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

DRUG INTERACTION ( 1663 FDA reports)
RENAL FAILURE ACUTE ( 1660 FDA reports)
DYSPNOEA ( 1400 FDA reports)
VOMITING ( 1151 FDA reports)
DIARRHOEA ( 1145 FDA reports)
NAUSEA ( 1083 FDA reports)
HYPOTENSION ( 1037 FDA reports)
DIZZINESS ( 929 FDA reports)
FALL ( 927 FDA reports)
RENAL FAILURE ( 894 FDA reports)
ASTHENIA ( 872 FDA reports)
FATIGUE ( 822 FDA reports)
MALAISE ( 807 FDA reports)
MYOCARDIAL INFARCTION ( 777 FDA reports)
ATRIAL FIBRILLATION ( 768 FDA reports)
ANAEMIA ( 762 FDA reports)
CONFUSIONAL STATE ( 736 FDA reports)
HYPERTENSION ( 727 FDA reports)
DEHYDRATION ( 719 FDA reports)
PNEUMONIA ( 712 FDA reports)
CHEST PAIN ( 699 FDA reports)
PYREXIA ( 691 FDA reports)
SYNCOPE ( 654 FDA reports)
OEDEMA PERIPHERAL ( 637 FDA reports)
RHABDOMYOLYSIS ( 628 FDA reports)
BLOOD CREATININE INCREASED ( 621 FDA reports)
HEADACHE ( 607 FDA reports)
HYPERKALAEMIA ( 605 FDA reports)
CARDIAC FAILURE ( 596 FDA reports)
PAIN ( 591 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 588 FDA reports)
HAEMOGLOBIN DECREASED ( 585 FDA reports)
HYPONATRAEMIA ( 568 FDA reports)
PAIN IN EXTREMITY ( 541 FDA reports)
ABDOMINAL PAIN ( 492 FDA reports)
MYALGIA ( 490 FDA reports)
DRUG INEFFECTIVE ( 482 FDA reports)
PRURITUS ( 476 FDA reports)
THROMBOCYTOPENIA ( 473 FDA reports)
WEIGHT DECREASED ( 471 FDA reports)
SOMNOLENCE ( 458 FDA reports)
SEPSIS ( 445 FDA reports)
URINARY TRACT INFECTION ( 435 FDA reports)
BLOOD GLUCOSE INCREASED ( 434 FDA reports)
CEREBROVASCULAR ACCIDENT ( 434 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 433 FDA reports)
DEATH ( 433 FDA reports)
BLOOD PRESSURE INCREASED ( 430 FDA reports)
ARTHRALGIA ( 429 FDA reports)
CONDITION AGGRAVATED ( 426 FDA reports)
LOSS OF CONSCIOUSNESS ( 418 FDA reports)
COUGH ( 416 FDA reports)
DEPRESSION ( 416 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 416 FDA reports)
BACK PAIN ( 404 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 381 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 376 FDA reports)
ANXIETY ( 375 FDA reports)
BRADYCARDIA ( 372 FDA reports)
RENAL IMPAIRMENT ( 369 FDA reports)
RASH ( 350 FDA reports)
FLUSHING ( 348 FDA reports)
CARDIAC ARREST ( 344 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 337 FDA reports)
MUSCULAR WEAKNESS ( 336 FDA reports)
GAIT DISTURBANCE ( 330 FDA reports)
ABDOMINAL PAIN UPPER ( 329 FDA reports)
HYPOGLYCAEMIA ( 328 FDA reports)
PARAESTHESIA ( 327 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 325 FDA reports)
CONVULSION ( 323 FDA reports)
MUSCLE SPASMS ( 316 FDA reports)
CONSTIPATION ( 311 FDA reports)
HYPOAESTHESIA ( 308 FDA reports)
OVERDOSE ( 306 FDA reports)
PALPITATIONS ( 300 FDA reports)
ANGIOEDEMA ( 298 FDA reports)
PLEURAL EFFUSION ( 296 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 290 FDA reports)
PULMONARY EMBOLISM ( 290 FDA reports)
HYPERHIDROSIS ( 289 FDA reports)
TACHYCARDIA ( 287 FDA reports)
ANGINA PECTORIS ( 285 FDA reports)
TREMOR ( 278 FDA reports)
CORONARY ARTERY DISEASE ( 273 FDA reports)
ERYTHEMA ( 270 FDA reports)
INSOMNIA ( 268 FDA reports)
PLATELET COUNT DECREASED ( 267 FDA reports)
HALLUCINATION ( 264 FDA reports)
NEUTROPENIA ( 261 FDA reports)
LACTIC ACIDOSIS ( 259 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 259 FDA reports)
MULTI-ORGAN FAILURE ( 258 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 252 FDA reports)
PULMONARY OEDEMA ( 247 FDA reports)
DIABETES MELLITUS ( 246 FDA reports)
DECREASED APPETITE ( 245 FDA reports)
BLOOD UREA INCREASED ( 241 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 233 FDA reports)
INFECTION ( 232 FDA reports)
HYPOKALAEMIA ( 231 FDA reports)
BLOOD PRESSURE DECREASED ( 226 FDA reports)
RECTAL HAEMORRHAGE ( 226 FDA reports)
VISION BLURRED ( 226 FDA reports)
RESPIRATORY FAILURE ( 219 FDA reports)
DEEP VEIN THROMBOSIS ( 217 FDA reports)
ARRHYTHMIA ( 212 FDA reports)
PANCYTOPENIA ( 210 FDA reports)
FEELING ABNORMAL ( 209 FDA reports)
MEMORY IMPAIRMENT ( 209 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 203 FDA reports)
DYSPHAGIA ( 202 FDA reports)
LETHARGY ( 201 FDA reports)
CHILLS ( 196 FDA reports)
CARDIAC DISORDER ( 195 FDA reports)
HAEMATEMESIS ( 195 FDA reports)
VISUAL IMPAIRMENT ( 195 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 195 FDA reports)
VERTIGO ( 194 FDA reports)
WEIGHT INCREASED ( 193 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 193 FDA reports)
AGITATION ( 189 FDA reports)
SWOLLEN TONGUE ( 187 FDA reports)
CHEST DISCOMFORT ( 185 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 182 FDA reports)
MYOCARDIAL ISCHAEMIA ( 181 FDA reports)
EPISTAXIS ( 180 FDA reports)
HYPERGLYCAEMIA ( 179 FDA reports)
FEELING HOT ( 178 FDA reports)
HAEMORRHAGE ( 178 FDA reports)
HYPERSENSITIVITY ( 178 FDA reports)
LIP SWELLING ( 176 FDA reports)
RENAL FAILURE CHRONIC ( 176 FDA reports)
BLOOD POTASSIUM INCREASED ( 175 FDA reports)
MITRAL VALVE INCOMPETENCE ( 175 FDA reports)
MUSCULOSKELETAL PAIN ( 175 FDA reports)
HEART RATE INCREASED ( 170 FDA reports)
CIRCULATORY COLLAPSE ( 169 FDA reports)
JAUNDICE ( 169 FDA reports)
SWELLING FACE ( 169 FDA reports)
LEUKOPENIA ( 167 FDA reports)
HEPATIC FAILURE ( 163 FDA reports)
JOINT SWELLING ( 162 FDA reports)
ORTHOSTATIC HYPOTENSION ( 162 FDA reports)
COMA ( 161 FDA reports)
PANCREATITIS ACUTE ( 161 FDA reports)
HAEMATOMA ( 160 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 159 FDA reports)
MELAENA ( 158 FDA reports)
STAPHYLOCOCCAL INFECTION ( 158 FDA reports)
CONTUSION ( 155 FDA reports)
HAEMODIALYSIS ( 155 FDA reports)
ABDOMINAL DISCOMFORT ( 154 FDA reports)
PANCREATITIS ( 153 FDA reports)
AMNESIA ( 152 FDA reports)
AGGRESSION ( 150 FDA reports)
CORONARY ARTERY STENOSIS ( 148 FDA reports)
GASTRITIS ( 148 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 148 FDA reports)
DISORIENTATION ( 147 FDA reports)
CELLULITIS ( 146 FDA reports)
BLOOD BILIRUBIN INCREASED ( 145 FDA reports)
OEDEMA ( 143 FDA reports)
HYPERTENSIVE CRISIS ( 141 FDA reports)
SEPTIC SHOCK ( 141 FDA reports)
URTICARIA ( 141 FDA reports)
VENTRICULAR TACHYCARDIA ( 141 FDA reports)
BRONCHITIS ( 140 FDA reports)
CARDIOMEGALY ( 140 FDA reports)
CEREBRAL HAEMORRHAGE ( 140 FDA reports)
HEPATIC ENZYME INCREASED ( 139 FDA reports)
SINUS TACHYCARDIA ( 139 FDA reports)
NEUTROPHIL COUNT INCREASED ( 137 FDA reports)
SLEEP DISORDER ( 137 FDA reports)
DRUG HYPERSENSITIVITY ( 136 FDA reports)
METABOLIC ACIDOSIS ( 136 FDA reports)
SUICIDE ATTEMPT ( 136 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 136 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 136 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 134 FDA reports)
ACUTE CORONARY SYNDROME ( 133 FDA reports)
CHOLESTASIS ( 133 FDA reports)
VISUAL ACUITY REDUCED ( 133 FDA reports)
BALANCE DISORDER ( 132 FDA reports)
NASOPHARYNGITIS ( 132 FDA reports)
ABDOMINAL DISTENSION ( 130 FDA reports)
CHOLELITHIASIS ( 129 FDA reports)
HAEMATURIA ( 129 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 125 FDA reports)
SINUS BRADYCARDIA ( 125 FDA reports)
DISTURBANCE IN ATTENTION ( 124 FDA reports)
DYSARTHRIA ( 124 FDA reports)
ASCITES ( 123 FDA reports)
BREAST CANCER ( 123 FDA reports)
EJECTION FRACTION DECREASED ( 122 FDA reports)
HIATUS HERNIA ( 122 FDA reports)
VENTRICULAR FIBRILLATION ( 122 FDA reports)
BLOOD SODIUM DECREASED ( 121 FDA reports)
INJURY ( 121 FDA reports)
ANOREXIA ( 120 FDA reports)
CORONARY ARTERY OCCLUSION ( 120 FDA reports)
FEBRILE NEUTROPENIA ( 120 FDA reports)
HYPOXIA ( 120 FDA reports)
GASTRIC ULCER ( 119 FDA reports)
HYPOPHAGIA ( 119 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 118 FDA reports)
THROMBOSIS ( 118 FDA reports)
DYSPEPSIA ( 117 FDA reports)
SUICIDAL IDEATION ( 117 FDA reports)
INCORRECT DOSE ADMINISTERED ( 115 FDA reports)
METASTASES TO SPINE ( 115 FDA reports)
MOBILITY DECREASED ( 115 FDA reports)
PRESYNCOPE ( 114 FDA reports)
RESTLESSNESS ( 114 FDA reports)
INFLUENZA LIKE ILLNESS ( 113 FDA reports)
SKIN EXFOLIATION ( 113 FDA reports)
CARDIOGENIC SHOCK ( 112 FDA reports)
DISEASE PROGRESSION ( 112 FDA reports)
EPILEPSY ( 112 FDA reports)
INTERSTITIAL LUNG DISEASE ( 112 FDA reports)
MYOSITIS ( 112 FDA reports)
PULMONARY FIBROSIS ( 112 FDA reports)
SINUSITIS ( 112 FDA reports)
SPEECH DISORDER ( 112 FDA reports)
SWELLING ( 112 FDA reports)
BLISTER ( 111 FDA reports)
DRUG TOXICITY ( 111 FDA reports)
DRY MOUTH ( 111 FDA reports)
GOUT ( 111 FDA reports)
ANURIA ( 110 FDA reports)
BREAST ABSCESS ( 110 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 110 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 109 FDA reports)
HAEMATOCRIT DECREASED ( 109 FDA reports)
HEMIPARESIS ( 109 FDA reports)
CARDIO-RESPIRATORY ARREST ( 108 FDA reports)
CEREBRAL INFARCTION ( 108 FDA reports)
DELIRIUM ( 108 FDA reports)
EMOTIONAL DISTRESS ( 106 FDA reports)
SKIN DISORDER ( 106 FDA reports)
PALLOR ( 105 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 104 FDA reports)
HEAD INJURY ( 104 FDA reports)
INFLAMMATION ( 104 FDA reports)
PULMONARY HYPERTENSION ( 104 FDA reports)
HEPATITIS ( 103 FDA reports)
OFF LABEL USE ( 103 FDA reports)
SKIN ULCER ( 103 FDA reports)
ACIDOSIS ( 101 FDA reports)
ANGINA UNSTABLE ( 101 FDA reports)
BLOOD POTASSIUM DECREASED ( 101 FDA reports)
ABSCESS ( 100 FDA reports)
ALOPECIA ( 100 FDA reports)
APHASIA ( 100 FDA reports)
IMPAIRED HEALING ( 100 FDA reports)
RHEUMATOID ARTHRITIS ( 100 FDA reports)
ASTHMA ( 99 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 99 FDA reports)
NEUROPATHY PERIPHERAL ( 99 FDA reports)
RASH ERYTHEMATOUS ( 99 FDA reports)
CARDIAC MURMUR ( 98 FDA reports)
PROTEINURIA ( 98 FDA reports)
PROTHROMBIN TIME PROLONGED ( 98 FDA reports)
DIALYSIS ( 97 FDA reports)
LEFT VENTRICULAR FAILURE ( 97 FDA reports)
MENTAL IMPAIRMENT ( 97 FDA reports)
TRANSAMINASES INCREASED ( 97 FDA reports)
URINARY RETENTION ( 97 FDA reports)
BONE PAIN ( 96 FDA reports)
BURNING SENSATION ( 96 FDA reports)
CARDIOMYOPATHY ( 96 FDA reports)
OSTEONECROSIS OF JAW ( 96 FDA reports)
LUNG DISORDER ( 95 FDA reports)
CYTOLYTIC HEPATITIS ( 94 FDA reports)
HEART RATE DECREASED ( 94 FDA reports)
URINARY INCONTINENCE ( 94 FDA reports)
LEUKOCYTOSIS ( 93 FDA reports)
RASH GENERALISED ( 93 FDA reports)
PNEUMONITIS ( 92 FDA reports)
PRURITUS GENERALISED ( 90 FDA reports)
ABASIA ( 89 FDA reports)
EOSINOPHILIA ( 89 FDA reports)
IRON DEFICIENCY ANAEMIA ( 89 FDA reports)
MYOPATHY ( 89 FDA reports)
OSTEOARTHRITIS ( 89 FDA reports)
SHOCK ( 88 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 88 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 87 FDA reports)
LUNG INFILTRATION ( 87 FDA reports)
RASH PRURITIC ( 86 FDA reports)
BLOOD ALBUMIN DECREASED ( 85 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 85 FDA reports)
OSTEONECROSIS ( 85 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 85 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 84 FDA reports)
DRUG INTOLERANCE ( 84 FDA reports)
NASAL CONGESTION ( 84 FDA reports)
PERICARDIAL EFFUSION ( 84 FDA reports)
RESPIRATORY DISORDER ( 84 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 84 FDA reports)
INTENTIONAL OVERDOSE ( 83 FDA reports)
MIOSIS ( 83 FDA reports)
MYOCLONUS ( 83 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 82 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 82 FDA reports)
DYSKINESIA ( 82 FDA reports)
HEART RATE IRREGULAR ( 82 FDA reports)
NEPHROLITHIASIS ( 82 FDA reports)
OROPHARYNGEAL PAIN ( 82 FDA reports)
DIPLOPIA ( 81 FDA reports)
FLATULENCE ( 81 FDA reports)
HEPATIC STEATOSIS ( 81 FDA reports)
LYMPHADENOPATHY ( 81 FDA reports)
TREATMENT NONCOMPLIANCE ( 81 FDA reports)
BONE MARROW FAILURE ( 80 FDA reports)
CHROMATURIA ( 80 FDA reports)
LIVER DISORDER ( 80 FDA reports)
MYELODYSPLASTIC SYNDROME ( 80 FDA reports)
OSTEOMYELITIS ( 80 FDA reports)
DYSPHONIA ( 79 FDA reports)
SUDDEN DEATH ( 79 FDA reports)
ARTHRITIS ( 78 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 78 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 78 FDA reports)
GASTROENTERITIS ( 78 FDA reports)
HALLUCINATION, VISUAL ( 78 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 78 FDA reports)
COMPLETED SUICIDE ( 77 FDA reports)
HEPATITIS ACUTE ( 77 FDA reports)
UROSEPSIS ( 77 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 76 FDA reports)
INJECTION SITE PAIN ( 76 FDA reports)
NARCOTIC INTOXICATION ( 76 FDA reports)
NEUTROPHIL COUNT DECREASED ( 76 FDA reports)
RENAL DISORDER ( 76 FDA reports)
SKIN LESION ( 76 FDA reports)
ACCIDENTAL OVERDOSE ( 75 FDA reports)
ARTERIOSCLEROSIS ( 75 FDA reports)
BLOOD GLUCOSE DECREASED ( 75 FDA reports)
DYSGEUSIA ( 75 FDA reports)
HAEMODYNAMIC INSTABILITY ( 75 FDA reports)
RHINORRHOEA ( 75 FDA reports)
STEVENS-JOHNSON SYNDROME ( 75 FDA reports)
HYPOTHYROIDISM ( 74 FDA reports)
POST PROCEDURAL COMPLICATION ( 74 FDA reports)
ECONOMIC PROBLEM ( 73 FDA reports)
FAECES DISCOLOURED ( 73 FDA reports)
NECK PAIN ( 73 FDA reports)
OXYGEN SATURATION DECREASED ( 73 FDA reports)
PSORIASIS ( 73 FDA reports)
ENCEPHALOPATHY ( 72 FDA reports)
TYPE 2 DIABETES MELLITUS ( 72 FDA reports)
VENTRICULAR HYPERTROPHY ( 72 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 71 FDA reports)
UNRESPONSIVE TO STIMULI ( 71 FDA reports)
BLOOD CALCIUM DECREASED ( 70 FDA reports)
CATARACT ( 70 FDA reports)
DIVERTICULITIS ( 70 FDA reports)
DYSPNOEA EXERTIONAL ( 70 FDA reports)
EYE SWELLING ( 70 FDA reports)
OLIGURIA ( 70 FDA reports)
RESPIRATORY DISTRESS ( 70 FDA reports)
WHEEZING ( 70 FDA reports)
WOUND INFECTION ( 70 FDA reports)
ANAPHYLACTIC REACTION ( 69 FDA reports)
LARYNGEAL OEDEMA ( 69 FDA reports)
NERVOUSNESS ( 69 FDA reports)
