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

ATRIAL FIBRILLATION ( 1148 FDA reports)
PAIN ( 1063 FDA reports)
RENAL FAILURE ( 969 FDA reports)
DYSPNOEA ( 963 FDA reports)
ANXIETY ( 871 FDA reports)
DRUG INTERACTION ( 805 FDA reports)
INJURY ( 789 FDA reports)
ASTHENIA ( 731 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 676 FDA reports)
HYPOTENSION ( 661 FDA reports)
DIZZINESS ( 636 FDA reports)
RENAL FAILURE ACUTE ( 632 FDA reports)
PNEUMONIA ( 611 FDA reports)
NAUSEA ( 609 FDA reports)
UNEVALUABLE EVENT ( 571 FDA reports)
FATIGUE ( 562 FDA reports)
OEDEMA PERIPHERAL ( 521 FDA reports)
EMOTIONAL DISTRESS ( 516 FDA reports)
DEATH ( 509 FDA reports)
FALL ( 496 FDA reports)
RENAL IMPAIRMENT ( 494 FDA reports)
MULTI-ORGAN FAILURE ( 480 FDA reports)
ANAEMIA ( 477 FDA reports)
VENTRICULAR TACHYCARDIA ( 465 FDA reports)
FEAR ( 458 FDA reports)
ANHEDONIA ( 432 FDA reports)
CARDIAC ARREST ( 430 FDA reports)
VOMITING ( 423 FDA reports)
BRADYCARDIA ( 405 FDA reports)
PLEURAL EFFUSION ( 402 FDA reports)
RENAL INJURY ( 401 FDA reports)
DIARRHOEA ( 396 FDA reports)
CHEST PAIN ( 380 FDA reports)
CARDIAC FAILURE ( 377 FDA reports)
STRESS ( 369 FDA reports)
CONDITION AGGRAVATED ( 365 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 363 FDA reports)
DEPRESSION ( 355 FDA reports)
DRUG INEFFECTIVE ( 352 FDA reports)
SYNCOPE ( 345 FDA reports)
MYOCARDIAL INFARCTION ( 334 FDA reports)
RESPIRATORY FAILURE ( 324 FDA reports)
WEIGHT DECREASED ( 307 FDA reports)
PYREXIA ( 296 FDA reports)
PAIN IN EXTREMITY ( 294 FDA reports)
ARRHYTHMIA ( 293 FDA reports)
HYPOTHYROIDISM ( 285 FDA reports)
ECONOMIC PROBLEM ( 284 FDA reports)
MALAISE ( 283 FDA reports)
HYPERTENSION ( 281 FDA reports)
DEHYDRATION ( 275 FDA reports)
COUGH ( 269 FDA reports)
ARTHRALGIA ( 263 FDA reports)
SEPSIS ( 261 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 261 FDA reports)
BACK PAIN ( 247 FDA reports)
BLOOD CREATININE INCREASED ( 243 FDA reports)
HYPERTHYROIDISM ( 241 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 240 FDA reports)
HEADACHE ( 239 FDA reports)
CONFUSIONAL STATE ( 237 FDA reports)
HAEMOGLOBIN DECREASED ( 237 FDA reports)
ABDOMINAL PAIN ( 232 FDA reports)
CEREBROVASCULAR ACCIDENT ( 232 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 229 FDA reports)
PULMONARY OEDEMA ( 229 FDA reports)
CARDIOMEGALY ( 228 FDA reports)
PALPITATIONS ( 227 FDA reports)
TORSADE DE POINTES ( 225 FDA reports)
DECREASED APPETITE ( 222 FDA reports)
INTERSTITIAL LUNG DISEASE ( 218 FDA reports)
PULMONARY FIBROSIS ( 217 FDA reports)
LOSS OF CONSCIOUSNESS ( 214 FDA reports)
HYPOKALAEMIA ( 210 FDA reports)
MUSCULAR WEAKNESS ( 208 FDA reports)
CORONARY ARTERY DISEASE ( 207 FDA reports)
PARAESTHESIA ( 204 FDA reports)
MITRAL VALVE INCOMPETENCE ( 201 FDA reports)
VENTRICULAR FIBRILLATION ( 200 FDA reports)
GAIT DISTURBANCE ( 199 FDA reports)
THROMBOCYTOPENIA ( 199 FDA reports)
URINARY TRACT INFECTION ( 197 FDA reports)
CONSTIPATION ( 195 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 190 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 188 FDA reports)
OEDEMA ( 187 FDA reports)
MULTIPLE INJURIES ( 184 FDA reports)
CARDIOGENIC SHOCK ( 183 FDA reports)
TACHYCARDIA ( 181 FDA reports)
TREMOR ( 179 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 177 FDA reports)
RENAL FAILURE CHRONIC ( 176 FDA reports)
ATRIAL FLUTTER ( 175 FDA reports)
HYPERKALAEMIA ( 174 FDA reports)
HYPONATRAEMIA ( 174 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 173 FDA reports)
PRURITUS ( 170 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 169 FDA reports)
CARDIAC DISORDER ( 169 FDA reports)
CHEST DISCOMFORT ( 169 FDA reports)
INSOMNIA ( 169 FDA reports)
RASH ( 166 FDA reports)
CARDIOMYOPATHY ( 165 FDA reports)
DRUG TOXICITY ( 162 FDA reports)
FEELING ABNORMAL ( 162 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 162 FDA reports)
LUNG DISORDER ( 160 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 155 FDA reports)
HEART RATE INCREASED ( 155 FDA reports)
RHABDOMYOLYSIS ( 154 FDA reports)
WEIGHT INCREASED ( 152 FDA reports)
BLOOD GLUCOSE INCREASED ( 151 FDA reports)
DYSPNOEA EXERTIONAL ( 149 FDA reports)
INFECTION ( 149 FDA reports)
HYPERHIDROSIS ( 148 FDA reports)
PULMONARY TOXICITY ( 148 FDA reports)
ERYTHEMA ( 146 FDA reports)
CARDIAC MURMUR ( 145 FDA reports)
HAEMORRHAGE ( 145 FDA reports)
MOBILITY DECREASED ( 145 FDA reports)
BLOOD BILIRUBIN INCREASED ( 143 FDA reports)
PERICARDIAL EFFUSION ( 143 FDA reports)
PULMONARY HYPERTENSION ( 142 FDA reports)
CONTUSION ( 140 FDA reports)
HEPATIC STEATOSIS ( 139 FDA reports)
ATELECTASIS ( 137 FDA reports)
BLOOD PRESSURE DECREASED ( 136 FDA reports)
BLOOD PRESSURE INCREASED ( 135 FDA reports)
DYSPHAGIA ( 132 FDA reports)
PULMONARY EMBOLISM ( 131 FDA reports)
SEPTIC SHOCK ( 129 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 128 FDA reports)
EJECTION FRACTION DECREASED ( 126 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 123 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 122 FDA reports)
SINUS BRADYCARDIA ( 121 FDA reports)
SKIN DISCOLOURATION ( 121 FDA reports)
HYPOXIA ( 120 FDA reports)
CARDIO-RESPIRATORY ARREST ( 119 FDA reports)
EPISTAXIS ( 118 FDA reports)
HEART RATE DECREASED ( 118 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 118 FDA reports)
HYPOAESTHESIA ( 117 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 117 FDA reports)
ABDOMINAL DISTENSION ( 116 FDA reports)
VISION BLURRED ( 115 FDA reports)
ABDOMINAL PAIN UPPER ( 114 FDA reports)
BLOOD UREA INCREASED ( 112 FDA reports)
HYPOGLYCAEMIA ( 112 FDA reports)
NEUROPATHY PERIPHERAL ( 112 FDA reports)
UNRESPONSIVE TO STIMULI ( 112 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 111 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 111 FDA reports)
LETHARGY ( 111 FDA reports)
PLATELET COUNT DECREASED ( 111 FDA reports)
CELLULITIS ( 109 FDA reports)
LUNG INFILTRATION ( 109 FDA reports)
HEART RATE IRREGULAR ( 107 FDA reports)
MYALGIA ( 107 FDA reports)
OSTEOARTHRITIS ( 105 FDA reports)
DEEP VEIN THROMBOSIS ( 104 FDA reports)
DISEASE PROGRESSION ( 103 FDA reports)
HEPATIC FAILURE ( 103 FDA reports)
MENTAL STATUS CHANGES ( 103 FDA reports)
PNEUMONITIS ( 103 FDA reports)
HYPERLIPIDAEMIA ( 102 FDA reports)
SOMNOLENCE ( 102 FDA reports)
TREATMENT NONCOMPLIANCE ( 102 FDA reports)
ANGINA PECTORIS ( 101 FDA reports)
BRONCHITIS ( 101 FDA reports)
COMA ( 101 FDA reports)
DRY SKIN ( 100 FDA reports)
LEUKOCYTOSIS ( 100 FDA reports)
PANCYTOPENIA ( 100 FDA reports)
DIABETES MELLITUS ( 99 FDA reports)
FLUID OVERLOAD ( 99 FDA reports)
HAEMATOCRIT DECREASED ( 99 FDA reports)
HAEMATURIA ( 99 FDA reports)
ABDOMINAL DISCOMFORT ( 97 FDA reports)
RECTAL HAEMORRHAGE ( 96 FDA reports)
BALANCE DISORDER ( 94 FDA reports)
WHEEZING ( 94 FDA reports)
ACUTE RESPIRATORY FAILURE ( 93 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 93 FDA reports)
CONVULSION ( 92 FDA reports)
LIVER DISORDER ( 92 FDA reports)
RESPIRATORY DISTRESS ( 92 FDA reports)
OVERDOSE ( 90 FDA reports)
SKIN INDURATION ( 89 FDA reports)
SKIN ULCER ( 88 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 87 FDA reports)
HAEMATOMA ( 86 FDA reports)
ABASIA ( 85 FDA reports)
PROTHROMBIN TIME PROLONGED ( 85 FDA reports)
MYOCARDIAL ISCHAEMIA ( 83 FDA reports)
COAGULOPATHY ( 82 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 82 FDA reports)
ANOREXIA ( 81 FDA reports)
CHILLS ( 80 FDA reports)
HAEMODIALYSIS ( 79 FDA reports)
HAEMOPTYSIS ( 79 FDA reports)
ILL-DEFINED DISORDER ( 79 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 79 FDA reports)
NECK PAIN ( 79 FDA reports)
CHOLELITHIASIS ( 78 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 77 FDA reports)
DYSPEPSIA ( 77 FDA reports)
SKIN HYPERTROPHY ( 77 FDA reports)
STAPHYLOCOCCAL INFECTION ( 77 FDA reports)
THROMBOSIS ( 77 FDA reports)
VERTIGO ( 77 FDA reports)
SLEEP APNOEA SYNDROME ( 76 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 75 FDA reports)
RESPIRATORY ARREST ( 75 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 74 FDA reports)
SKIN TIGHTNESS ( 74 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 73 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 73 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 73 FDA reports)
JOINT SWELLING ( 73 FDA reports)
ALOPECIA ( 71 FDA reports)
VISUAL IMPAIRMENT ( 71 FDA reports)
EMOTIONAL DISORDER ( 70 FDA reports)
ARTERIOSCLEROSIS ( 69 FDA reports)
DIALYSIS ( 69 FDA reports)
FLUSHING ( 69 FDA reports)
HEPATOTOXICITY ( 69 FDA reports)
HYPERSENSITIVITY ( 69 FDA reports)
