC ATROPHY ( 13 FDA reports)
ABDOMINAL SEPSIS ( 12 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 12 FDA reports)
ACUTE SINUSITIS ( 12 FDA reports)
ADRENAL DISORDER ( 12 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 12 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 12 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 12 FDA reports)
AORTIC ATHEROSCLEROSIS ( 12 FDA reports)
ASEPTIC NECROSIS BONE ( 12 FDA reports)
ATRIAL SEPTAL DEFECT ( 12 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 12 FDA reports)
BLOOD IRON INCREASED ( 12 FDA reports)
BLOOD LACTIC ACID INCREASED ( 12 FDA reports)
BONE FORMATION INCREASED ( 12 FDA reports)
BONE LOSS ( 12 FDA reports)
BONE SCAN ABNORMAL ( 12 FDA reports)
BRAIN COMPRESSION ( 12 FDA reports)
BREAST LUMP REMOVAL ( 12 FDA reports)
CARBON DIOXIDE DECREASED ( 12 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 12 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 12 FDA reports)
CATHETER SITE PAIN ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
CHOKING SENSATION ( 12 FDA reports)
CHONDROCALCINOSIS ( 12 FDA reports)
CONCUSSION ( 12 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 12 FDA reports)
DEPRESSION SUICIDAL ( 12 FDA reports)
DERMATITIS ACNEIFORM ( 12 FDA reports)
DEVICE OCCLUSION ( 12 FDA reports)
DIABETIC COMPLICATION ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
ECZEMA EYELIDS ( 12 FDA reports)
EFFUSION ( 12 FDA reports)
EOSINOPHILIC PNEUMONIA ( 12 FDA reports)
FOOD POISONING ( 12 FDA reports)
GASTROENTERITIS RADIATION ( 12 FDA reports)
HOSTILITY ( 12 FDA reports)
INCISION SITE COMPLICATION ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 12 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 12 FDA reports)
IRON OVERLOAD ( 12 FDA reports)
KIDNEY ENLARGEMENT ( 12 FDA reports)
KNEE OPERATION ( 12 FDA reports)
LIP DRY ( 12 FDA reports)
LIPOMATOSIS ( 12 FDA reports)
LOWER EXTREMITY MASS ( 12 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 12 FDA reports)
MENIERE'S DISEASE ( 12 FDA reports)
METAPLASIA ( 12 FDA reports)
METASTASES TO PERITONEUM ( 12 FDA reports)
MUSCLE NECROSIS ( 12 FDA reports)
MUSCLE SPASTICITY ( 12 FDA reports)
MUSCULAR DYSTROPHY ( 12 FDA reports)
MYOCARDIAL FIBROSIS ( 12 FDA reports)
NEURODERMATITIS ( 12 FDA reports)
NEUROPATHIC PAIN ( 12 FDA reports)
OCCULT BLOOD ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 12 FDA reports)
OROPHARYNGEAL BLISTERING ( 12 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 12 FDA reports)
ORTHOPEDIC PROCEDURE ( 12 FDA reports)
OTORRHOEA ( 12 FDA reports)
PARESIS ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
PELVIC FLUID COLLECTION ( 12 FDA reports)
PERIPHERAL EMBOLISM ( 12 FDA reports)
PERITONEAL ADHESIONS ( 12 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 12 FDA reports)
PLATELET COUNT ABNORMAL ( 12 FDA reports)
POLYCYTHAEMIA ( 12 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 12 FDA reports)
POTENTIATING DRUG INTERACTION ( 12 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 12 FDA reports)
PROSTATIC OBSTRUCTION ( 12 FDA reports)
PROTEIN URINE ( 12 FDA reports)
PYODERMA GANGRENOSUM ( 12 FDA reports)
PYOGENIC GRANULOMA ( 12 FDA reports)
PYURIA ( 12 FDA reports)
QUADRIPARESIS ( 12 FDA reports)
RENAL HYPERTROPHY ( 12 FDA reports)
RIGHT ATRIAL DILATATION ( 12 FDA reports)
SCLERAL OPERATION ( 12 FDA reports)
SCREAMING ( 12 FDA reports)
SEPTIC EMBOLUS ( 12 FDA reports)
SKIN OEDEMA ( 12 FDA reports)
SKULL FRACTURE ( 12 FDA reports)
SLUGGISHNESS ( 12 FDA reports)
SNEEZING ( 12 FDA reports)
SPONDYLOARTHROPATHY ( 12 FDA reports)
STEAL SYNDROME ( 12 FDA reports)
SYNOVITIS ( 12 FDA reports)
TENSION ( 12 FDA reports)
THERMAL BURN ( 12 FDA reports)
URATE NEPHROPATHY ( 12 FDA reports)
URETERAL STENT INSERTION ( 12 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 12 FDA reports)
VASCULITIC RASH ( 12 FDA reports)
XEROSIS ( 12 FDA reports)
PARAPLEGIA ( 11 FDA reports)
PENIS DISORDER ( 11 FDA reports)
PERIOSTITIS ( 11 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 11 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 11 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 11 FDA reports)
POISONING ( 11 FDA reports)
POLYMYOSITIS ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PROSTATE CANCER RECURRENT ( 11 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 11 FDA reports)
PSYCHOMOTOR RETARDATION ( 11 FDA reports)
RENAL COLIC ( 11 FDA reports)
SELF-MEDICATION ( 11 FDA reports)
SENSATION OF PRESSURE ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SICCA SYNDROME ( 11 FDA reports)
SKELETAL INJURY ( 11 FDA reports)
SKIN NEOPLASM EXCISION ( 11 FDA reports)
SKIN TURGOR DECREASED ( 11 FDA reports)
SPLEEN DISORDER ( 11 FDA reports)
SPLENECTOMY ( 11 FDA reports)
STENT OCCLUSION ( 11 FDA reports)
TERMINAL STATE ( 11 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 11 FDA reports)
THYROID NEOPLASM ( 11 FDA reports)
TIBIA FRACTURE ( 11 FDA reports)
TONGUE OEDEMA ( 11 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 11 FDA reports)
VITAMIN D DECREASED ( 11 FDA reports)
VITH NERVE PARALYSIS ( 11 FDA reports)
WHEELCHAIR USER ( 11 FDA reports)
ABDOMINAL INFECTION ( 11 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 11 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 11 FDA reports)
ALCOHOL ABUSE ( 11 FDA reports)
ALKALOSIS ( 11 FDA reports)
ANAPHYLACTOID REACTION ( 11 FDA reports)
ANEURYSM REPAIR ( 11 FDA reports)
AREFLEXIA ( 11 FDA reports)
ARTERIAL HAEMORRHAGE ( 11 FDA reports)
ASPIRATION PLEURAL CAVITY ( 11 FDA reports)
ASTERIXIS ( 11 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 11 FDA reports)
BONE MARROW OEDEMA ( 11 FDA reports)
BRAIN MIDLINE SHIFT ( 11 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BREAST OEDEMA ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 11 FDA reports)
CAROTID ARTERY OCCLUSION ( 11 FDA reports)
CEREBRAL THROMBOSIS ( 11 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 11 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 11 FDA reports)
COELIAC DISEASE ( 11 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 11 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 11 FDA reports)
DRESSLER'S SYNDROME ( 11 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 11 FDA reports)
FEELING OF DESPAIR ( 11 FDA reports)
FEMORAL ARTERY OCCLUSION ( 11 FDA reports)
FOOD INTERACTION ( 11 FDA reports)
GLUCOSE URINE PRESENT ( 11 FDA reports)
HEAD BANGING ( 11 FDA reports)
HEART SOUNDS ABNORMAL ( 11 FDA reports)
HOMICIDAL IDEATION ( 11 FDA reports)
HYPERAMMONAEMIA ( 11 FDA reports)
HYPERMETABOLISM ( 11 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 11 FDA reports)
INJECTION SITE BRUISING ( 11 FDA reports)
INJECTION SITE INFECTION ( 11 FDA reports)
INJECTION SITE NODULE ( 11 FDA reports)
INTENTIONAL SELF-INJURY ( 11 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 11 FDA reports)
KIDNEY FIBROSIS ( 11 FDA reports)
LEUKOCYTURIA ( 11 FDA reports)
LOOSE STOOLS ( 11 FDA reports)
LUNG ADENOCARCINOMA ( 11 FDA reports)
MICROALBUMINURIA ( 11 FDA reports)
MITRAL VALVE STENOSIS ( 11 FDA reports)
MONOPLEGIA ( 11 FDA reports)
NECK MASS ( 11 FDA reports)
NEOPLASM RECURRENCE ( 11 FDA reports)
NEOPLASM SKIN ( 11 FDA reports)
NODAL RHYTHM ( 11 FDA reports)
ONYCHOLYSIS ( 11 FDA reports)
ORAL FUNGAL INFECTION ( 11 FDA reports)
PANCREATIC ENZYMES INCREASED ( 11 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 10 FDA reports)
ACUTE PSYCHOSIS ( 10 FDA reports)
ADENOVIRUS INFECTION ( 10 FDA reports)
APPLICATION SITE IRRITATION ( 10 FDA reports)
APPLICATION SITE PRURITUS ( 10 FDA reports)
APPLICATION SITE VESICLES ( 10 FDA reports)
APRAXIA ( 10 FDA reports)
ARTERIAL DISORDER ( 10 FDA reports)
ARTHRITIS INFECTIVE ( 10 FDA reports)
BACTERIA URINE IDENTIFIED ( 10 FDA reports)
BACTERIAL DISEASE CARRIER ( 10 FDA reports)
BASOPHIL COUNT DECREASED ( 10 FDA reports)
BLOOD GASES ABNORMAL ( 10 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 10 FDA reports)
BLOOD UREA ABNORMAL ( 10 FDA reports)
BRAIN CONTUSION ( 10 FDA reports)
CELL DEATH ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CERVIX CARCINOMA ( 10 FDA reports)
COLON CANCER METASTATIC ( 10 FDA reports)
COMPLEX PARTIAL SEIZURES ( 10 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 10 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 10 FDA reports)
DENTAL CARE ( 10 FDA reports)
DERMATITIS PSORIASIFORM ( 10 FDA reports)
DISSOCIATION ( 10 FDA reports)
DIZZINESS EXERTIONAL ( 10 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
FUNGAL DNA TEST POSITIVE ( 10 FDA reports)
FUSOBACTERIUM INFECTION ( 10 FDA reports)
GAMMOPATHY ( 10 FDA reports)
GASTRIC PH DECREASED ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 10 FDA reports)
GASTROINTESTINAL TOXICITY ( 10 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 10 FDA reports)
GENERAL SYMPTOM ( 10 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 10 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 10 FDA reports)
HAEMATOMA INFECTION ( 10 FDA reports)
HAEMOGLOBINURIA ( 10 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 10 FDA reports)
HERPES ZOSTER DISSEMINATED ( 10 FDA reports)
HYPERAEMIA ( 10 FDA reports)
IATROGENIC INJURY ( 10 FDA reports)
ILEAL ULCER ( 10 FDA reports)
INFECTED SKIN ULCER ( 10 FDA reports)
INFUSION SITE PAIN ( 10 FDA reports)
INJECTION SITE URTICARIA ( 10 FDA reports)
INJECTION SITE WARMTH ( 10 FDA reports)
INTESTINAL DILATATION ( 10 FDA reports)
ISCHAEMIC HEPATITIS ( 10 FDA reports)
JOINT INSTABILITY ( 10 FDA reports)
KLEBSIELLA BACTERAEMIA ( 10 FDA reports)
LAPAROTOMY ( 10 FDA reports)
LARYNGEAL OEDEMA ( 10 FDA reports)
LICHEN PLANUS ( 10 FDA reports)
LOCALISED OSTEOARTHRITIS ( 10 FDA reports)
MENINGITIS VIRAL ( 10 FDA reports)
MENORRHAGIA ( 10 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 10 FDA reports)
MICROPHTHALMOS ( 10 FDA reports)
MULTIPLE FRACTURES ( 10 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 10 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 10 FDA reports)
MYELOPATHY ( 10 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 10 FDA reports)
NOCARDIOSIS ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 10 FDA reports)
OBSTRUCTION ( 10 FDA reports)
OOPHORECTOMY ( 10 FDA reports)
ORAL SOFT TISSUE DISORDER ( 10 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 10 FDA reports)
PCO2 INCREASED ( 10 FDA reports)
PELVIC ABSCESS ( 10 FDA reports)
PERIDIVERTICULAR ABSCESS ( 10 FDA reports)
PHLEBOLITH ( 10 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 10 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 10 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 10 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 10 FDA reports)
