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

MYOCARDIAL INFARCTION ( 20362 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12783 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7615 FDA reports)
CORONARY ARTERY DISEASE ( 5625 FDA reports)
DEATH ( 5236 FDA reports)
CARDIAC DISORDER ( 4676 FDA reports)
CARDIOVASCULAR DISORDER ( 2948 FDA reports)
BLOOD GLUCOSE INCREASED ( 2607 FDA reports)
DYSPNOEA ( 2596 FDA reports)
INJURY ( 2469 FDA reports)
PAIN ( 2456 FDA reports)
CHEST PAIN ( 2095 FDA reports)
NAUSEA ( 2072 FDA reports)
WEIGHT INCREASED ( 1905 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1893 FDA reports)
HEART INJURY ( 1714 FDA reports)
HYPERTENSION ( 1683 FDA reports)
WEIGHT DECREASED ( 1669 FDA reports)
OEDEMA PERIPHERAL ( 1610 FDA reports)
ATRIAL FIBRILLATION ( 1504 FDA reports)
FATIGUE ( 1487 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1455 FDA reports)
RENAL FAILURE ( 1421 FDA reports)
ADVERSE EVENT ( 1399 FDA reports)
ANXIETY ( 1276 FDA reports)
DIZZINESS ( 1257 FDA reports)
ASTHENIA ( 1199 FDA reports)
CARDIAC ARREST ( 1186 FDA reports)
CORONARY ARTERY BYPASS ( 1139 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1090 FDA reports)
CARDIAC FAILURE ( 1046 FDA reports)
DEPRESSION ( 993 FDA reports)
OEDEMA ( 968 FDA reports)
BLOOD GLUCOSE DECREASED ( 967 FDA reports)
ANAEMIA ( 943 FDA reports)
FLUID RETENTION ( 938 FDA reports)
STENT PLACEMENT ( 929 FDA reports)
DRUG INEFFECTIVE ( 908 FDA reports)
DIARRHOEA ( 890 FDA reports)
ARTERIOSCLEROSIS ( 887 FDA reports)
VOMITING ( 876 FDA reports)
ARRHYTHMIA ( 862 FDA reports)
HEADACHE ( 840 FDA reports)
DECREASED APPETITE ( 824 FDA reports)
CARDIOMYOPATHY ( 736 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 729 FDA reports)
HYPERLIPIDAEMIA ( 698 FDA reports)
PNEUMONIA ( 685 FDA reports)
FALL ( 678 FDA reports)
DIABETES MELLITUS ( 652 FDA reports)
PAIN IN EXTREMITY ( 636 FDA reports)
RENAL FAILURE ACUTE ( 606 FDA reports)
ACUTE CORONARY SYNDROME ( 572 FDA reports)
HYPOGLYCAEMIA ( 568 FDA reports)
ANGINA PECTORIS ( 567 FDA reports)
ANGINA UNSTABLE ( 557 FDA reports)
CARDIOMEGALY ( 553 FDA reports)
VISION BLURRED ( 544 FDA reports)
BACK PAIN ( 527 FDA reports)
PULMONARY OEDEMA ( 524 FDA reports)
CORONARY ARTERY OCCLUSION ( 520 FDA reports)
PLEURAL EFFUSION ( 496 FDA reports)
AMNESIA ( 494 FDA reports)
PALPITATIONS ( 488 FDA reports)
THROMBOSIS ( 480 FDA reports)
CONDITION AGGRAVATED ( 477 FDA reports)
SWELLING ( 476 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 475 FDA reports)
HYPOAESTHESIA ( 475 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 474 FDA reports)
EMOTIONAL DISTRESS ( 447 FDA reports)
GAIT DISTURBANCE ( 446 FDA reports)
MALAISE ( 442 FDA reports)
MITRAL VALVE INCOMPETENCE ( 437 FDA reports)
ARTHRALGIA ( 436 FDA reports)
CARDIO-RESPIRATORY ARREST ( 434 FDA reports)
RESPIRATORY FAILURE ( 422 FDA reports)
TREMOR ( 421 FDA reports)
MACULAR OEDEMA ( 418 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 414 FDA reports)
ABDOMINAL PAIN UPPER ( 412 FDA reports)
BLINDNESS ( 407 FDA reports)
PULMONARY HYPERTENSION ( 397 FDA reports)
HEART RATE IRREGULAR ( 396 FDA reports)
CONSTIPATION ( 391 FDA reports)
SYNCOPE ( 387 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 382 FDA reports)
INSOMNIA ( 378 FDA reports)
ABDOMINAL DISTENSION ( 375 FDA reports)
ABDOMINAL PAIN ( 370 FDA reports)
LOSS OF CONSCIOUSNESS ( 368 FDA reports)
HYPERHIDROSIS ( 346 FDA reports)
COUGH ( 345 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 334 FDA reports)
RENAL FAILURE CHRONIC ( 333 FDA reports)
CARDIAC PACEMAKER INSERTION ( 325 FDA reports)
HEPATIC FAILURE ( 325 FDA reports)
JOINT SWELLING ( 324 FDA reports)
RENAL DISORDER ( 324 FDA reports)
MUSCLE SPASMS ( 322 FDA reports)
HEART RATE INCREASED ( 321 FDA reports)
FEELING ABNORMAL ( 320 FDA reports)
HYPOTENSION ( 320 FDA reports)
VISUAL ACUITY REDUCED ( 316 FDA reports)
DEHYDRATION ( 314 FDA reports)
PYREXIA ( 314 FDA reports)
FLUID OVERLOAD ( 299 FDA reports)
RASH ( 298 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 296 FDA reports)
CONVULSION ( 291 FDA reports)
CHEST DISCOMFORT ( 289 FDA reports)
SOMNOLENCE ( 287 FDA reports)
TYPE 2 DIABETES MELLITUS ( 287 FDA reports)
DYSPEPSIA ( 282 FDA reports)
ANOREXIA ( 280 FDA reports)
PARAESTHESIA ( 280 FDA reports)
URINARY TRACT INFECTION ( 280 FDA reports)
MUSCULAR WEAKNESS ( 278 FDA reports)
NEUROPATHY PERIPHERAL ( 275 FDA reports)
CARDIAC OPERATION ( 273 FDA reports)
VENTRICULAR TACHYCARDIA ( 273 FDA reports)
HYPERGLYCAEMIA ( 271 FDA reports)
ECONOMIC PROBLEM ( 267 FDA reports)
CONFUSIONAL STATE ( 263 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 259 FDA reports)
SUDDEN CARDIAC DEATH ( 257 FDA reports)
PULMONARY EMBOLISM ( 256 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 255 FDA reports)
ANHEDONIA ( 254 FDA reports)
SEPSIS ( 253 FDA reports)
CATARACT ( 252 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 249 FDA reports)
MYALGIA ( 243 FDA reports)
DRUG EFFECT DECREASED ( 239 FDA reports)
ISCHAEMIC STROKE ( 235 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 234 FDA reports)
PRURITUS ( 234 FDA reports)
RENAL IMPAIRMENT ( 230 FDA reports)
SINUSITIS ( 230 FDA reports)
STRESS ( 230 FDA reports)
PANCREATITIS ( 229 FDA reports)
BALANCE DISORDER ( 227 FDA reports)
HAEMOGLOBIN DECREASED ( 227 FDA reports)
INJECTION SITE BRUISING ( 226 FDA reports)
OSTEOMYELITIS ( 223 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 222 FDA reports)
BRONCHITIS ( 220 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 217 FDA reports)
INTRACARDIAC THROMBUS ( 216 FDA reports)
INJECTION SITE PAIN ( 213 FDA reports)
SLEEP APNOEA SYNDROME ( 213 FDA reports)
LUNG DISORDER ( 212 FDA reports)
DYSPNOEA EXERTIONAL ( 209 FDA reports)
VISUAL IMPAIRMENT ( 207 FDA reports)
TACHYCARDIA ( 206 FDA reports)
DEEP VEIN THROMBOSIS ( 205 FDA reports)
CATHETERISATION CARDIAC ( 204 FDA reports)
CELLULITIS ( 203 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 203 FDA reports)
FLATULENCE ( 201 FDA reports)
BLOOD PRESSURE INCREASED ( 200 FDA reports)
CORONARY ARTERY STENOSIS ( 200 FDA reports)
FEAR ( 199 FDA reports)
RENAL INJURY ( 199 FDA reports)
CAROTID ARTERY STENOSIS ( 197 FDA reports)
LIVER INJURY ( 196 FDA reports)
CARDIOGENIC SHOCK ( 195 FDA reports)
CHOLELITHIASIS ( 195 FDA reports)
BLOOD CREATININE INCREASED ( 193 FDA reports)
PERICARDIAL EFFUSION ( 190 FDA reports)
VASCULAR GRAFT ( 190 FDA reports)
INFECTION ( 189 FDA reports)
CARDIAC VALVE DISEASE ( 188 FDA reports)
FRACTURE ( 188 FDA reports)
OSTEOARTHRITIS ( 186 FDA reports)
UNEVALUABLE EVENT ( 186 FDA reports)
CONTUSION ( 185 FDA reports)
DISABILITY ( 185 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 184 FDA reports)
ILL-DEFINED DISORDER ( 183 FDA reports)
OSTEONECROSIS OF JAW ( 182 FDA reports)
SPINAL OSTEOARTHRITIS ( 182 FDA reports)
DYSPHAGIA ( 179 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 179 FDA reports)
BRADYCARDIA ( 176 FDA reports)
VENTRICULAR FIBRILLATION ( 175 FDA reports)
DIABETIC NEUROPATHY ( 174 FDA reports)
NERVOUSNESS ( 172 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 172 FDA reports)
CEREBROVASCULAR DISORDER ( 169 FDA reports)
ATRIOVENTRICULAR BLOCK ( 168 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 168 FDA reports)
ATELECTASIS ( 167 FDA reports)
CEREBRAL INFARCTION ( 167 FDA reports)
OBESITY ( 167 FDA reports)
ATRIAL FLUTTER ( 165 FDA reports)
ARTHRITIS ( 162 FDA reports)
MULTI-ORGAN FAILURE ( 160 FDA reports)
DIABETIC RETINOPATHY ( 159 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 159 FDA reports)
ERECTILE DYSFUNCTION ( 158 FDA reports)
HYPERCHOLESTEROLAEMIA ( 158 FDA reports)
MULTIPLE INJURIES ( 156 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 155 FDA reports)
ASTHMA ( 155 FDA reports)
ABASIA ( 154 FDA reports)
CARDIAC MURMUR ( 154 FDA reports)
INJECTION SITE HAEMORRHAGE ( 152 FDA reports)
MEDICATION ERROR ( 151 FDA reports)
MEMORY IMPAIRMENT ( 151 FDA reports)
HYPERKALAEMIA ( 149 FDA reports)
CHILLS ( 148 FDA reports)
LIVER DISORDER ( 148 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 147 FDA reports)
EYE DISORDER ( 145 FDA reports)
THROMBOCYTOPENIA ( 145 FDA reports)
DYSGEUSIA ( 143 FDA reports)
GASTRITIS ( 142 FDA reports)
BONE DISORDER ( 141 FDA reports)
HEMIPARESIS ( 141 FDA reports)
HYPOXIA ( 140 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 139 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 138 FDA reports)
OVERDOSE ( 138 FDA reports)
COMA ( 137 FDA reports)
DRUG INTERACTION ( 136 FDA reports)
IMPAIRED HEALING ( 136 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 136 FDA reports)
STOMACH DISCOMFORT ( 135 FDA reports)
ISCHAEMIA ( 134 FDA reports)
NASOPHARYNGITIS ( 134 FDA reports)
MUSCULOSKELETAL PAIN ( 133 FDA reports)
ERUCTATION ( 132 FDA reports)
NECK PAIN ( 131 FDA reports)
ALOPECIA ( 130 FDA reports)
HEPATIC STEATOSIS ( 130 FDA reports)
URTICARIA ( 130 FDA reports)
HEPATIC CIRRHOSIS ( 128 FDA reports)
SPEECH DISORDER ( 128 FDA reports)
HYPERSENSITIVITY ( 127 FDA reports)
PARALYSIS ( 127 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 127 FDA reports)
CAROTID ARTERY DISEASE ( 125 FDA reports)
MENTAL STATUS CHANGES ( 124 FDA reports)
POLLAKIURIA ( 124 FDA reports)
EMOTIONAL DISORDER ( 123 FDA reports)
ERYTHEMA ( 123 FDA reports)
OSTEOPOROSIS ( 123 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 123 FDA reports)
NEPHROLITHIASIS ( 120 FDA reports)
JAUNDICE ( 119 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 118 FDA reports)
PANCREATITIS ACUTE ( 118 FDA reports)
ANGIOPLASTY ( 117 FDA reports)
EJECTION FRACTION DECREASED ( 117 FDA reports)
INCORRECT DOSE ADMINISTERED ( 117 FDA reports)
FEELING JITTERY ( 116 FDA reports)
HEPATIC ENZYME INCREASED ( 116 FDA reports)
WHEEZING ( 116 FDA reports)
SICK SINUS SYNDROME ( 115 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 114 FDA reports)
LEFT ATRIAL DILATATION ( 114 FDA reports)
PAIN IN JAW ( 114 FDA reports)
VERTIGO ( 114 FDA reports)
VISUAL DISTURBANCE ( 114 FDA reports)
DIASTOLIC DYSFUNCTION ( 113 FDA reports)
SWELLING FACE ( 113 FDA reports)
SURGERY ( 112 FDA reports)
ANGIOPATHY ( 111 FDA reports)
HAEMORRHAGE ( 111 FDA reports)
HYPOTHYROIDISM ( 111 FDA reports)
DEFORMITY ( 110 FDA reports)
CARDIAC DEATH ( 109 FDA reports)
TREATMENT NONCOMPLIANCE ( 109 FDA reports)
LACUNAR INFARCTION ( 108 FDA reports)
LETHARGY ( 108 FDA reports)
MOBILITY DECREASED ( 108 FDA reports)
PANCYTOPENIA ( 108 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 107 FDA reports)