ABDOMINAL TENDERNESS ( 68 FDA reports)
OBESITY ( 68 FDA reports)
PULMONARY CONGESTION ( 68 FDA reports)
DEMENTIA ( 67 FDA reports)
DERMATITIS EXFOLIATIVE ( 67 FDA reports)
FLUID RETENTION ( 67 FDA reports)
LUNG INFECTION ( 67 FDA reports)
MEDICATION ERROR ( 67 FDA reports)
MENTAL STATUS CHANGES ( 67 FDA reports)
OESOPHAGITIS ( 67 FDA reports)
PRODUCTIVE COUGH ( 67 FDA reports)
SPINAL OSTEOARTHRITIS ( 67 FDA reports)
UNEVALUABLE EVENT ( 67 FDA reports)
AGRANULOCYTOSIS ( 66 FDA reports)
DERMATITIS ALLERGIC ( 66 FDA reports)
ISCHAEMIC STROKE ( 66 FDA reports)
PAIN IN JAW ( 66 FDA reports)
SKIN DISCOLOURATION ( 66 FDA reports)
THIRST ( 66 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 66 FDA reports)
WHITE BLOOD CELL DISORDER ( 66 FDA reports)
ACUTE PULMONARY OEDEMA ( 65 FDA reports)
COGNITIVE DISORDER ( 65 FDA reports)
BRONCHOPNEUMONIA ( 64 FDA reports)
STRESS ( 64 FDA reports)
COAGULOPATHY ( 63 FDA reports)
CYANOSIS ( 63 FDA reports)
DYSURIA ( 63 FDA reports)
GASTROINTESTINAL DISORDER ( 63 FDA reports)
HOT FLUSH ( 63 FDA reports)
HYPOCALCAEMIA ( 63 FDA reports)
MUCOSAL INFLAMMATION ( 63 FDA reports)
NEPHROTIC SYNDROME ( 63 FDA reports)
PHARYNGEAL OEDEMA ( 63 FDA reports)
PSYCHOTIC DISORDER ( 63 FDA reports)
ABNORMAL BEHAVIOUR ( 62 FDA reports)
ATELECTASIS ( 62 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 62 FDA reports)
HERPES ZOSTER ( 62 FDA reports)
HYPOMAGNESAEMIA ( 62 FDA reports)
PANIC ATTACK ( 62 FDA reports)
PROSTATE CANCER ( 62 FDA reports)
RASH MACULO-PAPULAR ( 62 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 62 FDA reports)
ACUTE HEPATIC FAILURE ( 61 FDA reports)
CARDIOVASCULAR DISORDER ( 61 FDA reports)
HAEMOPTYSIS ( 61 FDA reports)
HEPATIC NECROSIS ( 61 FDA reports)
HIP FRACTURE ( 61 FDA reports)
HYPOTHERMIA ( 61 FDA reports)
PRODUCT QUALITY ISSUE ( 61 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 60 FDA reports)
DIABETIC KETOACIDOSIS ( 60 FDA reports)
DUODENAL ULCER ( 60 FDA reports)
NEOPLASM MALIGNANT ( 60 FDA reports)
PURPURA ( 60 FDA reports)
SLEEP APNOEA SYNDROME ( 60 FDA reports)
CONJUNCTIVITIS ( 59 FDA reports)
DEPRESSED MOOD ( 59 FDA reports)
DERMATITIS ( 59 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 59 FDA reports)
MENTAL DISORDER ( 59 FDA reports)
PERIPHERAL COLDNESS ( 59 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 59 FDA reports)
RESPIRATORY ARREST ( 59 FDA reports)
SUBDURAL HAEMATOMA ( 59 FDA reports)
BRONCHOSPASM ( 58 FDA reports)
GRAND MAL CONVULSION ( 58 FDA reports)
HAEMORRHOIDS ( 58 FDA reports)
HEPATOMEGALY ( 58 FDA reports)
ROAD TRAFFIC ACCIDENT ( 58 FDA reports)
THROMBOCYTOSIS ( 58 FDA reports)
CAROTID ARTERY STENOSIS ( 57 FDA reports)
COLD SWEAT ( 57 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 57 FDA reports)
HYPERLIPIDAEMIA ( 57 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 57 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 57 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 56 FDA reports)
BODY TEMPERATURE INCREASED ( 56 FDA reports)
DRUG LEVEL INCREASED ( 56 FDA reports)
HAEMATOCHEZIA ( 56 FDA reports)
JOINT STIFFNESS ( 56 FDA reports)
MEAN CELL VOLUME DECREASED ( 56 FDA reports)
APLASIA PURE RED CELL ( 55 FDA reports)
MONOCYTE COUNT INCREASED ( 55 FDA reports)
PNEUMONIA ASPIRATION ( 55 FDA reports)
SURGERY ( 55 FDA reports)
ANGIONEUROTIC OEDEMA ( 54 FDA reports)
ANHEDONIA ( 54 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 54 FDA reports)
BODY MASS INDEX DECREASED ( 54 FDA reports)
DISEASE RECURRENCE ( 54 FDA reports)
FACE OEDEMA ( 54 FDA reports)
GUILLAIN-BARRE SYNDROME ( 54 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 54 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 54 FDA reports)
BLOOD AMYLASE INCREASED ( 53 FDA reports)
CANDIDIASIS ( 53 FDA reports)
COLITIS ( 53 FDA reports)
GASTRITIS EROSIVE ( 53 FDA reports)
LIVER INJURY ( 53 FDA reports)
LUNG NEOPLASM MALIGNANT ( 53 FDA reports)
ORTHOPNOEA ( 53 FDA reports)
POLYNEUROPATHY ( 53 FDA reports)
RASH MACULAR ( 53 FDA reports)
SQUAMOUS CELL CARCINOMA ( 53 FDA reports)
ABDOMINAL PAIN LOWER ( 52 FDA reports)
ECZEMA ( 52 FDA reports)
FACIAL PAIN ( 52 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 52 FDA reports)
HEPATIC CIRRHOSIS ( 52 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 52 FDA reports)
NEUTROPENIC SEPSIS ( 52 FDA reports)
RALES ( 52 FDA reports)
TORSADE DE POINTES ( 52 FDA reports)
ATRIAL FLUTTER ( 51 FDA reports)
BRADYARRHYTHMIA ( 51 FDA reports)
DYSSTASIA ( 51 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 51 FDA reports)
HOSPITALISATION ( 51 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 51 FDA reports)
MUSCLE ATROPHY ( 51 FDA reports)
VASCULITIS ( 51 FDA reports)
VENTRICULAR DYSFUNCTION ( 51 FDA reports)
AORTIC VALVE INCOMPETENCE ( 50 FDA reports)
CEREBRAL ISCHAEMIA ( 50 FDA reports)
DRY SKIN ( 50 FDA reports)
FEAR ( 50 FDA reports)
HYPERCHOLESTEROLAEMIA ( 50 FDA reports)
SKIN NECROSIS ( 50 FDA reports)
TINNITUS ( 50 FDA reports)
ANAPHYLACTIC SHOCK ( 49 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 49 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 49 FDA reports)
COORDINATION ABNORMAL ( 49 FDA reports)
FAECAL INCONTINENCE ( 49 FDA reports)
HYPERTHYROIDISM ( 49 FDA reports)
HYPOKINESIA ( 49 FDA reports)
INFLUENZA ( 49 FDA reports)
TACHYARRHYTHMIA ( 49 FDA reports)
HEPATITIS CHOLESTATIC ( 48 FDA reports)
HYPERCALCAEMIA ( 48 FDA reports)
METASTASES TO LIVER ( 48 FDA reports)
TENDON RUPTURE ( 48 FDA reports)
BODY TEMPERATURE DECREASED ( 47 FDA reports)
FEELING COLD ( 47 FDA reports)
GOITRE ( 47 FDA reports)
ILL-DEFINED DISORDER ( 47 FDA reports)
LIPASE INCREASED ( 47 FDA reports)
OEDEMA MOUTH ( 47 FDA reports)
PEMPHIGOID ( 47 FDA reports)
BLOOD CREATINE INCREASED ( 46 FDA reports)
CEREBRAL HAEMATOMA ( 46 FDA reports)
COLITIS ISCHAEMIC ( 46 FDA reports)
PARALYSIS ( 46 FDA reports)
PERITONITIS ( 46 FDA reports)
PNEUMOTHORAX ( 46 FDA reports)
SHOCK HAEMORRHAGIC ( 46 FDA reports)
TACHYPNOEA ( 46 FDA reports)
VENTRICULAR HYPOKINESIA ( 46 FDA reports)
CYSTITIS ( 45 FDA reports)
DROOLING ( 45 FDA reports)
DRUG ADMINISTRATION ERROR ( 45 FDA reports)
DRY EYE ( 45 FDA reports)
DUODENITIS ( 45 FDA reports)
ELECTROLYTE IMBALANCE ( 45 FDA reports)
HEPATOTOXICITY ( 45 FDA reports)
INFUSION RELATED REACTION ( 45 FDA reports)
IRRITABILITY ( 45 FDA reports)
MULTIPLE MYELOMA ( 45 FDA reports)
MUSCLE STRAIN ( 45 FDA reports)
NIGHTMARE ( 45 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 45 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 45 FDA reports)
SPINAL DISORDER ( 45 FDA reports)
TROPONIN INCREASED ( 45 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 44 FDA reports)
INTESTINAL OBSTRUCTION ( 44 FDA reports)
OSTEOPOROSIS ( 44 FDA reports)
RIGHT VENTRICULAR FAILURE ( 44 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 44 FDA reports)
VIRAL INFECTION ( 44 FDA reports)
CARPAL TUNNEL SYNDROME ( 43 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 43 FDA reports)
FLUID OVERLOAD ( 43 FDA reports)
MIGRAINE ( 43 FDA reports)
MOVEMENT DISORDER ( 43 FDA reports)
MULTIPLE INJURIES ( 43 FDA reports)
MUSCLE TWITCHING ( 43 FDA reports)
POLLAKIURIA ( 43 FDA reports)
SENSORY DISTURBANCE ( 43 FDA reports)
TOXIC SKIN ERUPTION ( 43 FDA reports)
TUBERCULOSIS ( 43 FDA reports)
AGEUSIA ( 42 FDA reports)
CREPITATIONS ( 42 FDA reports)
EYELID OEDEMA ( 42 FDA reports)
HYPOVOLAEMIA ( 42 FDA reports)
METASTASES TO BONE ( 42 FDA reports)
MOUTH ULCERATION ( 42 FDA reports)
MUSCLE DISORDER ( 42 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 42 FDA reports)
RIB FRACTURE ( 42 FDA reports)
BRADYPHRENIA ( 41 FDA reports)
COLITIS ULCERATIVE ( 41 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 41 FDA reports)
JAW DISORDER ( 41 FDA reports)
OESOPHAGITIS ULCERATIVE ( 41 FDA reports)
PANCREATIC CARCINOMA ( 41 FDA reports)
PERIPHERAL ISCHAEMIA ( 41 FDA reports)
PETECHIAE ( 41 FDA reports)
ARTHROPATHY ( 40 FDA reports)
BONE DISORDER ( 40 FDA reports)
DRUG EFFECT DECREASED ( 40 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 40 FDA reports)
EMPHYSEMA ( 40 FDA reports)
HALLUCINATION, AUDITORY ( 40 FDA reports)
INTESTINAL PERFORATION ( 40 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 40 FDA reports)
NOCTURIA ( 40 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 40 FDA reports)
PHYSICAL ASSAULT ( 40 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 40 FDA reports)
RESTLESS LEGS SYNDROME ( 40 FDA reports)
ACUTE PRERENAL FAILURE ( 39 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 39 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 39 FDA reports)
AREFLEXIA ( 39 FDA reports)
CEREBRAL ATROPHY ( 39 FDA reports)
CHOLECYSTITIS ( 39 FDA reports)
HEPATITIS TOXIC ( 39 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 39 FDA reports)
INTRACARDIAC THROMBUS ( 39 FDA reports)
LOBAR PNEUMONIA ( 39 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 39 FDA reports)
PLATELET COUNT INCREASED ( 39 FDA reports)
PLEURISY ( 39 FDA reports)
RENAL CYST ( 39 FDA reports)
RESPIRATORY TRACT INFECTION ( 39 FDA reports)
STOMATITIS ( 39 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 38 FDA reports)
ATRIOVENTRICULAR BLOCK ( 38 FDA reports)
CARDIAC FAILURE ACUTE ( 38 FDA reports)
CRYING ( 38 FDA reports)
EAR PAIN ( 38 FDA reports)
ERYSIPELAS ( 38 FDA reports)
FOOT FRACTURE ( 38 FDA reports)
MOOD SWINGS ( 38 FDA reports)
NERVOUS SYSTEM DISORDER ( 38 FDA reports)
NIGHT SWEATS ( 38 FDA reports)
PARANOIA ( 38 FDA reports)
SKIN BURNING SENSATION ( 38 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 37 FDA reports)
CYST ( 37 FDA reports)
EATING DISORDER ( 37 FDA reports)
SALIVARY HYPERSECRETION ( 37 FDA reports)
SINUS DISORDER ( 37 FDA reports)
SPINAL COMPRESSION FRACTURE ( 37 FDA reports)
SYNCOPE VASOVAGAL ( 37 FDA reports)
TENDONITIS ( 37 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 36 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 36 FDA reports)
CACHEXIA ( 36 FDA reports)
DRUG ERUPTION ( 36 FDA reports)
DYSLIPIDAEMIA ( 36 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 36 FDA reports)
HYPERVENTILATION ( 36 FDA reports)
MYASTHENIA GRAVIS ( 36 FDA reports)
ODYNOPHAGIA ( 36 FDA reports)
PATHOLOGICAL FRACTURE ( 36 FDA reports)
PYELONEPHRITIS ( 36 FDA reports)
RASH PAPULAR ( 36 FDA reports)
RENAL TUBULAR DISORDER ( 36 FDA reports)
SEROTONIN SYNDROME ( 36 FDA reports)
TENDERNESS ( 36 FDA reports)
BASAL CELL CARCINOMA ( 35 FDA reports)
BLOOD LACTIC ACID INCREASED ( 35 FDA reports)
DIVERTICULUM ( 35 FDA reports)
DRUG DOSE OMISSION ( 35 FDA reports)
MOTOR DYSFUNCTION ( 35 FDA reports)
MULTIPLE DRUG OVERDOSE ( 35 FDA reports)
NO THERAPEUTIC RESPONSE ( 35 FDA reports)
SENSATION OF HEAVINESS ( 35 FDA reports)
SPINAL FRACTURE ( 35 FDA reports)
ACUTE RESPIRATORY FAILURE ( 34 FDA reports)
APNOEA ( 34 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 34 FDA reports)
BONE LESION ( 34 FDA reports)
BURSITIS ( 34 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 34 FDA reports)
DILATATION VENTRICULAR ( 34 FDA reports)
DISCOMFORT ( 34 FDA reports)
LOOSE TOOTH ( 34 FDA reports)
MIDDLE INSOMNIA ( 34 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 34 FDA reports)
SOPOR ( 34 FDA reports)
STENT PLACEMENT ( 34 FDA reports)
THROAT IRRITATION ( 34 FDA reports)
ANGER ( 33 FDA reports)
BLINDNESS ( 33 FDA reports)
COMPRESSION FRACTURE ( 33 FDA reports)
ERECTILE DYSFUNCTION ( 33 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 33 FDA reports)
HYPOACUSIS ( 33 FDA reports)
INJECTION SITE ERYTHEMA ( 33 FDA reports)
LACERATION ( 33 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 33 FDA reports)
LOWER LIMB FRACTURE ( 33 FDA reports)
NEPHROPATHY ( 33 FDA reports)
NEPHROPATHY TOXIC ( 33 FDA reports)
RENAL TUBULAR NECROSIS ( 33 FDA reports)
SEDATION ( 33 FDA reports)
SENSORY LOSS ( 33 FDA reports)
SICK SINUS SYNDROME ( 33 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 33 FDA reports)
BACTERIAL INFECTION ( 32 FDA reports)
CHOLANGITIS ( 32 FDA reports)
HAEMORRHAGIC ANAEMIA ( 32 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 32 FDA reports)
LYMPHOMA ( 32 FDA reports)
PARKINSONISM ( 32 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 32 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 32 FDA reports)
SPLENOMEGALY ( 32 FDA reports)
SUDDEN CARDIAC DEATH ( 32 FDA reports)
VIITH NERVE PARALYSIS ( 32 FDA reports)
ABSCESS JAW ( 31 FDA reports)
BLOOD URINE PRESENT ( 31 FDA reports)
CORONARY ARTERY THROMBOSIS ( 31 FDA reports)
FALLOT'S TETRALOGY ( 31 FDA reports)
HEPATIC ENCEPHALOPATHY ( 31 FDA reports)
HERNIA ( 31 FDA reports)
HYPERTENSIVE HEART DISEASE ( 31 FDA reports)
LEG AMPUTATION ( 31 FDA reports)
PARTIAL SEIZURES ( 31 FDA reports)
THROMBOSIS IN DEVICE ( 31 FDA reports)
AORTIC ANEURYSM ( 30 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 30 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 30 FDA reports)
CLOSTRIDIAL INFECTION ( 30 FDA reports)
COLON CANCER ( 30 FDA reports)
COMPARTMENT SYNDROME ( 30 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 30 FDA reports)
DIASTOLIC DYSFUNCTION ( 30 FDA reports)
DRUG RESISTANCE ( 30 FDA reports)
FEMUR FRACTURE ( 30 FDA reports)
FISTULA ( 30 FDA reports)
GINGIVAL BLEEDING ( 30 FDA reports)
GYNAECOMASTIA ( 30 FDA reports)
HAEMORRHAGIC STROKE ( 30 FDA reports)
HEMIPLEGIA ( 30 FDA reports)
INJECTION SITE HAEMORRHAGE ( 30 FDA reports)
KLEBSIELLA INFECTION ( 30 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 30 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 30 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 30 FDA reports)
OSTEITIS ( 30 FDA reports)