RENAL HAEMORRHAGE ( 10 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 10 FDA reports)
SENSITIVITY OF TEETH ( 10 FDA reports)
SEROMA ( 10 FDA reports)
SHOULDER OPERATION ( 10 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 10 FDA reports)
SKIN INFLAMMATION ( 10 FDA reports)
SKIN MASS ( 10 FDA reports)
STAG HORN CALCULUS ( 10 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
TESTICULAR SWELLING ( 10 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 10 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 10 FDA reports)
URINE COLOUR ABNORMAL ( 10 FDA reports)
VASCULAR INSUFFICIENCY ( 10 FDA reports)
VASCULITIS NECROTISING ( 10 FDA reports)
VEIN DISORDER ( 10 FDA reports)
VERTIGO POSITIONAL ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
WEIGHT FLUCTUATION ( 10 FDA reports)
WOUND DEBRIDEMENT ( 10 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PHLEBITIS SUPERFICIAL ( 9 FDA reports)
PILONIDAL CYST ( 9 FDA reports)
PLANTAR FASCIITIS ( 9 FDA reports)
PNEUMOCONIOSIS ( 9 FDA reports)
PNEUMONIA ESCHERICHIA ( 9 FDA reports)
PORTAL VEIN THROMBOSIS ( 9 FDA reports)
POST LAMINECTOMY SYNDROME ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
POSTPARTUM HAEMORRHAGE ( 9 FDA reports)
PREGNANCY ( 9 FDA reports)
PROCTITIS ( 9 FDA reports)
PROTEUS INFECTION ( 9 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
PULSE ABNORMAL ( 9 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 9 FDA reports)
PUSTULAR PSORIASIS ( 9 FDA reports)
PYELONEPHRITIS ACUTE ( 9 FDA reports)
QUADRIPLEGIA ( 9 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 9 FDA reports)
RENAL EMBOLISM ( 9 FDA reports)
SINUS ARREST ( 9 FDA reports)
SKIN CHAPPED ( 9 FDA reports)
SKIN GRAFT ( 9 FDA reports)
SMALL INTESTINAL PERFORATION ( 9 FDA reports)
SPINAL CORD INJURY THORACIC ( 9 FDA reports)
STARING ( 9 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 9 FDA reports)
STRESS SYMPTOMS ( 9 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 9 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 9 FDA reports)
TEARFULNESS ( 9 FDA reports)
THROAT CANCER ( 9 FDA reports)
TONGUE PARALYSIS ( 9 FDA reports)
TOOTH REPAIR ( 9 FDA reports)
TRAUMATIC BRAIN INJURY ( 9 FDA reports)
TUMOUR INVASION ( 9 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 9 FDA reports)
URAEMIC ENCEPHALOPATHY ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
VOLUME BLOOD DECREASED ( 9 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 9 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 9 FDA reports)
ADHESIOLYSIS ( 9 FDA reports)
AMAUROSIS ( 9 FDA reports)
ANAL ABSCESS ( 9 FDA reports)
APALLIC SYNDROME ( 9 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
AUTOIMMUNE THYROIDITIS ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BACTERIAL TEST ( 9 FDA reports)
BASOPHIL COUNT INCREASED ( 9 FDA reports)
BLADDER DISTENSION ( 9 FDA reports)
BLOOD CALCIUM ABNORMAL ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 9 FDA reports)
BOWEL SOUNDS ABNORMAL ( 9 FDA reports)
BRADYPHRENIA ( 9 FDA reports)
BRAIN DEATH ( 9 FDA reports)
BREAST CANCER METASTATIC ( 9 FDA reports)
CANDIDURIA ( 9 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 9 FDA reports)
CARDIAC DEATH ( 9 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATARACT NUCLEAR ( 9 FDA reports)
CELL MARKER INCREASED ( 9 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 9 FDA reports)
CITROBACTER INFECTION ( 9 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 9 FDA reports)
COAGULATION TEST ABNORMAL ( 9 FDA reports)
CRYPTORCHISM ( 9 FDA reports)
CULTURE STOOL POSITIVE ( 9 FDA reports)
CUTANEOUS VASCULITIS ( 9 FDA reports)
DEAFNESS BILATERAL ( 9 FDA reports)
DENTAL DISCOMFORT ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DIET REFUSAL ( 9 FDA reports)
DIPLEGIA ( 9 FDA reports)
DRUG TOLERANCE ( 9 FDA reports)
DYSMENORRHOEA ( 9 FDA reports)
DYSTONIA ( 9 FDA reports)
EPICONDYLITIS ( 9 FDA reports)
EPIDERMOLYSIS BULLOSA ( 9 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 9 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 9 FDA reports)
EYE ROLLING ( 9 FDA reports)
FACIAL PARESIS ( 9 FDA reports)
FAT EMBOLISM ( 9 FDA reports)
FEELING DRUNK ( 9 FDA reports)
FIBRIN INCREASED ( 9 FDA reports)
FRACTURE NONUNION ( 9 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 9 FDA reports)
FUNGAL SEPSIS ( 9 FDA reports)
FUNGAL SKIN INFECTION ( 9 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 9 FDA reports)
GINGIVAL EROSION ( 9 FDA reports)
GLOSSITIS ( 9 FDA reports)
GUN SHOT WOUND ( 9 FDA reports)
HAEMORRHAGIC DISORDER ( 9 FDA reports)
HAIR GROWTH ABNORMAL ( 9 FDA reports)
HEART DISEASE CONGENITAL ( 9 FDA reports)
HEPATIC ARTERY STENOSIS ( 9 FDA reports)
HEPATIC MASS ( 9 FDA reports)
HEPATITIS A ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HYPERTELORISM OF ORBIT ( 9 FDA reports)
HYPERTROPHY ( 9 FDA reports)
HYPERVISCOSITY SYNDROME ( 9 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 9 FDA reports)
ILEITIS ( 9 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 9 FDA reports)
INCISION SITE HAEMORRHAGE ( 9 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 9 FDA reports)
INTESTINAL RESECTION ( 9 FDA reports)
INTESTINAL ULCER ( 9 FDA reports)
INTRACRANIAL HAEMATOMA ( 9 FDA reports)
JOINT ARTHROPLASTY ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 9 FDA reports)
LIP PAIN ( 9 FDA reports)
LOW TURNOVER OSTEOPATHY ( 9 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 9 FDA reports)
LYMPHADENECTOMY ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MEDIASTINAL MASS ( 9 FDA reports)
MEGACOLON ( 9 FDA reports)
METASTASES TO OVARY ( 9 FDA reports)
METASTASES TO SKIN ( 9 FDA reports)
METRORRHAGIA ( 9 FDA reports)
MICROTIA ( 9 FDA reports)
NASAL CYST ( 9 FDA reports)
NASAL DISORDER ( 9 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 9 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 9 FDA reports)
NEUTROPHIL COUNT ( 9 FDA reports)
NEUTROPHILIA ( 9 FDA reports)
NODULE ON EXTREMITY ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 9 FDA reports)
OBSTRUCTIVE UROPATHY ( 9 FDA reports)
OESOPHAGEAL CARCINOMA ( 9 FDA reports)
OSTEORADIONECROSIS ( 9 FDA reports)
ABDOMINAL HAEMATOMA ( 8 FDA reports)
ABDOMINAL RIGIDITY ( 8 FDA reports)
ABDOMINAL SYMPTOM ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 8 FDA reports)
ABORTION SPONTANEOUS ( 8 FDA reports)
ADENOCARCINOMA PANCREAS ( 8 FDA reports)
ADNEXA UTERI MASS ( 8 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 8 FDA reports)
AMBLYOPIA ( 8 FDA reports)
ANGIOSARCOMA ( 8 FDA reports)
ANION GAP INCREASED ( 8 FDA reports)
ANORECTAL DISCOMFORT ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
APPENDIX DISORDER ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
ARTERIOVENOUS MALFORMATION ( 8 FDA reports)
ARTERITIS ( 8 FDA reports)
ASPERGILLUS TEST POSITIVE ( 8 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 8 FDA reports)
AXILLARY VEIN THROMBOSIS ( 8 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 8 FDA reports)
BIOPSY LIVER ABNORMAL ( 8 FDA reports)
BIOPSY LYMPH GLAND ( 8 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 8 FDA reports)
BLADDER DILATATION ( 8 FDA reports)
BLAST CELLS PRESENT ( 8 FDA reports)
BLOOD AMYLASE DECREASED ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BRADYKINESIA ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
BRAIN STEM SYNDROME ( 8 FDA reports)
BREAST CANCER RECURRENT ( 8 FDA reports)
BRONCHOSCOPY ABNORMAL ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CARDIOVERSION ( 8 FDA reports)
CAROTID ARTERY ANEURYSM ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CEREBELLAR ATAXIA ( 8 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 8 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 8 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 8 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 8 FDA reports)
CLEFT LIP AND PALATE ( 8 FDA reports)
COLITIS COLLAGENOUS ( 8 FDA reports)
COLOBOMA ( 8 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 8 FDA reports)
CONJUNCTIVITIS VIRAL ( 8 FDA reports)
CORONARY ARTERY SURGERY ( 8 FDA reports)
CRYOGLOBULINAEMIA ( 8 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DELIRIUM TREMENS ( 8 FDA reports)
DEPRESSIVE SYMPTOM ( 8 FDA reports)
DERMATITIS ATOPIC ( 8 FDA reports)
DERMATOMYOSITIS ( 8 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 8 FDA reports)
DIARRHOEA INFECTIOUS ( 8 FDA reports)
DRUG-INDUCED LIVER INJURY ( 8 FDA reports)
DYSPHORIA ( 8 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 8 FDA reports)
ENCEPHALITIS VIRAL ( 8 FDA reports)
EPIDERMAL NECROSIS ( 8 FDA reports)
ERYTHEMA OF EYELID ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 8 FDA reports)
FOOT AMPUTATION ( 8 FDA reports)
FRACTURE DELAYED UNION ( 8 FDA reports)
FRACTURED COCCYX ( 8 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 8 FDA reports)
GASTROENTERITIS NOROVIRUS ( 8 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 8 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 8 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 8 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 8 FDA reports)
GLIOBLASTOMA ( 8 FDA reports)
HAEMOGLOBIN ABNORMAL ( 8 FDA reports)
HEPATORENAL FAILURE ( 8 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 8 FDA reports)
HYPEROSMOLAR STATE ( 8 FDA reports)
HYPERPROTEINAEMIA ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
HYPOCAPNIA ( 8 FDA reports)
HYPOCHROMIC ANAEMIA ( 8 FDA reports)
HYPOPARATHYROIDISM ( 8 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 8 FDA reports)
INCISION SITE INFECTION ( 8 FDA reports)
LIP HAEMORRHAGE ( 8 FDA reports)
LIPIDS INCREASED ( 8 FDA reports)
LISTERIOSIS ( 8 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
MASS EXCISION ( 8 FDA reports)
MEAN CELL VOLUME DECREASED ( 8 FDA reports)
MENINGORRHAGIA ( 8 FDA reports)
MICROCYTOSIS ( 8 FDA reports)
MICTURITION DISORDER ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MONOCYTE COUNT DECREASED ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
NECROTISING COLITIS ( 8 FDA reports)
NERVE ROOT COMPRESSION ( 8 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 8 FDA reports)
NONSPECIFIC REACTION ( 8 FDA reports)
OESOPHAGEAL DILATATION ( 8 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PANCREATITIS RELAPSING ( 8 FDA reports)
PANNICULITIS ( 8 FDA reports)
PAPILLOMA ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PARTIAL SEIZURES ( 8 FDA reports)
PERICARDITIS CONSTRICTIVE ( 8 FDA reports)
PHARYNGEAL ERYTHEMA ( 8 FDA reports)
PILOERECTION ( 8 FDA reports)