DYSLIPIDAEMIA ( 106 FDA reports)
AORTIC STENOSIS ( 105 FDA reports)
MENTAL DISORDER ( 105 FDA reports)
RECTAL HAEMORRHAGE ( 105 FDA reports)
BLINDNESS UNILATERAL ( 104 FDA reports)
FOOT FRACTURE ( 104 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 104 FDA reports)
PRODUCTIVE COUGH ( 104 FDA reports)
DISORIENTATION ( 103 FDA reports)
HAEMATOCRIT DECREASED ( 103 FDA reports)
HEMIPLEGIA ( 103 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 102 FDA reports)
DIALYSIS ( 102 FDA reports)
HYPOKALAEMIA ( 100 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 100 FDA reports)
ACUTE RESPIRATORY FAILURE ( 99 FDA reports)
INCREASED APPETITE ( 99 FDA reports)
ORTHOPNOEA ( 99 FDA reports)
DYSARTHRIA ( 98 FDA reports)
DRY MOUTH ( 97 FDA reports)
EPISTAXIS ( 97 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 97 FDA reports)
BLOOD UREA INCREASED ( 95 FDA reports)
SUICIDAL IDEATION ( 95 FDA reports)
UPPER LIMB FRACTURE ( 95 FDA reports)
ABDOMINAL DISCOMFORT ( 94 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 94 FDA reports)
PRESYNCOPE ( 94 FDA reports)
SEPTIC SHOCK ( 94 FDA reports)
SKIN ULCER ( 93 FDA reports)
TINNITUS ( 93 FDA reports)
FLUSHING ( 92 FDA reports)
LIFE EXPECTANCY SHORTENED ( 91 FDA reports)
CARPAL TUNNEL SYNDROME ( 90 FDA reports)
HYPONATRAEMIA ( 89 FDA reports)
NEPHROPATHY ( 88 FDA reports)
OSTEONECROSIS ( 88 FDA reports)
FEELING HOT ( 87 FDA reports)
GENERALISED OEDEMA ( 87 FDA reports)
HAEMORRHOIDS ( 87 FDA reports)
STAPHYLOCOCCAL INFECTION ( 87 FDA reports)
ARTHROPATHY ( 86 FDA reports)
DIABETIC KETOACIDOSIS ( 86 FDA reports)
EXOSTOSIS ( 86 FDA reports)
GLAUCOMA ( 86 FDA reports)
HYPERTENSIVE HEART DISEASE ( 86 FDA reports)
RESPIRATORY ARREST ( 86 FDA reports)
RIB FRACTURE ( 86 FDA reports)
ROAD TRAFFIC ACCIDENT ( 86 FDA reports)
SLEEP DISORDER ( 86 FDA reports)
ANKLE FRACTURE ( 85 FDA reports)
BRAIN INJURY ( 85 FDA reports)
RENAL CYST ( 85 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 84 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 84 FDA reports)
SINUS TACHYCARDIA ( 84 FDA reports)
VENTRICULAR HYPERTROPHY ( 84 FDA reports)
PULMONARY CONGESTION ( 83 FDA reports)
APHASIA ( 82 FDA reports)
CHOLECYSTITIS ( 82 FDA reports)
DECREASED ACTIVITY ( 82 FDA reports)
DECREASED INTEREST ( 82 FDA reports)
RESPIRATORY DISORDER ( 82 FDA reports)
ASCITES ( 81 FDA reports)
EARLY SATIETY ( 81 FDA reports)
LUNG INFILTRATION ( 81 FDA reports)
QUALITY OF LIFE DECREASED ( 81 FDA reports)
TOOTH EXTRACTION ( 81 FDA reports)
WRIST FRACTURE ( 81 FDA reports)
ACUTE PULMONARY OEDEMA ( 80 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 79 FDA reports)
INFLUENZA LIKE ILLNESS ( 78 FDA reports)
MOVEMENT DISORDER ( 78 FDA reports)
EYE SWELLING ( 77 FDA reports)
HAEMATURIA ( 77 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 77 FDA reports)
MULTIPLE FRACTURES ( 77 FDA reports)
OSTEOPENIA ( 77 FDA reports)
SCAR ( 77 FDA reports)
ARTERIAL DISORDER ( 76 FDA reports)
HEART RATE DECREASED ( 76 FDA reports)
ROTATOR CUFF SYNDROME ( 76 FDA reports)
HAEMATOCHEZIA ( 75 FDA reports)
DYSURIA ( 74 FDA reports)
GASTRIC DISORDER ( 74 FDA reports)
HEAD INJURY ( 74 FDA reports)
LUMBAR SPINAL STENOSIS ( 74 FDA reports)
HAEMATOMA ( 73 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 73 FDA reports)
AORTIC VALVE INCOMPETENCE ( 72 FDA reports)
BLOOD PRESSURE DECREASED ( 72 FDA reports)
IRRITABILITY ( 72 FDA reports)
PROTHROMBIN TIME PROLONGED ( 72 FDA reports)
RHABDOMYOLYSIS ( 72 FDA reports)
BLOOD BILIRUBIN INCREASED ( 71 FDA reports)
IRON DEFICIENCY ANAEMIA ( 71 FDA reports)
INJECTION SITE IRRITATION ( 70 FDA reports)
RESPIRATORY DISTRESS ( 70 FDA reports)
RETINAL HAEMORRHAGE ( 70 FDA reports)
ANEURYSM ( 69 FDA reports)
NEOPLASM MALIGNANT ( 69 FDA reports)
NERVE INJURY ( 69 FDA reports)
NEURALGIA ( 69 FDA reports)
PULMONARY FIBROSIS ( 69 FDA reports)
DEMENTIA ( 68 FDA reports)
HIATUS HERNIA ( 68 FDA reports)
HIP FRACTURE ( 68 FDA reports)
HUNGER ( 68 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 68 FDA reports)
AORTIC VALVE REPLACEMENT ( 67 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 67 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 67 FDA reports)
DIPLOPIA ( 67 FDA reports)
INJECTION SITE ERYTHEMA ( 67 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 67 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 66 FDA reports)
BURNING SENSATION ( 66 FDA reports)
CAROTID ARTERY OCCLUSION ( 66 FDA reports)
HEPATITIS ( 66 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 66 FDA reports)
UNRESPONSIVE TO STIMULI ( 66 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 65 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 65 FDA reports)
DIVERTICULUM INTESTINAL ( 65 FDA reports)
DRUG HYPERSENSITIVITY ( 65 FDA reports)
HEART VALVE INCOMPETENCE ( 65 FDA reports)
HEPATOMEGALY ( 65 FDA reports)
METABOLIC ACIDOSIS ( 65 FDA reports)
OSTEOLYSIS ( 65 FDA reports)
PLATELET COUNT DECREASED ( 65 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 65 FDA reports)
TYPE 1 DIABETES MELLITUS ( 65 FDA reports)
CEREBRAL HAEMORRHAGE ( 64 FDA reports)
DEAFNESS ( 64 FDA reports)
HYPOCALCAEMIA ( 64 FDA reports)
MITRAL VALVE DISEASE ( 64 FDA reports)
MULTIPLE MYELOMA ( 64 FDA reports)
SINUS BRADYCARDIA ( 64 FDA reports)
URINARY INCONTINENCE ( 64 FDA reports)
HYPOPHAGIA ( 63 FDA reports)
DENTAL CARIES ( 62 FDA reports)
HEPATOCELLULAR DAMAGE ( 62 FDA reports)
LIMB INJURY ( 62 FDA reports)
AGITATION ( 61 FDA reports)
BLOOD DISORDER ( 61 FDA reports)
CHROMATURIA ( 61 FDA reports)
ENCEPHALOPATHY ( 61 FDA reports)
EYE HAEMORRHAGE ( 61 FDA reports)
GOITRE ( 61 FDA reports)
HYPOVOLAEMIA ( 61 FDA reports)
RETINOPATHY ( 61 FDA reports)
SINUS DISORDER ( 61 FDA reports)
DISTURBANCE IN ATTENTION ( 60 FDA reports)
LEUKOCYTOSIS ( 60 FDA reports)
PNEUMONIA ASPIRATION ( 60 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 59 FDA reports)
NASAL CONGESTION ( 59 FDA reports)
OBSTRUCTION ( 59 FDA reports)
ACCIDENTAL OVERDOSE ( 58 FDA reports)
CORONARY ANGIOPLASTY ( 58 FDA reports)
DIVERTICULUM ( 58 FDA reports)
FAECES DISCOLOURED ( 58 FDA reports)
GALLBLADDER DISORDER ( 58 FDA reports)
INFLUENZA ( 58 FDA reports)
SUDDEN DEATH ( 58 FDA reports)
VENTRICULAR DYSFUNCTION ( 58 FDA reports)
CARDIAC HYPERTROPHY ( 57 FDA reports)
FEELING COLD ( 57 FDA reports)
NERVOUS SYSTEM DISORDER ( 57 FDA reports)
PHYSICAL DISABILITY ( 57 FDA reports)
RHINORRHOEA ( 57 FDA reports)
TOOTH LOSS ( 57 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 56 FDA reports)
AZOTAEMIA ( 56 FDA reports)
BLISTER ( 56 FDA reports)
GASTROENTERITIS ( 56 FDA reports)
POST PROCEDURAL COMPLICATION ( 56 FDA reports)
SHOCK ( 56 FDA reports)
COLD SWEAT ( 55 FDA reports)
INJECTION SITE URTICARIA ( 55 FDA reports)
LEG AMPUTATION ( 55 FDA reports)
MENTAL IMPAIRMENT ( 55 FDA reports)
MUSCULOSKELETAL DISORDER ( 55 FDA reports)
CARDIAC FLUTTER ( 54 FDA reports)
IMPAIRED WORK ABILITY ( 54 FDA reports)
JOINT INJURY ( 54 FDA reports)
HALLUCINATION ( 53 FDA reports)
INFLAMMATION ( 53 FDA reports)
CEREBRAL ATROPHY ( 52 FDA reports)
GASTRIC ULCER ( 52 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 52 FDA reports)
MITRAL VALVE PROLAPSE ( 52 FDA reports)
PANIC ATTACK ( 52 FDA reports)
RHINITIS ALLERGIC ( 52 FDA reports)
BLOOD POTASSIUM INCREASED ( 51 FDA reports)
DIABETIC COMPLICATION ( 51 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 51 FDA reports)
MACULAR DEGENERATION ( 51 FDA reports)
METASTASES TO BONE ( 51 FDA reports)
MUSCLE TWITCHING ( 51 FDA reports)
OXYGEN SUPPLEMENTATION ( 51 FDA reports)
KIDNEY INFECTION ( 50 FDA reports)
LYMPHADENOPATHY ( 50 FDA reports)
MIGRAINE ( 50 FDA reports)
OFF LABEL USE ( 50 FDA reports)
PROSTATE CANCER ( 50 FDA reports)
SENSORY LOSS ( 50 FDA reports)
BONE PAIN ( 49 FDA reports)
CYSTITIS ( 49 FDA reports)
DYSPHONIA ( 49 FDA reports)
EAR PAIN ( 49 FDA reports)
ECCHYMOSIS ( 49 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 49 FDA reports)
RASH GENERALISED ( 49 FDA reports)
AORTIC ANEURYSM ( 48 FDA reports)
BRAIN STEM INFARCTION ( 48 FDA reports)
EYE PAIN ( 48 FDA reports)
FACIAL PALSY ( 48 FDA reports)
HAEMATEMESIS ( 48 FDA reports)
LOWER LIMB FRACTURE ( 48 FDA reports)
ONYCHOMYCOSIS ( 48 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 48 FDA reports)
SKIN DISORDER ( 48 FDA reports)
VIITH NERVE PARALYSIS ( 48 FDA reports)
VISUAL FIELD DEFECT ( 48 FDA reports)
CARDIAC FAILURE CHRONIC ( 47 FDA reports)
CEREBRAL ISCHAEMIA ( 47 FDA reports)
DIFFICULTY IN WALKING ( 47 FDA reports)
DIVERTICULITIS ( 47 FDA reports)
GASTROINTESTINAL DISORDER ( 47 FDA reports)
HYPOAESTHESIA ORAL ( 47 FDA reports)
JAW FRACTURE ( 47 FDA reports)
LEUKOPENIA ( 47 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 47 FDA reports)
DILATATION ATRIAL ( 46 FDA reports)
FEMUR FRACTURE ( 46 FDA reports)
GOUT ( 46 FDA reports)
HERPES ZOSTER ( 46 FDA reports)
LACRIMATION INCREASED ( 46 FDA reports)
LACTIC ACIDOSIS ( 46 FDA reports)
TACHYARRHYTHMIA ( 46 FDA reports)
CARDIOPULMONARY FAILURE ( 45 FDA reports)
CIRCULATORY COLLAPSE ( 45 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 45 FDA reports)
DIABETIC NEPHROPATHY ( 45 FDA reports)
DRUG ADMINISTRATION ERROR ( 45 FDA reports)
HAEMORRHAGIC STROKE ( 45 FDA reports)
MYELODYSPLASTIC SYNDROME ( 45 FDA reports)
PHLEBITIS ( 45 FDA reports)
ADVERSE DRUG REACTION ( 44 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 44 FDA reports)
BURSITIS ( 44 FDA reports)
COAGULOPATHY ( 44 FDA reports)
OPEN WOUND ( 44 FDA reports)
TOOTH ABSCESS ( 44 FDA reports)
EMPHYSEMA ( 43 FDA reports)
HOT FLUSH ( 43 FDA reports)
OROPHARYNGEAL PAIN ( 43 FDA reports)
RETCHING ( 43 FDA reports)
DISEASE PROGRESSION ( 42 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 42 FDA reports)
DYSSTASIA ( 42 FDA reports)
MUSCLE STRAIN ( 42 FDA reports)
MYOSITIS ( 42 FDA reports)
NOCTURIA ( 42 FDA reports)
RALES ( 42 FDA reports)
TARDIVE DYSKINESIA ( 42 FDA reports)
TENDONITIS ( 42 FDA reports)
VENTRICULAR HYPOKINESIA ( 42 FDA reports)
ABDOMINAL PAIN LOWER ( 41 FDA reports)
CANDIDIASIS ( 41 FDA reports)
HYPERSOMNIA ( 41 FDA reports)
INTERSTITIAL LUNG DISEASE ( 41 FDA reports)
LIBIDO DECREASED ( 41 FDA reports)
MENISCUS LESION ( 41 FDA reports)
PITTING OEDEMA ( 41 FDA reports)
SKIN DISCOLOURATION ( 41 FDA reports)
AORTIC VALVE STENOSIS ( 40 FDA reports)
COLONIC POLYP ( 40 FDA reports)
DRUG TOXICITY ( 40 FDA reports)
FEMORAL NECK FRACTURE ( 40 FDA reports)
HYPOAESTHESIA FACIAL ( 40 FDA reports)
NEUTROPENIA ( 40 FDA reports)
NON-CARDIAC CHEST PAIN ( 40 FDA reports)
SCOLIOSIS ( 40 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 40 FDA reports)