PANCREATITIS NECROTISING ( 30 FDA reports)
PHOTOPHOBIA ( 30 FDA reports)
RHINITIS ALLERGIC ( 30 FDA reports)
SKIN REACTION ( 30 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 30 FDA reports)
VISUAL DISTURBANCE ( 30 FDA reports)
ALVEOLITIS ( 29 FDA reports)
ANKLE FRACTURE ( 29 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 29 FDA reports)
ARTHRITIS BACTERIAL ( 29 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 29 FDA reports)
EMBOLISM ( 29 FDA reports)
ENDOCARDITIS ( 29 FDA reports)
EYE HAEMORRHAGE ( 29 FDA reports)
EYE PAIN ( 29 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 29 FDA reports)
GENERALISED OEDEMA ( 29 FDA reports)
LACUNAR INFARCTION ( 29 FDA reports)
MYOCARDITIS ( 29 FDA reports)
NAEVUS FLAMMEUS ( 29 FDA reports)
ORAL PAIN ( 29 FDA reports)
PHOTOSENSITIVITY REACTION ( 29 FDA reports)
SINUS ARRHYTHMIA ( 29 FDA reports)
ANAEMIA MACROCYTIC ( 28 FDA reports)
ATAXIA ( 28 FDA reports)
BLOOD PRESSURE ABNORMAL ( 28 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 28 FDA reports)
DERMATITIS BULLOUS ( 28 FDA reports)
DILATATION ATRIAL ( 28 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 28 FDA reports)
EXERCISE TOLERANCE DECREASED ( 28 FDA reports)
EXTRASYSTOLES ( 28 FDA reports)
FIBRIN D DIMER INCREASED ( 28 FDA reports)
FLANK PAIN ( 28 FDA reports)
HYPERSOMNIA ( 28 FDA reports)
HYPOTONIA ( 28 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 28 FDA reports)
ISCHAEMIA ( 28 FDA reports)
JAW FRACTURE ( 28 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 28 FDA reports)
ONYCHOMYCOSIS ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 28 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 28 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 28 FDA reports)
TARDIVE DYSKINESIA ( 28 FDA reports)
URINE COLOUR ABNORMAL ( 28 FDA reports)
WOUND DEHISCENCE ( 28 FDA reports)
WOUND SECRETION ( 28 FDA reports)
VASCULAR PSEUDOANEURYSM ( 27 FDA reports)
WOUND ( 27 FDA reports)
AKATHISIA ( 27 FDA reports)
ASTERIXIS ( 27 FDA reports)
DRUG PRESCRIBING ERROR ( 27 FDA reports)
DUODENAL ULCER PERFORATION ( 27 FDA reports)
ESCHERICHIA SEPSIS ( 27 FDA reports)
FOOD POISONING ( 27 FDA reports)
FUNGAL INFECTION ( 27 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 27 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 27 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 27 FDA reports)
LARGE INTESTINE PERFORATION ( 27 FDA reports)
LOCALISED INFECTION ( 27 FDA reports)
NEOPLASM PROGRESSION ( 27 FDA reports)
PULSE ABSENT ( 27 FDA reports)
SCAR ( 27 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 26 FDA reports)
BRAIN OEDEMA ( 26 FDA reports)
CARDIAC FAILURE CHRONIC ( 26 FDA reports)
CARDIOPULMONARY FAILURE ( 26 FDA reports)
CATARACT OPERATION ( 26 FDA reports)
COLONIC POLYP ( 26 FDA reports)
DIABETIC NEPHROPATHY ( 26 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 26 FDA reports)
HEPATOCELLULAR INJURY ( 26 FDA reports)
ILEUS ( 26 FDA reports)
LABORATORY TEST ABNORMAL ( 26 FDA reports)
MASS ( 26 FDA reports)
MENINGITIS ( 26 FDA reports)
MUSCLE HAEMORRHAGE ( 26 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 26 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 26 FDA reports)
RAYNAUD'S PHENOMENON ( 26 FDA reports)
RENAL INJURY ( 26 FDA reports)
ACCIDENTAL EXPOSURE ( 25 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 25 FDA reports)
BRADYKINESIA ( 25 FDA reports)
CAESAREAN SECTION ( 25 FDA reports)
COMA SCALE ABNORMAL ( 25 FDA reports)
EAR DISCOMFORT ( 25 FDA reports)
EPIGLOTTIC OEDEMA ( 25 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 25 FDA reports)
FAECALOMA ( 25 FDA reports)
HYPERCAPNIA ( 25 FDA reports)
INTESTINAL ISCHAEMIA ( 25 FDA reports)
LOCAL SWELLING ( 25 FDA reports)
PARAESTHESIA ORAL ( 25 FDA reports)
PARKINSON'S DISEASE ( 25 FDA reports)
PELVIC PAIN ( 25 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 25 FDA reports)
RENAL CANCER ( 25 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 25 FDA reports)
TONGUE OEDEMA ( 25 FDA reports)
TOOTH EXTRACTION ( 25 FDA reports)
ULCER ( 25 FDA reports)
URINE OUTPUT DECREASED ( 25 FDA reports)
ABNORMAL DREAMS ( 24 FDA reports)
ANGIOPATHY ( 24 FDA reports)
AZOTAEMIA ( 24 FDA reports)
BILIARY COLIC ( 24 FDA reports)
BONE MARROW DISORDER ( 24 FDA reports)
BREATH SOUNDS ABNORMAL ( 24 FDA reports)
CORONARY ARTERY BYPASS ( 24 FDA reports)
DEAFNESS ( 24 FDA reports)
DECREASED ACTIVITY ( 24 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 24 FDA reports)
FIBROMYALGIA ( 24 FDA reports)
GASTRIC DISORDER ( 24 FDA reports)
GASTRITIS HAEMORRHAGIC ( 24 FDA reports)
GASTROINTESTINAL INFECTION ( 24 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 24 FDA reports)
HIP ARTHROPLASTY ( 24 FDA reports)
HYPERTONIA ( 24 FDA reports)
INCONTINENCE ( 24 FDA reports)
INFARCTION ( 24 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 24 FDA reports)
JAUNDICE CHOLESTATIC ( 24 FDA reports)
JOINT EFFUSION ( 24 FDA reports)
MITRAL VALVE DISEASE ( 24 FDA reports)
OROPHARYNGEAL BLISTERING ( 24 FDA reports)
PERIODONTAL DISEASE ( 24 FDA reports)
POLYURIA ( 24 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 24 FDA reports)
SKIN CANCER ( 24 FDA reports)
THROAT TIGHTNESS ( 24 FDA reports)
TOOTH LOSS ( 24 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 23 FDA reports)
ANOSMIA ( 23 FDA reports)
AORTIC STENOSIS ( 23 FDA reports)
AORTIC VALVE DISEASE ( 23 FDA reports)
BEDRIDDEN ( 23 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 23 FDA reports)
BLADDER CANCER ( 23 FDA reports)
BLOOD CHLORIDE DECREASED ( 23 FDA reports)
ESCHERICHIA INFECTION ( 23 FDA reports)
HAEMOLYSIS ( 23 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 23 FDA reports)
HOSTILITY ( 23 FDA reports)
MEGAKARYOCYTES INCREASED ( 23 FDA reports)
MUSCLE INJURY ( 23 FDA reports)
RASH MORBILLIFORM ( 23 FDA reports)
REFLUX OESOPHAGITIS ( 23 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 23 FDA reports)
SPINAL COLUMN STENOSIS ( 23 FDA reports)
VAGINAL HAEMORRHAGE ( 23 FDA reports)
WITHDRAWAL SYNDROME ( 23 FDA reports)
VASCULAR PURPURA ( 22 FDA reports)
ATRIAL TACHYCARDIA ( 22 FDA reports)
BLOOD SODIUM INCREASED ( 22 FDA reports)
CARDIAC FLUTTER ( 22 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 22 FDA reports)
DIFFICULTY IN WALKING ( 22 FDA reports)
ERYTHEMA MULTIFORME ( 22 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 22 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 22 FDA reports)
HUMERUS FRACTURE ( 22 FDA reports)
HYPERBILIRUBINAEMIA ( 22 FDA reports)
LEUKOENCEPHALOPATHY ( 22 FDA reports)
MANIA ( 22 FDA reports)
MOUTH HAEMORRHAGE ( 22 FDA reports)
NIKOLSKY'S SIGN ( 22 FDA reports)
NODULE ( 22 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 22 FDA reports)
RESPIRATORY RATE INCREASED ( 22 FDA reports)
RESUSCITATION ( 22 FDA reports)
RETCHING ( 22 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 22 FDA reports)
SUBCUTANEOUS ABSCESS ( 22 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 22 FDA reports)
ABNORMAL FAECES ( 21 FDA reports)
AMYLASE INCREASED ( 21 FDA reports)
BLOOD CHLORIDE INCREASED ( 21 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 21 FDA reports)
DELUSION ( 21 FDA reports)
DIABETIC NEUROPATHY ( 21 FDA reports)
DRUG EFFECT INCREASED ( 21 FDA reports)
DRY THROAT ( 21 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 21 FDA reports)
GINGIVAL PAIN ( 21 FDA reports)
GLYCOSURIA ( 21 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 21 FDA reports)
HYPOREFLEXIA ( 21 FDA reports)
IATROGENIC INJURY ( 21 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 21 FDA reports)
INTENTIONAL SELF-INJURY ( 21 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 21 FDA reports)
MULTI-ORGAN DISORDER ( 21 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 21 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 21 FDA reports)
OLIGOHYDRAMNIOS ( 21 FDA reports)
ORAL CANDIDIASIS ( 21 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 21 FDA reports)
RENAL PAIN ( 21 FDA reports)
SKIN TIGHTNESS ( 21 FDA reports)
STATUS EPILEPTICUS ( 21 FDA reports)
VENTRICULAR ARRHYTHMIA ( 21 FDA reports)
VITAMIN B12 DEFICIENCY ( 20 FDA reports)
AFFECTIVE DISORDER ( 20 FDA reports)
ARTERIOSPASM CORONARY ( 20 FDA reports)
BIPOLAR I DISORDER ( 20 FDA reports)
BODY HEIGHT DECREASED ( 20 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 20 FDA reports)
CERUMEN IMPACTION ( 20 FDA reports)
CONDUCTION DISORDER ( 20 FDA reports)
DEVICE RELATED INFECTION ( 20 FDA reports)
DYSPNOEA AT REST ( 20 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 20 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 20 FDA reports)
EPIGASTRIC DISCOMFORT ( 20 FDA reports)
ERUCTATION ( 20 FDA reports)
FLUID INTAKE REDUCED ( 20 FDA reports)
GLAUCOMA ( 20 FDA reports)
HEMIANOPIA HOMONYMOUS ( 20 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 20 FDA reports)
IMPAIRED DRIVING ABILITY ( 20 FDA reports)
INJECTION SITE SWELLING ( 20 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 20 FDA reports)
KNEE ARTHROPLASTY ( 20 FDA reports)
LICHENOID KERATOSIS ( 20 FDA reports)
LUNG CONSOLIDATION ( 20 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 20 FDA reports)
MICTURITION URGENCY ( 20 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 20 FDA reports)
NAIL DISORDER ( 20 FDA reports)
PANIC REACTION ( 20 FDA reports)
PARAPLEGIA ( 20 FDA reports)
PARESIS ( 20 FDA reports)
PEPTIC ULCER ( 20 FDA reports)
PERSONALITY CHANGE ( 20 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 20 FDA reports)
POOR QUALITY SLEEP ( 20 FDA reports)
PUSTULAR PSORIASIS ( 20 FDA reports)
RED BLOOD CELL ABNORMALITY ( 20 FDA reports)
RENAL CELL CARCINOMA ( 20 FDA reports)
SELF-MEDICATION ( 20 FDA reports)
SKULL FRACTURE ( 20 FDA reports)
SPUTUM DISCOLOURED ( 20 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 20 FDA reports)
TOOTH DISORDER ( 20 FDA reports)
TOXIC SHOCK SYNDROME ( 20 FDA reports)
ADVERSE DRUG REACTION ( 19 FDA reports)
ASPIRATION ( 19 FDA reports)
BIPOLAR DISORDER ( 19 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 19 FDA reports)
BREAST CANCER FEMALE ( 19 FDA reports)
BRONCHIAL CARCINOMA ( 19 FDA reports)
CARDIAC TAMPONADE ( 19 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 19 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 19 FDA reports)
DEVICE FAILURE ( 19 FDA reports)
DIVERTICULUM INTESTINAL ( 19 FDA reports)
EXCORIATION ( 19 FDA reports)
EYE MOVEMENT DISORDER ( 19 FDA reports)
HEPATIC CONGESTION ( 19 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 19 FDA reports)
HYPOVOLAEMIC SHOCK ( 19 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 19 FDA reports)
INFECTIOUS PERITONITIS ( 19 FDA reports)
INJECTION SITE HAEMATOMA ( 19 FDA reports)
INJECTION SITE REACTION ( 19 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
LYMPHOCELE ( 19 FDA reports)
LYMPHOCYTOSIS ( 19 FDA reports)
MALLORY-WEISS SYNDROME ( 19 FDA reports)
MEDICATION RESIDUE ( 19 FDA reports)
MICROCYTIC ANAEMIA ( 19 FDA reports)
NECROSIS ( 19 FDA reports)
NEUROLOGICAL SYMPTOM ( 19 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 19 FDA reports)
OCULAR HYPERTENSION ( 19 FDA reports)
PREGNANCY ( 19 FDA reports)
PROTEIN TOTAL DECREASED ( 19 FDA reports)
PSYCHOMOTOR RETARDATION ( 19 FDA reports)
RENAL ARTERY STENOSIS ( 19 FDA reports)
RETINAL ARTERY OCCLUSION ( 19 FDA reports)
ROTATOR CUFF SYNDROME ( 19 FDA reports)
SKIN PLAQUE ( 19 FDA reports)
SYNOVIAL RUPTURE ( 19 FDA reports)
THERAPY NON-RESPONDER ( 19 FDA reports)
UPPER LIMB FRACTURE ( 19 FDA reports)
VASCULITIC RASH ( 19 FDA reports)
VENOUS THROMBOSIS ( 19 FDA reports)
VISUAL FIELD DEFECT ( 19 FDA reports)
WHEELCHAIR USER ( 18 FDA reports)
ADVERSE EVENT ( 18 FDA reports)
ALCOHOL USE ( 18 FDA reports)
BLOOD CREATININE DECREASED ( 18 FDA reports)
BLOOD DISORDER ( 18 FDA reports)
BLOOD URIC ACID INCREASED ( 18 FDA reports)
BREAST PAIN ( 18 FDA reports)
CAROTID ARTERY OCCLUSION ( 18 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 18 FDA reports)
DEAFNESS NEUROSENSORY ( 18 FDA reports)
DIAPHRAGMATIC DISORDER ( 18 FDA reports)
ECCHYMOSIS ( 18 FDA reports)
EMPYEMA ( 18 FDA reports)
EXPOSED BONE IN JAW ( 18 FDA reports)
FACIAL PARESIS ( 18 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
GASTRIC POLYPS ( 18 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 18 FDA reports)
GLUCOSE URINE PRESENT ( 18 FDA reports)
HEPATIC FIBROSIS ( 18 FDA reports)
HYPOALBUMINAEMIA ( 18 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 18 FDA reports)
INJECTION SITE PRURITUS ( 18 FDA reports)
INTENTIONAL DRUG MISUSE ( 18 FDA reports)
JUGULAR VEIN THROMBOSIS ( 18 FDA reports)
LARYNGOSPASM ( 18 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 18 FDA reports)
METABOLIC ENCEPHALOPATHY ( 18 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 18 FDA reports)
MUSCLE RIGIDITY ( 18 FDA reports)
NERVE INJURY ( 18 FDA reports)
NEUROPATHIC ULCER ( 18 FDA reports)
NOCTURNAL DYSPNOEA ( 18 FDA reports)
OCULAR HYPERAEMIA ( 18 FDA reports)
OPTIC DISC DISORDER ( 18 FDA reports)
PITTING OEDEMA ( 18 FDA reports)
POTENTIATING DRUG INTERACTION ( 18 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 18 FDA reports)
PSEUDOMONAS INFECTION ( 18 FDA reports)
QRS AXIS ABNORMAL ( 18 FDA reports)
SERUM FERRITIN INCREASED ( 18 FDA reports)
SMALL FOR DATES BABY ( 18 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 18 FDA reports)
THYMUS DISORDER ( 18 FDA reports)
TOOTH INFECTION ( 18 FDA reports)
ABORTION SPONTANEOUS ( 17 FDA reports)
ACTINOMYCOSIS ( 17 FDA reports)
APLASTIC ANAEMIA ( 17 FDA reports)
B-CELL LYMPHOMA ( 17 FDA reports)