PLEURAL ADHESION ( 8 FDA reports)
PNEUMONIA LEGIONELLA ( 8 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 8 FDA reports)
PROSTATE INFECTION ( 8 FDA reports)
PROSTATIC DISORDER ( 8 FDA reports)
PROSTATISM ( 8 FDA reports)
PSEUDOLYMPHOMA ( 8 FDA reports)
PSYCHOTIC BEHAVIOUR ( 8 FDA reports)
RECTAL ULCER ( 8 FDA reports)
RENAL INFARCT ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RETICULOCYTE COUNT DECREASED ( 8 FDA reports)
RETICULOCYTE COUNT INCREASED ( 8 FDA reports)
RETINAL TEAR ( 8 FDA reports)
RETINOIC ACID SYNDROME ( 8 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 8 FDA reports)
RICHTER'S SYNDROME ( 8 FDA reports)
SCROTAL IRRITATION ( 8 FDA reports)
SERUM FERRITIN DECREASED ( 8 FDA reports)
SIALOADENITIS ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SKULL FRACTURED BASE ( 8 FDA reports)
SLEEP INERTIA ( 8 FDA reports)
SPINAL CORD COMPRESSION ( 8 FDA reports)
SPINAL DEFORMITY ( 8 FDA reports)
STRESS ULCER ( 8 FDA reports)
SYSTEMIC MYCOSIS ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
TESTICULAR PAIN ( 8 FDA reports)
THALAMUS HAEMORRHAGE ( 8 FDA reports)
THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TONGUE COATED ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 8 FDA reports)
ULNA FRACTURE ( 8 FDA reports)
URETERIC STENOSIS ( 8 FDA reports)
URETHRITIS ( 8 FDA reports)
VESTIBULAR DISORDER ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
WHIPLASH INJURY ( 8 FDA reports)
YAWNING ( 8 FDA reports)
PARASOMNIA ( 7 FDA reports)
PENILE HAEMORRHAGE ( 7 FDA reports)
PERITONEAL DISORDER ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 7 FDA reports)
PNEUMONIA HERPES VIRAL ( 7 FDA reports)
POST PROCEDURAL PAIN ( 7 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
POSTURE ABNORMAL ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PRINZMETAL ANGINA ( 7 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 7 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
PULMONARY HYPOPLASIA ( 7 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 7 FDA reports)
PULSE PRESSURE DECREASED ( 7 FDA reports)
RENAL TUBULAR ATROPHY ( 7 FDA reports)
RESORPTION BONE INCREASED ( 7 FDA reports)
RESPIRATION ABNORMAL ( 7 FDA reports)
RESPIRATORY ALKALOSIS ( 7 FDA reports)
RHINITIS SEASONAL ( 7 FDA reports)
SELF ESTEEM DECREASED ( 7 FDA reports)
SHOCK HYPOGLYCAEMIC ( 7 FDA reports)
SIMPLE PARTIAL SEIZURES ( 7 FDA reports)
SKIN FRAGILITY ( 7 FDA reports)
SPLENIC RUPTURE ( 7 FDA reports)
SPONTANEOUS HAEMATOMA ( 7 FDA reports)
STRONGYLOIDIASIS ( 7 FDA reports)
SUNBURN ( 7 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 7 FDA reports)
TEMPORAL LOBE EPILEPSY ( 7 FDA reports)
TENOSYNOVITIS STENOSANS ( 7 FDA reports)
THYROIDITIS ( 7 FDA reports)
THYROXINE INCREASED ( 7 FDA reports)
TOBACCO ABUSE ( 7 FDA reports)
TROPONIN T INCREASED ( 7 FDA reports)
TUMOUR PAIN ( 7 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 7 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
URINE KETONE BODY PRESENT ( 7 FDA reports)
URINE OUTPUT INCREASED ( 7 FDA reports)
VENOUS STASIS ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VENTRICULAR FAILURE ( 7 FDA reports)
VERTEBROPLASTY ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
VULVAL ULCERATION ( 7 FDA reports)
WALKING DISABILITY ( 7 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 7 FDA reports)
ACARODERMATITIS ( 7 FDA reports)
ACCELERATED HYPERTENSION ( 7 FDA reports)
ACUTE LUNG INJURY ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 7 FDA reports)
ADJUSTMENT DISORDER ( 7 FDA reports)
AKATHISIA ( 7 FDA reports)
AKINESIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
ALLERGY TO ARTHROPOD STING ( 7 FDA reports)
ANGIODYSPLASIA ( 7 FDA reports)
ANGIOGRAM ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
ANTITHROMBIN III DECREASED ( 7 FDA reports)
AORTIC BRUIT ( 7 FDA reports)
ARTERIAL THROMBOSIS ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
ATRIAL THROMBOSIS ( 7 FDA reports)
BACTERIURIA ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BETA GLOBULIN INCREASED ( 7 FDA reports)
BLADDER PAIN ( 7 FDA reports)
BLADDER SPASM ( 7 FDA reports)
BLEPHAROSPASM ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 7 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 7 FDA reports)
BLOOD URIC ACID ABNORMAL ( 7 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 7 FDA reports)
BOVINE TUBERCULOSIS ( 7 FDA reports)
BRAIN ABSCESS ( 7 FDA reports)
BREAST SWELLING ( 7 FDA reports)
BREATH ODOUR ( 7 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
BULIMIA NERVOSA ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CALCULUS BLADDER ( 7 FDA reports)
CALCULUS URINARY ( 7 FDA reports)
CANCER PAIN ( 7 FDA reports)
CARBON DIOXIDE INCREASED ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
CATHETER SITE RELATED REACTION ( 7 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CHOLESTATIC LIVER INJURY ( 7 FDA reports)
CHONDROPATHY ( 7 FDA reports)
CLAUSTROPHOBIA ( 7 FDA reports)
CLUBBING ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
COLORECTAL CANCER ( 7 FDA reports)
COLOSTOMY ( 7 FDA reports)
COMA SCALE ABNORMAL ( 7 FDA reports)
CONTRAST MEDIA REACTION ( 7 FDA reports)
CORNEAL DYSTROPHY ( 7 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 7 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
CUTIS LAXA ( 7 FDA reports)
CYTOGENETIC ABNORMALITY ( 7 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 7 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 7 FDA reports)
DEVICE RELATED SEPSIS ( 7 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 7 FDA reports)
DIABETIC ULCER ( 7 FDA reports)
DROOLING ( 7 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 7 FDA reports)
DRUG EFFECT INCREASED ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
DYSCHEZIA ( 7 FDA reports)
DYSENTERY ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
DYSPHEMIA ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
ECZEMA ASTEATOTIC ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EXSANGUINATION ( 7 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 7 FDA reports)
EXTRADURAL HAEMATOMA ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
FAECES HARD ( 7 FDA reports)
FOAMING AT MOUTH ( 7 FDA reports)
FOETAL GROWTH RESTRICTION ( 7 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 7 FDA reports)
GALLBLADDER POLYP ( 7 FDA reports)
GASTROINTESTINAL OEDEMA ( 7 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 7 FDA reports)
GENITAL LESION ( 7 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 7 FDA reports)
GRAFT DYSFUNCTION ( 7 FDA reports)
HIDRADENITIS ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 7 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 7 FDA reports)
HYDROURETER ( 7 FDA reports)
HYPERCHLORAEMIA ( 7 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 7 FDA reports)
HYPOCHROMASIA ( 7 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
IMPRISONMENT ( 7 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
INGUINAL MASS ( 7 FDA reports)
INJECTION SITE EXTRAVASATION ( 7 FDA reports)
INNER EAR DISORDER ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 7 FDA reports)
JOINT LOCK ( 7 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 7 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 7 FDA reports)
METASTASES TO THE MEDIASTINUM ( 7 FDA reports)
MICROGNATHIA ( 7 FDA reports)
MITRAL VALVE REPLACEMENT ( 7 FDA reports)
MIXED LIVER INJURY ( 7 FDA reports)
MONARTHRITIS ( 7 FDA reports)
MUCOSAL DRYNESS ( 7 FDA reports)
MUCOSAL HAEMORRHAGE ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
MYCOSIS FUNGOIDES ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
NEPHROANGIOSCLEROSIS ( 7 FDA reports)
NICOTINE DEPENDENCE ( 7 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
OESOPHAGEAL RUPTURE ( 7 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 7 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 7 FDA reports)
OPTIC NEURITIS ( 7 FDA reports)
ORAL FIBROMA ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
OTITIS MEDIA CHRONIC ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
OVERLAP SYNDROME ( 7 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 7 FDA reports)
PAIN EXACERBATED ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ABDOMINAL WALL INFECTION ( 6 FDA reports)
ACANTHOSIS NIGRICANS ( 6 FDA reports)
AIR EMBOLISM ( 6 FDA reports)
ALVEOLAR OSTEITIS ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 6 FDA reports)
APNOEIC ATTACK ( 6 FDA reports)
APPARENT LIFE THREATENING EVENT ( 6 FDA reports)
APPLICATION SITE DISCOLOURATION ( 6 FDA reports)
ARACHNOID CYST ( 6 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 6 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
AXILLARY MASS ( 6 FDA reports)
B-CELL LYMPHOMA STAGE I ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BLASTOMYCOSIS ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 6 FDA reports)
BONE MARROW NECROSIS ( 6 FDA reports)
BREAST CANCER STAGE III ( 6 FDA reports)
BUTTERFLY RASH ( 6 FDA reports)
CANDIDA SEPSIS ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
CAROTID ARTERY ATHEROMA ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 6 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 6 FDA reports)
CERVICAL DYSPLASIA ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CHOLANGITIS ACUTE ( 6 FDA reports)
CHOREA ( 6 FDA reports)
CHRONIC HEPATITIS ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 6 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 6 FDA reports)
CORNEAL ABSCESS ( 6 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 6 FDA reports)
CREATININE URINE INCREASED ( 6 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 6 FDA reports)
CYANOPSIA ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 6 FDA reports)
DELUSION OF GRANDEUR ( 6 FDA reports)
DIABETES INSIPIDUS ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DUODENITIS HAEMORRHAGIC ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
EJECTION FRACTION ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 6 FDA reports)
ENDOMETRIAL DISORDER ( 6 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 6 FDA reports)
ENTERITIS INFECTIOUS ( 6 FDA reports)
EPIDERMOLYSIS ( 6 FDA reports)
ERYTHRODERMIC PSORIASIS ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
FALLOPIAN TUBE OPERATION ( 6 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 6 FDA reports)
FIBROUS HISTIOCYTOMA ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FINGER AMPUTATION ( 6 FDA reports)
FISTULA DISCHARGE ( 6 FDA reports)
FLUID IMBALANCE ( 6 FDA reports)
FOOD AVERSION ( 6 FDA reports)