MUSCULOSKELETAL PAIN ( 69 FDA reports)
MYOSITIS ( 69 FDA reports)
SCAR ( 69 FDA reports)
ATAXIA ( 68 FDA reports)
HEPATIC ENZYME INCREASED ( 68 FDA reports)
POST PROCEDURAL COMPLICATION ( 68 FDA reports)
PULMONARY CONGESTION ( 68 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 68 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 67 FDA reports)
MYOPATHY ( 67 FDA reports)
OBESITY ( 67 FDA reports)
AGITATION ( 66 FDA reports)
BLOOD POTASSIUM DECREASED ( 66 FDA reports)
HEPATITIS ACUTE ( 66 FDA reports)
MUSCLE SPASMS ( 66 FDA reports)
SURGERY ( 66 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 65 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 65 FDA reports)
METABOLIC ACIDOSIS ( 65 FDA reports)
NEUTROPENIA ( 65 FDA reports)
RALES ( 65 FDA reports)
BLOOD POTASSIUM INCREASED ( 64 FDA reports)
CEREBRAL HAEMORRHAGE ( 64 FDA reports)
BURNING SENSATION ( 63 FDA reports)
SHOCK ( 63 FDA reports)
BLOOD SODIUM DECREASED ( 62 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 62 FDA reports)
LEUKOPENIA ( 62 FDA reports)
ASCITES ( 61 FDA reports)
ASTHMA ( 61 FDA reports)
ATRIOVENTRICULAR BLOCK ( 61 FDA reports)
OSTEONECROSIS OF JAW ( 61 FDA reports)
OXYGEN SATURATION DECREASED ( 61 FDA reports)
THYROID DISORDER ( 61 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 60 FDA reports)
ORTHOSTATIC HYPOTENSION ( 60 FDA reports)
SINUSITIS ( 60 FDA reports)
HALLUCINATION ( 59 FDA reports)
MEDICATION ERROR ( 59 FDA reports)
PRESYNCOPE ( 59 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 59 FDA reports)
IMPAIRED HEALING ( 58 FDA reports)
INCORRECT DOSE ADMINISTERED ( 58 FDA reports)
JAUNDICE ( 58 FDA reports)
MELAENA ( 58 FDA reports)
MEMORY IMPAIRMENT ( 58 FDA reports)
CARDIAC PACEMAKER INSERTION ( 57 FDA reports)
HYPOKINESIA ( 57 FDA reports)
JOINT STIFFNESS ( 57 FDA reports)
SKIN DISORDER ( 57 FDA reports)
BONE DISORDER ( 56 FDA reports)
CIRCULATORY COLLAPSE ( 56 FDA reports)
MENTAL DISORDER ( 56 FDA reports)
OROPHARYNGEAL PAIN ( 56 FDA reports)
OSTEOMYELITIS ( 56 FDA reports)
RENAL DISORDER ( 56 FDA reports)
SKIN HYPERPIGMENTATION ( 56 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 56 FDA reports)
VENTRICULAR HYPOKINESIA ( 56 FDA reports)
VISUAL ACUITY REDUCED ( 56 FDA reports)
DEFORMITY ( 55 FDA reports)
AORTIC VALVE INCOMPETENCE ( 54 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 54 FDA reports)
DILATATION VENTRICULAR ( 54 FDA reports)
HEAD INJURY ( 54 FDA reports)
HYPERGLYCAEMIA ( 54 FDA reports)
NASOPHARYNGITIS ( 54 FDA reports)
ORTHOPNOEA ( 54 FDA reports)
PRODUCTIVE COUGH ( 54 FDA reports)
SPINAL OSTEOARTHRITIS ( 54 FDA reports)
URINARY RETENTION ( 54 FDA reports)
BLOOD GLUCOSE DECREASED ( 53 FDA reports)
FEBRILE NEUTROPENIA ( 53 FDA reports)
FLUID RETENTION ( 53 FDA reports)
LYMPHADENOPATHY ( 53 FDA reports)
SUBDURAL HAEMATOMA ( 53 FDA reports)
BLISTER ( 52 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 52 FDA reports)
GOUT ( 52 FDA reports)
OFF LABEL USE ( 52 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 52 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 52 FDA reports)
CEREBRAL INFARCTION ( 51 FDA reports)
DISABILITY ( 51 FDA reports)
GASTRITIS ( 51 FDA reports)
HAEMORRHOIDS ( 51 FDA reports)
PALLOR ( 51 FDA reports)
RESTLESSNESS ( 51 FDA reports)
AMNESIA ( 50 FDA reports)
CARDIAC VALVE DISEASE ( 50 FDA reports)
GASTROINTESTINAL DISORDER ( 50 FDA reports)
MULTIPLE MYELOMA ( 50 FDA reports)
NERVOUSNESS ( 50 FDA reports)
TYPE 2 DIABETES MELLITUS ( 50 FDA reports)
DRUG HYPERSENSITIVITY ( 49 FDA reports)
INFLAMMATION ( 49 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 48 FDA reports)
DISCOMFORT ( 48 FDA reports)
DYSGEUSIA ( 48 FDA reports)
DYSPHONIA ( 48 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 48 FDA reports)
PHLEBITIS ( 48 FDA reports)
SICK SINUS SYNDROME ( 48 FDA reports)
SLEEP DISORDER ( 48 FDA reports)
URINARY INCONTINENCE ( 48 FDA reports)
CHEST X-RAY ABNORMAL ( 47 FDA reports)
CHOLESTASIS ( 47 FDA reports)
DYSURIA ( 47 FDA reports)
FIBROSIS ( 47 FDA reports)
SKIN EXFOLIATION ( 47 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 46 FDA reports)
FLATULENCE ( 46 FDA reports)
SWELLING ( 46 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 45 FDA reports)
NERVOUS SYSTEM DISORDER ( 45 FDA reports)
RASH GENERALISED ( 45 FDA reports)
SPEECH DISORDER ( 45 FDA reports)
TINNITUS ( 45 FDA reports)
DYSARTHRIA ( 44 FDA reports)
EMPHYSEMA ( 44 FDA reports)
ENTEROCOCCAL INFECTION ( 44 FDA reports)
HAEMATOCHEZIA ( 44 FDA reports)
HEMIPARESIS ( 44 FDA reports)
LABORATORY TEST ABNORMAL ( 44 FDA reports)
MALNUTRITION ( 44 FDA reports)
PULSE ABSENT ( 44 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 43 FDA reports)
BREATH SOUNDS ABNORMAL ( 43 FDA reports)
HYPOPHAGIA ( 43 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 43 FDA reports)
OSTEOPOROSIS ( 43 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 43 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 42 FDA reports)
AORTIC STENOSIS ( 42 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 42 FDA reports)
FEELING HOT ( 42 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 42 FDA reports)
INTENTIONAL OVERDOSE ( 42 FDA reports)
LEFT ATRIAL DILATATION ( 42 FDA reports)
NO THERAPEUTIC RESPONSE ( 42 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 42 FDA reports)
RHEUMATOID ARTHRITIS ( 42 FDA reports)
ANURIA ( 41 FDA reports)
APHASIA ( 41 FDA reports)
BONE PAIN ( 41 FDA reports)
DEAFNESS ( 41 FDA reports)
DISORIENTATION ( 41 FDA reports)
DRY MOUTH ( 41 FDA reports)
DYSLIPIDAEMIA ( 41 FDA reports)
ECCHYMOSIS ( 41 FDA reports)
HAEMATEMESIS ( 41 FDA reports)
HIP FRACTURE ( 41 FDA reports)
NEUROTOXICITY ( 41 FDA reports)
PSYCHOTIC DISORDER ( 41 FDA reports)
RIGHT VENTRICULAR FAILURE ( 41 FDA reports)
CEREBRAL ATROPHY ( 40 FDA reports)
CORONARY ARTERY OCCLUSION ( 40 FDA reports)
DIVERTICULUM ( 40 FDA reports)
EAR PAIN ( 40 FDA reports)
FAILURE TO THRIVE ( 40 FDA reports)
OSTEONECROSIS ( 40 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 40 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 39 FDA reports)
GANGRENE ( 39 FDA reports)
GENERALISED OEDEMA ( 39 FDA reports)
HEPATIC CIRRHOSIS ( 39 FDA reports)
JOINT CONTRACTURE ( 39 FDA reports)
PNEUMOTHORAX ( 39 FDA reports)
TOOTH EXTRACTION ( 39 FDA reports)
VENTRICULAR ARRHYTHMIA ( 39 FDA reports)
ACUTE CORONARY SYNDROME ( 38 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 38 FDA reports)
BRONCHOPNEUMONIA ( 38 FDA reports)
BRONCHOSPASM ( 38 FDA reports)
DISEASE RECURRENCE ( 38 FDA reports)
LONG QT SYNDROME ( 38 FDA reports)
VENTRICULAR DYSFUNCTION ( 38 FDA reports)
ACUTE PULMONARY OEDEMA ( 37 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 37 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 37 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 37 FDA reports)
CATARACT ( 37 FDA reports)
DECUBITUS ULCER ( 37 FDA reports)
DELUSION ( 37 FDA reports)
DRUG EFFECT DECREASED ( 37 FDA reports)
DRUG LEVEL INCREASED ( 37 FDA reports)
DYSKINESIA ( 37 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 37 FDA reports)
HYPOMAGNESAEMIA ( 37 FDA reports)
RASH ERYTHEMATOUS ( 37 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 37 FDA reports)
TACHYPNOEA ( 37 FDA reports)
ARTHRITIS ( 36 FDA reports)
AZOTAEMIA ( 36 FDA reports)
BLOOD ALBUMIN DECREASED ( 36 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 36 FDA reports)
CHOLECYSTITIS ( 36 FDA reports)
ENCEPHALOPATHY ( 36 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 36 FDA reports)
LOBAR PNEUMONIA ( 36 FDA reports)
METASTASES TO BONE ( 36 FDA reports)
NEPHROLITHIASIS ( 36 FDA reports)
NODAL RHYTHM ( 36 FDA reports)
PERIPHERAL COLDNESS ( 36 FDA reports)
PNEUMONIA ASPIRATION ( 36 FDA reports)
RIB FRACTURE ( 36 FDA reports)
SUDDEN DEATH ( 36 FDA reports)
COLITIS ( 35 FDA reports)
COMPLETED SUICIDE ( 35 FDA reports)
EXTRASYSTOLES ( 35 FDA reports)
LEFT VENTRICULAR FAILURE ( 35 FDA reports)
MOTOR DYSFUNCTION ( 35 FDA reports)
PANCREATITIS ( 35 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 35 FDA reports)
POLLAKIURIA ( 35 FDA reports)
SINUS TACHYCARDIA ( 35 FDA reports)
URINE OUTPUT DECREASED ( 35 FDA reports)
APNOEA ( 34 FDA reports)
BLINDNESS ( 34 FDA reports)
CARDIOVERSION ( 34 FDA reports)
COORDINATION ABNORMAL ( 34 FDA reports)
EXERCISE TOLERANCE DECREASED ( 34 FDA reports)
INFUSION RELATED REACTION ( 34 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 34 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 34 FDA reports)
URTICARIA ( 34 FDA reports)
ACCIDENTAL OVERDOSE ( 33 FDA reports)