THIRST ( 40 FDA reports)
VENTRICULAR ARRHYTHMIA ( 40 FDA reports)
AORTIC VALVE SCLEROSIS ( 39 FDA reports)
BLOOD SODIUM DECREASED ( 39 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 39 FDA reports)
GINGIVAL PAIN ( 39 FDA reports)
LOCAL SWELLING ( 39 FDA reports)
PERICARDITIS ( 39 FDA reports)
PRURITUS GENERALISED ( 39 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 39 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 39 FDA reports)
AGGRESSION ( 38 FDA reports)
COLITIS ISCHAEMIC ( 38 FDA reports)
DILATATION VENTRICULAR ( 38 FDA reports)
DRY SKIN ( 38 FDA reports)
FUNGAL INFECTION ( 38 FDA reports)
LUNG NEOPLASM ( 38 FDA reports)
AORTIC CALCIFICATION ( 37 FDA reports)
BLADDER DISORDER ( 37 FDA reports)
BLOOD POTASSIUM DECREASED ( 37 FDA reports)
COR PULMONALE ( 37 FDA reports)
DEPRESSED MOOD ( 37 FDA reports)
EATING DISORDER ( 37 FDA reports)
GINGIVAL INFECTION ( 37 FDA reports)
HAEMODIALYSIS ( 37 FDA reports)
MELAENA ( 37 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 37 FDA reports)
RASH PRURITIC ( 37 FDA reports)
SKIN EXFOLIATION ( 37 FDA reports)
ANOXIC ENCEPHALOPATHY ( 36 FDA reports)
AORTIC VALVE DISEASE ( 36 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 36 FDA reports)
ENERGY INCREASED ( 36 FDA reports)
EXTRASYSTOLES ( 36 FDA reports)
FEBRILE NEUTROPENIA ( 36 FDA reports)
HYDRONEPHROSIS ( 36 FDA reports)
MITRAL VALVE CALCIFICATION ( 36 FDA reports)
MOOD SWINGS ( 36 FDA reports)
MUCOSAL INFLAMMATION ( 36 FDA reports)
PRESCRIBED OVERDOSE ( 36 FDA reports)
BLOOD URINE PRESENT ( 35 FDA reports)
CHOLECYSTECTOMY ( 35 FDA reports)
FAECAL INCONTINENCE ( 35 FDA reports)
HUMERUS FRACTURE ( 35 FDA reports)
ORTHOSTATIC HYPOTENSION ( 35 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 35 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 35 FDA reports)
ULCER ( 35 FDA reports)
VITAMIN D DEFICIENCY ( 35 FDA reports)
CONJUNCTIVITIS ( 34 FDA reports)
DYSKINESIA ( 34 FDA reports)
HEART VALVE REPLACEMENT ( 34 FDA reports)
INJECTION SITE PRURITUS ( 34 FDA reports)
MOUTH ULCERATION ( 34 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 34 FDA reports)
OESOPHAGITIS ( 34 FDA reports)
PROTEINURIA ( 34 FDA reports)
PULMONARY THROMBOSIS ( 34 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 34 FDA reports)
RETINAL DETACHMENT ( 34 FDA reports)
SPINAL COMPRESSION FRACTURE ( 34 FDA reports)
BRONCHOPNEUMONIA ( 33 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 33 FDA reports)
FACE OEDEMA ( 33 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 33 FDA reports)
HAND FRACTURE ( 33 FDA reports)
INJECTION SITE EXTRAVASATION ( 33 FDA reports)
LOCALISED OSTEOARTHRITIS ( 33 FDA reports)
LYMPHOEDEMA ( 33 FDA reports)
PLEURAL FIBROSIS ( 33 FDA reports)
PSYCHOTIC DISORDER ( 33 FDA reports)
RADICULOPATHY ( 33 FDA reports)
RASH ERYTHEMATOUS ( 33 FDA reports)
RENAL TUBULAR NECROSIS ( 33 FDA reports)
SUBDURAL HAEMATOMA ( 33 FDA reports)
TOOTH FRACTURE ( 33 FDA reports)
TOOTHACHE ( 33 FDA reports)
TRAUMATIC LUNG INJURY ( 33 FDA reports)
BACK DISORDER ( 32 FDA reports)
BIPOLAR DISORDER ( 32 FDA reports)
CORONARY ARTERY THROMBOSIS ( 32 FDA reports)
DEBRIDEMENT ( 32 FDA reports)
DENTURE WEARER ( 32 FDA reports)
DYSAESTHESIA ( 32 FDA reports)
EXCORIATION ( 32 FDA reports)
GROIN PAIN ( 32 FDA reports)
HALLUCINATION, AUDITORY ( 32 FDA reports)
INTERMITTENT CLAUDICATION ( 32 FDA reports)
PANCREATITIS CHRONIC ( 32 FDA reports)
SPLENOMEGALY ( 32 FDA reports)
SWOLLEN TONGUE ( 32 FDA reports)
THROAT IRRITATION ( 32 FDA reports)
WEIGHT LOSS POOR ( 32 FDA reports)
APPARENT DEATH ( 31 FDA reports)
BACTERAEMIA ( 31 FDA reports)
BLOOD ALBUMIN DECREASED ( 31 FDA reports)
BONE LOSS ( 31 FDA reports)
BUNDLE BRANCH BLOCK ( 31 FDA reports)
COLITIS ( 31 FDA reports)
DIABETIC COMA ( 31 FDA reports)
DRY EYE ( 31 FDA reports)
ESSENTIAL HYPERTENSION ( 31 FDA reports)
EXPOSED BONE IN JAW ( 31 FDA reports)
GYNAECOMASTIA ( 31 FDA reports)
ILEUS ( 31 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 31 FDA reports)
LOBAR PNEUMONIA ( 31 FDA reports)
MIDDLE INSOMNIA ( 31 FDA reports)
MYOPATHY ( 31 FDA reports)
NECK INJURY ( 31 FDA reports)
NEUROPATHY ( 31 FDA reports)
PALLOR ( 31 FDA reports)
PANCREATIC CARCINOMA ( 31 FDA reports)
PATHOLOGICAL FRACTURE ( 31 FDA reports)
PELVIC FRACTURE ( 31 FDA reports)
RESPIRATORY TRACT CONGESTION ( 31 FDA reports)
RHEUMATOID ARTHRITIS ( 31 FDA reports)
RIGHT VENTRICULAR FAILURE ( 31 FDA reports)
SPINAL FRACTURE ( 31 FDA reports)
TENDERNESS ( 31 FDA reports)
TOOTH DISORDER ( 31 FDA reports)
VITREOUS FLOATERS ( 31 FDA reports)
ABDOMINAL HERNIA ( 30 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 30 FDA reports)
ADRENAL INSUFFICIENCY ( 30 FDA reports)
EXERCISE TOLERANCE DECREASED ( 30 FDA reports)
HAEMOPTYSIS ( 30 FDA reports)
HEPATIC ENCEPHALOPATHY ( 30 FDA reports)
HYDROCELE ( 30 FDA reports)
HYPERTENSIVE CRISIS ( 30 FDA reports)
INJECTION SITE RASH ( 30 FDA reports)
LYMPHOMA ( 30 FDA reports)
NODULE ( 30 FDA reports)
OXYGEN SATURATION DECREASED ( 30 FDA reports)
PERIODONTAL DISEASE ( 30 FDA reports)
PNEUMONITIS ( 30 FDA reports)
PURULENT DISCHARGE ( 30 FDA reports)
RENAL ISCHAEMIA ( 30 FDA reports)
RESTLESS LEGS SYNDROME ( 30 FDA reports)
SKIN LACERATION ( 30 FDA reports)
SKIN TIGHTNESS ( 30 FDA reports)
STOMATITIS ( 30 FDA reports)
URINE OUTPUT DECREASED ( 30 FDA reports)
VIRAL INFECTION ( 30 FDA reports)
ACIDOSIS ( 29 FDA reports)
ASPIRATION ( 29 FDA reports)
COMPRESSION FRACTURE ( 29 FDA reports)
DERMAL CYST ( 29 FDA reports)
DISCOMFORT ( 29 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 29 FDA reports)
INCONTINENCE ( 29 FDA reports)
POOR PERIPHERAL CIRCULATION ( 29 FDA reports)
SPINAL COLUMN STENOSIS ( 29 FDA reports)
THYROID DISORDER ( 29 FDA reports)
TOE AMPUTATION ( 29 FDA reports)
UTERINE LEIOMYOMA ( 29 FDA reports)
VARICOSE VEIN ( 29 FDA reports)
BLOOD CHLORIDE DECREASED ( 28 FDA reports)
BREAST CANCER ( 28 FDA reports)
CARDIAC VALVE ABSCESS ( 28 FDA reports)
CATHETER PLACEMENT ( 28 FDA reports)
DEVICE MALFUNCTION ( 28 FDA reports)
DRUG DISPENSING ERROR ( 28 FDA reports)
FEAR OF DEATH ( 28 FDA reports)
GINGIVAL SWELLING ( 28 FDA reports)
OSTEITIS ( 28 FDA reports)
PERIPHERAL EMBOLISM ( 28 FDA reports)
PYELONEPHRITIS ( 28 FDA reports)
RECTAL POLYP ( 28 FDA reports)
TESTICULAR SWELLING ( 28 FDA reports)
BLOOD CALCIUM DECREASED ( 27 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 27 FDA reports)
CATARACT OPERATION ( 27 FDA reports)
CRYING ( 27 FDA reports)
FACET JOINT SYNDROME ( 27 FDA reports)
HERNIA ( 27 FDA reports)
KNEE ARTHROPLASTY ( 27 FDA reports)
LABORATORY TEST ABNORMAL ( 27 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
MOTOR DYSFUNCTION ( 27 FDA reports)
ORAL CANDIDIASIS ( 27 FDA reports)
POLYURIA ( 27 FDA reports)
PRIMARY SEQUESTRUM ( 27 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 27 FDA reports)
TOE DEFORMITY ( 27 FDA reports)
URINARY RETENTION ( 27 FDA reports)
ABNORMAL BEHAVIOUR ( 26 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 26 FDA reports)
BONE MARROW FAILURE ( 26 FDA reports)
BREATH ODOUR ( 26 FDA reports)
BRONCHITIS CHRONIC ( 26 FDA reports)
COGNITIVE DISORDER ( 26 FDA reports)
CONDUCTION DISORDER ( 26 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 26 FDA reports)
EPIDIDYMITIS ( 26 FDA reports)
FIBROMYALGIA ( 26 FDA reports)
HYPERCALCAEMIA ( 26 FDA reports)
HYPOMAGNESAEMIA ( 26 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 26 FDA reports)
JOINT SPRAIN ( 26 FDA reports)
LOCALISED INFECTION ( 26 FDA reports)
MICTURITION URGENCY ( 26 FDA reports)
MONOPLEGIA ( 26 FDA reports)
MUSCLE CRAMP ( 26 FDA reports)
PEPTIC ULCER ( 26 FDA reports)
RESTLESSNESS ( 26 FDA reports)
VASCULAR CALCIFICATION ( 26 FDA reports)
VITAMIN B12 DEFICIENCY ( 26 FDA reports)
WOUND INFECTION ( 26 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 26 FDA reports)
ACUTE PRERENAL FAILURE ( 25 FDA reports)
ARTERIOSPASM CORONARY ( 25 FDA reports)
BACK INJURY ( 25 FDA reports)
BLOOD AMYLASE INCREASED ( 25 FDA reports)
BLOOD IRON DECREASED ( 25 FDA reports)
BONE LESION ( 25 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 25 FDA reports)
CHOKING ( 25 FDA reports)
CHOLESTASIS ( 25 FDA reports)
EMBOLIC STROKE ( 25 FDA reports)
GASTROINTESTINAL PAIN ( 25 FDA reports)
INCREASED TENDENCY TO BRUISE ( 25 FDA reports)
JOINT STIFFNESS ( 25 FDA reports)
LIPASE INCREASED ( 25 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 25 FDA reports)
OEDEMA MOUTH ( 25 FDA reports)
PARANOIA ( 25 FDA reports)
PLEURISY ( 25 FDA reports)
PORTAL HYPERTENSION ( 25 FDA reports)
STRESS FRACTURE ( 25 FDA reports)
TESTICULAR PAIN ( 25 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 24 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 24 FDA reports)
BONE DEBRIDEMENT ( 24 FDA reports)
CHRONIC SINUSITIS ( 24 FDA reports)
COORDINATION ABNORMAL ( 24 FDA reports)
DECUBITUS ULCER ( 24 FDA reports)
DEVICE FAILURE ( 24 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 24 FDA reports)
ENTEROCOCCAL INFECTION ( 24 FDA reports)
FLANK PAIN ( 24 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 24 FDA reports)
HYPOACUSIS ( 24 FDA reports)
LIMB DISCOMFORT ( 24 FDA reports)
LUNG NEOPLASM MALIGNANT ( 24 FDA reports)
PERIPHERAL COLDNESS ( 24 FDA reports)
PROCEDURAL PAIN ( 24 FDA reports)
PSORIASIS ( 24 FDA reports)
RETINAL DISORDER ( 24 FDA reports)
TACHYPNOEA ( 24 FDA reports)
WHIPLASH INJURY ( 24 FDA reports)
ANGIONEUROTIC OEDEMA ( 23 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 23 FDA reports)
DENTAL FISTULA ( 23 FDA reports)
DRUG DOSE OMISSION ( 23 FDA reports)
ELECTROLYTE IMBALANCE ( 23 FDA reports)
ENDOTRACHEAL INTUBATION ( 23 FDA reports)
GASTROENTERITIS VIRAL ( 23 FDA reports)
HYPOTONIA ( 23 FDA reports)
LEFT VENTRICULAR FAILURE ( 23 FDA reports)
MASTICATION DISORDER ( 23 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 23 FDA reports)
OCCULT BLOOD POSITIVE ( 23 FDA reports)
OCULAR HYPERAEMIA ( 23 FDA reports)
ORCHITIS ( 23 FDA reports)
PULSE ABSENT ( 23 FDA reports)
PURPURA ( 23 FDA reports)
RASH MACULO-PAPULAR ( 23 FDA reports)
SCIATICA ( 23 FDA reports)
SEASONAL ALLERGY ( 23 FDA reports)
SEXUAL DYSFUNCTION ( 23 FDA reports)
SPONDYLOLISTHESIS ( 23 FDA reports)
SUBCUTANEOUS ABSCESS ( 23 FDA reports)
ABSCESS ( 22 FDA reports)
ANAPHYLACTIC REACTION ( 22 FDA reports)
ANGIOEDEMA ( 22 FDA reports)
BACTERIAL INFECTION ( 22 FDA reports)
BEDRIDDEN ( 22 FDA reports)
BLADDER CANCER ( 22 FDA reports)
BONE NEOPLASM MALIGNANT ( 22 FDA reports)
COLITIS ULCERATIVE ( 22 FDA reports)
COLLAPSE OF LUNG ( 22 FDA reports)