FUNGAL OESOPHAGITIS ( 6 FDA reports)
FUNGAL TEST POSITIVE ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTROENTERITIS BACTERIAL ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
GIANT CELL EPULIS ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
GOODPASTURE'S SYNDROME ( 6 FDA reports)
GRAFT LOSS ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 6 FDA reports)
HAEMORRHOID OPERATION ( 6 FDA reports)
HAEMOSIDEROSIS ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HERNIA OBSTRUCTIVE ( 6 FDA reports)
HYPERCHLORHYDRIA ( 6 FDA reports)
HYPERINSULINAEMIA ( 6 FDA reports)
HYPERTRANSAMINASAEMIA ( 6 FDA reports)
HYPOGONADISM ( 6 FDA reports)
HYPOMETABOLISM ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INJECTION SITE VESICLES ( 6 FDA reports)
INSULIN RESISTANCE ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 6 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 6 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 6 FDA reports)
INTUBATION ( 6 FDA reports)
IRIDOCELE ( 6 FDA reports)
JAUNDICE NEONATAL ( 6 FDA reports)
JC VIRUS INFECTION ( 6 FDA reports)
KAPOSI'S SARCOMA ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
KNEE DEFORMITY ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
LARYNGEAL CANCER ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 6 FDA reports)
LIP ULCERATION ( 6 FDA reports)
LITHOTRIPSY ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 6 FDA reports)
MACULE ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MEIBOMIANITIS ( 6 FDA reports)
MELANODERMIA ( 6 FDA reports)
MENSTRUATION IRREGULAR ( 6 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 6 FDA reports)
METASTASES TO STOMACH ( 6 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 6 FDA reports)
MONOCYTOSIS ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 6 FDA reports)
MYOGLOBIN URINE PRESENT ( 6 FDA reports)
MYOPATHY TOXIC ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
NEPHRECTOMY ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
NEUROSIS ( 6 FDA reports)
OCULAR VASCULAR DISORDER ( 6 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 6 FDA reports)
OESOPHAGITIS ULCERATIVE ( 6 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 6 FDA reports)
OVARIAN CANCER RECURRENT ( 6 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 6 FDA reports)
PAINFUL RESPIRATION ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 6 FDA reports)
PAPILLOPHLEBITIS ( 6 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 6 FDA reports)
PELVIC HAEMATOMA ( 6 FDA reports)
PENILE PAIN ( 6 FDA reports)
PERIANAL ABSCESS ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERICARDIAL DISEASE ( 6 FDA reports)
PERSECUTORY DELUSION ( 6 FDA reports)
PEYRONIE'S DISEASE ( 6 FDA reports)
PHARYNGEAL DISORDER ( 6 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 6 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 6 FDA reports)
PITUITARY TUMOUR ( 6 FDA reports)
PNEUMONIA INFLUENZAL ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
POST THROMBOTIC SYNDROME ( 6 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 6 FDA reports)
POSTICTAL STATE ( 6 FDA reports)
POSTOPERATIVE ABSCESS ( 6 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 6 FDA reports)
PREMATURE LABOUR ( 6 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 6 FDA reports)
PSEUDOHYPERKALAEMIA ( 6 FDA reports)
PSYCHOLOGICAL TRAUMA ( 6 FDA reports)
PULMONARY VASCULAR DISORDER ( 6 FDA reports)
RADICULITIS CERVICAL ( 6 FDA reports)
RECTAL CANCER STAGE 0 ( 6 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 6 FDA reports)
RHEUMATOID NODULE ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SCEDOSPORIUM INFECTION ( 6 FDA reports)
SCLERAL HAEMORRHAGE ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 6 FDA reports)
SELF-INJURIOUS IDEATION ( 6 FDA reports)
SERONEGATIVE ARTHRITIS ( 6 FDA reports)
SERRATIA BACTERAEMIA ( 6 FDA reports)
SJOGREN'S SYNDROME ( 6 FDA reports)
SKIN CANCER METASTATIC ( 6 FDA reports)
SKIN INJURY ( 6 FDA reports)
SPINAL CORD INJURY ( 6 FDA reports)
SPONDYLOLYSIS ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
TETANY ( 6 FDA reports)
THYROGLOBULIN INCREASED ( 6 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TONIC CLONIC MOVEMENTS ( 6 FDA reports)
TOOTH DEPOSIT ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
URTICARIA GENERALISED ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
WHITE CLOT SYNDROME ( 6 FDA reports)
WISDOM TEETH REMOVAL ( 6 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 5 FDA reports)
PARAKERATOSIS ( 5 FDA reports)
PARAPSORIASIS ( 5 FDA reports)
PARATHYROIDECTOMY ( 5 FDA reports)
PERICARDIAL DRAINAGE ( 5 FDA reports)
PERIORBITAL CELLULITIS ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
PLACENTAL DISORDER ( 5 FDA reports)
PLANTAR ERYTHEMA ( 5 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 5 FDA reports)
PNEUMOMEDIASTINUM ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POLYSEROSITIS ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 5 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 5 FDA reports)
POSTURING ( 5 FDA reports)
PRECANCEROUS CELLS PRESENT ( 5 FDA reports)
PROCEDURAL HYPERTENSION ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PSYCHOMOTOR AGITATION ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY HILUM MASS ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
RASH SCARLATINIFORM ( 5 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
REFLEXES ABNORMAL ( 5 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 5 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 5 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL ARTERY THROMBOSIS ( 5 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 5 FDA reports)
RHEUMATOID FACTOR INCREASED ( 5 FDA reports)
ROTAVIRUS TEST POSITIVE ( 5 FDA reports)
SALMONELLOSIS ( 5 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SERUM SEROTONIN INCREASED ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN BACTERIAL INFECTION ( 5 FDA reports)
SKIN DEGENERATIVE DISORDER ( 5 FDA reports)
SLOW RESPONSE TO STIMULI ( 5 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 5 FDA reports)
SMALL INTESTINE ULCER ( 5 FDA reports)
SOFT TISSUE NECROSIS ( 5 FDA reports)
SPUTUM RETENTION ( 5 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 5 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 5 FDA reports)
SUPRANUCLEAR PALSY ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
SUTURE RUPTURE ( 5 FDA reports)
SYNOVIAL SARCOMA ( 5 FDA reports)
TACHYCARDIA PAROXYSMAL ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 5 FDA reports)
THYROXINE DECREASED ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 5 FDA reports)
TUMOUR HAEMORRHAGE ( 5 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 5 FDA reports)
URETHRAL HAEMORRHAGE ( 5 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VASCULAR ENCEPHALOPATHY ( 5 FDA reports)
VASOSPASM ( 5 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VESICOURETERIC REFLUX ( 5 FDA reports)
VIRAL CARDIOMYOPATHY ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
VULVAL DISORDER ( 5 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
ZYGOMYCOSIS ( 5 FDA reports)
ABDOMINAL NEOPLASM ( 5 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 5 FDA reports)
ABSCESS BACTERIAL ( 5 FDA reports)
ACCESSORY SPLEEN ( 5 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 5 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ALCOHOL INTERACTION ( 5 FDA reports)
ALDOLASE INCREASED ( 5 FDA reports)
ANAL DISCOMFORT ( 5 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 5 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 5 FDA reports)
ANTIBODY TEST POSITIVE ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APHERESIS ( 5 FDA reports)
APPLICATION SITE EXFOLIATION ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
APPLICATION SITE URTICARIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
BACTERIAL TOXAEMIA ( 5 FDA reports)
BASE EXCESS DECREASED ( 5 FDA reports)
BEHCET'S SYNDROME ( 5 FDA reports)
BLADDER DIVERTICULUM ( 5 FDA reports)
BLADDER NEOPLASM ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD CREATININE ( 5 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 5 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 5 FDA reports)
BONE SWELLING ( 5 FDA reports)
BRAIN CANCER METASTATIC ( 5 FDA reports)
BREAST CALCIFICATIONS ( 5 FDA reports)
BRONCHOPULMONARY DISEASE ( 5 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 5 FDA reports)
BURN INFECTION ( 5 FDA reports)
CANDIDA OSTEOMYELITIS ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CAUSTIC INJURY ( 5 FDA reports)
CEREBELLAR SYNDROME ( 5 FDA reports)
CEREBRAL FUNGAL INFECTION ( 5 FDA reports)
CEREBRAL HYPOPERFUSION ( 5 FDA reports)
CHLOROMA ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 5 FDA reports)
COOMBS TEST POSITIVE ( 5 FDA reports)
CORNEAL ABRASION ( 5 FDA reports)
CRANIOPHARYNGIOMA ( 5 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 5 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 5 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 5 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 5 FDA reports)
DEVICE LEAKAGE ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DROP ATTACKS ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
EJACULATION DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 5 FDA reports)
ENDOMETRIAL CANCER ( 5 FDA reports)
ENERGY INCREASED ( 5 FDA reports)
ENTHESOPATHY ( 5 FDA reports)
EPIDERMAL NAEVUS ( 5 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 5 FDA reports)
ERYTHEMA INFECTIOSUM ( 5 FDA reports)
ERYTHEMA MIGRANS ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXTERNAL EAR DISORDER ( 5 FDA reports)
EYE REDNESS ( 5 FDA reports)
FACIAL WASTING ( 5 FDA reports)
FAT NECROSIS ( 5 FDA reports)
FEBRILE INFECTION ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FEELINGS OF WORTHLESSNESS ( 5 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 5 FDA reports)
FIBRIN DECREASED ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 5 FDA reports)
FOOT OPERATION ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC VARICES ( 5 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GINGIVAL OPERATION ( 5 FDA reports)
GLARE ( 5 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 5 FDA reports)
GLOBULINS DECREASED ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMANGIOMA OF SKIN ( 5 FDA reports)
HAIR COLOUR CHANGES ( 5 FDA reports)
HALO VISION ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HEART TRANSPLANT REJECTION ( 5 FDA reports)
HEAT RASH ( 5 FDA reports)
HEMIANOPIA ( 5 FDA reports)