CORONARY ARTERY STENOSIS ( 33 FDA reports)
CYTOLYTIC HEPATITIS ( 33 FDA reports)
DELIRIUM ( 33 FDA reports)
DIASTOLIC DYSFUNCTION ( 33 FDA reports)
GASTRIC ULCER ( 33 FDA reports)
JUGULAR VEIN DISTENSION ( 33 FDA reports)
PHOTOSENSITIVITY REACTION ( 33 FDA reports)
SKIN LESION ( 33 FDA reports)
AGEUSIA ( 32 FDA reports)
ANGINA UNSTABLE ( 32 FDA reports)
CORNEAL DEPOSITS ( 32 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 32 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 32 FDA reports)
FEAR OF DEATH ( 32 FDA reports)
FRACTURE ( 32 FDA reports)
HERPES ZOSTER ( 32 FDA reports)
IRRITABLE BOWEL SYNDROME ( 32 FDA reports)
NIGHT SWEATS ( 32 FDA reports)
OSTEOPENIA ( 32 FDA reports)
RASH MACULO-PAPULAR ( 32 FDA reports)
RENAL CYST ( 32 FDA reports)
RESPIRATORY DISORDER ( 32 FDA reports)
ROTATOR CUFF SYNDROME ( 32 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 32 FDA reports)
CYANOSIS ( 31 FDA reports)
DERMATITIS ( 31 FDA reports)
DEVICE RELATED INFECTION ( 31 FDA reports)
DISSOCIATION ( 31 FDA reports)
DISTURBANCE IN ATTENTION ( 31 FDA reports)
DIVERTICULUM INTESTINAL ( 31 FDA reports)
ECZEMA ( 31 FDA reports)
GOITRE ( 31 FDA reports)
IRRITABILITY ( 31 FDA reports)
PRODUCT QUALITY ISSUE ( 31 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 31 FDA reports)
PURPURA ( 31 FDA reports)
RASH PAPULAR ( 31 FDA reports)
TOOTH ABSCESS ( 31 FDA reports)
CARDIAC FAILURE ACUTE ( 30 FDA reports)
CORONARY ARTERY BYPASS ( 30 FDA reports)
CREPITATIONS ( 30 FDA reports)
EXTRAVASATION ( 30 FDA reports)
HEPATIC CONGESTION ( 30 FDA reports)
HEPATIC CYST ( 30 FDA reports)
HYPERCHOLESTEROLAEMIA ( 30 FDA reports)
LACERATION ( 30 FDA reports)
LUNG NEOPLASM MALIGNANT ( 30 FDA reports)
MUSCLE TIGHTNESS ( 30 FDA reports)
PAIN IN JAW ( 30 FDA reports)
PERIPHERAL ISCHAEMIA ( 30 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 30 FDA reports)
PULMONARY HAEMORRHAGE ( 30 FDA reports)
SKIN FIBROSIS ( 30 FDA reports)
BACTERAEMIA ( 29 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 29 FDA reports)
DILATATION ATRIAL ( 29 FDA reports)
DRUG INTOLERANCE ( 29 FDA reports)
DYSSTASIA ( 29 FDA reports)
EXCORIATION ( 29 FDA reports)
EXTREMITY CONTRACTURE ( 29 FDA reports)
HEPATITIS ( 29 FDA reports)
HYPERGLOBULINAEMIA ( 29 FDA reports)
KERATOPATHY ( 29 FDA reports)
KLEBSIELLA INFECTION ( 29 FDA reports)
NASAL CONGESTION ( 29 FDA reports)
PSEUDOMONAS INFECTION ( 29 FDA reports)
RESPIRATORY TRACT INFECTION ( 29 FDA reports)
SINUS HEADACHE ( 29 FDA reports)
TENDERNESS ( 29 FDA reports)
TRANSAMINASES INCREASED ( 29 FDA reports)
ACUTE HEPATIC FAILURE ( 28 FDA reports)
ADVERSE DRUG REACTION ( 28 FDA reports)
CACHEXIA ( 28 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 28 FDA reports)
EXOSTOSIS ( 28 FDA reports)
HEPATITIS FULMINANT ( 28 FDA reports)
INTRACARDIAC THROMBUS ( 28 FDA reports)
LUNG NEOPLASM ( 28 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 28 FDA reports)
CANDIDIASIS ( 27 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 27 FDA reports)
COLONIC POLYP ( 27 FDA reports)
EYE DISORDER ( 27 FDA reports)
HAEMODYNAMIC INSTABILITY ( 27 FDA reports)
IMPAIRED WORK ABILITY ( 27 FDA reports)
INFLUENZA ( 27 FDA reports)
INTESTINAL ISCHAEMIA ( 27 FDA reports)
MOVEMENT DISORDER ( 27 FDA reports)
NEOPLASM MALIGNANT ( 27 FDA reports)
PANCREATITIS ACUTE ( 27 FDA reports)
THYROIDITIS ( 27 FDA reports)
ABNORMAL BEHAVIOUR ( 26 FDA reports)
COGNITIVE DISORDER ( 26 FDA reports)
DEVICE MALFUNCTION ( 26 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 26 FDA reports)
IRON DEFICIENCY ANAEMIA ( 26 FDA reports)
LACTIC ACIDOSIS ( 26 FDA reports)
LIMB INJURY ( 26 FDA reports)
MITRAL VALVE CALCIFICATION ( 26 FDA reports)
OLIGURIA ( 26 FDA reports)
ORGAN FAILURE ( 26 FDA reports)
PARKINSONISM ( 26 FDA reports)
POLYNEUROPATHY ( 26 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 26 FDA reports)
RENAL TUBULAR NECROSIS ( 26 FDA reports)
SKIN NECROSIS ( 26 FDA reports)
UROSEPSIS ( 26 FDA reports)
VASCULITIS ( 26 FDA reports)
BREAST CANCER ( 25 FDA reports)
CARDIOVASCULAR DISORDER ( 25 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 25 FDA reports)
DEMENTIA ( 25 FDA reports)
HYPOTONIA ( 25 FDA reports)
HYPOVOLAEMIA ( 25 FDA reports)
JOINT INJURY ( 25 FDA reports)
LYMPHOMA ( 25 FDA reports)
ODYNOPHAGIA ( 25 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 25 FDA reports)
SKIN PLAQUE ( 25 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
CEREBRAL ISCHAEMIA ( 24 FDA reports)
FEMUR FRACTURE ( 24 FDA reports)
HIATUS HERNIA ( 24 FDA reports)
HYPOCALCAEMIA ( 24 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 24 FDA reports)
INFLUENZA LIKE ILLNESS ( 24 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 24 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 24 FDA reports)
ISCHAEMIC STROKE ( 24 FDA reports)
JAW FRACTURE ( 24 FDA reports)
MUSCLE ATROPHY ( 24 FDA reports)
OPTIC NEUROPATHY ( 24 FDA reports)
PERITONITIS ( 24 FDA reports)
RASH MACULAR ( 24 FDA reports)
RHINORRHOEA ( 24 FDA reports)
SPLENOMEGALY ( 24 FDA reports)
AORTIC VALVE DISEASE ( 23 FDA reports)
ASPIRATION ( 23 FDA reports)
ATRIAL TACHYCARDIA ( 23 FDA reports)
BLOOD CULTURE POSITIVE ( 23 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 23 FDA reports)
BRADYARRHYTHMIA ( 23 FDA reports)
BRUGADA SYNDROME ( 23 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 23 FDA reports)
CAROTID ARTERY STENOSIS ( 23 FDA reports)
CLOSTRIDIAL INFECTION ( 23 FDA reports)
CONDUCTION DISORDER ( 23 FDA reports)
DRUG ADMINISTRATION ERROR ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 23 FDA reports)
INJECTION SITE ERYTHEMA ( 23 FDA reports)
PANIC ATTACK ( 23 FDA reports)
PAPILLOEDEMA ( 23 FDA reports)
SINUS ARRHYTHMIA ( 23 FDA reports)
SKIN SWELLING ( 23 FDA reports)
SPINAL COLUMN STENOSIS ( 23 FDA reports)
VENTRICULAR HYPERTROPHY ( 23 FDA reports)
VISUAL DISTURBANCE ( 23 FDA reports)
WALKING AID USER ( 23 FDA reports)
ALVEOLITIS ( 22 FDA reports)
ANGIOEDEMA ( 22 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 22 FDA reports)
BLOOD PRESSURE ABNORMAL ( 22 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 22 FDA reports)
DEPRESSED MOOD ( 22 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 22 FDA reports)
EXPOSED BONE IN JAW ( 22 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 22 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 22 FDA reports)
MICTURITION URGENCY ( 22 FDA reports)
NYSTAGMUS ( 22 FDA reports)
PETECHIAE ( 22 FDA reports)
SOCIAL PROBLEM ( 22 FDA reports)
SWELLING FACE ( 22 FDA reports)
WOUND ( 22 FDA reports)
BLOOD CALCIUM DECREASED ( 21 FDA reports)
BLOOD MAGNESIUM DECREASED ( 21 FDA reports)
CARDIAC FAILURE CHRONIC ( 21 FDA reports)
COLON CANCER ( 21 FDA reports)
DIVERTICULITIS ( 21 FDA reports)
GASTROENTERITIS ( 21 FDA reports)
GINGIVAL SWELLING ( 21 FDA reports)
HAEMORRHAGIC ANAEMIA ( 21 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 21 FDA reports)
LARGE INTESTINE PERFORATION ( 21 FDA reports)
LIVER INJURY ( 21 FDA reports)
LUNG INFECTION ( 21 FDA reports)
MAJOR DEPRESSION ( 21 FDA reports)
MASS ( 21 FDA reports)
MOUTH ULCERATION ( 21 FDA reports)
NEUROMYOPATHY ( 21 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 21 FDA reports)
OCCULT BLOOD POSITIVE ( 21 FDA reports)
PSYCHIATRIC SYMPTOM ( 21 FDA reports)
PULMONARY MASS ( 21 FDA reports)
QUALITY OF LIFE DECREASED ( 21 FDA reports)
RETROPERITONEAL HAEMATOMA ( 21 FDA reports)
SENSORY DISTURBANCE ( 21 FDA reports)
SPINAL FRACTURE ( 21 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 21 FDA reports)
STREPTOCOCCAL INFECTION ( 21 FDA reports)
THROAT IRRITATION ( 21 FDA reports)
WOUND INFECTION ( 21 FDA reports)
WOUND SECRETION ( 21 FDA reports)
ADVERSE EVENT ( 20 FDA reports)
BLOOD DISORDER ( 20 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 20 FDA reports)
CARDIAC TAMPONADE ( 20 FDA reports)
COLITIS ISCHAEMIC ( 20 FDA reports)
DERMATITIS BULLOUS ( 20 FDA reports)
DIPLOPIA ( 20 FDA reports)
DRUG DOSE OMISSION ( 20 FDA reports)
ELECTROLYTE IMBALANCE ( 20 FDA reports)
EYE HAEMORRHAGE ( 20 FDA reports)
FAMILY STRESS ( 20 FDA reports)
GINGIVAL DISORDER ( 20 FDA reports)
HEART INJURY ( 20 FDA reports)
INTESTINAL OBSTRUCTION ( 20 FDA reports)
MACULAR DEGENERATION ( 20 FDA reports)
MENTAL IMPAIRMENT ( 20 FDA reports)
ORGANISING PNEUMONIA ( 20 FDA reports)
PERITONITIS BACTERIAL ( 20 FDA reports)
PROCEDURAL COMPLICATION ( 20 FDA reports)
RHONCHI ( 20 FDA reports)
SPINAL COMPRESSION FRACTURE ( 20 FDA reports)
STEVENS-JOHNSON SYNDROME ( 20 FDA reports)
ACIDOSIS ( 19 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
