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

PAIN ( 703 FDA reports)
ANXIETY ( 645 FDA reports)
DYSPNOEA ( 583 FDA reports)
NAUSEA ( 535 FDA reports)
FATIGUE ( 513 FDA reports)
ASTHENIA ( 503 FDA reports)
DEPRESSION ( 457 FDA reports)
BACK PAIN ( 442 FDA reports)
FALL ( 440 FDA reports)
HEADACHE ( 407 FDA reports)
ANAEMIA ( 399 FDA reports)
CHEST PAIN ( 396 FDA reports)
WEIGHT DECREASED ( 385 FDA reports)
ARTHRALGIA ( 382 FDA reports)
DIZZINESS ( 381 FDA reports)
INJURY ( 373 FDA reports)
DIARRHOEA ( 367 FDA reports)
PAIN IN EXTREMITY ( 366 FDA reports)
OSTEOARTHRITIS ( 360 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 341 FDA reports)
VOMITING ( 335 FDA reports)
MYOCARDIAL INFARCTION ( 333 FDA reports)
HYPERTENSION ( 322 FDA reports)
OEDEMA PERIPHERAL ( 320 FDA reports)
BONE DISORDER ( 311 FDA reports)
PNEUMONIA ( 310 FDA reports)
TOOTH EXTRACTION ( 310 FDA reports)
HYPOAESTHESIA ( 294 FDA reports)
ABDOMINAL PAIN ( 292 FDA reports)
CEREBROVASCULAR ACCIDENT ( 279 FDA reports)
OSTEONECROSIS OF JAW ( 273 FDA reports)
PAIN IN JAW ( 273 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 271 FDA reports)
INSOMNIA ( 264 FDA reports)
PYREXIA ( 264 FDA reports)
URINARY TRACT INFECTION ( 249 FDA reports)
OSTEOMYELITIS ( 245 FDA reports)
EMOTIONAL DISTRESS ( 244 FDA reports)
DEHYDRATION ( 243 FDA reports)
HYPOTENSION ( 240 FDA reports)
OSTEONECROSIS ( 232 FDA reports)
CONSTIPATION ( 228 FDA reports)
CORONARY ARTERY DISEASE ( 222 FDA reports)
PARAESTHESIA ( 216 FDA reports)
ANHEDONIA ( 212 FDA reports)
DYSPHAGIA ( 209 FDA reports)
NEUROPATHY PERIPHERAL ( 205 FDA reports)
BRONCHITIS ( 202 FDA reports)
SINUSITIS ( 196 FDA reports)
SWELLING ( 192 FDA reports)
PLEURAL EFFUSION ( 191 FDA reports)
CELLULITIS ( 189 FDA reports)
RENAL FAILURE ( 185 FDA reports)
GAIT DISTURBANCE ( 184 FDA reports)
ATRIAL FIBRILLATION ( 183 FDA reports)
COUGH ( 182 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 181 FDA reports)
CONFUSIONAL STATE ( 174 FDA reports)
SPINAL OSTEOARTHRITIS ( 173 FDA reports)
DEBRIDEMENT ( 172 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 166 FDA reports)
MUSCLE SPASMS ( 166 FDA reports)
DRUG INEFFECTIVE ( 161 FDA reports)
INFECTION ( 159 FDA reports)
DECREASED APPETITE ( 157 FDA reports)
RASH ( 155 FDA reports)
DEEP VEIN THROMBOSIS ( 154 FDA reports)
DENTAL CARIES ( 152 FDA reports)
IMPAIRED HEALING ( 150 FDA reports)
BLOOD GLUCOSE INCREASED ( 149 FDA reports)
WEIGHT INCREASED ( 149 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 148 FDA reports)
HYPERLIPIDAEMIA ( 148 FDA reports)
ABDOMINAL PAIN UPPER ( 147 FDA reports)
HAEMOGLOBIN DECREASED ( 147 FDA reports)