HEPATIC CALCIFICATION ( 5 FDA reports)
HERPES OESOPHAGITIS ( 5 FDA reports)
HISTIOCYTOSIS ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HOMICIDE ( 5 FDA reports)
HYDROPNEUMOTHORAX ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 5 FDA reports)
HYPERPROLACTINAEMIA ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
HYPOCHOLESTEROLAEMIA ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
IGA NEPHROPATHY ( 5 FDA reports)
ILIAC ARTERY STENOSIS ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
INCORRECT PRODUCT STORAGE ( 5 FDA reports)
INFLAMMATORY MARKER INCREASED ( 5 FDA reports)
INFUSION SITE EXTRAVASATION ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE OEDEMA ( 5 FDA reports)
INJECTION SITE PAPULE ( 5 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 5 FDA reports)
INTERCOSTAL NEURALGIA ( 5 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 5 FDA reports)
IODINE ALLERGY ( 5 FDA reports)
JOINT CREPITATION ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
KIDNEY SMALL ( 5 FDA reports)
LABYRINTHITIS ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LARYNGEAL HAEMORRHAGE ( 5 FDA reports)
LEUKAEMOID REACTION ( 5 FDA reports)
LIGAMENT DISORDER ( 5 FDA reports)
LIP BLISTER ( 5 FDA reports)
LIPOATROPHY ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LYMPHANGITIS ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MARASMUS ( 5 FDA reports)
MEDIASTINUM NEOPLASM ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENINGITIS ASEPTIC ( 5 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METASTASES TO MUSCLE ( 5 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 5 FDA reports)
MIDDLE EAR EFFUSION ( 5 FDA reports)
MITOCHONDRIAL MYOPATHY ( 5 FDA reports)
MITRAL VALVE SCLEROSIS ( 5 FDA reports)
MUSCLE FIBROSIS ( 5 FDA reports)
MYODESOPSIA ( 5 FDA reports)
MYOSCLEROSIS ( 5 FDA reports)
MYXOEDEMA COMA ( 5 FDA reports)
NAIL HYPERTROPHY ( 5 FDA reports)
NAIL PIGMENTATION ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NASAL SEPTUM PERFORATION ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 5 FDA reports)
NO ADVERSE EFFECT ( 5 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
OPEN FRACTURE ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
OPTIC NERVE DISORDER ( 5 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
PALATAL DISORDER ( 5 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 4 FDA reports)
ABDOMINAL WALL DISORDER ( 4 FDA reports)
ABNORMAL WEIGHT GAIN ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACOUSTIC NEUROMA ( 4 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 4 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 4 FDA reports)
AGONAL RHYTHM ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 4 FDA reports)
AMYOTROPHY ( 4 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAL EROSION ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 4 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC ELONGATION ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
APPLICATION SITE HAEMATOMA ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 4 FDA reports)
AXILLARY PAIN ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BALANOPOSTHITIS ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLADDER CONSTRICTION ( 4 FDA reports)
BLEEDING VARICOSE VEIN ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 4 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 4 FDA reports)
BLOOD FOLATE DECREASED ( 4 FDA reports)
BLOOD SODIUM ABNORMAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BLOODY DISCHARGE ( 4 FDA reports)
BODY TINEA ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST ENLARGEMENT ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 4 FDA reports)
CANDIDA PNEUMONIA ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 4 FDA reports)
CARCINOID SYNDROME ( 4 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 4 FDA reports)
CARCINOMA ( 4 FDA reports)
CARDIAC ABLATION ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 4 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 4 FDA reports)
CARDIAC VENTRICULOGRAM ( 4 FDA reports)
CATHETER SITE ERYTHEMA ( 4 FDA reports)
CELLULITIS ORBITAL ( 4 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHLAMYDIAL INFECTION ( 4 FDA reports)
CHOLURIA ( 4 FDA reports)
CHROMATOPSIA ( 4 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 4 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
CNS VENTRICULITIS ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONGENITAL HYDROCEPHALUS ( 4 FDA reports)
CONJUNCTIVAL OEDEMA ( 4 FDA reports)
CONJUNCTIVAL PALLOR ( 4 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CORONARY ARTERY DISSECTION ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
CRANIOCEREBRAL INJURY ( 4 FDA reports)
CRUSH SYNDROME ( 4 FDA reports)
CYSTOCELE ( 4 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 4 FDA reports)
DANDRUFF ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DEVICE CONNECTION ISSUE ( 4 FDA reports)
DIABETIC GANGRENE ( 4 FDA reports)
DIAGNOSTIC PROCEDURE ( 4 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 4 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DUODENAL NEOPLASM ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
EAR HAEMORRHAGE ( 4 FDA reports)
EAR MALFORMATION ( 4 FDA reports)
EDENTULOUS ( 4 FDA reports)
EJECTION FRACTION ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 4 FDA reports)
EMBOLISM ARTERIAL ( 4 FDA reports)
EMPTY SELLA SYNDROME ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 4 FDA reports)
ENDOTOXIC SHOCK ( 4 FDA reports)
ENTEROVESICAL FISTULA ( 4 FDA reports)
ENZYME ABNORMALITY ( 4 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 4 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 4 FDA reports)
ERYTHROPENIA ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
FAECAL VOMITING ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FUNGAL RASH ( 4 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 4 FDA reports)
FUSARIUM INFECTION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTRIC INFECTION ( 4 FDA reports)
GASTRIC MUCOSAL LESION ( 4 FDA reports)
GASTRIC OPERATION ( 4 FDA reports)
GASTROINTESTINAL EROSION ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GENITAL BURNING SENSATION ( 4 FDA reports)
GENITAL EROSION ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GINGIVAL HYPERPLASIA ( 4 FDA reports)
GLOMERULONEPHROPATHY ( 4 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
GRAFT THROMBOSIS ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 4 FDA reports)
HAEMATOMA EVACUATION ( 4 FDA reports)
HAEMOBILIA ( 4 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATIC SIDEROSIS ( 4 FDA reports)
HEPATITIS ALCOHOLIC ( 4 FDA reports)
HEPATITIS C POSITIVE ( 4 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 4 FDA reports)
HEPATITIS E ( 4 FDA reports)
HOMANS' SIGN ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPOGLOBULINAEMIA ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 4 FDA reports)
IMPLANT SITE INFECTION ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INCISIONAL HERNIA REPAIR ( 4 FDA reports)
INFLAMMATION OF WOUND ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
INTESTINAL OPERATION ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LACTOBACILLUS INFECTION ( 4 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 4 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 4 FDA reports)
LEUKOSTASIS ( 4 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 4 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 4 FDA reports)
LIP DISORDER ( 4 FDA reports)
LOSS OF CONTROL OF LEGS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 4 FDA reports)
LUNG TRANSPLANT ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
LYMPHOCYTE COUNT ( 4 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
LYMPHOMA TRANSFORMATION ( 4 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 4 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
MENINGITIS HERPES ( 4 FDA reports)
METASTASES TO PLEURA ( 4 FDA reports)
METASTASES TO THORAX ( 4 FDA reports)
METASTATIC CARCINOID TUMOUR ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MOUTH BREATHING ( 4 FDA reports)
MUSCLE HYPERTROPHY ( 4 FDA reports)
MUSCLE SWELLING ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOCARDIAL RUPTURE ( 4 FDA reports)
NASAL SEPTUM DISORDER ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NECROSIS ISCHAEMIC ( 4 FDA reports)
NEOVASCULARISATION ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
NEURODEGENERATIVE DISORDER ( 4 FDA reports)
NEUROENDOCRINE TUMOUR ( 4 FDA reports)
NEUROPATHIC ARTHROPATHY ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OCULAR PEMPHIGOID ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
OEDEMATOUS PANCREATITIS ( 4 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORAL DYSAESTHESIA ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
OSTEOMA CUTIS ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PARATHYROID DISORDER ( 4 FDA reports)
PARATHYROID TUMOUR BENIGN ( 4 FDA reports)
PAROPHTHALMIA ( 4 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 4 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 4 FDA reports)
PHLEBITIS DEEP ( 4 FDA reports)
PHONOPHOBIA ( 4 FDA reports)
PHRENIC NERVE PARALYSIS ( 4 FDA reports)
PHYSICAL ASSAULT ( 4 FDA reports)
PITUITARY ENLARGEMENT ( 4 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 4 FDA reports)
PLEUROTHOTONUS ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
PO2 ABNORMAL ( 4 FDA reports)
POLYP COLORECTAL ( 4 FDA reports)
POST PROCEDURAL BILE LEAK ( 4 FDA reports)
POST PROCEDURAL HAEMATURIA ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PROSTATECTOMY ( 4 FDA reports)
PSYCHOSOMATIC DISEASE ( 4 FDA reports)
PULMONARY VALVE STENOSIS ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 4 FDA reports)
RASH PAPULOSQUAMOUS ( 4 FDA reports)
RASH SCALY ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RECALL PHENOMENON ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 4 FDA reports)
RED BLOOD CELL ABNORMALITY ( 4 FDA reports)
RED BLOOD CELLS URINE ( 4 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 4 FDA reports)
REHABILITATION THERAPY ( 4 FDA reports)
REITER'S SYNDROME ( 4 FDA reports)
RELAPSING FEVER ( 4 FDA reports)
RENAL ARTERY OCCLUSION ( 4 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 4 FDA reports)
RENAL CYST INFECTION ( 4 FDA reports)
RENAL ISCHAEMIA ( 4 FDA reports)
RENAL VEIN THROMBOSIS ( 4 FDA reports)
RENAL VESSEL DISORDER ( 4 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 4 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