BLOOD CREATINE INCREASED ( 19 FDA reports)
COLD SWEAT ( 19 FDA reports)
CYST ( 19 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 19 FDA reports)
ENDOTRACHEAL INTUBATION ( 19 FDA reports)
ESCHERICHIA INFECTION ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
FOOT DEFORMITY ( 19 FDA reports)
H1N1 INFLUENZA ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
ILEUS ( 19 FDA reports)
ISCHAEMIA ( 19 FDA reports)
ISCHAEMIC HEPATITIS ( 19 FDA reports)
JOINT DISLOCATION ( 19 FDA reports)
OESOPHAGITIS ( 19 FDA reports)
ORAL CANDIDIASIS ( 19 FDA reports)
RASH PRURITIC ( 19 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 19 FDA reports)
RHINITIS ALLERGIC ( 19 FDA reports)
SCAB ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 19 FDA reports)
TACHYARRHYTHMIA ( 19 FDA reports)
THROMBOPHLEBITIS ( 19 FDA reports)
TREATMENT FAILURE ( 19 FDA reports)
ABDOMINAL PAIN LOWER ( 18 FDA reports)
ABSCESS ( 18 FDA reports)
ANKLE FRACTURE ( 18 FDA reports)
BACTERIAL INFECTION ( 18 FDA reports)
BLOOD CHLORIDE DECREASED ( 18 FDA reports)
FAECES DISCOLOURED ( 18 FDA reports)
FLANK PAIN ( 18 FDA reports)
HEART RATE ABNORMAL ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
ILEUS PARALYTIC ( 18 FDA reports)
INFUSION SITE EXTRAVASATION ( 18 FDA reports)
INTERMITTENT CLAUDICATION ( 18 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
MUCOSAL INFLAMMATION ( 18 FDA reports)
PERICARDIAL HAEMORRHAGE ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
RESPIRATORY RATE INCREASED ( 18 FDA reports)
SKIN FISSURES ( 18 FDA reports)
TOOTH LOSS ( 18 FDA reports)
TOOTHACHE ( 18 FDA reports)
ANGIOPLASTY ( 17 FDA reports)
ARTHROPATHY ( 17 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 17 FDA reports)
BODY TEMPERATURE INCREASED ( 17 FDA reports)
CARDIOPULMONARY FAILURE ( 17 FDA reports)
CATHETERISATION CARDIAC ( 17 FDA reports)
CEREBROVASCULAR DISORDER ( 17 FDA reports)
CRYING ( 17 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 17 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 17 FDA reports)
EMBOLISM ( 17 FDA reports)
EOSINOPHILIA ( 17 FDA reports)
FISTULA ( 17 FDA reports)
HAEMOLYTIC ANAEMIA ( 17 FDA reports)
HAEMOTHORAX ( 17 FDA reports)
HALLUCINATION, AUDITORY ( 17 FDA reports)
HEPATOCELLULAR INJURY ( 17 FDA reports)
HOT FLUSH ( 17 FDA reports)
HYPERBILIRUBINAEMIA ( 17 FDA reports)
HYPOPERFUSION ( 17 FDA reports)
INCONTINENCE ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
LOCAL SWELLING ( 17 FDA reports)
MECHANICAL VENTILATION ( 17 FDA reports)
MYELODYSPLASTIC SYNDROME ( 17 FDA reports)
PERICARDITIS ( 17 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 17 FDA reports)
SKIN EROSION ( 17 FDA reports)
SKIN LACERATION ( 17 FDA reports)
VASCULAR PSEUDOANEURYSM ( 17 FDA reports)
VENOUS INSUFFICIENCY ( 17 FDA reports)
ANAPHYLACTIC REACTION ( 16 FDA reports)
ANAPHYLACTIC SHOCK ( 16 FDA reports)
AORTIC VALVE SCLEROSIS ( 16 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 16 FDA reports)
ATROPHY ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 16 FDA reports)
BLOOD URINE PRESENT ( 16 FDA reports)
BUNDLE BRANCH BLOCK ( 16 FDA reports)
CHOLECYSTITIS ACUTE ( 16 FDA reports)
COMPRESSION FRACTURE ( 16 FDA reports)
CYSTITIS ( 16 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 16 FDA reports)
EATING DISORDER ( 16 FDA reports)
ESSENTIAL HYPERTENSION ( 16 FDA reports)
GLOSSODYNIA ( 16 FDA reports)
GROIN PAIN ( 16 FDA reports)
HALO VISION ( 16 FDA reports)
HEMIPLEGIA ( 16 FDA reports)
HEPATIC ENCEPHALOPATHY ( 16 FDA reports)
HYPOAESTHESIA ORAL ( 16 FDA reports)
INJECTION SITE PAIN ( 16 FDA reports)
LEG AMPUTATION ( 16 FDA reports)
MYOCLONUS ( 16 FDA reports)
NEPHROPATHY ( 16 FDA reports)
ORAL PAIN ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
RASH PUSTULAR ( 16 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 16 FDA reports)
SKIN HYPOPIGMENTATION ( 16 FDA reports)
STENT PLACEMENT ( 16 FDA reports)
SWOLLEN TONGUE ( 16 FDA reports)
TRAUMATIC HAEMATOMA ( 16 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 16 FDA reports)
ULCER ( 16 FDA reports)
ABSCESS LIMB ( 15 FDA reports)
BLINDNESS UNILATERAL ( 15 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 15 FDA reports)
BRAIN OEDEMA ( 15 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 15 FDA reports)
CATHETER RELATED INFECTION ( 15 FDA reports)
DECREASED INTEREST ( 15 FDA reports)
DIABETIC NEUROPATHY ( 15 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 15 FDA reports)
FAECAL INCONTINENCE ( 15 FDA reports)
FEELING COLD ( 15 FDA reports)
GASTRITIS EROSIVE ( 15 FDA reports)
HEARING IMPAIRED ( 15 FDA reports)
HEPATOCELLULAR DAMAGE ( 15 FDA reports)
HYPOTHERMIA ( 15 FDA reports)
INCREASED TENDENCY TO BRUISE ( 15 FDA reports)
INJECTION SITE WARMTH ( 15 FDA reports)
INTESTINAL HAEMORRHAGE ( 15 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 15 FDA reports)
JAW DISORDER ( 15 FDA reports)
LIP HAEMORRHAGE ( 15 FDA reports)
LUNG CONSOLIDATION ( 15 FDA reports)
NOCTURIA ( 15 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 15 FDA reports)
RESUSCITATION ( 15 FDA reports)
RETCHING ( 15 FDA reports)
RHINITIS ( 15 FDA reports)
ROAD TRAFFIC ACCIDENT ( 15 FDA reports)
STASIS DERMATITIS ( 15 FDA reports)
SUBDURAL HAEMORRHAGE ( 15 FDA reports)
THERAPY NON-RESPONDER ( 15 FDA reports)
TOE AMPUTATION ( 15 FDA reports)
TROPONIN INCREASED ( 15 FDA reports)
URGE INCONTINENCE ( 15 FDA reports)
VASCULAR GRAFT ( 15 FDA reports)
ABSCESS DRAINAGE ( 14 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 14 FDA reports)
AORTIC ANEURYSM ( 14 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 14 FDA reports)
BRAIN INJURY ( 14 FDA reports)
CARPAL TUNNEL SYNDROME ( 14 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 14 FDA reports)
DEVELOPMENTAL DELAY ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 14 FDA reports)
ERUCTATION ( 14 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 14 FDA reports)
HEART TRANSPLANT ( 14 FDA reports)
HEPATIC NEOPLASM ( 14 FDA reports)
HOSPITALISATION ( 14 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 14 FDA reports)
LIGAMENT SPRAIN ( 14 FDA reports)
LOSS OF EMPLOYMENT ( 14 FDA reports)
MALIGNANT MELANOMA ( 14 FDA reports)
MYOCARDIAL FIBROSIS ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
NODAL ARRHYTHMIA ( 14 FDA reports)
PROSTATE CANCER METASTATIC ( 14 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 14 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 14 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 14 FDA reports)
SKIN BURNING SENSATION ( 14 FDA reports)
STRESS URINARY INCONTINENCE ( 14 FDA reports)
THIRST ( 14 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 14 FDA reports)
THYROTOXIC CRISIS ( 14 FDA reports)
UPPER LIMB FRACTURE ( 14 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 14 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 13 FDA reports)
ADRENAL INSUFFICIENCY ( 13 FDA reports)
ADRENAL NEOPLASM ( 13 FDA reports)
AORTIC VALVE CALCIFICATION ( 13 FDA reports)
AORTIC VALVE STENOSIS ( 13 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 13 FDA reports)
BLADDER DISORDER ( 13 FDA reports)
BODY TEMPERATURE DECREASED ( 13 FDA reports)
BONE MARROW FAILURE ( 13 FDA reports)
CARDIAC FLUTTER ( 13 FDA reports)
CAROTID BRUIT ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 13 FDA reports)
DIZZINESS POSTURAL ( 13 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FUNGAL INFECTION ( 13 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 13 FDA reports)
HAEMORRHAGIC STROKE ( 13 FDA reports)
HEART SOUNDS ABNORMAL ( 13 FDA reports)
HYPERCAPNIA ( 13 FDA reports)
HYPERNATRAEMIA ( 13 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 13 FDA reports)
LOCALISED INFECTION ( 13 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE ( 13 FDA reports)
NECROSIS ( 13 FDA reports)
NEPHROGENIC ANAEMIA ( 13 FDA reports)
OESOPHAGEAL STENOSIS ( 13 FDA reports)
OPTIC ATROPHY ( 13 FDA reports)
PHARYNGEAL OEDEMA ( 13 FDA reports)
PIGMENTATION DISORDER ( 13 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 13 FDA reports)
PROTEINURIA ( 13 FDA reports)
PROTHROMBIN TIME SHORTENED ( 13 FDA reports)
RADICULOPATHY ( 13 FDA reports)
RASH MORBILLIFORM ( 13 FDA reports)
RESPIRATORY ACIDOSIS ( 13 FDA reports)
RESPIRATORY TRACT CONGESTION ( 13 FDA reports)
SCOLIOSIS ( 13 FDA reports)
SHOCK HAEMORRHAGIC ( 13 FDA reports)
SKIN OEDEMA ( 13 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
TEMPERATURE INTOLERANCE ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