DIABETES MELLITUS ( 141 FDA reports)
PRIMARY SEQUESTRUM ( 140 FDA reports)
RESPIRATORY FAILURE ( 139 FDA reports)
BONE PAIN ( 138 FDA reports)
MITRAL VALVE INCOMPETENCE ( 138 FDA reports)
MYALGIA ( 138 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 137 FDA reports)
RENAL FAILURE ACUTE ( 137 FDA reports)
MALAISE ( 135 FDA reports)
CONVULSION ( 134 FDA reports)
MUSCULOSKELETAL PAIN ( 133 FDA reports)
VISION BLURRED ( 132 FDA reports)
TOOTH FRACTURE ( 131 FDA reports)
OSTEOPOROSIS ( 129 FDA reports)
SEPSIS ( 129 FDA reports)
CONDITION AGGRAVATED ( 128 FDA reports)
TREMOR ( 128 FDA reports)
CHOLELITHIASIS ( 127 FDA reports)
OSTEOPENIA ( 127 FDA reports)
PALPITATIONS ( 126 FDA reports)
RIB FRACTURE ( 126 FDA reports)
SUICIDAL IDEATION ( 126 FDA reports)
BLOOD PRESSURE INCREASED ( 125 FDA reports)
CARDIAC DISORDER ( 124 FDA reports)
GASTRITIS ( 124 FDA reports)
METASTASES TO BONE ( 122 FDA reports)
THROMBOCYTOPENIA ( 122 FDA reports)
ASTHMA ( 121 FDA reports)
HIATUS HERNIA ( 121 FDA reports)
NECK PAIN ( 121 FDA reports)
SOMNOLENCE ( 119 FDA reports)
TOOTH LOSS ( 119 FDA reports)
ANGINA PECTORIS ( 118 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 117 FDA reports)
BURSITIS ( 115 FDA reports)
ERYTHEMA ( 115 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 115 FDA reports)
AMNESIA ( 114 FDA reports)
HYPOKALAEMIA ( 114 FDA reports)
CATARACT ( 113 FDA reports)
CONTUSION ( 113 FDA reports)
HYPERGLYCAEMIA ( 113 FDA reports)
MEMORY IMPAIRMENT ( 113 FDA reports)
CHEST DISCOMFORT ( 112 FDA reports)
DEATH ( 112 FDA reports)
CARDIOMEGALY ( 111 FDA reports)
DYSPEPSIA ( 111 FDA reports)
TOOTH DISORDER ( 110 FDA reports)
HYPOPHAGIA ( 109 FDA reports)
SYNCOPE ( 108 FDA reports)
OEDEMA ( 107 FDA reports)
PURULENT DISCHARGE ( 107 FDA reports)
DEFORMITY ( 106 FDA reports)
EXOSTOSIS ( 106 FDA reports)
JOINT SWELLING ( 105 FDA reports)
BALANCE DISORDER ( 102 FDA reports)
BONE DEBRIDEMENT ( 102 FDA reports)
HYPERHIDROSIS ( 102 FDA reports)
DIVERTICULUM ( 100 FDA reports)
DRY MOUTH ( 100 FDA reports)
PULMONARY EMBOLISM ( 100 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 100 FDA reports)
ENDODONTIC PROCEDURE ( 99 FDA reports)
HYPOXIA ( 98 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 97 FDA reports)
LOSS OF CONSCIOUSNESS ( 97 FDA reports)
EAR PAIN ( 95 FDA reports)
RENAL FAILURE CHRONIC ( 94 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 94 FDA reports)
HOT FLUSH ( 93 FDA reports)
ARTHRITIS ( 92 FDA reports)
DYSURIA ( 92 FDA reports)
MUSCULAR WEAKNESS ( 92 FDA reports)
MOUTH ULCERATION ( 91 FDA reports)
RECTAL HAEMORRHAGE ( 91 FDA reports)