RETROGRADE AMNESIA ( 4 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
SCIATIC NERVE NEUROPATHY ( 4 FDA reports)
SCROTAL INFECTION ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SHUNT OCCLUSION ( 4 FDA reports)
SIGMOIDECTOMY ( 4 FDA reports)
SINUSITIS FUNGAL ( 4 FDA reports)
SKIN GRAFT FAILURE ( 4 FDA reports)
SKIN TEST NEGATIVE ( 4 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 4 FDA reports)
SPLENIC LESION ( 4 FDA reports)
SPONTANEOUS PENILE ERECTION ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STENT EMBOLISATION ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 4 FDA reports)
TESTICULAR DISORDER ( 4 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
THYROXINE FREE DECREASED ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TOLOSA-HUNT SYNDROME ( 4 FDA reports)
TONGUE INJURY ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 4 FDA reports)
TUMOUR MARKER INCREASED ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URETHRAL MEATUS STENOSIS ( 4 FDA reports)
UROBILIN URINE PRESENT ( 4 FDA reports)
UROGENITAL DISORDER ( 4 FDA reports)
VARICOSE VEIN RUPTURED ( 4 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 4 FDA reports)
VASOMOTOR RHINITIS ( 4 FDA reports)
VEILLONELLA INFECTION ( 4 FDA reports)
VENTRICULAR FLUTTER ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
VULVOVAGINAL PRURITUS ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
XANTHOPSIA ( 4 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PARKINSONIAN GAIT ( 3 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PENIS CARCINOMA ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PERIPROCTITIS ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PHLEBOTHROMBOSIS ( 3 FDA reports)
PINEAL GERMINOMA ( 3 FDA reports)
PITUITARY CYST ( 3 FDA reports)
PLEURAL INFECTION ( 3 FDA reports)
PLEURAL INFECTION BACTERIAL ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PNEUMONIA NECROTISING ( 3 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 3 FDA reports)
PNEUMOPERICARDIUM ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POOR PERSONAL HYGIENE ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST PROCEDURAL NAUSEA ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PROCTITIS HAEMORRHAGIC ( 3 FDA reports)
PROCTITIS ULCERATIVE ( 3 FDA reports)
PROCTOCOLITIS ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PROSTATE CANCER STAGE IV ( 3 FDA reports)
PROTEIN C DEFICIENCY ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PRURITUS GENITAL ( 3 FDA reports)
PSEUDO-BARTTER SYNDROME ( 3 FDA reports)
PSEUDOPORPHYRIA ( 3 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 3 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
RADICULAR PAIN ( 3 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 3 FDA reports)
RENAL CYST HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SCROTAL HAEMATOCOELE ( 3 FDA reports)
SEBORRHOEA ( 3 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 3 FDA reports)
SEMEN VOLUME DECREASED ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SKIN BLEEDING ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SOLAR ELASTOSIS ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL CORD HAEMORRHAGE ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPLENIC VEIN THROMBOSIS ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STENT-GRAFT ENDOLEAK ( 3 FDA reports)
STILL'S DISEASE ADULT ONSET ( 3 FDA reports)
STOMACH MASS ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUPERINFECTION LUNG ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SURFACTANT PROTEIN INCREASED ( 3 FDA reports)
SUTURE INSERTION ( 3 FDA reports)
SWEAT GLAND DISORDER ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 3 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TERATOMA ( 3 FDA reports)
TESTICULAR NEOPLASM ( 3 FDA reports)
THROMBIN TIME PROLONGED ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOOTH MALFORMATION ( 3 FDA reports)
TORUS FRACTURE ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
URETERAL NECROSIS ( 3 FDA reports)
URETERAL NEOPLASM ( 3 FDA reports)
URETHRAL DISORDER ( 3 FDA reports)
URINARY BLADDER POLYP ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 3 FDA reports)
URINE AMYLASE INCREASED ( 3 FDA reports)
URINE SODIUM DECREASED ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
URTICARIA PAPULAR ( 3 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VENTRICLE RUPTURE ( 3 FDA reports)
VENTRICULAR DYSKINESIA ( 3 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 3 FDA reports)
VISUAL BRIGHTNESS ( 3 FDA reports)
VISUAL PATHWAY DISORDER ( 3 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 3 FDA reports)
VITAMIN D INCREASED ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND DECOMPOSITION ( 3 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
WOUND SEPSIS ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
XANTHOMA ( 3 FDA reports)
XERODERMA ( 3 FDA reports)
ABDOMINAL INJURY ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACID BASE BALANCE ABNORMAL ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE TONSILLITIS ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALBUMINURIA ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANAPHYLACTOID SHOCK ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 3 FDA reports)
APPENDICEAL ABSCESS ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 3 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
ASPIRATION BRONCHIAL ( 3 FDA reports)
ATONIC URINARY BLADDER ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
ATROPHIE BLANCHE ( 3 FDA reports)
AUTOIMMUNE PANCREATITIS ( 3 FDA reports)
AZOOSPERMIA ( 3 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 3 FDA reports)
BASE EXCESS INCREASED ( 3 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 3 FDA reports)
BENIGN NEOPLASM OF SKIN ( 3 FDA reports)
BILE DUCT NECROSIS ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLADDER CATHETER REPLACEMENT ( 3 FDA reports)
BLADDER HYPERTROPHY ( 3 FDA reports)
BLADDER NEOPLASM SURGERY ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER TAMPONADE ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BONE METABOLISM DISORDER ( 3 FDA reports)
BONE TRIMMING ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRAIN STEM ISCHAEMIA ( 3 FDA reports)
BREAST CANCER MALE ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATABOLIC STATE ( 3 FDA reports)
CATAPLEXY ( 3 FDA reports)
CATARACT DIABETIC ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CATHETER REMOVAL ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CATHETER SITE INFLAMMATION ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHEST WALL MASS ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COAGULATION TIME SHORTENED ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLITIS MICROSCOPIC ( 3 FDA reports)
COLON CANCER RECURRENT ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLONIC HAEMORRHAGE ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONDYLOMA ACUMINATUM ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CREST SYNDROME ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
CYCLIC VOMITING SYNDROME ( 3 FDA reports)
CYST RUPTURE ( 3 FDA reports)
CYTOKINE STORM ( 3 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 3 FDA reports)
DACRYOCYSTITIS ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DESQUAMATION MOUTH ( 3 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 3 FDA reports)
DEVICE INTERACTION ( 3 FDA reports)
DIABETIC GASTROENTEROPATHY ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 3 FDA reports)
DIAPHRAGMATIC APLASIA ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DRUG CLEARANCE DECREASED ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG INTERACTION INHIBITION ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DUODENAL STENOSIS ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EPIGLOTTITIS ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EVAN'S SYNDROME ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
EYELID BLEEDING ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FEAR OF FALLING ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FROSTBITE ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GALLBLADDER EMPYEMA ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTRIC VOLVULUS ( 3 FDA reports)
GASTROENTERITIS BACILLUS ( 3 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 3 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 3 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 3 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ( 3 FDA reports)
GENITAL PRURITUS MALE ( 3 FDA reports)
GENITAL SWELLING ( 3 FDA reports)
GIARDIASIS ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLOSSOPTOSIS ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 3 FDA reports)
GLYCOGEN STORAGE DISORDER ( 3 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HALITOSIS ( 3 FDA reports)
HALLUCINATION, TACTILE ( 3 FDA reports)
HANTAVIRAL INFECTION ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEPATIC ENZYME DECREASED ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HEPATIC INFECTION FUNGAL ( 3 FDA reports)
HEPATIC VEIN DILATATION ( 3 FDA reports)
HEPATITIS B ANTIBODY ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 3 FDA reports)
HOUSE DUST ALLERGY ( 3 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 3 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERPHOSPHATASAEMIA ( 3 FDA reports)
HYPOTENSIVE TRANSFUSION REACTION ( 3 FDA reports)
HYPOURICAEMIA ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
HYPOZINCAEMIA ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
ILEOSTOMY ( 3 FDA reports)
ILEOSTOMY CLOSURE ( 3 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 3 FDA reports)
IMPLANTABLE PLEURAL CATHETER INSERTION ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INFECTED DERMAL CYST ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INGUINAL HERNIA REPAIR ( 3 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL GANGRENE ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
IRIS ATROPHY ( 3 FDA reports)
JEALOUS DELUSION ( 3 FDA reports)
JOINT ANKYLOSIS ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
KUSSMAUL RESPIRATION ( 3 FDA reports)
LARGE INTESTINAL STRICTURE ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LEIOMYOSARCOMA ( 3 FDA reports)
LENS IMPLANT ( 3 FDA reports)
LEUKOENCEPHALOMYELITIS ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LINEAR IGA DISEASE ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LOCALISED EXFOLIATION ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LOOSE ASSOCIATIONS ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 3 FDA reports)