DISEASE RECURRENCE ( 22 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 22 FDA reports)
EYE INJURY ( 22 FDA reports)
GASTRIC HAEMORRHAGE ( 22 FDA reports)
HEART DISEASE CONGENITAL ( 22 FDA reports)
HEPATIC NECROSIS ( 22 FDA reports)
IMMOBILE ( 22 FDA reports)
INFARCTION ( 22 FDA reports)
JOINT DISLOCATION ( 22 FDA reports)
KYPHOSIS ( 22 FDA reports)
LOSS OF EMPLOYMENT ( 22 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 22 FDA reports)
RENAL TRANSPLANT ( 22 FDA reports)
SENSATION OF HEAVINESS ( 22 FDA reports)
SNEEZING ( 22 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 22 FDA reports)
TENSION ( 22 FDA reports)
THALAMIC INFARCTION ( 22 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 22 FDA reports)
UROSEPSIS ( 22 FDA reports)
ABNORMAL DREAMS ( 21 FDA reports)
BASAL CELL CARCINOMA ( 21 FDA reports)
BLOOD MAGNESIUM DECREASED ( 21 FDA reports)
BLOOD PRESSURE ABNORMAL ( 21 FDA reports)
BREAST MASS ( 21 FDA reports)
DRUG INTOLERANCE ( 21 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 21 FDA reports)
FAECALOMA ( 21 FDA reports)
FRACTURED SACRUM ( 21 FDA reports)
GANGRENE ( 21 FDA reports)
HEPATOTOXICITY ( 21 FDA reports)
MAJOR DEPRESSION ( 21 FDA reports)
MICTURITION DISORDER ( 21 FDA reports)
MUSCLE ATROPHY ( 21 FDA reports)
MUSCLE TIGHTNESS ( 21 FDA reports)
NEOPLASM PROGRESSION ( 21 FDA reports)
OESOPHAGEAL DISORDER ( 21 FDA reports)
ORAL DISORDER ( 21 FDA reports)
PROSTATOMEGALY ( 21 FDA reports)
SINUS CONGESTION ( 21 FDA reports)
SUICIDE ATTEMPT ( 21 FDA reports)
THINKING ABNORMAL ( 21 FDA reports)
VARICES OESOPHAGEAL ( 21 FDA reports)
VASCULAR OCCLUSION ( 21 FDA reports)
WALKING AID USER ( 21 FDA reports)
APPENDICITIS ( 20 FDA reports)
BRONCHITIS ACUTE ( 20 FDA reports)
CARDIAC ANEURYSM ( 20 FDA reports)
CEREBELLAR INFARCTION ( 20 FDA reports)
CERUMEN IMPACTION ( 20 FDA reports)
COLON CANCER ( 20 FDA reports)
CORNEAL ABRASION ( 20 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 20 FDA reports)
HYPOGLYCAEMIC COMA ( 20 FDA reports)
HYPOKINESIA ( 20 FDA reports)
HYPOVENTILATION ( 20 FDA reports)
JAW DISORDER ( 20 FDA reports)
JUGULAR VEIN DISTENSION ( 20 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 20 FDA reports)
MALIGNANT MELANOMA ( 20 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 20 FDA reports)
MALNUTRITION ( 20 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 20 FDA reports)
ORAL INFECTION ( 20 FDA reports)
PNEUMOTHORAX ( 20 FDA reports)
SERUM FERRITIN INCREASED ( 20 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 20 FDA reports)
VENOUS INSUFFICIENCY ( 20 FDA reports)
ACTINIC KERATOSIS ( 19 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 19 FDA reports)
BODY HEIGHT DECREASED ( 19 FDA reports)
BREATH SOUNDS ABNORMAL ( 19 FDA reports)
BUNION ( 19 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 19 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 19 FDA reports)
DIABETIC FOOT ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
EYE IRRITATION ( 19 FDA reports)
FACIAL PAIN ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 19 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 19 FDA reports)
LIGAMENT INJURY ( 19 FDA reports)
NIGHT SWEATS ( 19 FDA reports)
OLIGURIA ( 19 FDA reports)
OPEN ANGLE GLAUCOMA ( 19 FDA reports)
ORGAN FAILURE ( 19 FDA reports)
PARKINSON'S DISEASE ( 19 FDA reports)
PERIPHERAL ISCHAEMIA ( 19 FDA reports)
PHOTOPHOBIA ( 19 FDA reports)
PHOTOPSIA ( 19 FDA reports)
POLYDIPSIA ( 19 FDA reports)
PRODUCT QUALITY ISSUE ( 19 FDA reports)
RASH MACULAR ( 19 FDA reports)
SINUS ARRHYTHMIA ( 19 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 19 FDA reports)
SPINAL DISORDER ( 19 FDA reports)
THYROID NEOPLASM ( 19 FDA reports)
TOOTH INFECTION ( 19 FDA reports)
TRANSFUSION ( 19 FDA reports)
VAGINAL HAEMORRHAGE ( 19 FDA reports)
VASCULITIS ( 19 FDA reports)
VITREOUS HAEMORRHAGE ( 19 FDA reports)
WHEELCHAIR USER ( 19 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 19 FDA reports)
ANAEMIA MACROCYTIC ( 18 FDA reports)
ANGER ( 18 FDA reports)
ANGIOGRAM ( 18 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 18 FDA reports)
ANURIA ( 18 FDA reports)
APLASIA PURE RED CELL ( 18 FDA reports)
ARTERIAL STENOSIS ( 18 FDA reports)
BLINDNESS TRANSIENT ( 18 FDA reports)
CARDIAC TAMPONADE ( 18 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 18 FDA reports)
DELIRIUM ( 18 FDA reports)
DELUSION ( 18 FDA reports)
DENTAL OPERATION ( 18 FDA reports)
DYSPNOEA EXACERBATED ( 18 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 18 FDA reports)
FOOD CRAVING ( 18 FDA reports)
GINGIVAL BLEEDING ( 18 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 18 FDA reports)
HAEMOLYTIC ANAEMIA ( 18 FDA reports)
HEARING IMPAIRED ( 18 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 18 FDA reports)
HOSPITALISATION ( 18 FDA reports)
INJECTION SITE NODULE ( 18 FDA reports)
INSULIN RESISTANCE ( 18 FDA reports)
INTESTINAL OBSTRUCTION ( 18 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 18 FDA reports)
MALIGNANT HYPERTENSION ( 18 FDA reports)
METABOLIC SYNDROME ( 18 FDA reports)
METASTATIC NEOPLASM ( 18 FDA reports)
NIGHT BLINDNESS ( 18 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 18 FDA reports)
RETINAL OEDEMA ( 18 FDA reports)
SKIN ATROPHY ( 18 FDA reports)
THERAPY NON-RESPONDER ( 18 FDA reports)
TROPONIN INCREASED ( 18 FDA reports)
VASCULAR INJURY ( 18 FDA reports)
VASODILATATION ( 18 FDA reports)
VITAMIN D DECREASED ( 18 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 17 FDA reports)
APNOEA ( 17 FDA reports)
ATHEROSCLEROSIS ( 17 FDA reports)
DIABETIC EYE DISEASE ( 17 FDA reports)
DIABETIC GASTROPARESIS ( 17 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 17 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 17 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 17 FDA reports)
EYE OEDEMA ( 17 FDA reports)
GASTRITIS EROSIVE ( 17 FDA reports)
GINGIVITIS ( 17 FDA reports)
IMPAIRED DRIVING ABILITY ( 17 FDA reports)
INJECTION SITE HAEMATOMA ( 17 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 17 FDA reports)
METASTASES TO LIVER ( 17 FDA reports)
MONARTHRITIS ( 17 FDA reports)
MOOD ALTERED ( 17 FDA reports)
MUMPS ( 17 FDA reports)
MYOCARDITIS ( 17 FDA reports)
NIGHTMARE ( 17 FDA reports)
OSTEOGENESIS IMPERFECTA ( 17 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 17 FDA reports)
PERIODONTITIS ( 17 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 17 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 17 FDA reports)
RENAL ARTERY STENOSIS ( 17 FDA reports)
RENAL CANCER ( 17 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 17 FDA reports)
SKIN FIBROSIS ( 17 FDA reports)
SKIN INDURATION ( 17 FDA reports)
SNORING ( 17 FDA reports)
TOBACCO ABUSE ( 17 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 17 FDA reports)
ACTINOMYCOSIS ( 16 FDA reports)
ATAXIA ( 16 FDA reports)
ATRIAL TACHYCARDIA ( 16 FDA reports)
BASAL GANGLIA INFARCTION ( 16 FDA reports)
BLOOD URIC ACID INCREASED ( 16 FDA reports)
BRAIN STEM STROKE ( 16 FDA reports)
BRONCHOSPASM ( 16 FDA reports)
CALCULUS URINARY ( 16 FDA reports)
DIABETIC MICROANGIOPATHY ( 16 FDA reports)
ESCHERICHIA INFECTION ( 16 FDA reports)
FAILURE TO THRIVE ( 16 FDA reports)
GINGIVAL ERYTHEMA ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
HYPERKERATOSIS ( 16 FDA reports)
INJECTION SITE REACTION ( 16 FDA reports)
INTESTINAL ISCHAEMIA ( 16 FDA reports)
IRRITABLE BOWEL SYNDROME ( 16 FDA reports)
LOCALISED OEDEMA ( 16 FDA reports)
LUMBAR RADICULOPATHY ( 16 FDA reports)
LUNG HYPERINFLATION ( 16 FDA reports)
MEDICATION RESIDUE ( 16 FDA reports)
MENINGIOMA ( 16 FDA reports)
MITRAL VALVE REPAIR ( 16 FDA reports)
ORAL PAIN ( 16 FDA reports)
PIGMENTATION DISORDER ( 16 FDA reports)
POOR DENTAL CONDITION ( 16 FDA reports)
RETINAL TEAR ( 16 FDA reports)
RUBELLA ( 16 FDA reports)
SLUGGISHNESS ( 16 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 16 FDA reports)
THROAT TIGHTNESS ( 16 FDA reports)
TIBIA FRACTURE ( 16 FDA reports)
VENOUS OCCLUSION ( 16 FDA reports)
VITREOUS DETACHMENT ( 16 FDA reports)
WOUND DEHISCENCE ( 16 FDA reports)
ABNORMAL SENSATION IN EYE ( 15 FDA reports)
ACETABULUM FRACTURE ( 15 FDA reports)
ACROCHORDON ( 15 FDA reports)
ANAPHYLACTIC SHOCK ( 15 FDA reports)
BODY TEMPERATURE INCREASED ( 15 FDA reports)
BREAST CANCER RECURRENT ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
CAROTID BRUIT ( 15 FDA reports)
CHOLECYSTITIS CHRONIC ( 15 FDA reports)
CORONARY ARTERY RESTENOSIS ( 15 FDA reports)
ENDOCARDITIS ( 15 FDA reports)
ENTERITIS ( 15 FDA reports)
EYELID OEDEMA ( 15 FDA reports)
EYELID PTOSIS ( 15 FDA reports)
FIBULA FRACTURE ( 15 FDA reports)
FORMICATION ( 15 FDA reports)
GINGIVAL RECESSION ( 15 FDA reports)
HAEMOLYSIS ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
HEPATOSPLENOMEGALY ( 15 FDA reports)
HYPERMETABOLISM ( 15 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 15 FDA reports)
IMPAIRED SELF-CARE ( 15 FDA reports)
LACERATION ( 15 FDA reports)
LIGAMENT SPRAIN ( 15 FDA reports)
MEDICAL DEVICE COMPLICATION ( 15 FDA reports)
MENIERE'S DISEASE ( 15 FDA reports)
MULTIPLE SCLEROSIS ( 15 FDA reports)
ORAL INTAKE REDUCED ( 15 FDA reports)
PAPILLOEDEMA ( 15 FDA reports)
PARTNER STRESS ( 15 FDA reports)
PETECHIAE ( 15 FDA reports)
PHARYNGITIS ( 15 FDA reports)
PHOTOSENSITIVITY REACTION ( 15 FDA reports)
PROCEDURAL COMPLICATION ( 15 FDA reports)
PROCTALGIA ( 15 FDA reports)
PROSTATITIS ( 15 FDA reports)
RADIUS FRACTURE ( 15 FDA reports)
RESPIRATORY RATE INCREASED ( 15 FDA reports)
RETINAL VEIN OCCLUSION ( 15 FDA reports)
RIGHT ATRIAL DILATATION ( 15 FDA reports)
ROSACEA ( 15 FDA reports)
SCARLET FEVER ( 15 FDA reports)
SKIN BURNING SENSATION ( 15 FDA reports)
STRESS URINARY INCONTINENCE ( 15 FDA reports)
TERMINAL STATE ( 15 FDA reports)
UTERINE POLYP ( 15 FDA reports)
ACNE ( 14 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 14 FDA reports)
BONE NEOPLASM ( 14 FDA reports)
CARDIAC OUTPUT DECREASED ( 14 FDA reports)
CLOSTRIDIAL INFECTION ( 14 FDA reports)
CONCUSSION ( 14 FDA reports)
CYANOSIS ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
DRESSLER'S SYNDROME ( 14 FDA reports)
ENDODONTIC PROCEDURE ( 14 FDA reports)
FACIAL BONES FRACTURE ( 14 FDA reports)
FAECES HARD ( 14 FDA reports)
GLOSSODYNIA ( 14 FDA reports)
HEPATIC CYST ( 14 FDA reports)
HICCUPS ( 14 FDA reports)
HIP ARTHROPLASTY ( 14 FDA reports)
HYPERTHYROIDISM ( 14 FDA reports)
LOSS OF LIBIDO ( 14 FDA reports)
LUNG CONSOLIDATION ( 14 FDA reports)
METASTASES TO LUNG ( 14 FDA reports)
NASAL SEPTUM DEVIATION ( 14 FDA reports)