SLEEP APNOEA SYNDROME ( 91 FDA reports)
ABDOMINAL DISTENSION ( 90 FDA reports)
ATELECTASIS ( 90 FDA reports)
HAEMORRHOIDS ( 89 FDA reports)
PRURITUS ( 89 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 88 FDA reports)
HAEMATOCRIT DECREASED ( 88 FDA reports)
PANCYTOPENIA ( 88 FDA reports)
SPINAL COLUMN STENOSIS ( 88 FDA reports)
STOMATITIS ( 88 FDA reports)
SCOLIOSIS ( 87 FDA reports)
THROMBOSIS ( 87 FDA reports)
DISABILITY ( 86 FDA reports)
LUMBAR SPINAL STENOSIS ( 86 FDA reports)
TOOTHACHE ( 86 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 84 FDA reports)
GINGIVAL SWELLING ( 84 FDA reports)
PULMONARY OEDEMA ( 84 FDA reports)
ABASIA ( 83 FDA reports)
GINGIVAL PAIN ( 83 FDA reports)
MENTAL STATUS CHANGES ( 83 FDA reports)
TACHYCARDIA ( 83 FDA reports)
FEELING ABNORMAL ( 81 FDA reports)
JAW OPERATION ( 81 FDA reports)
TOOTH ABSCESS ( 81 FDA reports)
ABDOMINAL DISCOMFORT ( 80 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 80 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 80 FDA reports)
DECREASED INTEREST ( 79 FDA reports)
SWELLING FACE ( 79 FDA reports)
HYPERCHOLESTEROLAEMIA ( 78 FDA reports)
CHILLS ( 77 FDA reports)
DENTAL OPERATION ( 77 FDA reports)
EMPHYSEMA ( 77 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 77 FDA reports)
NERVOUSNESS ( 77 FDA reports)
SPINAL COMPRESSION FRACTURE ( 77 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 76 FDA reports)
HERPES ZOSTER ( 76 FDA reports)
PERIODONTITIS ( 76 FDA reports)
HAEMORRHAGE ( 75 FDA reports)
LUNG NEOPLASM ( 75 FDA reports)
STAPHYLOCOCCAL INFECTION ( 75 FDA reports)
NEUTROPENIA ( 74 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 74 FDA reports)
PULMONARY HYPERTENSION ( 74 FDA reports)
ROTATOR CUFF SYNDROME ( 74 FDA reports)
ADVERSE EVENT ( 73 FDA reports)
CYST ( 73 FDA reports)
HAEMATOCHEZIA ( 72 FDA reports)
LETHARGY ( 72 FDA reports)
TYPE 2 DIABETES MELLITUS ( 72 FDA reports)
BONE DENSITY DECREASED ( 71 FDA reports)
BONE LESION ( 71 FDA reports)
HEPATIC STEATOSIS ( 71 FDA reports)
WALKING AID USER ( 71 FDA reports)
ABSCESS ( 70 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 70 FDA reports)
CARDIOMYOPATHY ( 70 FDA reports)
DIVERTICULUM INTESTINAL ( 70 FDA reports)
LUNG INFILTRATION ( 70 FDA reports)
NEPHROLITHIASIS ( 70 FDA reports)
TENDERNESS ( 70 FDA reports)
CARDIAC ARREST ( 69 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 69 FDA reports)
OVERDOSE ( 69 FDA reports)
ARTHROPATHY ( 68 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 68 FDA reports)
LOOSE TOOTH ( 68 FDA reports)
RHEUMATOID ARTHRITIS ( 68 FDA reports)
TOOTH INFECTION ( 68 FDA reports)