BLOOD CULTURE POSITIVE ( 17 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 17 FDA reports)
BREAST CANCER METASTATIC ( 17 FDA reports)
CARDIAC VALVE DISEASE ( 17 FDA reports)
CATHETERISATION CARDIAC ( 17 FDA reports)
CHANGE OF BOWEL HABIT ( 17 FDA reports)
CHOLECYSTECTOMY ( 17 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 17 FDA reports)
DENTAL FISTULA ( 17 FDA reports)
EDENTULOUS ( 17 FDA reports)
ENCEPHALITIS ( 17 FDA reports)
ENTEROBACTER INFECTION ( 17 FDA reports)
GLOMERULONEPHRITIS ( 17 FDA reports)
HAEMARTHROSIS ( 17 FDA reports)
HYPERKERATOSIS ( 17 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 17 FDA reports)
INCOHERENT ( 17 FDA reports)
LARGE INTESTINAL ULCER ( 17 FDA reports)
LEFT ATRIAL DILATATION ( 17 FDA reports)
LUPUS-LIKE SYNDROME ( 17 FDA reports)
LYMPHOPENIA ( 17 FDA reports)
MACULOPATHY ( 17 FDA reports)
METASTASES TO LUNG ( 17 FDA reports)
NON-CARDIAC CHEST PAIN ( 17 FDA reports)
OPEN WOUND ( 17 FDA reports)
PRIMARY SEQUESTRUM ( 17 FDA reports)
RASH PUSTULAR ( 17 FDA reports)
SKIN FISSURES ( 17 FDA reports)
TONGUE INJURY ( 17 FDA reports)
ANXIETY DISORDER ( 16 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 16 FDA reports)
CHEST X-RAY ABNORMAL ( 16 FDA reports)
CHOLECYSTITIS ACUTE ( 16 FDA reports)
DECUBITUS ULCER ( 16 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
EYE PRURITUS ( 16 FDA reports)
FEMORAL NECK FRACTURE ( 16 FDA reports)
GANGRENE ( 16 FDA reports)
GRAFT LOSS ( 16 FDA reports)
GROIN PAIN ( 16 FDA reports)
HAIR GROWTH ABNORMAL ( 16 FDA reports)
HELICOBACTER GASTRITIS ( 16 FDA reports)
HEPATOCELLULAR DAMAGE ( 16 FDA reports)
HYPERTRANSAMINASAEMIA ( 16 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 16 FDA reports)
HYPOPHOSPHATAEMIA ( 16 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 16 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 16 FDA reports)
LACRIMATION INCREASED ( 16 FDA reports)
LIMB DISCOMFORT ( 16 FDA reports)
LUNG NEOPLASM ( 16 FDA reports)
LYMPH NODE PAIN ( 16 FDA reports)
MUSCULOSKELETAL DISORDER ( 16 FDA reports)
MYDRIASIS ( 16 FDA reports)
NEUTROPHILIA ( 16 FDA reports)
OESOPHAGEAL CARCINOMA ( 16 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 16 FDA reports)
PANCREATITIS CHRONIC ( 16 FDA reports)
PERICARDITIS ( 16 FDA reports)
PHLEBITIS ( 16 FDA reports)
POST PROCEDURAL INFECTION ( 16 FDA reports)
PROCEDURAL COMPLICATION ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
RADICULOPATHY ( 16 FDA reports)
RETINAL VEIN OCCLUSION ( 16 FDA reports)
SINUS HEADACHE ( 16 FDA reports)
STRIDOR ( 16 FDA reports)
SUPERINFECTION ( 16 FDA reports)
THYROID NEOPLASM ( 16 FDA reports)
TUMOUR LYSIS SYNDROME ( 16 FDA reports)
WRONG DRUG ADMINISTERED ( 16 FDA reports)
ABORTION INDUCED ( 15 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 15 FDA reports)
ANGIOPLASTY ( 15 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 15 FDA reports)
APATHY ( 15 FDA reports)
BACTERAEMIA ( 15 FDA reports)
BLINDNESS UNILATERAL ( 15 FDA reports)
BLOOD BLISTER ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 15 FDA reports)
CARDIAC DEATH ( 15 FDA reports)
CATHETER RELATED COMPLICATION ( 15 FDA reports)
CEREBROVASCULAR DISORDER ( 15 FDA reports)
CUBITAL TUNNEL SYNDROME ( 15 FDA reports)
DECREASED INTEREST ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
DROP ATTACKS ( 15 FDA reports)
DRUG DEPENDENCE ( 15 FDA reports)
DRUG DISPENSING ERROR ( 15 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
ENTEROCOCCAL INFECTION ( 15 FDA reports)
EXPIRED DRUG ADMINISTERED ( 15 FDA reports)
EXTREMITY CONTRACTURE ( 15 FDA reports)
FRACTURE ( 15 FDA reports)
GALLBLADDER DISORDER ( 15 FDA reports)
GASTRIC HAEMORRHAGE ( 15 FDA reports)
GLIOBLASTOMA ( 15 FDA reports)
HEMIANOPIA ( 15 FDA reports)
HYDROCEPHALUS ( 15 FDA reports)
HYPERSEXUALITY ( 15 FDA reports)
HYPERTHERMIA ( 15 FDA reports)
HYPOGLYCAEMIC COMA ( 15 FDA reports)
IMMUNOSUPPRESSION ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 15 FDA reports)
LIMB INJURY ( 15 FDA reports)
MENSTRUATION IRREGULAR ( 15 FDA reports)
NEURALGIA ( 15 FDA reports)
NODAL ARRHYTHMIA ( 15 FDA reports)
ORAL INTAKE REDUCED ( 15 FDA reports)
PARAPARESIS ( 15 FDA reports)
PERICARDIAL HAEMORRHAGE ( 15 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 15 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 15 FDA reports)
POLYARTHRITIS ( 15 FDA reports)
POLYDIPSIA ( 15 FDA reports)
PROSTATITIS ( 15 FDA reports)
RECTAL CANCER ( 15 FDA reports)
SCIATICA ( 15 FDA reports)
SKIN HYPERTROPHY ( 15 FDA reports)
SUBDURAL HAEMORRHAGE ( 15 FDA reports)
SUBILEUS ( 15 FDA reports)
TENSION ( 15 FDA reports)
THROMBOPHLEBITIS ( 15 FDA reports)
TOOTH FRACTURE ( 15 FDA reports)
BLADDER CATHETERISATION ( 14 FDA reports)
BLOOD BICARBONATE DECREASED ( 14 FDA reports)
CEREBRAL THROMBOSIS ( 14 FDA reports)
CHOKING ( 14 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 14 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 14 FDA reports)
CORONARY ARTERY RESTENOSIS ( 14 FDA reports)
DEVICE MALFUNCTION ( 14 FDA reports)
DYSAESTHESIA ( 14 FDA reports)
EXFOLIATIVE RASH ( 14 FDA reports)
EYE IRRITATION ( 14 FDA reports)
FIBULA FRACTURE ( 14 FDA reports)
GRAFT DYSFUNCTION ( 14 FDA reports)
GRANULOCYTOPENIA ( 14 FDA reports)
HAEMOTHORAX ( 14 FDA reports)
HEART VALVE INCOMPETENCE ( 14 FDA reports)
HEPATIC LESION ( 14 FDA reports)
HEPATITIS FULMINANT ( 14 FDA reports)
IMPAIRED WORK ABILITY ( 14 FDA reports)
INJECTION SITE IRRITATION ( 14 FDA reports)
JOINT INJURY ( 14 FDA reports)
LOCALISED OEDEMA ( 14 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 14 FDA reports)
MACULAR DEGENERATION ( 14 FDA reports)
MAJOR DEPRESSION ( 14 FDA reports)
MENINGIOMA ( 14 FDA reports)
METASTASIS ( 14 FDA reports)
MULTIPLE SCLEROSIS ( 14 FDA reports)
MUSCLE MASS ( 14 FDA reports)
MUSCLE RUPTURE ( 14 FDA reports)
NEONATAL ANURIA ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
ORAL DISORDER ( 14 FDA reports)
PAPILLOEDEMA ( 14 FDA reports)
PAROTITIS ( 14 FDA reports)
PELVIC FRACTURE ( 14 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 14 FDA reports)
PLEURAL FIBROSIS ( 14 FDA reports)
PNEUMONIA FUNGAL ( 14 FDA reports)
QUADRIPARESIS ( 14 FDA reports)
RENAL APLASIA ( 14 FDA reports)
RENAL COLIC ( 14 FDA reports)
RESPIRATORY TRACT CONGESTION ( 14 FDA reports)
SKIN HAEMORRHAGE ( 14 FDA reports)
SYNOVITIS ( 14 FDA reports)
TEARFULNESS ( 14 FDA reports)
THINKING ABNORMAL ( 14 FDA reports)
THYROID CANCER ( 14 FDA reports)
TONGUE DISORDER ( 14 FDA reports)
TROPONIN I INCREASED ( 14 FDA reports)
TROPONIN T INCREASED ( 14 FDA reports)
TUBERCULIN TEST POSITIVE ( 14 FDA reports)
URINARY TRACT DISORDER ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
UVEITIS ( 14 FDA reports)
VENOUS THROMBOSIS LIMB ( 14 FDA reports)
WRIST FRACTURE ( 14 FDA reports)
VERBAL ABUSE ( 13 FDA reports)
ACNE ( 13 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 13 FDA reports)
ALVEOLITIS ALLERGIC ( 13 FDA reports)
ANASTOMOTIC LEAK ( 13 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 13 FDA reports)
AUTOIMMUNE DISORDER ( 13 FDA reports)
BLEPHARITIS ( 13 FDA reports)
BLOOD IRON DECREASED ( 13 FDA reports)
BLOOD OSMOLARITY DECREASED ( 13 FDA reports)
BONE CYST ( 13 FDA reports)
BONE MARROW DEPRESSION ( 13 FDA reports)
BURNS THIRD DEGREE ( 13 FDA reports)
COAGULATION TIME PROLONGED ( 13 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 13 FDA reports)
CRANIAL SUTURES WIDENING ( 13 FDA reports)
CRYSTAL URINE ( 13 FDA reports)
DERMATOMYOSITIS ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 13 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 13 FDA reports)
HEART TRANSPLANT ( 13 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 13 FDA reports)
HYPOCHROMIC ANAEMIA ( 13 FDA reports)
ILEUS PARALYTIC ( 13 FDA reports)
IMMOBILE ( 13 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 13 FDA reports)
INCREASED APPETITE ( 13 FDA reports)
INJECTION SITE RASH ( 13 FDA reports)
INTERVERTEBRAL DISCITIS ( 13 FDA reports)
JEALOUS DELUSION ( 13 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 13 FDA reports)
LIPOMA ( 13 FDA reports)
LUMBAR SPINAL STENOSIS ( 13 FDA reports)
MEGACOLON ( 13 FDA reports)
METABOLIC ALKALOSIS ( 13 FDA reports)
METRORRHAGIA ( 13 FDA reports)
MUCOSAL ULCERATION ( 13 FDA reports)
NEOPLASM ( 13 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 13 FDA reports)
OEDEMATOUS PANCREATITIS ( 13 FDA reports)
OESOPHAGEAL ULCER ( 13 FDA reports)
ORAL HERPES ( 13 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 13 FDA reports)
PLASMACYTOMA ( 13 FDA reports)
PLEURITIC PAIN ( 13 FDA reports)
PO2 DECREASED ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
PREMATURE BABY ( 13 FDA reports)
PROSTATOMEGALY ( 13 FDA reports)
RENAL TRANSPLANT ( 13 FDA reports)
RESPIRATION ABNORMAL ( 13 FDA reports)
RESPIRATORY DEPRESSION ( 13 FDA reports)
SCAB ( 13 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 13 FDA reports)
SKIN WARM ( 13 FDA reports)
SLEEP TERROR ( 13 FDA reports)
SNORING ( 13 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 13 FDA reports)
STENT OCCLUSION ( 13 FDA reports)
STRESS CARDIOMYOPATHY ( 13 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 13 FDA reports)
THYROID DISORDER ( 13 FDA reports)
TRANSPLANT REJECTION ( 13 FDA reports)
ABDOMINAL SEPSIS ( 12 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 12 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 12 FDA reports)
ANAPHYLACTOID REACTION ( 12 FDA reports)
ANEURYSM ( 12 FDA reports)
AORTIC VALVE SCLEROSIS ( 12 FDA reports)
APHAGIA ( 12 FDA reports)
AUTOIMMUNE HEPATITIS ( 12 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 12 FDA reports)
BILE DUCT STONE ( 12 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 12 FDA reports)
BLOOD PH DECREASED ( 12 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 12 FDA reports)
BONE DENSITY DECREASED ( 12 FDA reports)
BONE INFARCTION ( 12 FDA reports)
BREAST HYPERPLASIA ( 12 FDA reports)
CARDIAC ENZYMES INCREASED ( 12 FDA reports)
CARDIAC PACEMAKER INSERTION ( 12 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 12 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 12 FDA reports)
CROHN'S DISEASE ( 12 FDA reports)
CULTURE URINE POSITIVE ( 12 FDA reports)
DEAFNESS UNILATERAL ( 12 FDA reports)
DEFORMITY ( 12 FDA reports)
DEPENDENCE ( 12 FDA reports)
DIABETIC RETINOPATHY ( 12 FDA reports)
DIZZINESS POSTURAL ( 12 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
EAR INFECTION ( 12 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 12 FDA reports)
ENDOMETRIAL CANCER ( 12 FDA reports)
EXOSTOSIS ( 12 FDA reports)
FACIAL PALSY ( 12 FDA reports)
FEAR OF DEATH ( 12 FDA reports)
FIBROSIS ( 12 FDA reports)
FINGER DEFORMITY ( 12 FDA reports)
GASTRIC ULCER PERFORATION ( 12 FDA reports)
GENERALISED ERYTHEMA ( 12 FDA reports)
GINGIVITIS ( 12 FDA reports)
GRANULOMA ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HEPATIC CYST ( 12 FDA reports)
HYPERAESTHESIA ( 12 FDA reports)
HYPERPHOSPHATAEMIA ( 12 FDA reports)
HYPOMANIA ( 12 FDA reports)
IRITIS ( 12 FDA reports)
JUGULAR VEIN DISTENSION ( 12 FDA reports)
LUNG CANCER METASTATIC ( 12 FDA reports)
METASTASES TO LYMPH NODES ( 12 FDA reports)
MUCOSAL INFECTION ( 12 FDA reports)
NEPHRITIS ( 12 FDA reports)
NO ADVERSE EVENT ( 12 FDA reports)
NODAL RHYTHM ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
PANIC DISORDER ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
PCO2 DECREASED ( 12 FDA reports)
PERONEAL NERVE PALSY ( 12 FDA reports)
PITUITARY TUMOUR BENIGN ( 12 FDA reports)
POLYMYALGIA RHEUMATICA ( 12 FDA reports)
POLYMYOSITIS ( 12 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 12 FDA reports)
SINOATRIAL BLOCK ( 12 FDA reports)
SOFT TISSUE DISORDER ( 12 FDA reports)
STOMACH DISCOMFORT ( 12 FDA reports)
TEMPORAL ARTERITIS ( 12 FDA reports)
TIBIA FRACTURE ( 12 FDA reports)
TOOTH ABSCESS ( 12 FDA reports)
TRANSPLANT FAILURE ( 12 FDA reports)
TRIGGER FINGER ( 12 FDA reports)
ULCER HAEMORRHAGE ( 12 FDA reports)
UNDERDOSE ( 12 FDA reports)
URETERIC STENOSIS ( 12 FDA reports)
VASCULAR GRAFT ( 12 FDA reports)
WATER INTOXICATION ( 12 FDA reports)
URINARY HESITATION ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 11 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 11 FDA reports)
ANAPHYLACTOID SHOCK ( 11 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 11 FDA reports)
BLADDER NEOPLASM ( 11 FDA reports)
BLOOD MAGNESIUM DECREASED ( 11 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 11 FDA reports)
BLOOD TEST ABNORMAL ( 11 FDA reports)
CARDIAC OUTPUT DECREASED ( 11 FDA reports)
CATHETER RELATED INFECTION ( 11 FDA reports)
CEREBRAL DISORDER ( 11 FDA reports)
CEREBRAL MICROANGIOPATHY ( 11 FDA reports)
CERVIX CARCINOMA ( 11 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 11 FDA reports)
COAGULATION TEST ABNORMAL ( 11 FDA reports)
CONCUSSION ( 11 FDA reports)
DEVICE RELATED SEPSIS ( 11 FDA reports)
DIABETIC FOOT ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DYSTONIA ( 11 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 11 FDA reports)
ELECTROLYTE DEPLETION ( 11 FDA reports)
EMBOLIC STROKE ( 11 FDA reports)
EOSINOPHIL COUNT INCREASED ( 11 FDA reports)
ESSENTIAL HYPERTENSION ( 11 FDA reports)
EXANTHEM ( 11 FDA reports)
EYE DISORDER ( 11 FDA reports)
FAECES PALE ( 11 FDA reports)
GASTROINTESTINAL NECROSIS ( 11 FDA reports)
GINGIVAL DISORDER ( 11 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 11 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 11 FDA reports)
HELICOBACTER INFECTION ( 11 FDA reports)
HEPATITIS A ( 11 FDA reports)
HICCUPS ( 11 FDA reports)
HYPERKINESIA ( 11 FDA reports)
HYPERPYREXIA ( 11 FDA reports)