URINE ANALYSIS ABNORMAL ( 13 FDA reports)
WRONG DRUG ADMINISTERED ( 13 FDA reports)
ABDOMINAL HERNIA ( 12 FDA reports)
ABDOMINAL TENDERNESS ( 12 FDA reports)
ACCIDENT ( 12 FDA reports)
ACUTE PRERENAL FAILURE ( 12 FDA reports)
ANGIONEUROTIC OEDEMA ( 12 FDA reports)
APATHY ( 12 FDA reports)
AREFLEXIA ( 12 FDA reports)
BACTERIAL SEPSIS ( 12 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 12 FDA reports)
BLOOD URIC ACID INCREASED ( 12 FDA reports)
BURSITIS ( 12 FDA reports)
CARDIAC OUTPUT DECREASED ( 12 FDA reports)
CARDIORENAL SYNDROME ( 12 FDA reports)
COLON ADENOMA ( 12 FDA reports)
CULTURE URINE POSITIVE ( 12 FDA reports)
DEBRIDEMENT ( 12 FDA reports)
DENTAL CARIES ( 12 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 12 FDA reports)
DRY EYE ( 12 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 12 FDA reports)
EMBOLIC STROKE ( 12 FDA reports)
ENDODONTIC PROCEDURE ( 12 FDA reports)
ERECTILE DYSFUNCTION ( 12 FDA reports)
GASTRIC HAEMORRHAGE ( 12 FDA reports)
HEPATIC NECROSIS ( 12 FDA reports)
HEPATOJUGULAR REFLUX ( 12 FDA reports)
HUMERUS FRACTURE ( 12 FDA reports)
HYPERTENSIVE CRISIS ( 12 FDA reports)
HYPERTENSIVE HEART DISEASE ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
LACRIMATION INCREASED ( 12 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
LOWER LIMB FRACTURE ( 12 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 12 FDA reports)
MEDICAL DEVICE COMPLICATION ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
MIGRAINE ( 12 FDA reports)
MITRAL VALVE PROLAPSE ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
PAIN OF SKIN ( 12 FDA reports)
PELVIC FRACTURE ( 12 FDA reports)
PERFORMANCE STATUS DECREASED ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
PUPIL FIXED ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
SINUS ARREST ( 12 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 12 FDA reports)
SPUTUM CULTURE POSITIVE ( 12 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 12 FDA reports)
TENDON RUPTURE ( 12 FDA reports)
THYROXINE FREE INCREASED ( 12 FDA reports)
TOBACCO ABUSE ( 12 FDA reports)
TOBACCO USER ( 12 FDA reports)
TROPONIN I INCREASED ( 12 FDA reports)
TUMOUR HAEMORRHAGE ( 12 FDA reports)
ULCER HAEMORRHAGE ( 12 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 12 FDA reports)
VIRAL INFECTION ( 12 FDA reports)
VISUAL FIELD DEFECT ( 12 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 11 FDA reports)
ADDISON'S DISEASE ( 11 FDA reports)
AGGRESSION ( 11 FDA reports)
ALCOHOL ABUSE ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
ANOXIC ENCEPHALOPATHY ( 11 FDA reports)
AORTIC VALVE REPLACEMENT ( 11 FDA reports)
BASAL CELL CARCINOMA ( 11 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 11 FDA reports)
BODY HEIGHT DECREASED ( 11 FDA reports)
BRONCHIECTASIS ( 11 FDA reports)
CARDIAC OPERATION ( 11 FDA reports)
CATHETER RELATED COMPLICATION ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CEREBRAL HAEMATOMA ( 11 FDA reports)
CHOLECYSTECTOMY ( 11 FDA reports)
CHROMATURIA ( 11 FDA reports)
DERMATITIS ALLERGIC ( 11 FDA reports)
DISEASE COMPLICATION ( 11 FDA reports)
DRUG DISPENSING ERROR ( 11 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
EFFUSION ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 11 FDA reports)
ESCHERICHIA SEPSIS ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
GINGIVAL PAIN ( 11 FDA reports)
GLAUCOMA ( 11 FDA reports)
GYNAECOMASTIA ( 11 FDA reports)
HAEMATOMA INFECTION ( 11 FDA reports)
HEPATIC FIBROSIS ( 11 FDA reports)
HERNIA ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPOREFLEXIA ( 11 FDA reports)
INTENTIONAL DRUG MISUSE ( 11 FDA reports)
LARYNGEAL CYST ( 11 FDA reports)
LARYNGITIS ( 11 FDA reports)
LUNG INJURY ( 11 FDA reports)
LYMPHOCELE ( 11 FDA reports)
MALIGNANT HYPERTENSION ( 11 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 11 FDA reports)
MOUTH HAEMORRHAGE ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
NON-CARDIAC CHEST PAIN ( 11 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 11 FDA reports)
PEMPHIGOID ( 11 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 11 FDA reports)
PHOTOPHOBIA ( 11 FDA reports)
PHYSICAL DISABILITY ( 11 FDA reports)
PROSTATE CANCER ( 11 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 11 FDA reports)
SCIATICA ( 11 FDA reports)
SINUS CONGESTION ( 11 FDA reports)
SKIN ATROPHY ( 11 FDA reports)
SNORING ( 11 FDA reports)
SPUTUM DISCOLOURED ( 11 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 11 FDA reports)
TENDONITIS ( 11 FDA reports)
TOOTH FRACTURE ( 11 FDA reports)
URINE ABNORMALITY ( 11 FDA reports)
VOCAL CORD THICKENING ( 11 FDA reports)
WITHDRAWAL SYNDROME ( 11 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 10 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 10 FDA reports)
BASAL GANGLIA INFARCTION ( 10 FDA reports)
BEDRIDDEN ( 10 FDA reports)
BLOOD AMYLASE INCREASED ( 10 FDA reports)
BLOOD PH INCREASED ( 10 FDA reports)
BONE NEOPLASM ( 10 FDA reports)
CARDIAC DEATH ( 10 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 10 FDA reports)
CAROTID ARTERY ANEURYSM ( 10 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 10 FDA reports)
COAGULATION TIME PROLONGED ( 10 FDA reports)
DIFFICULTY IN WALKING ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 10 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FOOT FRACTURE ( 10 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 10 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 10 FDA reports)
HALLUCINATION, VISUAL ( 10 FDA reports)
HEPATIC LESION ( 10 FDA reports)
HEPATITIS CHOLESTATIC ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
HYPOVENTILATION ( 10 FDA reports)
IATROGENIC INJURY ( 10 FDA reports)
ILIAC ARTERY STENOSIS ( 10 FDA reports)
INJECTION SITE HAEMATOMA ( 10 FDA reports)
JAUNDICE CHOLESTATIC ( 10 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 10 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
METASTASES TO LIVER ( 10 FDA reports)
MUSCLE HAEMORRHAGE ( 10 FDA reports)
MYOCARDITIS ( 10 FDA reports)
NEOPLASM PROGRESSION ( 10 FDA reports)
NEUROPATHIC ARTHROPATHY ( 10 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 10 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 10 FDA reports)
PEPTIC ULCER ( 10 FDA reports)
PERITONEAL HAEMORRHAGE ( 10 FDA reports)
PERONEAL NERVE PALSY ( 10 FDA reports)
PITTING OEDEMA ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
PROCEDURAL PAIN ( 10 FDA reports)
PRURITUS GENERALISED ( 10 FDA reports)
PSORIASIS ( 10 FDA reports)
PSYCHOLOGICAL TRAUMA ( 10 FDA reports)
PULMONARY SEPSIS ( 10 FDA reports)
RIGHT ATRIAL DILATATION ( 10 FDA reports)
SCLERODACTYLIA ( 10 FDA reports)
SENSORY LOSS ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SKIN HAEMORRHAGE ( 10 FDA reports)
SMALL INTESTINE OPERATION ( 10 FDA reports)
SPINAL LAMINECTOMY ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
VARICOSE VEIN ( 10 FDA reports)
VIITH NERVE PARALYSIS ( 10 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 10 FDA reports)
WRIST FRACTURE ( 10 FDA reports)
X-RAY ABNORMAL ( 10 FDA reports)
AFFECTIVE DISORDER ( 9 FDA reports)
ALCOHOL USE ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
AORTIC CALCIFICATION ( 9 FDA reports)
APLASIA PURE RED CELL ( 9 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
BLEPHARITIS ( 9 FDA reports)
BLOOD PH DECREASED ( 9 FDA reports)
BRONCHITIS CHRONIC ( 9 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 9 FDA reports)
CATARACT OPERATION ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 9 FDA reports)
COMMUNICATION DISORDER ( 9 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 9 FDA reports)
CONJUNCTIVITIS ( 9 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DEPRESSION SUICIDAL ( 9 FDA reports)
DEVICE FAILURE ( 9 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
DRUG LEVEL DECREASED ( 9 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 9 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 9 FDA reports)
ESSENTIAL TREMOR ( 9 FDA reports)
FACIAL PALSY ( 9 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 9 FDA reports)
GASTRITIS ATROPHIC ( 9 FDA reports)
GLOMERULONEPHRITIS ( 9 FDA reports)
GRAND MAL CONVULSION ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HYPERSOMNIA ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LAZINESS ( 9 FDA reports)
LIGAMENT RUPTURE ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
MALLORY-WEISS SYNDROME ( 9 FDA reports)
MENISCUS LESION ( 9 FDA reports)
MIDDLE INSOMNIA ( 9 FDA reports)
MITRAL VALVE DISEASE ( 9 FDA reports)