NO THERAPEUTIC RESPONSE ( 14 FDA reports)
ORAL FIBROMA ( 14 FDA reports)
PARAESTHESIA ORAL ( 14 FDA reports)
PERITONITIS ( 14 FDA reports)
PLATELET COUNT INCREASED ( 14 FDA reports)
POOR QUALITY SLEEP ( 14 FDA reports)
POST HERPETIC NEURALGIA ( 14 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 14 FDA reports)
PROTEIN TOTAL DECREASED ( 14 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RESUSCITATION ( 14 FDA reports)
RHINITIS ( 14 FDA reports)
SCAB ( 14 FDA reports)
SCROTAL SWELLING ( 14 FDA reports)
SEPSIS SYNDROME ( 14 FDA reports)
SHOULDER PAIN ( 14 FDA reports)
SINUS HEADACHE ( 14 FDA reports)
SKIN CANCER ( 14 FDA reports)
STREPTOCOCCAL INFECTION ( 14 FDA reports)
TONGUE OEDEMA ( 14 FDA reports)
TRANSAMINASES INCREASED ( 14 FDA reports)
VOCAL CORD PARALYSIS ( 14 FDA reports)
WEIGHT FLUCTUATION ( 14 FDA reports)
ACUTE SINUSITIS ( 13 FDA reports)
AMENORRHOEA ( 13 FDA reports)
AORTIC VALVE CALCIFICATION ( 13 FDA reports)
ARTERIOVENOUS MALFORMATION ( 13 FDA reports)
BASOSQUAMOUS CARCINOMA ( 13 FDA reports)
BLEPHARITIS ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 13 FDA reports)
BRONCHIECTASIS ( 13 FDA reports)
CEREBRAL THROMBOSIS ( 13 FDA reports)
CHEST X-RAY ABNORMAL ( 13 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 13 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 13 FDA reports)
EJECTION FRACTION ABNORMAL ( 13 FDA reports)
EYE PRURITUS ( 13 FDA reports)
FAMILY STRESS ( 13 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 13 FDA reports)
HEPATIC LESION ( 13 FDA reports)
HEPATITIS C ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HILAR LYMPHADENOPATHY ( 13 FDA reports)
HISTOPLASMOSIS ( 13 FDA reports)
HYPERPHAGIA ( 13 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 13 FDA reports)
IRON DEFICIENCY ( 13 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 13 FDA reports)
KIDNEY ENLARGEMENT ( 13 FDA reports)
LABYRINTHITIS ( 13 FDA reports)
LIPIDS INCREASED ( 13 FDA reports)
MACULOPATHY ( 13 FDA reports)
MECHANICAL VENTILATION ( 13 FDA reports)
MICROALBUMINURIA ( 13 FDA reports)
NEPHROGENIC ANAEMIA ( 13 FDA reports)
NEPHROTIC SYNDROME ( 13 FDA reports)
OCCULT BLOOD ( 13 FDA reports)
ONYCHOCLASIS ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
PAIN OF SKIN ( 13 FDA reports)
PENILE SWELLING ( 13 FDA reports)
PERIRECTAL ABSCESS ( 13 FDA reports)
PICKWICKIAN SYNDROME ( 13 FDA reports)
PLEURITIC PAIN ( 13 FDA reports)
POLYMYALGIA RHEUMATICA ( 13 FDA reports)
POLYNEUROPATHY ( 13 FDA reports)
POLYP ( 13 FDA reports)
PROSTATE CANCER METASTATIC ( 13 FDA reports)
PROSTATIC DISORDER ( 13 FDA reports)
RAYNAUD'S PHENOMENON ( 13 FDA reports)
SKIN HYPERTROPHY ( 13 FDA reports)
SYSTOLIC DYSFUNCTION ( 13 FDA reports)
WEGENER'S GRANULOMATOSIS ( 13 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
ACUTE HEPATIC FAILURE ( 12 FDA reports)
ADDISON'S DISEASE ( 12 FDA reports)
AFFECTIVE DISORDER ( 12 FDA reports)
AMMONIA INCREASED ( 12 FDA reports)
BENIGN COLONIC NEOPLASM ( 12 FDA reports)
BILE DUCT OBSTRUCTION ( 12 FDA reports)
BONE MARROW OEDEMA ( 12 FDA reports)
BREAST CANCER FEMALE ( 12 FDA reports)
BREAST PAIN ( 12 FDA reports)
CARDIAC ENZYMES INCREASED ( 12 FDA reports)
CHONDROCALCINOSIS ( 12 FDA reports)
COMPLETED SUICIDE ( 12 FDA reports)
COR PULMONALE CHRONIC ( 12 FDA reports)
DEVICE OCCLUSION ( 12 FDA reports)
DIABETIC RETINAL OEDEMA ( 12 FDA reports)
DIABETIC ULCER ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 12 FDA reports)
FIBROSIS ( 12 FDA reports)
FRACTURE NONUNION ( 12 FDA reports)
GASTRODUODENITIS ( 12 FDA reports)
GRAND MAL CONVULSION ( 12 FDA reports)
HAEMANGIOMA ( 12 FDA reports)
HAEMOTHORAX ( 12 FDA reports)
HYDROCEPHALUS ( 12 FDA reports)
ILIAC ARTERY STENOSIS ( 12 FDA reports)
INCOHERENT ( 12 FDA reports)
INTRACRANIAL ANEURYSM ( 12 FDA reports)
IRITIS ( 12 FDA reports)
KETOACIDOSIS ( 12 FDA reports)
LIP HAEMORRHAGE ( 12 FDA reports)
MENSTRUAL DISORDER ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
NASAL POLYPS ( 12 FDA reports)
NEOVASCULARISATION ( 12 FDA reports)
NEUTROPHIL COUNT DECREASED ( 12 FDA reports)
ORAL DISCOMFORT ( 12 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 12 FDA reports)
PAPULE ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
PATELLA FRACTURE ( 12 FDA reports)
PELVIC PAIN ( 12 FDA reports)
POST PROCEDURAL INFECTION ( 12 FDA reports)
RASH PAPULAR ( 12 FDA reports)
REFLUX OESOPHAGITIS ( 12 FDA reports)
SCLERODERMA ( 12 FDA reports)
SKIN INJURY ( 12 FDA reports)
SKIN NECROSIS ( 12 FDA reports)
SOFT TISSUE DISORDER ( 12 FDA reports)
SPINAL COLUMN INJURY ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
TENOSYNOVITIS STENOSANS ( 12 FDA reports)
TINEA PEDIS ( 12 FDA reports)
TONGUE DISCOLOURATION ( 12 FDA reports)
VASCULAR PSEUDOANEURYSM ( 12 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 12 FDA reports)
WRONG DRUG ADMINISTERED ( 12 FDA reports)
ACCIDENTAL EXPOSURE ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 11 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 11 FDA reports)
BLOOD CULTURE POSITIVE ( 11 FDA reports)
BLOODY DISCHARGE ( 11 FDA reports)
BONE FRAGMENTATION ( 11 FDA reports)
BRADYARRHYTHMIA ( 11 FDA reports)
CARDIAC ABLATION ( 11 FDA reports)
CARDIAC SEPTAL DEFECT ( 11 FDA reports)
CATHETER RELATED INFECTION ( 11 FDA reports)
CREPITATIONS ( 11 FDA reports)
DENTAL DISCOMFORT ( 11 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 11 FDA reports)
DERMATITIS CONTACT ( 11 FDA reports)
DERMOID CYST ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 11 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 11 FDA reports)
FEELING DRUNK ( 11 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 11 FDA reports)
HYPERCAPNIA ( 11 FDA reports)
HYPERTENSIVE EMERGENCY ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
INJECTION SITE DISCOMFORT ( 11 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 11 FDA reports)
LARYNGEAL CYST ( 11 FDA reports)
LIP SWELLING ( 11 FDA reports)
LUNG INJURY ( 11 FDA reports)
MENORRHAGIA ( 11 FDA reports)
MUCOSAL ULCERATION ( 11 FDA reports)
NAIL DYSTROPHY ( 11 FDA reports)
ORAL HERPES ( 11 FDA reports)
OSTEOMALACIA ( 11 FDA reports)
OTITIS EXTERNA ( 11 FDA reports)
PERFORMANCE STATUS DECREASED ( 11 FDA reports)
PHARYNGEAL OEDEMA ( 11 FDA reports)
POSTNASAL DRIP ( 11 FDA reports)
POSTOPERATIVE INFECTION ( 11 FDA reports)
PRESBYOPIA ( 11 FDA reports)
PROTEIN URINE PRESENT ( 11 FDA reports)
RESPIRATORY TRACT INFECTION ( 11 FDA reports)
RETINAL ANEURYSM ( 11 FDA reports)
SINUS POLYP ( 11 FDA reports)
SKIN LESION ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 11 FDA reports)
STAPHYLOMA ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TRACHEAL DEVIATION ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
UTERINE ENLARGEMENT ( 11 FDA reports)
VASCULAR GRAFT OCCLUSION ( 11 FDA reports)
VENOUS STASIS ( 11 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
VOCAL CORD THICKENING ( 11 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 11 FDA reports)
ABDOMINAL TENDERNESS ( 10 FDA reports)
ABNORMAL FAECES ( 10 FDA reports)
ADRENAL MASS ( 10 FDA reports)
AFFECT LABILITY ( 10 FDA reports)
AGEUSIA ( 10 FDA reports)
ANAL FISSURE ( 10 FDA reports)
ANAL FISTULA ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
AORTIC DISSECTION ( 10 FDA reports)
APTYALISM ( 10 FDA reports)
ARTERIAL BYPASS OPERATION ( 10 FDA reports)
AUTOIMMUNE HEPATITIS ( 10 FDA reports)
BLOOD PRESSURE ( 10 FDA reports)
BONE DENSITY DECREASED ( 10 FDA reports)
BONE EROSION ( 10 FDA reports)
BORDERLINE GLAUCOMA ( 10 FDA reports)
CARDIAC FIBRILLATION ( 10 FDA reports)
CARDIAC VALVE SCLEROSIS ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 10 FDA reports)
COLOUR BLINDNESS ( 10 FDA reports)
DEAFNESS NEUROSENSORY ( 10 FDA reports)
DERMATITIS ( 10 FDA reports)
DYSGRAPHIA ( 10 FDA reports)
EAR INFECTION ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 10 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 10 FDA reports)
FACIAL NEURALGIA ( 10 FDA reports)
FAT TISSUE INCREASED ( 10 FDA reports)
FISTULA ( 10 FDA reports)
HEART TRANSPLANT ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HOARSENESS ( 10 FDA reports)
HYPERPARATHYROIDISM ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
INFECTED SKIN ULCER ( 10 FDA reports)
INGROWING NAIL ( 10 FDA reports)
INJECTION SITE SWELLING ( 10 FDA reports)
INTESTINAL HAEMORRHAGE ( 10 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 10 FDA reports)
KYPHOSCOLIOSIS ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
MALOCCLUSION ( 10 FDA reports)
MASTOIDITIS ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
NOCTURNAL DYSPNOEA ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
OSTEITIS DEFORMANS ( 10 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 10 FDA reports)
PEAU D'ORANGE ( 10 FDA reports)
PERSONALITY CHANGE ( 10 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 10 FDA reports)
PLANTAR FASCIITIS ( 10 FDA reports)
PLASMACYTOSIS ( 10 FDA reports)
PULPITIS DENTAL ( 10 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 10 FDA reports)
PYELOCALIECTASIS ( 10 FDA reports)
RENAL ATROPHY ( 10 FDA reports)
RESORPTION BONE INCREASED ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
SPONDYLOLYSIS ( 10 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 10 FDA reports)
TEMPERATURE INTOLERANCE ( 10 FDA reports)
TENSION HEADACHE ( 10 FDA reports)
THROMBOCYTOSIS ( 10 FDA reports)
TONGUE DISORDER ( 10 FDA reports)
TOOTH INJURY ( 10 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 10 FDA reports)
VAGINAL INFECTION ( 10 FDA reports)
ADVERSE REACTION ( 9 FDA reports)
ANAEMIA POSTOPERATIVE ( 9 FDA reports)
APPENDIX DISORDER ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
BLEPHAROSPASM ( 9 FDA reports)
BLOOD COUNT ABNORMAL ( 9 FDA reports)
BLOOD TEST ABNORMAL ( 9 FDA reports)
BONE OPERATION ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 9 FDA reports)
CALCULUS URETERIC ( 9 FDA reports)
CAROTID ENDARTERECTOMY ( 9 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 9 FDA reports)
CUTIS LAXA ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 9 FDA reports)
DROOLING ( 9 FDA reports)
DRUG DEPENDENCE ( 9 FDA reports)
DYSTONIA ( 9 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 9 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 9 FDA reports)
EMBOLISM ( 9 FDA reports)
FACE INJURY ( 9 FDA reports)
FEMORAL ARTERY OCCLUSION ( 9 FDA reports)
FOETAL ARRHYTHMIA ( 9 FDA reports)
FOOD POISONING ( 9 FDA reports)
GALLOP RHYTHM PRESENT ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