DYSARTHRIA ( 67 FDA reports)
GINGIVAL BLEEDING ( 67 FDA reports)
GINGIVITIS ( 67 FDA reports)
TENDONITIS ( 67 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 67 FDA reports)
ARTERIOSCLEROSIS ( 66 FDA reports)
DYSGEUSIA ( 66 FDA reports)
RHINITIS ALLERGIC ( 66 FDA reports)
DISCOMFORT ( 65 FDA reports)
DRUG HYPERSENSITIVITY ( 65 FDA reports)
RENAL CYST ( 65 FDA reports)
URTICARIA ( 65 FDA reports)
ARRHYTHMIA ( 64 FDA reports)
HALLUCINATION ( 64 FDA reports)
HEART RATE INCREASED ( 64 FDA reports)
HYPOGLYCAEMIA ( 64 FDA reports)
PERIODONTAL DISEASE ( 64 FDA reports)
RADICULOPATHY ( 64 FDA reports)
SKIN ULCER ( 64 FDA reports)
SPONDYLOLISTHESIS ( 64 FDA reports)
BASAL CELL CARCINOMA ( 63 FDA reports)
DIVERTICULITIS ( 63 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 63 FDA reports)
OSTEOSCLEROSIS ( 63 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 63 FDA reports)
ANGINA UNSTABLE ( 62 FDA reports)
BLOOD CREATININE INCREASED ( 62 FDA reports)
INFLAMMATION ( 62 FDA reports)
OBESITY ( 62 FDA reports)
ROAD TRAFFIC ACCIDENT ( 62 FDA reports)
SCAR ( 62 FDA reports)
VERTIGO ( 62 FDA reports)
ALOPECIA ( 61 FDA reports)
COLITIS ( 61 FDA reports)
HIP FRACTURE ( 61 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 61 FDA reports)
DYSPNOEA EXERTIONAL ( 60 FDA reports)
HYPONATRAEMIA ( 60 FDA reports)
MALNUTRITION ( 60 FDA reports)
MUCOSAL INFLAMMATION ( 60 FDA reports)
PHYSICAL DISABILITY ( 60 FDA reports)
BRADYCARDIA ( 59 FDA reports)
FIBROMYALGIA ( 59 FDA reports)
OSTEOLYSIS ( 59 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 59 FDA reports)
SINUS DISORDER ( 59 FDA reports)
CEREBRAL ATROPHY ( 58 FDA reports)
HAEMATURIA ( 58 FDA reports)
ACUTE SINUSITIS ( 57 FDA reports)
BLOOD UREA INCREASED ( 57 FDA reports)
CARDIAC FAILURE ( 57 FDA reports)
HEART RATE IRREGULAR ( 57 FDA reports)
LACUNAR INFARCTION ( 57 FDA reports)
UTERINE LEIOMYOMA ( 57 FDA reports)
FOOT FRACTURE ( 56 FDA reports)
KYPHOSIS ( 56 FDA reports)
SINUS TACHYCARDIA ( 56 FDA reports)
CARPAL TUNNEL SYNDROME ( 55 FDA reports)
LYMPHADENOPATHY ( 55 FDA reports)
WHEEZING ( 55 FDA reports)
CARDIAC MURMUR ( 54 FDA reports)
GINGIVAL INFECTION ( 54 FDA reports)
METASTATIC NEOPLASM ( 54 FDA reports)
HAEMATEMESIS ( 53 FDA reports)
HYPERSENSITIVITY ( 53 FDA reports)
ORTHOSTATIC HYPOTENSION ( 53 FDA reports)
OSTEITIS ( 53 FDA reports)
PHARYNGITIS ( 53 FDA reports)
PLATELET COUNT DECREASED ( 53 FDA reports)
POLLAKIURIA ( 53 FDA reports)
URINARY RETENTION ( 53 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 53 FDA reports)
JOINT SPRAIN ( 52 FDA reports)
MIGRAINE ( 52 FDA reports)
PANCREATITIS ( 52 FDA reports)