LUNG CYST ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
LYMPHATIC OBSTRUCTION ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MECHANICAL ILEUS ( 3 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
MENINGITIS LISTERIA ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 3 FDA reports)
METAPNEUMOVIRUS INFECTION ( 3 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
METASTASES TO SPLEEN ( 3 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 3 FDA reports)
MICROCOCCUS INFECTION ( 3 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 3 FDA reports)
MONONUCLEOSIS SYNDROME ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MOTOR NEURONE DISEASE ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MYCOPLASMA TEST POSITIVE ( 3 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 3 FDA reports)
MYOGLOBINAEMIA ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NASAL OPERATION ( 3 FDA reports)
NASAL VESTIBULITIS ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEAR DROWNING ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NERVE BLOCK ( 3 FDA reports)
NEURILEMMOMA ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 3 FDA reports)
OPTIC NERVE HYPOPLASIA ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
OROPHARYNGITIS FUNGAL ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PALLANAESTHESIA ( 3 FDA reports)
PALLIDOTOMY ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACQUIRED MACROGLOSSIA ( 2 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALCOHOL DETOXIFICATION ( 2 FDA reports)
ALLERGIC PHARYNGITIS ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALLOIMMUNISATION ( 2 FDA reports)
ALOPECIA TOTALIS ( 2 FDA reports)
ALOPECIA UNIVERSALIS ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL SPHINCTEROTOMY ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANEURYSM ARTERIOVENOUS ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 2 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTI-HBS ANTIBODY ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
APOLIPOPROTEIN INCREASED ( 2 FDA reports)
APPLICATION SITE CELLULITIS ( 2 FDA reports)
APPLICATION SITE PAPULES ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE ABSCESS ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 2 FDA reports)
ARTERITIS CORONARY ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ASCITES INFECTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BARTHOLIN'S CYST ( 2 FDA reports)
BARTTER'S SYNDROME ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASOPHILIA ( 2 FDA reports)
BENIGN MESENTERIC NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY LUNG ABNORMAL ( 2 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 2 FDA reports)
BLADDER CANCER STAGE II ( 2 FDA reports)
BLADDER GRANULOMA ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD LACTIC ACID ( 2 FDA reports)
BLOOD MAGNESIUM ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 2 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD TRYPSIN INCREASED ( 2 FDA reports)
BLOOD UREA ( 2 FDA reports)
BONE FISTULA ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE MARROW ISCHAEMIA ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BURKHOLDERIA TEST POSITIVE ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
C-REACTIVE PROTEIN ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIOMYOPATHY ACUTE ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CATHETER SITE PHLEBITIS ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 2 FDA reports)
CEREBELLAR ISCHAEMIA ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVICAL ROOT PAIN ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHEMICAL CYSTITIS ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHROMOSOMAL DELETION ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COELIAC ARTERY STENOSIS ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
COLONOSCOPY NORMAL ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONGENITAL ACROCHORDON ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONJUNCTIVAL SCAR ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONSTRICTED AFFECT ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
COOMBS TEST NEGATIVE ( 2 FDA reports)
CORNEAL LESION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CRYSTAL ARTHROPATHY ( 2 FDA reports)
CSF PROTEIN DECREASED ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYSTOSCOPY ABNORMAL ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
CYTARABINE SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DENGUE FEVER ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DIALYSIS DEVICE INSERTION ( 2 FDA reports)
DIASTOLIC HYPOTENSION ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DISEASE PRODROMAL STAGE ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DISUSE SYNDROME ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DYSLOGIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
DYSPROSODY ( 2 FDA reports)
EAR INFECTION BACTERIAL ( 2 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECHINOCOCCIASIS ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOMETRIAL ABLATION ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENDOVENOUS ABLATION ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
ENTEROCELE ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
ENZYME INDUCTION ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
ERYTHROID SERIES ABNORMAL ( 2 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 2 FDA reports)
EXECUTIVE DYSFUNCTION ( 2 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FAECAL DISIMPACTION ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FIBRIN D DIMER DECREASED ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTURE MALUNION ( 2 FDA reports)
FUNGAL ENDOCARDITIS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC ULCER HELICOBACTER ( 2 FDA reports)
GASTRITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMOGLOBINOPATHY ( 2 FDA reports)
HAEMORRHOID INFECTION ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
HEPATITIS INFECTIOUS ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY NEGATIVE ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HIV TEST POSITIVE ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 2 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 2 FDA reports)
HYALOSIS ASTEROID ( 2 FDA reports)
HYDROCHOLECYSTIS ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOPLASTIC ANAEMIA ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILIAC VEIN THROMBOSIS ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE DISCHARGE ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INBORN ERROR OF METABOLISM ( 2 FDA reports)
INCISION SITE PAIN ( 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)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INJECTION RELATED REACTION ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL ADENOCARCINOMA ( 2 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IODINE UPTAKE INCREASED ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
ISCHAEMIC NEPHROPATHY ( 2 FDA reports)
IVTH NERVE PARESIS ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LAPAROSCOPY ( 2 FDA reports)
LARYNGEAL POLYP ( 2 FDA reports)
LARYNGOPHARYNGITIS ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 2 FDA reports)
LEUKODERMA ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LIVER GRAFT LOSS ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 2 FDA reports)
MALIGNANT MELANOMA STAGE III ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
METHYLOBACTERIUM INFECTION ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MIXED INCONTINENCE ( 2 FDA reports)
MOANING ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE REATTACHMENT ( 2 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOTIC ALLERGY ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYELOCYTOSIS ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 2 FDA reports)
MYOTONIC DYSTROPHY ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NECROLYTIC MIGRATORY ERYTHEMA ( 2 FDA reports)
NEONATAL CARDIAC FAILURE ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL FISTULA ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARESIS CRANIAL NERVE ( 2 FDA reports)
PCO2 ABNORMAL ( 2 FDA reports)
PEDAL PULSE ABSENT ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PENILE DISCHARGE ( 2 FDA reports)
PENILE INFECTION ( 2 FDA reports)
PENILE OPERATION ( 2 FDA reports)
PENILE SIZE REDUCED ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIORBITAL DISORDER ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERISTALSIS VISIBLE ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PH BODY FLUID DECREASED ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHAGOPHOBIA ( 2 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNGITIS BACTERIAL ( 2 FDA reports)
PHOBIA OF DRIVING ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLICATED TONGUE ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PORTAL HYPERTENSIVE ENTEROPATHY ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POSTMATURE BABY ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROSTATIC CALCIFICATION ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTHROMBIN TIME ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOALDOSTERONISM ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOENDOPHTHALMITIS ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PULMONARY APLASIA ( 2 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RECTAL CANCER STAGE I ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS SEMEN ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
RENAL HYPERTENSION ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETINAL DEPIGMENTATION ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHABDOMYOSARCOMA ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCAR PAIN ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SEBACEOUS ADENOMA ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SERRATIA SEPSIS ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SIGNET-RING CELL CARCINOMA ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SPERMATOCELE ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPLENIC VEIN OCCLUSION ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
SUBDURAL EMPYEMA ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUPPORTIVE CARE ( 2 FDA reports)
SURGICAL VASCULAR SHUNT ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
T-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