GINGIVAL EROSION ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEPATIC PAIN ( 9 FDA reports)
HIDRADENITIS ( 9 FDA reports)
HYPERCHLORHYDRIA ( 9 FDA reports)
HYPERKINESIA ( 9 FDA reports)
HYPERNATRAEMIA ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
HYPOTRICHOSIS ( 9 FDA reports)
INITIAL INSOMNIA ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
JAUNDICE NEONATAL ( 9 FDA reports)
LIGAMENT RUPTURE ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 9 FDA reports)
METAMORPHOPSIA ( 9 FDA reports)
MICROANGIOPATHY ( 9 FDA reports)
MICROCYTIC ANAEMIA ( 9 FDA reports)
MULTIPLE ALLERGIES ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
NEOPLASM ( 9 FDA reports)
NEPHRITIS ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEUROLOGICAL SYMPTOM ( 9 FDA reports)
OPTIC ATROPHY ( 9 FDA reports)
ORAL CAVITY FISTULA ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
OSTEORADIONECROSIS ( 9 FDA reports)
OTITIS MEDIA ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PAROSMIA ( 9 FDA reports)
PAROTID GLAND ENLARGEMENT ( 9 FDA reports)
PERONEAL NERVE PALSY ( 9 FDA reports)
PNEUMONIA BACTERIAL ( 9 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 9 FDA reports)
PREMATURE BABY ( 9 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
RENAL COLIC ( 9 FDA reports)
RENAL PAIN ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SOCIAL PROBLEM ( 9 FDA reports)
STERNAL FRACTURE ( 9 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 9 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 9 FDA reports)
TENDON RUPTURE ( 9 FDA reports)
URETHRAL STENOSIS ( 9 FDA reports)
URINARY TRACT DISORDER ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
UVEITIS ( 9 FDA reports)
VENTRICLE RUPTURE ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
VESTIBULAR DISORDER ( 9 FDA reports)
VITAMIN B12 DECREASED ( 9 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 9 FDA reports)
WOUND ( 9 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ACCIDENTAL NEEDLE STICK ( 8 FDA reports)
ADENOCARCINOMA PANCREAS ( 8 FDA reports)
AKINESIA ( 8 FDA reports)
AMPUTATION ( 8 FDA reports)
APATHY ( 8 FDA reports)
ARTHROSCOPIC SURGERY ( 8 FDA reports)
BARRETT'S OESOPHAGUS ( 8 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CARDIOVERSION ( 8 FDA reports)
CATARACT CORTICAL ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CHANGE OF BOWEL HABIT ( 8 FDA reports)
CHOLECYSTITIS ACUTE ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
COLON POLYPECTOMY ( 8 FDA reports)
CYSTITIS HAEMORRHAGIC ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIABETIC FOOT INFECTION ( 8 FDA reports)
DRUG SCREEN POSITIVE ( 8 FDA reports)
DRY THROAT ( 8 FDA reports)
DYSPLASIA ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
EXPOSURE TO TOXIC AGENT ( 8 FDA reports)
EYE LASER SURGERY ( 8 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 8 FDA reports)
FOOD AVERSION ( 8 FDA reports)
FOOT AMPUTATION ( 8 FDA reports)
GALLBLADDER ENLARGEMENT ( 8 FDA reports)
GASTRIC OPERATION ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
GRAVITATIONAL OEDEMA ( 8 FDA reports)
HAEMORRHAGE URINARY TRACT ( 8 FDA reports)
HAEMORRHAGIC DIATHESIS ( 8 FDA reports)
HAIR GROWTH ABNORMAL ( 8 FDA reports)
HAIR TEXTURE ABNORMAL ( 8 FDA reports)
HANGOVER ( 8 FDA reports)
HEART RATE ABNORMAL ( 8 FDA reports)
HEMIANOPIA HOMONYMOUS ( 8 FDA reports)
HEPATOJUGULAR REFLUX ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
HYPOCHROMIC ANAEMIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
IMMUNE SYSTEM DISORDER ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INCISIONAL DRAINAGE ( 8 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 8 FDA reports)
INTUBATION ( 8 FDA reports)
JUDGEMENT IMPAIRED ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
MASS ( 8 FDA reports)
METAPLASIA ( 8 FDA reports)
METASTASES TO SPINE ( 8 FDA reports)
MITRAL VALVE SCLEROSIS ( 8 FDA reports)
MUSCLE FATIGUE ( 8 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 8 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 8 FDA reports)
NO ADVERSE EFFECT ( 8 FDA reports)
OESOPHAGEAL PAIN ( 8 FDA reports)
OROPHARYNGEAL SWELLING ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PERIORBITAL OEDEMA ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
POLYTRAUMATISM ( 8 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 8 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 8 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 8 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 8 FDA reports)
RENAL CELL CARCINOMA ( 8 FDA reports)
RENAL HAEMORRHAGE ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SELF-MEDICATION ( 8 FDA reports)
SENSATION OF FOREIGN BODY ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SKIN REACTION ( 8 FDA reports)
SPUTUM DISCOLOURED ( 8 FDA reports)
STRESS CARDIOMYOPATHY ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
THROMBOPHLEBITIS ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
TRAUMATIC RENAL INJURY ( 8 FDA reports)
ULNA FRACTURE ( 8 FDA reports)
UNDERDOSE ( 8 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 8 FDA reports)
VASCULAR DEMENTIA ( 8 FDA reports)
VEIN DISORDER ( 8 FDA reports)
WALKING DISABILITY ( 8 FDA reports)
ALBUMIN URINE PRESENT ( 7 FDA reports)
ANGIOMYOLIPOMA ( 7 FDA reports)
APPENDICECTOMY ( 7 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 7 FDA reports)
ARTHROPOD BITE ( 7 FDA reports)
ASPIRATION PLEURAL CAVITY ( 7 FDA reports)
BLADDER CANCER STAGE IV ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD CALCIUM INCREASED ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BLOOD CHOLESTEROL ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD URINE ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BREAST CANCER METASTATIC ( 7 FDA reports)
BRONCHIAL DISORDER ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CALCINOSIS ( 7 FDA reports)
CARDIAC INFECTION ( 7 FDA reports)
CATARACT NUCLEAR ( 7 FDA reports)
CAUDA EQUINA SYNDROME ( 7 FDA reports)
CHEST INJURY ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 7 FDA reports)
COLON ADENOMA ( 7 FDA reports)
COMMUNICATION DISORDER ( 7 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
CORONARY ARTERY REOCCLUSION ( 7 FDA reports)
CORONARY ARTERY SURGERY ( 7 FDA reports)
COSTOCHONDRITIS ( 7 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
CYST ( 7 FDA reports)
DERMATITIS BULLOUS ( 7 FDA reports)
DEVICE LEAKAGE ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DRUG PRESCRIBING ERROR ( 7 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 7 FDA reports)
EMBOLISM ARTERIAL ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 7 FDA reports)
EYE DISCHARGE ( 7 FDA reports)
EYE OPERATION ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 7 FDA reports)
FOETAL GROWTH RETARDATION ( 7 FDA reports)
FRACTURED COCCYX ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
HEART VALVE STENOSIS ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HERNIA REPAIR ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 7 FDA reports)
HYPEROSMOLAR STATE ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
HYPOTONIA NEONATAL ( 7 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
INCISION SITE PAIN ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 7 FDA reports)
ISCHAEMIC HEPATITIS ( 7 FDA reports)
KNEE OPERATION ( 7 FDA reports)
LACRIMATION DECREASED ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
MACROCYTOSIS ( 7 FDA reports)
MANIA ( 7 FDA reports)
MEAN CELL VOLUME INCREASED ( 7 FDA reports)
MITRAL VALVE REPLACEMENT ( 7 FDA reports)
NASAL ULCER ( 7 FDA reports)
ODYNOPHAGIA ( 7 FDA reports)
OEDEMA GENITAL ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
PANCREATITIS RELAPSING ( 7 FDA reports)
PARESIS ( 7 FDA reports)
PERNICIOUS ANAEMIA ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
PRINZMETAL ANGINA ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
REGURGITATION ( 7 FDA reports)
RENAL SURGERY ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SHOULDER DEFORMITY ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SKIN HYPERPIGMENTATION ( 7 FDA reports)
SPINAL LAMINECTOMY ( 7 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
STARING ( 7 FDA reports)
TESTICULAR MASS ( 7 FDA reports)
TOOTH IMPACTED ( 7 FDA reports)
TRAUMATIC BRAIN INJURY ( 7 FDA reports)
ULCER HAEMORRHAGE ( 7 FDA reports)
UMBILICAL HERNIA ( 7 FDA reports)
URINE ABNORMALITY ( 7 FDA reports)
URINE OUTPUT INCREASED ( 7 FDA reports)
UTERINE CANCER ( 7 FDA reports)
VASCULAR STENOSIS ( 7 FDA reports)
VITAMIN K DEFICIENCY ( 7 FDA reports)
VOMITING PROJECTILE ( 7 FDA reports)
YELLOW SKIN ( 7 FDA reports)
ABSCESS JAW ( 6 FDA reports)
ABSCESS LIMB ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ANGIOGRAM ABNORMAL ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
AORTIC VALVE REPAIR ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
APPLICATION SITE REACTION ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BIOPSY LIVER ABNORMAL ( 6 FDA reports)
BLADDER NEOPLASM ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BONE GRAFT ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BREAST CYST ( 6 FDA reports)
BREAST NEOPLASM ( 6 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 6 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 6 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 6 FDA reports)
CAROTID ARTERY ANEURYSM ( 6 FDA reports)
CEREBELLAR HAEMORRHAGE ( 6 FDA reports)
CERVICOBRACHIAL SYNDROME ( 6 FDA reports)
CLOSTRIDIUM COLITIS ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 6 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
DIABETIC VASCULAR DISORDER ( 6 FDA reports)
DROP ATTACKS ( 6 FDA reports)
EAR DISCOMFORT ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
FRUSTRATION ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
GASTROSTOMY ( 6 FDA reports)
GLOBULINS INCREASED ( 6 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 6 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 6 FDA reports)
GRIP STRENGTH DECREASED ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HYPERCOAGULATION ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
ILIAC ARTERY OCCLUSION ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
INJECTION SITE MASS ( 6 FDA reports)
LIPOMA ( 6 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 6 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 6 FDA reports)
MALLORY-WEISS SYNDROME ( 6 FDA reports)
MAMMOGRAM ABNORMAL ( 6 FDA reports)