HYPOAESTHESIA ORAL ( 11 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 11 FDA reports)
INFERTILITY ( 11 FDA reports)
INFLAMMATION OF WOUND ( 11 FDA reports)
INGROWING NAIL ( 11 FDA reports)
IRRITABLE BOWEL SYNDROME ( 11 FDA reports)
LIBIDO DECREASED ( 11 FDA reports)
LIP OEDEMA ( 11 FDA reports)
MALNUTRITION ( 11 FDA reports)
MARROW HYPERPLASIA ( 11 FDA reports)
MEDICAL DEVICE COMPLICATION ( 11 FDA reports)
METASTASES TO PERITONEUM ( 11 FDA reports)
MONOPLEGIA ( 11 FDA reports)
MUCOUS STOOLS ( 11 FDA reports)
MUSCLE CRAMP ( 11 FDA reports)
MUSCLE NECROSIS ( 11 FDA reports)
MUSCLE TIGHTNESS ( 11 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 11 FDA reports)
NEPHROSCLEROSIS ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
OVARIAN CANCER ( 11 FDA reports)
PANCREATIC CYST ( 11 FDA reports)
PANCREATIC DISORDER ( 11 FDA reports)
PERIODONTITIS ( 11 FDA reports)
PERIORBITAL OEDEMA ( 11 FDA reports)
PETIT MAL EPILEPSY ( 11 FDA reports)
PLATELET COUNT ABNORMAL ( 11 FDA reports)
POISONING ( 11 FDA reports)
POLYCYSTIC OVARIES ( 11 FDA reports)
PORTAL HYPERTENSION ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 11 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 11 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
SCHIZOPHRENIA ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
STUPOR ( 11 FDA reports)
TONGUE BITING ( 11 FDA reports)
TONGUE PARALYSIS ( 11 FDA reports)
TRIGEMINAL NEURALGIA ( 11 FDA reports)
ABNORMAL SENSATION IN EYE ( 10 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 10 FDA reports)
ADENOCARCINOMA ( 10 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 10 FDA reports)
ANAL HAEMORRHAGE ( 10 FDA reports)
AORTIC DILATATION ( 10 FDA reports)
AORTIC VALVE STENOSIS ( 10 FDA reports)
APPLICATION SITE ERYTHEMA ( 10 FDA reports)
BLOOD CALCIUM INCREASED ( 10 FDA reports)
BONE FISTULA ( 10 FDA reports)
BREAST MASS ( 10 FDA reports)
BRONCHIAL OBSTRUCTION ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
CATATONIA ( 10 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 10 FDA reports)
CEREBELLAR SYNDROME ( 10 FDA reports)
CHEILITIS ( 10 FDA reports)
CHOLECYSTITIS CHRONIC ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 10 FDA reports)
CORONARY ANGIOPLASTY ( 10 FDA reports)
DEMYELINATION ( 10 FDA reports)
DIABETIC COMPLICATION ( 10 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 10 FDA reports)
ENTERITIS ( 10 FDA reports)
EXTREMITY NECROSIS ( 10 FDA reports)
FAECAL VOMITING ( 10 FDA reports)
FEBRILE BONE MARROW APLASIA ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 10 FDA reports)
GASTRIC CANCER ( 10 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 10 FDA reports)
GESTATIONAL DIABETES ( 10 FDA reports)
HAEMOGLOBIN INCREASED ( 10 FDA reports)
HAEMORRHAGIC DIATHESIS ( 10 FDA reports)
HEART RATE ABNORMAL ( 10 FDA reports)
HEPATOSPLENOMEGALY ( 10 FDA reports)
HYPERNATRAEMIA ( 10 FDA reports)
HYPERURICAEMIA ( 10 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 10 FDA reports)
INGUINAL HERNIA ( 10 FDA reports)
INJECTION SITE NODULE ( 10 FDA reports)
INTERMITTENT CLAUDICATION ( 10 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 10 FDA reports)
LICHEN PLANUS ( 10 FDA reports)
LYMPHOEDEMA ( 10 FDA reports)
MACROCYTOSIS ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
METASTATIC NEOPLASM ( 10 FDA reports)
MITRAL VALVE PROLAPSE ( 10 FDA reports)
MUCOSAL DRYNESS ( 10 FDA reports)
MYOGLOBINURIA ( 10 FDA reports)
NEOPLASM RECURRENCE ( 10 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 10 FDA reports)
NEUTROPENIC INFECTION ( 10 FDA reports)
OCULAR VASCULAR DISORDER ( 10 FDA reports)
OPERATIVE HAEMORRHAGE ( 10 FDA reports)
OPTIC ATROPHY ( 10 FDA reports)
ORAL DISCHARGE ( 10 FDA reports)
ORAL FUNGAL INFECTION ( 10 FDA reports)
OSTEOSCLEROSIS ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PARATHYROID TUMOUR BENIGN ( 10 FDA reports)
PENILE OEDEMA ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
POLYP ( 10 FDA reports)
PRODUCT TASTE ABNORMAL ( 10 FDA reports)
PROTEIN URINE PRESENT ( 10 FDA reports)
PROTEUS INFECTION ( 10 FDA reports)
PULMONARY HAEMORRHAGE ( 10 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 10 FDA reports)
RESPIRATORY ACIDOSIS ( 10 FDA reports)
SCLERAL DISCOLOURATION ( 10 FDA reports)
SINGLE UMBILICAL ARTERY ( 10 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 10 FDA reports)
SNEEZING ( 10 FDA reports)
SOCIAL PROBLEM ( 10 FDA reports)
SPLENIC INFARCTION ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
STRESS FRACTURE ( 10 FDA reports)
SYSTOLIC HYPERTENSION ( 10 FDA reports)
TETANY ( 10 FDA reports)
TOOTHACHE ( 10 FDA reports)
TRAUMATIC HAEMATOMA ( 10 FDA reports)
URINE ANALYSIS ABNORMAL ( 10 FDA reports)
VARICOSE VEIN ( 10 FDA reports)
VASCULAR GRAFT COMPLICATION ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
VITAMIN D DECREASED ( 10 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 10 FDA reports)
URINARY TRACT OBSTRUCTION ( 9 FDA reports)
VASCULAR DEMENTIA ( 9 FDA reports)
VASODILATATION ( 9 FDA reports)
VENOUS INSUFFICIENCY ( 9 FDA reports)
VENTRICULAR ASYSTOLE ( 9 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 9 FDA reports)
ABDOMINAL HERNIA ( 9 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 9 FDA reports)
ACINETOBACTER INFECTION ( 9 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 9 FDA reports)
ADENOCARCINOMA PANCREAS ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
AKINESIA ( 9 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
APPENDICITIS ( 9 FDA reports)
ARTERIAL DISORDER ( 9 FDA reports)
ARTERIAL STENOSIS ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BILIARY TRACT DISORDER ( 9 FDA reports)
BLINDNESS TRANSIENT ( 9 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 9 FDA reports)
BLOOD CORTISOL INCREASED ( 9 FDA reports)
BLOOD CREATININE ABNORMAL ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 9 FDA reports)
BLOOD UREA DECREASED ( 9 FDA reports)
BONE DEBRIDEMENT ( 9 FDA reports)
BONE FRAGMENTATION ( 9 FDA reports)
BOVINE TUBERCULOSIS ( 9 FDA reports)
BRADYPNOEA ( 9 FDA reports)
CATHETER SITE HAEMORRHAGE ( 9 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 9 FDA reports)
CERVICAL SPINAL STENOSIS ( 9 FDA reports)
CHOKING SENSATION ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
COMMUNICATION DISORDER ( 9 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 9 FDA reports)
CULTURE WOUND POSITIVE ( 9 FDA reports)
CYSTOCELE ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DEMENTIA WITH LEWY BODIES ( 9 FDA reports)
DERMATOPHYTOSIS ( 9 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 9 FDA reports)
DIVERTICULAR PERFORATION ( 9 FDA reports)
DIZZINESS EXERTIONAL ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
DYSPNOEA EXACERBATED ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ENTEROCOCCAL SEPSIS ( 9 FDA reports)
ENTEROVESICAL FISTULA ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GASTROINTESTINAL CARCINOMA ( 9 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 9 FDA reports)
GINGIVAL HYPERPLASIA ( 9 FDA reports)
GLOSSODYNIA ( 9 FDA reports)
HAEMATOMA INFECTION ( 9 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 9 FDA reports)
HALLUCINATIONS, MIXED ( 9 FDA reports)
HEARING DISABILITY ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 9 FDA reports)
HEPATORENAL SYNDROME ( 9 FDA reports)
HERPES SIMPLEX ( 9 FDA reports)
HYDRONEPHROSIS ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
HYPERLACTACIDAEMIA ( 9 FDA reports)
INCISIONAL HERNIA ( 9 FDA reports)
IRON DEFICIENCY ( 9 FDA reports)
JAUNDICE NEONATAL ( 9 FDA reports)
JAW OPERATION ( 9 FDA reports)
JOINT CONTRACTURE ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
LIFE EXPECTANCY SHORTENED ( 9 FDA reports)
LIVEDO RETICULARIS ( 9 FDA reports)
LIVER ABSCESS ( 9 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
MICROALBUMINURIA ( 9 FDA reports)
MIGRAINE WITH AURA ( 9 FDA reports)
MITRAL VALVE CALCIFICATION ( 9 FDA reports)
MIXED LIVER INJURY ( 9 FDA reports)
MUSCLE SWELLING ( 9 FDA reports)
NEPHROCALCINOSIS ( 9 FDA reports)
NEPHROGENIC ANAEMIA ( 9 FDA reports)
NERVE COMPRESSION ( 9 FDA reports)
NEUROTOXICITY ( 9 FDA reports)
NODULE ON EXTREMITY ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
OLFACTORY NERVE DISORDER ( 9 FDA reports)
ORAL NEOPLASM ( 9 FDA reports)
ORGAN FAILURE ( 9 FDA reports)
PERIORBITAL HAEMATOMA ( 9 FDA reports)
PERIPHERAL EMBOLISM ( 9 FDA reports)
PERITONEAL HAEMORRHAGE ( 9 FDA reports)
PERITONITIS BACTERIAL ( 9 FDA reports)
PERSECUTORY DELUSION ( 9 FDA reports)
POOR DENTAL CONDITION ( 9 FDA reports)
POSTURE ABNORMAL ( 9 FDA reports)
PROTEIN TOTAL INCREASED ( 9 FDA reports)
PROTHROMBIN TIME SHORTENED ( 9 FDA reports)
PURULENCE ( 9 FDA reports)
QUADRIPLEGIA ( 9 FDA reports)
QUALITY OF LIFE DECREASED ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
RETINOPATHY ( 9 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 9 FDA reports)
ROTAVIRUS TEST POSITIVE ( 9 FDA reports)
SECRETION DISCHARGE ( 9 FDA reports)
SEQUESTRECTOMY ( 9 FDA reports)
SKIN INDURATION ( 9 FDA reports)
STRABISMUS ( 9 FDA reports)
STREPTOCOCCAL SEPSIS ( 9 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 9 FDA reports)
TOURETTE'S DISORDER ( 9 FDA reports)
TREATMENT FAILURE ( 9 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 9 FDA reports)
ANAEMIA POSTOPERATIVE ( 8 FDA reports)
ANION GAP INCREASED ( 8 FDA reports)
ANORECTAL DISORDER ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
APRAXIA ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ATRIAL THROMBOSIS ( 8 FDA reports)
AURICULAR SWELLING ( 8 FDA reports)
BACK DISORDER ( 8 FDA reports)
BILE DUCT CANCER ( 8 FDA reports)
BLEPHAROSPASM ( 8 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 8 FDA reports)
BLOOD CALCITONIN INCREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 8 FDA reports)
BLOOD URINE ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
CARDIAC OPERATION ( 8 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CONGENITAL TERATOMA ( 8 FDA reports)
CONVERSION DISORDER ( 8 FDA reports)
CORONARY ARTERY DISSECTION ( 8 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 8 FDA reports)
EAR DISORDER ( 8 FDA reports)
EJECTION FRACTION ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 8 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
EYE INFLAMMATION ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 8 FDA reports)
FOOD INTERACTION ( 8 FDA reports)
FOREARM FRACTURE ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
GASTRIC PERFORATION ( 8 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 8 FDA reports)
HAEMOGLOBIN ABNORMAL ( 8 FDA reports)
HAEMORRHAGE URINARY TRACT ( 8 FDA reports)
HAIR DISORDER ( 8 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 8 FDA reports)
HORDEOLUM ( 8 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 8 FDA reports)
ILEOSTOMY ( 8 FDA reports)
IMPAIRED SELF-CARE ( 8 FDA reports)
INITIAL INSOMNIA ( 8 FDA reports)
INJECTION SITE EXTRAVASATION ( 8 FDA reports)
INJECTION SITE MASS ( 8 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 8 FDA reports)
LIGAMENT SPRAIN ( 8 FDA reports)
LIP EROSION ( 8 FDA reports)
LONG QT SYNDROME ( 8 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 8 FDA reports)
MEDIASTINITIS ( 8 FDA reports)
MIDDLE EAR EFFUSION ( 8 FDA reports)
MONOCLONAL GAMMOPATHY ( 8 FDA reports)
MOOD ALTERED ( 8 FDA reports)
MUCOUS MEMBRANE DISORDER ( 8 FDA reports)
MUSCLE ABSCESS ( 8 FDA reports)
NECROTISING FASCIITIS ( 8 FDA reports)
NYSTAGMUS ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
ORAL DYSAESTHESIA ( 8 FDA reports)
OSTEOPOROTIC FRACTURE ( 8 FDA reports)
PALATAL OEDEMA ( 8 FDA reports)
PATELLA FRACTURE ( 8 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 8 FDA reports)
PERFORMANCE STATUS DECREASED ( 8 FDA reports)
PHOTOPSIA ( 8 FDA reports)
PLEURAL DISORDER ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
PROSTATE CANCER METASTATIC ( 8 FDA reports)
PROSTATE INFECTION ( 8 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 8 FDA reports)
PRURIGO ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 8 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 8 FDA reports)
REFRACTORY ANAEMIA ( 8 FDA reports)
RESPIRATORY TRACT OEDEMA ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RETINOGRAM ABNORMAL ( 8 FDA reports)
RHINITIS ( 8 FDA reports)
SCOTOMA ( 8 FDA reports)
SENSATION OF FOREIGN BODY ( 8 FDA reports)
SINUS CONGESTION ( 8 FDA reports)
SJOGREN'S SYNDROME ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN PAPILLOMA ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 8 FDA reports)
SUDDEN HEARING LOSS ( 8 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
THROMBOCYTHAEMIA ( 8 FDA reports)
THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
THYROIDECTOMY ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
TRIGONITIS ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
URETHRITIS ( 8 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 8 FDA reports)
VAGINAL CANDIDIASIS ( 8 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
WOUND DRAINAGE ( 8 FDA reports)
URETHRAL HAEMORRHAGE ( 7 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 7 FDA reports)
VASCULAR GRAFT OCCLUSION ( 7 FDA reports)
VENTRICULAR FAILURE ( 7 FDA reports)
WEGENER'S GRANULOMATOSIS ( 7 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
ABDOMINAL NEOPLASM ( 7 FDA reports)
ABDOMINAL WALL CYST ( 7 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ACUTE PSYCHOSIS ( 7 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