MITRAL VALVE STENOSIS ( 9 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 9 FDA reports)
NEPHROSCLEROSIS ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
OBSTRUCTIVE UROPATHY ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
PANCREATITIS CHRONIC ( 9 FDA reports)
PARALYSIS ( 9 FDA reports)
PERIORBITAL HAEMATOMA ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
PNEUMONIA BACTERIAL ( 9 FDA reports)
POLYP ( 9 FDA reports)
RESPIRATORY DEPRESSION ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
SUDDEN CARDIAC DEATH ( 9 FDA reports)
SYSTEMIC CANDIDA ( 9 FDA reports)
TOOTH INFECTION ( 9 FDA reports)
TYPE 1 DIABETES MELLITUS ( 9 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 9 FDA reports)
VISUAL BRIGHTNESS ( 9 FDA reports)
ACINETOBACTER INFECTION ( 8 FDA reports)
AKINESIA ( 8 FDA reports)
APLASTIC ANAEMIA ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 8 FDA reports)
BONE MARROW DEPRESSION ( 8 FDA reports)
BREAST CANCER FEMALE ( 8 FDA reports)
CALCIPHYLAXIS ( 8 FDA reports)
CARDIAC ENZYMES INCREASED ( 8 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 8 FDA reports)
CHRONIC SINUSITIS ( 8 FDA reports)
CROHN'S DISEASE ( 8 FDA reports)
CYSTOCELE ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
DRUG LEVEL FLUCTUATING ( 8 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
ENDOCARDITIS ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
EYE ROLLING ( 8 FDA reports)
FEMORAL NECK FRACTURE ( 8 FDA reports)
FIBROMYALGIA ( 8 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
INFUSION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE DISCHARGE ( 8 FDA reports)
INJECTION SITE REACTION ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
JOINT SPRAIN ( 8 FDA reports)
LACUNAR INFARCTION ( 8 FDA reports)
LISTLESS ( 8 FDA reports)
LOOSE TOOTH ( 8 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 8 FDA reports)
LUMBAR SPINAL STENOSIS ( 8 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 8 FDA reports)
MACROCYTOSIS ( 8 FDA reports)
METASTASES TO LUNG ( 8 FDA reports)
MUSCLE CONTRACTURE ( 8 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 8 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 8 FDA reports)
NEUTROPENIC SEPSIS ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 8 FDA reports)
OPEN WOUND ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
OSTEORADIONECROSIS ( 8 FDA reports)
OXYGEN SUPPLEMENTATION ( 8 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PERIPHERAL EMBOLISM ( 8 FDA reports)
PHARYNGEAL ERYTHEMA ( 8 FDA reports)
PLATELET COUNT INCREASED ( 8 FDA reports)
PO2 DECREASED ( 8 FDA reports)
POST HERPETIC NEURALGIA ( 8 FDA reports)
POSTOPERATIVE ILEUS ( 8 FDA reports)
POTENTIATING DRUG INTERACTION ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 8 FDA reports)
PYELONEPHRITIS ACUTE ( 8 FDA reports)
RENAL ARTERY STENOSIS ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 8 FDA reports)
RESPIRATORY ALKALOSIS ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RETROPERITONEAL NEOPLASM ( 8 FDA reports)
SEBORRHOEIC DERMATITIS ( 8 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 8 FDA reports)
SPINAL OPERATION ( 8 FDA reports)
STRESS CARDIOMYOPATHY ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
VASCULAR CALCIFICATION ( 8 FDA reports)
VEIN DISORDER ( 8 FDA reports)
VITAMIN D DECREASED ( 8 FDA reports)
WOUND DRAINAGE ( 8 FDA reports)
ABNORMAL DREAMS ( 7 FDA reports)
ACUTE LUNG INJURY ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
ALVEOLITIS FIBROSING ( 7 FDA reports)
ANEURYSM REPAIR ( 7 FDA reports)
ANGER ( 7 FDA reports)
ANGIOPATHY ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 7 FDA reports)
AORTIC BYPASS ( 7 FDA reports)
APLASIA ( 7 FDA reports)
APPENDICECTOMY ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BLADDER CANCER ( 7 FDA reports)
BLADDER NEOPLASM ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 7 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 7 FDA reports)
BRONCHOSCOPY ABNORMAL ( 7 FDA reports)
CARDIAC FIBRILLATION ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIOTOXICITY ( 7 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 7 FDA reports)
CELL MARKER INCREASED ( 7 FDA reports)
CENTRAL LINE INFECTION ( 7 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
COMA HEPATIC ( 7 FDA reports)
CORONARY ARTERY THROMBOSIS ( 7 FDA reports)
DIAPHRAGMATIC HERNIA ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG PRESCRIBING ERROR ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
EJECTION FRACTION ABNORMAL ( 7 FDA reports)
EPIDIDYMITIS ( 7 FDA reports)
EYE PAIN ( 7 FDA reports)
EYELID OEDEMA ( 7 FDA reports)
FEEDING DISORDER ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
GALLBLADDER DISORDER ( 7 FDA reports)
GALLOP RHYTHM PRESENT ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GASTROENTERITIS RADIATION ( 7 FDA reports)
GINGIVAL ULCERATION ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
HEMIANOPIA ( 7 FDA reports)
HEPATIC MASS ( 7 FDA reports)
HEPATOSPLENOMEGALY ( 7 FDA reports)
HUNGER ( 7 FDA reports)
HYDROPNEUMOTHORAX ( 7 FDA reports)
HYPERKERATOSIS ( 7 FDA reports)
HYPERPARATHYROIDISM ( 7 FDA reports)
HYPERPHOSPHATAEMIA ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 7 FDA reports)
INFARCTION ( 7 FDA reports)
INFECTIOUS PERITONITIS ( 7 FDA reports)
INJECTION SITE INFECTION ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
LIP SWELLING ( 7 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MONOCLONAL GAMMOPATHY ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MULTIPLE ALLERGIES ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MUSCULAR DYSTROPHY ( 7 FDA reports)
NECK MASS ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
NOCTURNAL DYSPNOEA ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PNEUMONIA KLEBSIELLA ( 7 FDA reports)
POISONING ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 7 FDA reports)
PURULENCE ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RAYNAUD'S PHENOMENON ( 7 FDA reports)
RECTAL POLYP ( 7 FDA reports)
RESTLESS LEGS SYNDROME ( 7 FDA reports)
SARCOIDOSIS ( 7 FDA reports)
SEDATION ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SINUS DISORDER ( 7 FDA reports)
SKIN CANCER ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
SYNOVIAL CYST ( 7 FDA reports)
TONGUE DISCOLOURATION ( 7 FDA reports)
UNEMPLOYMENT ( 7 FDA reports)
UTERINE CANCER ( 7 FDA reports)
VASODILATATION ( 7 FDA reports)
XEROSIS ( 7 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 6 FDA reports)
ACUTE STRESS DISORDER ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
ANASTOMOTIC LEAK ( 6 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 6 FDA reports)
ANXIETY DISORDER ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPLICATION SITE PRURITUS ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 6 FDA reports)
BLADDER MASS ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 6 FDA reports)
BLOOD SODIUM INCREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BONE MARROW DISORDER ( 6 FDA reports)
BRADYPNOEA ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
CARDIAC ABLATION ( 6 FDA reports)
CARDIAC ANEURYSM ( 6 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CERUMEN IMPACTION ( 6 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 6 FDA reports)
CORNEAL OPACITY ( 6 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DIABETIC GASTROPARESIS ( 6 FDA reports)
DUPUYTREN'S CONTRACTURE ( 6 FDA reports)
ENDOCARDIAL FIBROSIS ( 6 FDA reports)
EOSINOPHILIA MYALGIA SYNDROME ( 6 FDA reports)
EXPOSURE TO TOXIC AGENT ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
FUNGAEMIA ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
GAZE PALSY ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GINGIVAL INFECTION ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GOUTY ARTHRITIS ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HAEMANGIOMA ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HEPATIC INFECTION FUNGAL ( 6 FDA reports)
HERPES VIRUS INFECTION ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 6 FDA reports)
HYPERACUSIS ( 6 FDA reports)
HYPERCOAGULATION ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOPNOEA ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
IMPAIRED DRIVING ABILITY ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
INITIAL INSOMNIA ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
INTRAOCULAR LENS IMPLANT ( 6 FDA reports)
JOINT INSTABILITY ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
MASTICATION DISORDER ( 6 FDA reports)