TACITURNITY ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY NAIVE ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROID OPERATION ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TROPONIN T ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINAL LACERATION ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 2 FDA reports)
VASCULAR SKIN DISORDER ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 2 FDA reports)
VENTILATION PERFUSION MISMATCH ( 2 FDA reports)
VERBAL ABUSE ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VESTIBULAR ATAXIA ( 2 FDA reports)
VESTIBULOPLASTY ( 2 FDA reports)
VIRAL MYOSITIS ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
VOCAL CORD PARESIS ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARAESTHESIA CIRCUMORAL ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE CURVATURE ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENILE VEIN THROMBOSIS ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PENIS INJURY ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDIOTOMY ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHAGOCYTOSIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PLATELET DISTRIBUTION WIDTH ( 1 FDA reports)
PLEURAL DECORTICATION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA MORAXELLA ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
PORCELAIN GALLBLADDER ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE DIZZINESS ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREAURICULAR CYST ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN URINE ABSENT ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PSEUDOANGINA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURINE METABOLISM DISORDER ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL CANCER STAGE IV ( 1 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHINOLARYNGITIS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND CANCER STAGE III ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 1 FDA reports)
SARCOMA UTERUS ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCIATIC NERVE PALSY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL PIGMENTATION ( 1 FDA reports)
SCLEREMA ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBACEOUS GLAND DISORDER ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SEPTIC NECROSIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN WOUND ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE ABNORMAL ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPIGELIAN HERNIA ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN MALFORMATION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOMACH SCAN ABNORMAL ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
STROKE IN EVOLUTION ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBASTHENIA ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOPHLEBITIS PELVIC VEIN ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 1 FDA reports)
TRANSPLANT EVALUATION ( 1 FDA reports)
TRANSURETHRAL RESECTION SYNDROME ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 1 FDA reports)
TRUNCUS COELIACUS THROMBOSIS ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS BLADDER ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URAEMIC PRURITUS ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL SPASM ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC DIVERSION OPERATION ( 1 FDA reports)
URETERIC INJURY ( 1 FDA reports)
URETERIC OPERATION ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY BLADDER ABSCESS ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CHLORIDE DECREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGENITAL INFECTION BACTERIAL ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VAGINAL PROLAPSE REPAIR ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL ABSCESS ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTIGO LABYRINTHINE ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITAMIN K INCREASED ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL X-RAY ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
ADRENOCORTICAL CARCINOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALCOHOLISATION PROCEDURE ( 1 FDA reports)
ALDOLASE DECREASED ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPHA 1 GLOBULIN DECREASED ( 1 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOGRAM RETINA ABNORMAL ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTIANGIOGENIC THERAPY ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASTEATOSIS ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL RUPTURE ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BARTHOLIN'S ABSCESS ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA GLOBULIN ABNORMAL ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILIARY ANASTOMOSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY MUSCLE ( 1 FDA reports)
BIOPSY PLEURA ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CANCER STAGE I, WITHOUT CANCER IN SITU ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 1 FDA reports)
BLINDNESS DAY ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN D DECREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORRELIA BURGDORFERI SEROLOGY POSITIVE ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIUM PHOSPHATE PRODUCT INCREASED ( 1 FDA reports)
CAMPTOCORMIA ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHIASMA SYNDROME ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHRONIC EOSINOPHILIC LEUKAEMIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC LEUKAEMIA ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLOSED FRACTURE MANIPULATION ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONY STIMULATING FACTOR THERAPY ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL JAW MALFORMATION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONUS MEDULLARIS SYNDROME ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COXIELLA TEST POSITIVE ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF GLUCOSE ABNORMAL ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CUTANEOUS TUBERCULOSIS ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 1 FDA reports)
DACRYOCYSTORHINOSTOMY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIFFUSE MESANGIAL SCLEROSIS ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRAIN REMOVAL ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUBIN-JOHNSON SYNDROME ( 1 FDA reports)
DUST INHALATION PNEUMOPATHY ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOPRAXIA ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM RR INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELECTROOCULOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENLARGED CEREBRAL PERIVASCULAR SPACES ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC CYSTITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EOSINOPHILIC PUSTULOSIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPINEPHRINE ABNORMAL ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPIPHYSEAL FRACTURE ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ERYTHROCYANOSIS ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXUDATIVE RETINOPATHY ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL MACROSOMIA ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOSTER-KENNEDY SYNDROME ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 1 FDA reports)
GANGLIONEUROBLASTOMA ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRITIS FUNGAL ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GINGIVAL HYPERPIGMENTATION ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOPHILUS SEPSIS ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART AND LUNG TRANSPLANT ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CANCER STAGE IV ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C RNA FLUCTUATION ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS NON-A NON-B ( 1 FDA reports)
HEPATITIS NON-A NON-B NON-C ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOBILIARY INFECTION ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HLA MARKER STUDY POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE TYPE STAGE UNSPECIFIED ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HTLV-1 TEST POSITIVE ( 1 FDA reports)
HY'S LAW CASE ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPERKALIURIA ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERSTHENURIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYSTEROCELE ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IDIOSYNCRATIC ALCOHOL INTOXICATION ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMUNE AGGLUTININS ( 1 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
IMPLANT TISSUE NECROSIS ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL FISTULA REPAIR ( 1 FDA reports)
INTESTINAL GASTRIC METAPLASIA ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYPECTOMY ( 1 FDA reports)
INTESTINAL STENT INSERTION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAVASCULAR PAPILLARY ENDOTHELIAL HYPERPLASIA ( 1 FDA reports)
IRIDOTOMY ( 1 FDA reports)
IRIS INJURY ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT CAPSULE RUPTURE ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT PROSTHESIS USER ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS VIRAL ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY ABLATION ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARYNGEAL CANCER STAGE IV ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEAD DISLODGEMENT ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDURIA ( 1 FDA reports)
LIPOEDEMA ( 1 FDA reports)
LISTERIA ENCEPHALITIS ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOIDECTOMY ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MAXILLOFACIAL OPERATION ( 1 FDA reports)
MEASLES ANTIBODY POSITIVE ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAMYELOCYTE COUNT DECREASED ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO DIAPHRAGM ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PITUITARY GLAND ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROBIOLOGY TEST ABNORMAL ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MINERAL SUPPLEMENTATION ( 1 FDA reports)
MINOR COGNITIVE MOTOR DISORDER ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL INFECTION ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIA URINE TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYECTOMY ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEEDLE BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NOROVIRUS TEST POSITIVE ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
ONYCHOGRYPHOSIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC SPHINCTEROTOMY ( 1 FDA reports)

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