MELANOSIS COLI ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MITRAL VALVE STENOSIS ( 6 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 6 FDA reports)
MIXED HYPERLIPIDAEMIA ( 6 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 6 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 6 FDA reports)
MUSCLE NECROSIS ( 6 FDA reports)
MYDRIASIS ( 6 FDA reports)
MYELOPATHY ( 6 FDA reports)
NARCOTIC INTOXICATION ( 6 FDA reports)
NASOPHARYNGEAL DISORDER ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 6 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER ( 6 FDA reports)
NYSTAGMUS ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OLIGOHYDRAMNIOS ( 6 FDA reports)
OMPHALITIS ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
ORAL SURGERY ( 6 FDA reports)
PANCREATIC INSUFFICIENCY ( 6 FDA reports)
PANCREATIC PSEUDOCYST ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PERSONALITY DISORDER ( 6 FDA reports)
PHYSICAL ASSAULT ( 6 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 6 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SCAPULA FRACTURE ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
SEBORRHOEIC KERATOSIS ( 6 FDA reports)
SELF MUTILATION ( 6 FDA reports)
SENSITIVITY OF TEETH ( 6 FDA reports)
SERUM FERRITIN DECREASED ( 6 FDA reports)
SKIN ODOUR ABNORMAL ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
STOOL ANALYSIS ABNORMAL ( 6 FDA reports)
STRABISMUS ( 6 FDA reports)
STRESS SYMPTOMS ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SYNOVIAL CYST ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
TOXIC ENCEPHALOPATHY ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
UNINTENDED PREGNANCY ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
VASCULAR BYPASS GRAFT ( 6 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 6 FDA reports)
ACCIDENT ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ADRENAL NEOPLASM ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALVEOLOPLASTY ( 5 FDA reports)
ANION GAP INCREASED ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APHONIA ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ATROPHY ( 5 FDA reports)
BACTERIA URINE IDENTIFIED ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BIPOLAR I DISORDER ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD ARSENIC INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD COPPER DECREASED ( 5 FDA reports)
BLOOD INSULIN INCREASED ( 5 FDA reports)
BLOOD IRON ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 5 FDA reports)
BRADYPHRENIA ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST INFECTION ( 5 FDA reports)
BREAST SWELLING ( 5 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 5 FDA reports)
CARBON DIOXIDE DECREASED ( 5 FDA reports)
CARCINOID TUMOUR ( 5 FDA reports)
CARDIAC STRESS TEST ( 5 FDA reports)
CEREBELLAR ATROPHY ( 5 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 5 FDA reports)
CEREBRAL ARTERY STENOSIS ( 5 FDA reports)
CEREBRAL HYPOPERFUSION ( 5 FDA reports)
CEREBRAL MICROANGIOPATHY ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CYSTOCELE ( 5 FDA reports)
CYSTOCELE REPAIR ( 5 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DRUG EFFECT INCREASED ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
DYSPHEMIA ( 5 FDA reports)
DYSPNOEA AT REST ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYE INFECTION VIRAL ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
EYEBALL AVULSION ( 5 FDA reports)
EYELID FUNCTION DISORDER ( 5 FDA reports)
FEBRILE BONE MARROW APLASIA ( 5 FDA reports)
FISTULA DISCHARGE ( 5 FDA reports)
FLUID IMBALANCE ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC MASS ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPERTROPHY ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INJECTION SITE COLDNESS ( 5 FDA reports)
INJECTION SITE DISCOLOURATION ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 5 FDA reports)
INTRAOCULAR LENS IMPLANT ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LIVER OPERATION ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MONOCYTOSIS ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NEUROPATHIC ARTHROPATHY ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
NIGHT CRAMPS ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OESOPHAGEAL CARCINOMA ( 5 FDA reports)
OPEN REDUCTION OF FRACTURE ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PERIARTHRITIS ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
POLYCYTHAEMIA ( 5 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
PROTEIN TOTAL INCREASED ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PYURIA ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
READING DISORDER ( 5 FDA reports)
REGURGITATION OF FOOD ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RETINAL EXUDATES ( 5 FDA reports)
RETINAL SCAR ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 5 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SKIN INFECTION ( 5 FDA reports)
SKIN MASS ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
SUBACUTE ENDOCARDITIS ( 5 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 5 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
TOOTH REPAIR ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 4 FDA reports)
ACUTE STRESS DISORDER ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
AGORAPHOBIA ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
ALVEOLITIS FIBROSING ( 4 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
APPLICATION SITE DERMATITIS ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
ATRIAL THROMBOSIS ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BENIGN HEPATIC NEOPLASM ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BITE ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLADDER PROLAPSE ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BREAST ABSCESS ( 4 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 4 FDA reports)
BURKITT'S LYMPHOMA ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CARDIAC VENTRICULOGRAM ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
CAROTID ARTERY DISSECTION ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CLOSED HEAD INJURY ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
COLONOSCOPY ABNORMAL ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CORONARY ARTERY EMBOLISM ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DYSMENORRHOEA ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
EJECTION FRACTION ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ENDARTERECTOMY ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXCESSIVE MASTURBATION ( 4 FDA reports)
EXFOLIATIVE RASH ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE REDNESS ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FISTULA REPAIR ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GESTATIONAL DIABETES ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT THROMBOSIS ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HAEMORRHAGIC INFARCTION ( 4 FDA reports)
HAIR COLOUR CHANGES ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEPATIC ADENOMA ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HOMICIDAL IDEATION ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 4 FDA reports)
INTESTINAL MASS ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LICHEN PLANUS ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LUNG CREPITATION ( 4 FDA reports)
MALE SEXUAL DYSFUNCTION ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MYELOMA RECURRENCE ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NEOPLASM PROSTATE ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OESOPHAGEAL STENOSIS ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
ONYCHOPHAGIA ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATIC DUCT DILATATION ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 4 FDA reports)
RECTAL FISTULA REPAIR ( 4 FDA reports)
REFLUX GASTRITIS ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RETINAL ARTERY EMBOLISM ( 4 FDA reports)
RETINAL PIGMENTATION ( 4 FDA reports)
RETINOPATHY PROLIFERATIVE ( 4 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN NODULE ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SKIN WARM ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUBCUTANEOUS NODULE ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SYMBOLIC DYSFUNCTION ( 4 FDA reports)
THALAMUS HAEMORRHAGE ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THIRST DECREASED ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 4 FDA reports)
THYROID MASS ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TORTICOLLIS ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TROPONIN I INCREASED ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
URETHRAL DISCHARGE ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
VERTEBROPLASTY ( 4 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 4 FDA reports)
VOLUME BLOOD DECREASED ( 4 FDA reports)
VULVOVAGINAL PRURITUS ( 4 FDA reports)
WALLENBERG SYNDROME ( 4 FDA reports)
WEIGHT ( 4 FDA reports)
WOUND DRAINAGE ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APOLIPOPROTEIN A-I DECREASED ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTERIAL REPAIR ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
AXILLARY VEIN THROMBOSIS ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BIOPSY BREAST ABNORMAL ( 3 FDA reports)
BLADDER ABLATION ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD KETONE BODY ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BODY HEIGHT BELOW NORMAL ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CALCIPHYLAXIS ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CENTRAL PAIN SYNDROME ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CERVICAL MYELOPATHY ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHRONIC FATIGUE SYNDROME ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
COLECTOMY PARTIAL ( 3 FDA reports)
COMMINUTED FRACTURE ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DIVORCED ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSACUSIS ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 3 FDA reports)
ERYTHROSIS ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 3 FDA reports)
EXTREMITY CONTRACTURE ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FATTY LIVER ALCOHOLIC ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
FUNGAL PERITONITIS ( 3 FDA reports)
GANGLION ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTRIC ILEUS ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HORMONE LEVEL ABNORMAL ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERINSULINAEMIA ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INJECTION SITE DESQUAMATION ( 3 FDA reports)