ADHESION ( 7 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 7 FDA reports)
ALBUMIN URINE PRESENT ( 7 FDA reports)
ARTERIAL HAEMORRHAGE ( 7 FDA reports)
ARTERIAL STENT INSERTION ( 7 FDA reports)
BACK INJURY ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BENCE JONES PROTEINURIA ( 7 FDA reports)
BICYTOPENIA ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BILIARY SEPSIS ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BLOOD MAGNESIUM INCREASED ( 7 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 7 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 7 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 7 FDA reports)
BONE MARROW TOXICITY ( 7 FDA reports)
BRAIN DEATH ( 7 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 7 FDA reports)
BRONCHIECTASIS ( 7 FDA reports)
BRONCHOPNEUMOPATHY ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
CALCINOSIS ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
CARDIAC FIBRILLATION ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIOTOXICITY ( 7 FDA reports)
CATHETER SITE INFECTION ( 7 FDA reports)
CELL DEATH ( 7 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 7 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 7 FDA reports)
CLONUS ( 7 FDA reports)
COLONOSCOPY ( 7 FDA reports)
COR PULMONALE ( 7 FDA reports)
CRUSH SYNDROME ( 7 FDA reports)
DEFAECATION URGENCY ( 7 FDA reports)
DIABETES INSIPIDUS ( 7 FDA reports)
DISSEMINATED TUBERCULOSIS ( 7 FDA reports)
DRUG INTERACTION POTENTIATION ( 7 FDA reports)
DRUG-INDUCED LIVER INJURY ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 7 FDA reports)
EMBOLISM ARTERIAL ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENTEROCOLITIS ( 7 FDA reports)
EYE INFECTION ( 7 FDA reports)
EYE ROLLING ( 7 FDA reports)
EYELID PTOSIS ( 7 FDA reports)
FOOD INTOLERANCE ( 7 FDA reports)
GASTROENTERITIS NOROVIRUS ( 7 FDA reports)
GASTROINTESTINAL PAIN ( 7 FDA reports)
GENITAL HERPES ( 7 FDA reports)
GINGIVAL INFECTION ( 7 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 7 FDA reports)
GLOSSITIS ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HAIR TEXTURE ABNORMAL ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HEART TRANSPLANT REJECTION ( 7 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 7 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 7 FDA reports)
HYPOPROTEINAEMIA ( 7 FDA reports)
ILEITIS ( 7 FDA reports)
INCISION SITE HAEMORRHAGE ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INFECTED SKIN ULCER ( 7 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
INTESTINAL INFARCTION ( 7 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 7 FDA reports)
KIDNEY FIBROSIS ( 7 FDA reports)
KIDNEY INFECTION ( 7 FDA reports)
LARYNGEAL CANCER ( 7 FDA reports)
LIGAMENT RUPTURE ( 7 FDA reports)
LIPIDS INCREASED ( 7 FDA reports)
LOSS OF LIBIDO ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
MALIGNANT MELANOMA ( 7 FDA reports)
MEAN CELL VOLUME INCREASED ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
METASTASES TO MENINGES ( 7 FDA reports)
MICROANGIOPATHY ( 7 FDA reports)
NAIL DISCOLOURATION ( 7 FDA reports)
NEPHRITIC SYNDROME ( 7 FDA reports)
NEUROPATHY ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
ORAL DISCOMFORT ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
OSTEOLYSIS ( 7 FDA reports)
OVERWEIGHT ( 7 FDA reports)
PARADOXICAL DRUG REACTION ( 7 FDA reports)
PATHOLOGICAL GAMBLING ( 7 FDA reports)
PERITONEAL DIALYSIS ( 7 FDA reports)
PLEUROTHOTONUS ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
PREMATURE LABOUR ( 7 FDA reports)
PROCTITIS ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PULMONARY ALVEOLAR MICROLITHIASIS ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
PURULENT DISCHARGE ( 7 FDA reports)
RADIUS FRACTURE ( 7 FDA reports)
RASH VESICULAR ( 7 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 7 FDA reports)
RENAL ATROPHY ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RENAL TUBULAR ACIDOSIS ( 7 FDA reports)
RETICULOCYTE COUNT DECREASED ( 7 FDA reports)
RETINAL INJURY ( 7 FDA reports)
RETROPERITONEAL HAEMATOMA ( 7 FDA reports)
SARCOIDOSIS ( 7 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SOFT TISSUE INJURY ( 7 FDA reports)
SPINAL FUSION SURGERY ( 7 FDA reports)
STASIS DERMATITIS ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
SYNOVIAL CYST ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
TONGUE ULCERATION ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
ABDOMINAL HAEMATOMA ( 6 FDA reports)
ABSCESS INTESTINAL ( 6 FDA reports)
ABSCESS LIMB ( 6 FDA reports)
ACTINIC KERATOSIS ( 6 FDA reports)
ACUTE ABDOMEN ( 6 FDA reports)
ACUTE STRESS DISORDER ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 6 FDA reports)
ANGIOGRAM ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
APPLICATION SITE IRRITATION ( 6 FDA reports)
APPLICATION SITE PAIN ( 6 FDA reports)
ARTERIAL THROMBOSIS ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
ASTHMA LATE ONSET ( 6 FDA reports)
ATHEROSCLEROSIS ( 6 FDA reports)
AXONAL NEUROPATHY ( 6 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLADDER DISTENSION ( 6 FDA reports)
BLADDER PROLAPSE ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BREAST CANCER MALE ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
BRONCHOSTENOSIS ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CEREBELLAR HAEMATOMA ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
CONTRAST MEDIA REACTION ( 6 FDA reports)
CREATININE URINE INCREASED ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DERMATOSIS ( 6 FDA reports)
DIABETIC MICROANGIOPATHY ( 6 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 6 FDA reports)
DYSLEXIA ( 6 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 6 FDA reports)
ECZEMA EYELIDS ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 6 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
ENTEROSTOMY ( 6 FDA reports)
EPIDERMAL NECROSIS ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
EXCESSIVE EYE BLINKING ( 6 FDA reports)
EXERCISE TEST ABNORMAL ( 6 FDA reports)
EXTRADURAL ABSCESS ( 6 FDA reports)
FACIAL BONES FRACTURE ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
FEELING DRUNK ( 6 FDA reports)
FEELING JITTERY ( 6 FDA reports)
FLOPPY IRIS SYNDROME ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
FOREIGN BODY ASPIRATION ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GALLBLADDER PAIN ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GLOMERULONEPHROPATHY ( 6 FDA reports)
HAEMOPHILUS INFECTION ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HAEMORRHAGIC URTICARIA ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HEART INJURY ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HERNIA REPAIR ( 6 FDA reports)
HYPERCREATININAEMIA ( 6 FDA reports)
HYPERVOLAEMIA ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOCAPNIA ( 6 FDA reports)
HYPOCOAGULABLE STATE ( 6 FDA reports)
HYPOGONADISM ( 6 FDA reports)
IGA NEPHROPATHY ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INJECTION SITE INFECTION ( 6 FDA reports)
INJECTION SITE URTICARIA ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LIBIDO INCREASED ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LIVIDITY ( 6 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MENINGORRHAGIA ( 6 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 6 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 6 FDA reports)
MOTOR NEURONE DISEASE ( 6 FDA reports)
MUCOSAL EROSION ( 6 FDA reports)
MUSCLE CONTRACTURE ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 6 FDA reports)
MYOPERICARDITIS ( 6 FDA reports)
NEOPLASM SKIN ( 6 FDA reports)
NEURODEGENERATIVE DISORDER ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 6 FDA reports)
OEDEMA MUCOSAL ( 6 FDA reports)
OESOPHAGEAL STENOSIS ( 6 FDA reports)
OPPORTUNISTIC INFECTION ( 6 FDA reports)
PARALYSIS FLACCID ( 6 FDA reports)
PARATHYROIDECTOMY ( 6 FDA reports)
PAROSMIA ( 6 FDA reports)
PEDAL PULSE DECREASED ( 6 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 6 FDA reports)
PHIMOSIS ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 6 FDA reports)
PNEUMONIA ESCHERICHIA ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 6 FDA reports)
PRIAPISM ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PRODUCT ODOUR ABNORMAL ( 6 FDA reports)
PROSTATE CANCER RECURRENT ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
PULMONARY SARCOIDOSIS ( 6 FDA reports)
PULMONARY SEPSIS ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RECTOSIGMOID CANCER ( 6 FDA reports)
RENAL NEOPLASM ( 6 FDA reports)
RESPIRATORY ALKALOSIS ( 6 FDA reports)
RHEUMATOID FACTOR INCREASED ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SCROTAL OEDEMA ( 6 FDA reports)
SHUNT OCCLUSION ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
SPINAL CORD HAEMORRHAGE ( 6 FDA reports)
STENOTROPHOMONAS INFECTION ( 6 FDA reports)
STERNAL FRACTURE ( 6 FDA reports)
SUNBURN ( 6 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 6 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 6 FDA reports)
TIC ( 6 FDA reports)
TRISMUS ( 6 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 6 FDA reports)
URETHRAL PROLAPSE ( 6 FDA reports)
URINE ODOUR ABNORMAL ( 6 FDA reports)
VASCULAR RUPTURE ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 6 FDA reports)
VITH NERVE PARALYSIS ( 6 FDA reports)
WALKING AID USER ( 6 FDA reports)
WEIGHT FLUCTUATION ( 6 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VARICOSE ULCERATION ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
VASCULITIS NECROTISING ( 5 FDA reports)
VENIPUNCTURE SITE SWELLING ( 5 FDA reports)
VESTIBULAR DISORDER ( 5 FDA reports)
VOCAL CORD POLYPECTOMY ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WHIPPLE'S DISEASE ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
ALKALOSIS ( 5 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 5 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
AMBLYOPIA ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANAESTHETIC COMPLICATION ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
ANTIBODY TEST POSITIVE ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 5 FDA reports)
ATROPHY ( 5 FDA reports)
AURA ( 5 FDA reports)
BINGE EATING ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD FOLATE INCREASED ( 5 FDA reports)
BLOOD GASES ABNORMAL ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BONE SWELLING ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BREAST CYST ( 5 FDA reports)
BREAST DISCHARGE ( 5 FDA reports)
BREAST TENDERNESS ( 5 FDA reports)
BRONCHIAL INJURY ( 5 FDA reports)
BRUXISM ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL ARTERY STENOSIS ( 5 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 5 FDA reports)
CLOSTRIDIUM COLITIS ( 5 FDA reports)
COLECTOMY ( 5 FDA reports)
COLORECTAL CANCER ( 5 FDA reports)
COMPLEX PARTIAL SEIZURES ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
CSF PROTEIN INCREASED ( 5 FDA reports)
CULTURE POSITIVE ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DENERVATION ATROPHY ( 5 FDA reports)
DEPRESSION SUICIDAL ( 5 FDA reports)
DEVICE DISLOCATION ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 5 FDA reports)
DIARRHOEA INFECTIOUS ( 5 FDA reports)
DISSOCIATION ( 5 FDA reports)
DUODENAL STENOSIS ( 5 FDA reports)
EAR HAEMORRHAGE ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 5 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EPIDERMOLYSIS ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
ERYTHROPENIA ( 5 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GASTROINTESTINAL TOXICITY ( 5 FDA reports)
HAEMANGIOMA ( 5 FDA reports)
HAPTOGLOBIN DECREASED ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HISTOLOGY ABNORMAL ( 5 FDA reports)
HUNGER ( 5 FDA reports)
HYDROTHORAX ( 5 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 5 FDA reports)
HYPOPROTHROMBINAEMIA ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
KETOACIDOSIS ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LABYRINTHITIS ( 5 FDA reports)
LARYNGEAL INJURY ( 5 FDA reports)
LIMB DEFORMITY ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MONOCYTE COUNT DECREASED ( 5 FDA reports)
MUSCLE ENZYME INCREASED ( 5 FDA reports)
MUSCLE FATIGUE ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
MYOCARDIAL RUPTURE ( 5 FDA reports)
MYOCARDIAL STRAIN ( 5 FDA reports)
NASAL DRYNESS ( 5 FDA reports)
NASAL INFLAMMATION ( 5 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 5 FDA reports)
NIPPLE DISORDER ( 5 FDA reports)
NITRITOID REACTION ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
NOSOCOMIAL INFECTION ( 5 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
OESOPHAGEAL SPASM ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
OSTEOCHONDROSIS ( 5 FDA reports)
OTORRHOEA ( 5 FDA reports)
PANCREATIC DUCT DILATATION ( 5 FDA reports)
PANCREATIC NECROSIS ( 5 FDA reports)
PANCREATIC NEOPLASM ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARAPSORIASIS ( 5 FDA reports)
PEPTIC ULCER PERFORATION ( 5 FDA reports)
PERIANAL ABSCESS ( 5 FDA reports)
PHARYNGEAL ABSCESS ( 5 FDA reports)
PITUITARY TUMOUR RECURRENT ( 5 FDA reports)
PLEURAL HAEMORRHAGE ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POLYCYSTIC LIVER DISEASE ( 5 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 5 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 5 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 5 FDA reports)
RENAL CANCER STAGE III ( 5 FDA reports)
RENAL VASCULITIS ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RETINOPATHY OF PREMATURITY ( 5 FDA reports)