MEDIASTINAL MASS ( 6 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 6 FDA reports)
MESENTERIC OCCLUSION ( 6 FDA reports)
METAPNEUMOVIRUS INFECTION ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
MUCOSAL DRYNESS ( 6 FDA reports)
MUCOSAL EROSION ( 6 FDA reports)
MULTI-ORGAN DISORDER ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MYDRIASIS ( 6 FDA reports)
NERVE INJURY ( 6 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER ( 6 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 6 FDA reports)
ORAL DISCOMFORT ( 6 FDA reports)
ORAL HERPES ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
OTITIS MEDIA CHRONIC ( 6 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
POSTURE ABNORMAL ( 6 FDA reports)
PROCEDURAL HYPOTENSION ( 6 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
RENAL INFARCT ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
RETINAL ARTERY OCCLUSION ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 6 FDA reports)
SURGICAL PROCEDURE REPEATED ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
SYNOVITIS ( 6 FDA reports)
TEMPORAL ARTERITIS ( 6 FDA reports)
TERMINAL STATE ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
TONGUE COATED ( 6 FDA reports)
TOOTH INJURY ( 6 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
TRAUMATIC LUNG INJURY ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VENOUS STENOSIS ( 6 FDA reports)
VITREOUS DETACHMENT ( 6 FDA reports)
WEANING FAILURE ( 6 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
ADRENAL MASS ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
ARTERIAL DISORDER ( 5 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CARDIAC SEPTAL DEFECT ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CHEYNE-STOKES RESPIRATION ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 5 FDA reports)
CUBITAL TUNNEL SYNDROME ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DENTAL OPERATION ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 5 FDA reports)
EMPYEMA ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FOAMING AT MOUTH ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 5 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 5 FDA reports)
GINGIVAL RECESSION ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
HEART DISEASE CONGENITAL ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEART VALVE REPLACEMENT ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HEPATORENAL SYNDROME ( 5 FDA reports)
HERNIA REPAIR ( 5 FDA reports)
HIDRADENITIS ( 5 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 5 FDA reports)
HYPERPLASIA ( 5 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 5 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INCISION SITE INFECTION ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LIFE EXPECTANCY SHORTENED ( 5 FDA reports)
LIFE SUPPORT ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MAGNESIUM DEFICIENCY ( 5 FDA reports)
MARROW HYPERPLASIA ( 5 FDA reports)
MEDIASTINITIS ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MENINGITIS ENTEROCOCCAL ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 5 FDA reports)
OBSTRUCTION ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 5 FDA reports)
OOPHORECTOMY ( 5 FDA reports)
OPTIC DISC DISORDER ( 5 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PATHOGEN RESISTANCE ( 5 FDA reports)
PATHOLOGICAL FRACTURE ( 5 FDA reports)
PEAU D'ORANGE ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PLASMACYTOMA ( 5 FDA reports)
PNEUMOMEDIASTINUM ( 5 FDA reports)
POOR PERIPHERAL CIRCULATION ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RETINAL SCAR ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SEQUESTRECTOMY ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SOPOR ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
SUPERINFECTION ( 5 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
TACHYCARDIA PAROXYSMAL ( 5 FDA reports)
THROMBOSIS IN DEVICE ( 5 FDA reports)
THYROXINE INCREASED ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TONGUE BITING ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 5 FDA reports)
UMBILICAL HERNIA ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URINE CYTOLOGY ABNORMAL ( 5 FDA reports)
VITAMIN D DEFICIENCY ( 5 FDA reports)
VOCAL CORD PARALYSIS ( 5 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
5Q MINUS SYNDROME ( 4 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CORTISOL DECREASED ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BREAST OEDEMA ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CANDIDA OSTEOMYELITIS ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CELL MARKER ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CORNEAL PIGMENTATION ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CORONARY ARTERY ANEURYSM ( 4 FDA reports)
CORONARY ARTERY SURGERY ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CYST REMOVAL ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EDENTULOUS ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 4 FDA reports)
EX-TOBACCO USER ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
FACET JOINT SYNDROME ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FOETAL DISORDER ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
FUSOBACTERIUM INFECTION ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
HAEMOCHROMATOSIS ( 4 FDA reports)
HAEMOGLOBIN ABNORMAL ( 4 FDA reports)
HAEMOSIDEROSIS ( 4 FDA reports)
HAIR GROWTH ABNORMAL ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPERTHERMIA MALIGNANT ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
ILIAC ARTERY OCCLUSION ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 4 FDA reports)
INFERTILITY ( 4 FDA reports)
INFUSION SITE PAIN ( 4 FDA reports)
INFUSION SITE PHLEBITIS ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIP DISORDER ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LUNG HYPERINFLATION ( 4 FDA reports)
LYMPHORRHOEA ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NAIL DISORDER ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NEOPLASM PROSTATE ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OCCULT BLOOD ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
OPEN REDUCTION OF FRACTURE ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PACEMAKER COMPLICATION ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PERICARDIAL EXCISION ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL INFECTION ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POOR PERSONAL HYGIENE ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROCEDURAL DIZZINESS ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 4 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
ROTAVIRUS INFECTION ( 4 FDA reports)
SALIVARY GLAND DISORDER ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SERRATIA BACTERAEMIA ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SKIN TURGOR DECREASED ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SPONDYLOLISTHESIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STEM CELL TRANSPLANT ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 4 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 4 FDA reports)
SYSTOLIC DYSFUNCTION ( 4 FDA reports)
TANGENTIALITY ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THORACIC CAVITY DRAINAGE ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TONGUE HAEMATOMA ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
VESTIBULAR DISORDER ( 4 FDA reports)
VITREOUS FLOATERS ( 4 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 4 FDA reports)
WOUND INFECTION FUNGAL ( 4 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABNORMAL CLOTTING FACTOR ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ADAMS-STOKES SYNDROME ( 3 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AIR EMBOLISM ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAEMIA POSTOPERATIVE ( 3 FDA reports)
ANIMAL BITE ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
AORTIC DISSECTION RUPTURE ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ( 3 FDA reports)
ATRIAL PRESSURE INCREASED ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BLADDER INJURY ( 3 FDA reports)
BLADDER NEOPLASM SURGERY ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE DEBRIDEMENT ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BUNION ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CAPILLARY FRAGILITY ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL ATAXIA ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