INJECTION SITE SCAR ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INTESTINAL GANGRENE ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LIMB OPERATION ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MACULAR PSEUDOHOLE ( 3 FDA reports)
MAMMARY DUCT ECTASIA ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MASTITIS ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MONONEURITIS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MYOCARDIAL RUPTURE ( 3 FDA reports)
MYODESOPSIA ( 3 FDA reports)
MYOGLOBINURIA ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 3 FDA reports)
NORMAL TENSION GLAUCOMA ( 3 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OPTIC NERVE CUPPING ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
ORTHOSTATIC INTOLERANCE ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREAS INFECTION ( 3 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PATIENT ISOLATION ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERICARDIAL CALCIFICATION ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
PHOTOCOAGULATION ( 3 FDA reports)
PLEURAL HAEMORRHAGE ( 3 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETINAL NEOVASCULARISATION ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SCIATIC NERVE INJURY ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SHIFT TO THE LEFT ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINOBRONCHITIS ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKULL X-RAY ABNORMAL ( 3 FDA reports)
SOFT TISSUE INFLAMMATION ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STENT MALFUNCTION ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
THYROID ADENOMA ( 3 FDA reports)
THYROID CYST ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TONGUE HAEMATOMA ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONGUE INJURY ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TRICUSPID VALVE REPAIR ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
TWIN PREGNANCY ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URETHRAL PAIN ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENA CAVA FILTER INSERTION ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VENTRICULAR ASYSTOLE ( 3 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VITRECTOMY ( 3 FDA reports)
VITREOUS DISORDER ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL CORTEX NECROSIS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
AMAUROSIS FUGAX ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE PUSTULES ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
BACK CRUSHING ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD CAFFEINE INCREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 2 FDA reports)
BREAST ATROPHY ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST CYST EXCISION ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST ENGORGEMENT ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATARACT DIABETIC ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLELITHOTOMY ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHONDROMATOSIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHOROIDITIS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR INCREASED ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
COX-MAZE PROCEDURE ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DENTAL NECROSIS ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DERMOGRAPHISM ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
EARLY RETIREMENT ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ELBOW DEFORMITY ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ENCHONDROMA ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EYE DEGENERATIVE DISORDER ( 2 FDA reports)
EYELID INFECTION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FAT NECROSIS OF BREAST ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC LAVAGE ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENITAL PRURITUS MALE ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 2 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HAND DERMATITIS ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HEPATITIS INFECTIOUS ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HETEROPHORIA ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HYPERCHROMASIA ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERINSULINISM ( 2 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
ILLITERACY ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFERTILITY FEMALE ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ( 2 FDA reports)
IODINE ALLERGY ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT LIGAMENT RUPTURE ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LAGOPHTHALMOS ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LERICHE SYNDROME ( 2 FDA reports)
LEUKOENCEPHALOMYELITIS ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LICE INFESTATION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MUCORMYCOSIS ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ONCOCYTOMA ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL DECORTICATION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
PROSTATE CANCER STAGE I ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL MICROANEURYSMS ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RHABDOMYOSARCOMA ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RIB DEFORMITY ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SCROTAL INFECTION ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THERMOHYPOAESTHESIA ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROMBOEMBOLIC STROKE ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC DILATATION OF COLON ( 2 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL OBSTRUCTION ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETERAL NEOPLASM ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URTICARIA LOCALISED ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VAGINAL ABSCESS ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR ASSIST DEVICE INSERTION ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VENTRICULAR REMODELING ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VIRAL TRACHEITIS ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VITREOUS INJURY ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION SPONTANEOUS INCOMPLETE ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-2 MACROGLOBULIN INCREASED ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMMONIA ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL CANCER STAGE 0 ( 1 FDA reports)
ANAL FISSURE EXCISION ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APOLIPOPROTEIN A-II DECREASED ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BERYLLIOSIS ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CATHETER REPLACEMENT ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA METASTATIC ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD SELENIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANCER IN REMISSION ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC AUTONOMIC NEUROPATHY ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OUTPUT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERITIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL JAW MALFORMATION ( 1 FDA reports)
CONGENITAL NAIL DISORDER ( 1 FDA reports)
CONJUNCTIVAL CYST ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY ENDARTERECTOMY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CORTISOL FREE URINE INCREASED ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED INSULIN REQUIREMENT ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC GLAUCOMA ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DURAL FISTULA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR NEOPLASM MALIGNANT ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMERGENCY CARE EXAMINATION ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALITIS POST VARICELLA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPENDYMOMA MALIGNANT ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULGURATION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL CYST ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOCRIT NORMAL ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOPHILUS SEPSIS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC ENZYME ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYDRAEMIA ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INADEQUATE LUBRICATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTIOUS DISEASE CARRIER ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRANASAL HYPOAESTHESIA ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ITCHING SCAR ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DUCT NEOPLASM ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LIPIDS ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT RENAL HYPERTENSION ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE GRAFT ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODDING OF HEAD ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OSTEOMYELITIS DRAINAGE ( 1 FDA reports)
OTITIS EXTERNA FUNGAL ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
OVULATION INDUCTION ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE PROSTHESIS INSERTION ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POTTER'S SYNDROME ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PREVENTIVE SURGERY ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE INDURATION ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REMOVAL OF FOREIGN BODY ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL TUMOUR EXCISION ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY SIGHS ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL CYST ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOMOGYI PHENOMENON ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBSTANCE ABUSER ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TIC ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA METASTATIC ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE ABNORMAL ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND SCAN ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE COPPER DECREASED ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROSTOMY COMPLICATION ( 1 FDA reports)
URTICARIA CONTACT ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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