RETROGRADE AMNESIA ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SEBORRHOEIC DERMATITIS ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SHUNT MALFUNCTION ( 5 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 5 FDA reports)
SKIN FRAGILITY ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
SPIDER VEIN ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPLENIC CYST ( 5 FDA reports)
SPLENIC RUPTURE ( 5 FDA reports)
STOOL PH DECREASED ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
SURGICAL PROCEDURE REPEATED ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
THROMBOEMBOLECTOMY ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
THYROID CYST ( 5 FDA reports)
TOE AMPUTATION ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRACHEAL INJURY ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
TUNNEL VISION ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACNE CYSTIC ( 4 FDA reports)
ACQUIRED HAEMOPHILIA ( 4 FDA reports)
ACTINIC ELASTOSIS ( 4 FDA reports)
ACUTE PHASE REACTION ( 4 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANAL ULCER ( 4 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ANOSOGNOSIA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC RUPTURE ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APLASIA ( 4 FDA reports)
APPARENT LIFE THREATENING EVENT ( 4 FDA reports)
APPLICATION SITE VESICLES ( 4 FDA reports)
ARTERIAL RESTENOSIS ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASBESTOSIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ATONIC URINARY BLADDER ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BENIGN BREAST NEOPLASM ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 4 FDA reports)
BLOOD CREATINE ABNORMAL ( 4 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 4 FDA reports)
BLOOD FOLATE ABNORMAL ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BREECH PRESENTATION ( 4 FDA reports)
BRONCHIAL INFECTION ( 4 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
BURNOUT SYNDROME ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 4 FDA reports)
CAROTID ARTERY DISSECTION ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CATAPLEXY ( 4 FDA reports)
CERVICAL MYELOPATHY ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
CLUBBING ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COCCIDIOIDOMYCOSIS ( 4 FDA reports)
COLON ADENOMA ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
CORONARY ARTERY PERFORATION ( 4 FDA reports)
CSF TEST ABNORMAL ( 4 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DELAYED SLEEP PHASE ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 4 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 4 FDA reports)
DRESSLER'S SYNDROME ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
DYSPRAXIA ( 4 FDA reports)
DYSTROPHIC CALCIFICATION ( 4 FDA reports)
EAR LOBE INFECTION ( 4 FDA reports)
ECZEMA INFECTED ( 4 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 4 FDA reports)
ENDOMETRITIS ( 4 FDA reports)
ENDOSCOPY BILIARY TRACT ( 4 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
EPICONDYLITIS ( 4 FDA reports)
ERECTION INCREASED ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA INFECTIOSUM ( 4 FDA reports)
EXTERNAL EAR DISORDER ( 4 FDA reports)
EYE LASER SURGERY ( 4 FDA reports)
EYELID INFECTION ( 4 FDA reports)
FACIAL ASYMMETRY ( 4 FDA reports)
FASCIOTOMY ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
FINE MOTOR DELAY ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
FUNGAL PERITONITIS ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GLIOBLASTOMA MULTIFORME ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMATOSPERMIA ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMOCHROMATOSIS ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAEMOGLOBINURIA ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPERTROPHY ( 4 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 4 FDA reports)
HYPOSPERMIA ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
ILEAL ULCER ( 4 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
IMPLANT SITE EFFUSION ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INHIBITORY DRUG INTERACTION ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INSULINOMA ( 4 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTRACRANIAL ANEURYSM ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
KETONURIA ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LAPAROTOMY ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEIOMYOSARCOMA ( 4 FDA reports)
LIGAMENT INJURY ( 4 FDA reports)
LIMB ASYMMETRY ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LINEAR IGA DISEASE ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LIPODYSTROPHY ACQUIRED ( 4 FDA reports)
LIPOPROTEIN (A) INCREASED ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LOW TURNOVER OSTEOPATHY ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
MACROGLOSSIA ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MAGNESIUM DEFICIENCY ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METAMORPHOPSIA ( 4 FDA reports)
METASTASES TO STOMACH ( 4 FDA reports)
MICTURITION DISORDER ( 4 FDA reports)
MONONEUROPATHY ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MYELOID MATURATION ARREST ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
MYOPATHY TOXIC ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NEUROENDOCRINE TUMOUR ( 4 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 4 FDA reports)
NEUROSURGERY ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 4 FDA reports)
ON AND OFF PHENOMENON ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 4 FDA reports)
PERITONEAL DISORDER ( 4 FDA reports)
PERITONEAL TUBERCULOSIS ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
PODAGRA ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
POST PROCEDURAL DISCHARGE ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
PROPOFOL INFUSION SYNDROME ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
RADICULAR SYNDROME ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 4 FDA reports)
RENAL ISCHAEMIA ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 4 FDA reports)
RETICULOCYTE COUNT INCREASED ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 4 FDA reports)
SELF-INJURIOUS IDEATION ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
STEATORRHOEA ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
SYSTEMIC SCLEROSIS ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THOUGHT INSERTION ( 4 FDA reports)
THYROXINE FREE DECREASED ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONGUE DISCOLOURATION ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
ULCERATIVE KERATITIS ( 4 FDA reports)
URAEMIC GASTROPATHY ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
URTICARIA PAPULAR ( 4 FDA reports)
UTERINE CERVIX STENOSIS ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
VIROLOGIC FAILURE ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
URETHRAL DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINE CALCIUM INCREASED ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
URINOMA ( 3 FDA reports)
UROGENITAL DISORDER ( 3 FDA reports)
UROGENITAL HAEMORRHAGE ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VACCINATION COMPLICATION ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 3 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 3 FDA reports)
VIIITH NERVE INJURY ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VITAL CAPACITY DECREASED ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VITREOUS DISORDER ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
VOLUME BLOOD DECREASED ( 3 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
WRIST SURGERY ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ABULIA ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AGITATED DEPRESSION ( 3 FDA reports)
AIDS ENCEPHALOPATHY ( 3 FDA reports)
ALBUMINURIA ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
ALOPECIA TOTALIS ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANGIODYSPLASIA ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTEROGRADE AMNESIA ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTO-DUODENAL FISTULA ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTERITIS CORONARY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 3 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AUTOMATISM ( 3 FDA reports)
BABINSKI REFLEX TEST ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BASE EXCESS NEGATIVE ( 3 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BILIRUBIN URINE ( 3 FDA reports)
BIOPSY KIDNEY ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD IRON INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 3 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BLOOD URIC ACID DECREASED ( 3 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 3 FDA reports)
BONE MARROW OEDEMA ( 3 FDA reports)
BORRELIA TEST POSITIVE ( 3 FDA reports)
BRACHIAL PLEXUS INJURY ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CAMPYLOBACTER INFECTION ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CARDIAC ABLATION ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CARTILAGE INJURY ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERULOPLASMIN INCREASED ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CERVIX INFLAMMATION ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLITIS MICROSCOPIC ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATED FRACTURE ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 3 FDA reports)
DELUSIONAL DISORDER, JEALOUS TYPE ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DENTURE WEARER ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
EDUCATIONAL PROBLEM ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
EMBOLISM VENOUS ( 3 FDA reports)
ENCEPHALITIS VIRAL ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROCOLITIS BACTERIAL ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FACTOR VIII DEFICIENCY ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 3 FDA reports)
FOETAL GROWTH RESTRICTION ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FROSTBITE ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTRIC CANCER RECURRENT ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTRIC STENOSIS ( 3 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GINGIVAL OPERATION ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
GLOBAL AMNESIA ( 3 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRANDIOSITY ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HAND DEFORMITY ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS B DNA INCREASED ( 3 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 3 FDA reports)
HIV TEST POSITIVE ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HORMONE LEVEL ABNORMAL ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERPARATHYROIDISM ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOPHARYNGEAL CANCER ( 3 FDA reports)
HYPOPYON ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
ILEAL STENOSIS ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
IMPLANT SITE ERYTHEMA ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INFUSION SITE ABSCESS ( 3 FDA reports)
INGUINAL HERNIA REPAIR ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
INTRACARDIAC MASS ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
INTRASPINAL ABSCESS ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JAUNDICE ACHOLURIC ( 3 FDA reports)
JOINT DESTRUCTION ( 3 FDA reports)
JOINT FLUID DRAINAGE ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KARNOFSKY SCALE WORSENED ( 3 FDA reports)
LDL/HDL RATIO ( 3 FDA reports)
LEISHMANIASIS ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
LIPOEDEMA ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MACULE ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MECHANICAL ILEUS ( 3 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 3 FDA reports)
MYELOCYTE COUNT DECREASED ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NEPHROANGIOSCLEROSIS ( 3 FDA reports)
NEURITIS ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
OESOPHAGEAL RUPTURE ( 3 FDA reports)
OPTIC NERVE DISORDER ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC ATROPHY ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PANOPHTHALMITIS ( 3 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 3 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIPHERAL PULSE DECREASED ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERITONITIS SCLEROSING ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PEYRONIE'S DISEASE ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PLACENTAL DISORDER ( 3 FDA reports)
PLANTAR ERYTHEMA ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PLEURAL CALCIFICATION ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTINFARCTION ANGINA ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PROCTITIS ULCERATIVE ( 3 FDA reports)
PROSTATIC ADENOMA ( 3 FDA reports)
PROSTATIC HAEMORRHAGE ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PSEUDOPOLYP ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
PULPITIS DENTAL ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 3 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL NEOVASCULARISATION ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
ROTATOR CUFF REPAIR ( 3 FDA reports)
ROTAVIRUS INFECTION ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SENILE DEMENTIA ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SEROLOGY ABNORMAL ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SICCA SYNDROME ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SINUS RHYTHM ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN SENSITISATION ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SMOKER ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SOMATIC DELUSION ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPLEEN SCAN ABNORMAL ( 3 FDA reports)