COCCYDYNIA ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONNECTIVE TISSUE DISORDER ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
COR PULMONALE ACUTE ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL REFLEX DECREASED ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CSF TEST ABNORMAL ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DEFIBRILLATION THRESHOLD INCREASED ( 3 FDA reports)
DEPOSIT EYE ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG INTERACTION POTENTIATION ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EAR LOBE INFECTION ( 3 FDA reports)
EJECTION FRACTION ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
EMPTY SELLA SYNDROME ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EXTERNAL EAR INFLAMMATION ( 3 FDA reports)
EYE INFECTION INTRAOCULAR ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FABRY'S DISEASE ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FISTULA REPAIR ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
GRUNTING ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HILAR LYMPHADENOPATHY ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
ILEAL ULCER PERFORATION ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFLAMMATION OF WOUND ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE THROMBOSIS ( 3 FDA reports)
INJECTION SITE VESICLES ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MASTITIS ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MITRAL VALVE SCLEROSIS ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MORTON'S NEUROMA ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOCARDIAL RUPTURE ( 3 FDA reports)
MYOGLOBINURIA ( 3 FDA reports)
MYXOEDEMA ( 3 FDA reports)
MYXOEDEMA COMA ( 3 FDA reports)
NAIL HYPERTROPHY ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
OPTIC NERVE CUPPING ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHANTOM PAIN ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHOTODERMATOSIS ( 3 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RADIAL PULSE ABNORMAL ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPLENIC GRANULOMA ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUTURE RELATED COMPLICATION ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBIN TIME PROLONGED ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THYROID CYST ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
THYROXINE DECREASED ( 3 FDA reports)
THYROXINE FREE DECREASED ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIRAL RASH ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
X-RAY LIMB ABNORMAL ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
ALVEOLOPLASTY ( 2 FDA reports)
AMPUTATION STUMP PAIN ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANKLE ARTHROPLASTY ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE NECROSIS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPERGILLOMA ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
AUTOANTIBODY POSITIVE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BILIRUBIN CONJUGATED ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCAGON ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE MARROW GRANULOMA ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC ARREST NEONATAL ( 2 FDA reports)
CARDIAC INDEX DECREASED ( 2 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CARDITIS ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CORNEAL CYST ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CREATININE RENAL CLEARANCE ( 2 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DEVICE INTOLERANCE ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DEVICE PACING ISSUE ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELEVATED PACING THRESHOLD ( 2 FDA reports)
EMERGENCY CARE ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE EXCISION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FIBRIN INCREASED ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GAMMA RADIATION THERAPY ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEMIANOPIA HETERONYMOUS ( 2 FDA reports)
HEPATIC ARTERY STENOSIS ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPLANT SITE ABSCESS ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTED SEBACEOUS CYST ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTRACRANIAL INJURY ( 2 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
INTUBATION COMPLICATION ( 2 FDA reports)
JAUNDICE HEPATOCELLULAR ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LUMBAR VERTEBRA INJURY ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUPUS VASCULITIS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MACROANGIOPATHY ( 2 FDA reports)
MALIGNANT MYOPIA ( 2 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDIASTINAL SHIFT ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NASAL TURBINATE ABNORMALITY ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROGENIC SHOCK ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NITRITE URINE ABSENT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NOSOPHOBIA ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTECTOMY ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVERSENSING ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL FISTULA REPAIR ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SIGMOIDOSCOPY ( 2 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STARING ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TISSUE ANOXIA ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TRACHEAL DILATATION ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TYPE II HYPERSENSITIVITY ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VESTIBULAR ATAXIA ( 2 FDA reports)
VIRAL CARDIOMYOPATHY ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCESSORY CARDIAC PATHWAY ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY CERVIX ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY PROSTATE ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX NEOPLASM ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHLAMYDIA SEROLOGY ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER STAGE I ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO VACCINATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DILUTIONAL COAGULOPATHY ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULECTOMY ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EISENMENGER'S SYNDROME ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDIDYMAL TENDERNESS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERCISE TEST ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC DYSPLASIA ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERALISED RESISTANCE TO THYROID HORMONE ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISORDER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOGLOBULIN G4 RELATED SCLEROSING DISEASE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE DERMATITIS ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IODINE UPTAKE INCREASED ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME ABNORMAL ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEFT VENTRICULAR HEAVE ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LONG QT SYNDROME CONGENITAL ( 1 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR PSEUDOHOLE ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL PIGMENTATION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA METASTATIC ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHYSICAL EXAMINATION ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET FACTOR 4 INCREASED ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
PORTAL TRIADITIS ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRIMARY AMYLOIDOSIS ( 1 FDA reports)
PRIMARY HYPOTHYROIDISM ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE CANCER STAGE 0 ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAN GALLIUM ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBIN TIME ABNORMAL ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROIDITIS ACUTE ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
UREA RENAL CLEARANCE DECREASED ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINISMUS ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS OXYGEN SATURATION INCREASED ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ASSIST DEVICE INSERTION ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR PRE-EXCITATION ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE CLOT IN BLOOD PRESENT ( 1 FDA reports)
WITHDRAWAL ARRHYTHMIA ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

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