SPONDYLITIC MYELOPATHY ( 3 FDA reports)
SPONTANEOUS HAEMATOMA ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STENOTROPHOMONAS SEPSIS ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TOE OPERATION ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TONGUE NECROSIS ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TROPONIN ( 3 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UMBILICAL CORD ABNORMALITY ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
ALVEOLAR SOFT PART SARCOMA METASTATIC ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL INJURY ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANGIOLIPOMA ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
AORTIC BYPASS ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC INTRAMURAL HAEMATOMA ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE HYPERAESTHESIA ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL CATHETERISATION ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ASCITES INFECTION ( 2 FDA reports)
ASPIRATION JOINT ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BENIGN OVARIAN TUMOUR ( 2 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 2 FDA reports)
BILE DUCT NECROSIS ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY BILE DUCT ABNORMAL ( 2 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLADDER SPHINCTER ATONY ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 2 FDA reports)
BLOOD CALCITONIN DECREASED ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GLUCAGON ABNORMAL ( 2 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIFFERENCE OF EXTREMITIES ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST NECROSIS ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHITIS PNEUMOCOCCAL ( 2 FDA reports)
BRONCHOPULMONARY DISEASE ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
BULBAR PALSY ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BUNION ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
C-REACTIVE PROTEIN ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CANDIDA OSTEOMYELITIS ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIOMYOPATHY ACUTE ( 2 FDA reports)
CARDIOPULMONARY BYPASS ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CAUDAL REGRESSION SYNDROME ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHOROIDAL EFFUSION ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLON CANCER STAGE III ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMA URAEMIC ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
CORNEAL ABSCESS ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYSTITIS BACTERIAL ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIGITAL ULCER ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DIVERTICULUM DUODENAL ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL FISTULA ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ECHOCARDIOGRAM ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENTERITIS NECROTICANS ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EOSINOPHILIC COLITIS ( 2 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ERYTHROBLASTOSIS ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXECUTIVE DYSFUNCTION ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXTRASKELETAL OSSIFICATION ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTRIC CYST ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 2 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HELMINTHIC INFECTION ( 2 FDA reports)
HEMIANOPIA HETERONYMOUS ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HIV ANTIBODY POSITIVE ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPERPHOSPHATURIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPONATRAEMIC SYNDROME ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINAL STRICTURE ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEIOMYOSARCOMA RECURRENT ( 2 FDA reports)
LERICHE SYNDROME ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIP HAEMATOMA ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPASE DECREASED ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
MALIGNANT HEPATOBILIARY NEOPLASM ( 2 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 2 FDA reports)
MALIGNANT PITUITARY TUMOUR ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDIAN NERVE INJURY ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESENTERIC NEOPLASM ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO EYE ( 2 FDA reports)
METASTASES TO PHARYNX ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MORGANELLA TEST POSITIVE ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NIPPLE EXUDATE BLOODY ( 2 FDA reports)
NITRITOID CRISIS ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NON-DIPPING ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PACHYMENINGITIS ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANEOPLASTIC ENCEPHALOMYELITIS ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC INFECTION ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENILE SIZE REDUCED ( 2 FDA reports)
PERFORATED DUODENAL ULCER REPAIR ( 2 FDA reports)
PERIARTICULAR DISORDER ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERITONEAL ADHESIONS DIVISION ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PLEURAL DECORTICATION ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PSEUDOENDOPHTHALMITIS ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTURE SITE PAIN ( 2 FDA reports)
PYELOTOMY ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL NEOPLASM ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL CYST HAEMORRHAGE ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RESECTION OF RECTUM ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINAL ANEURYSM ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL DEPOSITS ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCIATIC NERVE NEUROPATHY ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SENSORY LEVEL ABNORMAL ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPERM CONCENTRATION ZERO ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STARING ( 2 FDA reports)
STENT EMBOLISATION ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TENDON SHEATH INCISION ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYROIDITIS ACUTE ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE CYTOLOGY ABNORMAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE SODIUM ABNORMAL ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VIRAL CARDIOMYOPATHY ( 2 FDA reports)
VITAMIN B1 DEFICIENCY ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VOLVULUS OF SMALL BOWEL ( 2 FDA reports)
VON WILLEBRAND'S DISEASE ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
VULVOVAGINAL RASH ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URATE NEPHROPATHY ( 1 FDA reports)
URETERECTOMY ( 1 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER ABSCESS ( 1 FDA reports)
URINARY BLADDER EXCISION ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGENITAL INFECTION BACTERIAL ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS OPERATION ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VERTEBRAL ARTERY HYPOPLASIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOGT-KOYANAGI-HARADA SYNDROME ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL SWELLING ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
WOUND HEALING NORMAL ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
ADRENALITIS ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMMONIA ( 1 FDA reports)
AMOEBIC DYSENTERY ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOKERATOMA ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANOTIA ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 1 FDA reports)
ANTI-PLATELET ANTIBODY NEGATIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARRHYTHMIA NEONATAL ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS ABNORMAL ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY HEART ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY LYMPH GLAND ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER CANCER STAGE I, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY INCREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C1 ESTERASE INHIBITOR DECREASED ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CAPNOCYTOPHAGIA INFECTION ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE RASH ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL DECOMPRESSION ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CERVICAL CONISATION ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CHARLES BONNET SYNDROME ( 1 FDA reports)
CHEILITIS GRANULOMATOSA ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLANGIOADENOMA ( 1 FDA reports)
CHOLELITHIASIS MIGRATION ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLEMENT FACTOR C4 INCREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONTRAINDICATION TO SURGERY ( 1 FDA reports)
CONTRALATERAL BREAST CANCER ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL THICKENING ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CUTANEOUS LEISHMANIASIS ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DECREASED INSULIN REQUIREMENT ( 1 FDA reports)
DEHYDROEPIANDROSTERONE DECREASED ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPRESSIVE DELUSION ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC DERMOPATHY ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC MACROANGIOPATHY ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULITIS MECKEL'S ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DEFORMITY ACQUIRED ( 1 FDA reports)
EAR NEOPLASM MALIGNANT ( 1 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALITIS ALLERGIC ( 1 FDA reports)
ENCEPHALOCELE ( 1 FDA reports)
ENDOCARDIAL FIBROELASTOSIS ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL ADENOMA ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCLYSIS ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC PUSTULOSIS ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIDIDYMAL CYST ( 1 FDA reports)
EPIDURITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHROPLASIA ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID TUMOUR ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR XI DEFICIENCY ( 1 FDA reports)
FALLOT'S PENTALOGY ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FOSTER-KENNEDY SYNDROME ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRITIS FUNGAL ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOTTIS CARCINOMA ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GONADOTROPHIN DEFICIENCY ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHAGIC VASCULITIS ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATITIS D ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEAL ULCER PERFORATION ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED DRUG PRESCRIBING ERROR ( 1 FDA reports)
INTERMEDIATE UVEITIS ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
JEJUNAL ULCER PERFORATION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS VIRAL ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY ANASTOMOSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MALIGNANT NEOPLASM OF AURICULAR CARTILAGE ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MICROSURGERY TO HAND ( 1 FDA reports)
MIDDLE EAR INFLAMMATION ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDITIS POST INFECTION ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROBORRELIOSIS ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALPATORY FINDING ABNORMAL ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PARADOXICAL PRESSOR RESPONSE ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARAPHARYNGEAL ABSCESS ( 1 FDA reports)
PARASITIC INFECTION INTESTINAL ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PENILE CURVATURE ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIHEPATIC DISCOMFORT ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIPROSTHETIC OSTEOLYSIS ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PILONIDAL SINUS REPAIR ( 1 FDA reports)
PITUITARY INFARCTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL PYAEMIA ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCALCITONIN ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE BULBAR PALSY ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY VALVE SCLEROSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL CANCER STAGE I ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL FUNCTION TEST ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL MIGRAINE ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND ADENOMA ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERRATIA BACTERAEMIA ( 1 FDA reports)
SERUM PROCOLLAGEN TYPE III N-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPECIFIC GRAVITY URINE ABNORMAL ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL MENINGIOMA BENIGN ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON REPAIR ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR INFARCTION ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACOSTOMY ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX DECREASED ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID C-CELL HYPERPLASIA ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL FISTULA REPAIR ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRYPTASE DECREASED ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)