CATARACT OPERATION ( 51 FDA reports)
DENTURE WEARER ( 51 FDA reports)
DERMATITIS ( 51 FDA reports)
FISTULA ( 51 FDA reports)
LEUKOPENIA ( 51 FDA reports)
MULTIPLE MYELOMA ( 51 FDA reports)
RENAL DISORDER ( 51 FDA reports)
VIRAL INFECTION ( 51 FDA reports)
CEREBRAL INFARCTION ( 50 FDA reports)
DEAFNESS ( 50 FDA reports)
ENCEPHALOPATHY ( 50 FDA reports)
HAEMATOMA ( 50 FDA reports)
HEPATIC CYST ( 50 FDA reports)
NIGHT SWEATS ( 50 FDA reports)
ORAL PAIN ( 50 FDA reports)
JOINT DISLOCATION ( 49 FDA reports)
LEUKOCYTOSIS ( 49 FDA reports)
MYOCARDIAL ISCHAEMIA ( 49 FDA reports)
PRODUCTIVE COUGH ( 49 FDA reports)
ACTINOMYCOSIS ( 48 FDA reports)
BONE OPERATION ( 48 FDA reports)
CAROTID ARTERY STENOSIS ( 48 FDA reports)
COLONIC POLYP ( 48 FDA reports)
DIABETIC NEUROPATHY ( 48 FDA reports)
DIPLOPIA ( 48 FDA reports)
EATING DISORDER ( 48 FDA reports)
EPISTAXIS ( 48 FDA reports)
HYPOTHYROIDISM ( 48 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 48 FDA reports)
IRRITABLE BOWEL SYNDROME ( 48 FDA reports)
SLEEP DISORDER ( 48 FDA reports)
VISUAL IMPAIRMENT ( 48 FDA reports)
AGITATION ( 47 FDA reports)
BLOOD PRESSURE DECREASED ( 47 FDA reports)
COSTOCHONDRITIS ( 47 FDA reports)
JAW DISORDER ( 47 FDA reports)
NOCTURIA ( 47 FDA reports)
RESPIRATORY ARREST ( 47 FDA reports)
UNRESPONSIVE TO STIMULI ( 47 FDA reports)
VISUAL ACUITY REDUCED ( 47 FDA reports)
BLOOD CALCIUM DECREASED ( 46 FDA reports)
BLOOD CALCIUM INCREASED ( 46 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 46 FDA reports)
DYSKINESIA ( 46 FDA reports)
DYSPHONIA ( 46 FDA reports)
ERECTILE DYSFUNCTION ( 46 FDA reports)
INJECTION SITE ERYTHEMA ( 46 FDA reports)
LUNG DISORDER ( 46 FDA reports)
RESTLESS LEGS SYNDROME ( 46 FDA reports)
TREATMENT NONCOMPLIANCE ( 46 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 45 FDA reports)
DISORIENTATION ( 45 FDA reports)
FLUID RETENTION ( 45 FDA reports)
MUSCLE STRAIN ( 45 FDA reports)
OESOPHAGITIS ( 45 FDA reports)
PULMONARY CONGESTION ( 45 FDA reports)
STRESS ( 45 FDA reports)
WRIST FRACTURE ( 45 FDA reports)
AZOTAEMIA ( 44 FDA reports)
DISTURBANCE IN ATTENTION ( 44 FDA reports)
GASTRIC ULCER ( 44 FDA reports)
HYPOCALCAEMIA ( 44 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 44 FDA reports)
METASTASES TO SPINE ( 44 FDA reports)
MYOPATHY ( 44 FDA reports)
SPEECH DISORDER ( 44 FDA reports)
ALVEOLOPLASTY ( 43 FDA reports)
BLOOD POTASSIUM DECREASED ( 43 FDA reports)
COAGULOPATHY ( 43 FDA reports)
DERMATITIS CONTACT ( 43 FDA reports)
ESCHERICHIA INFECTION ( 43 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 43 FDA reports)
HEPATIC ENZYME INCREASED ( 43 FDA reports)
PATHOLOGICAL FRACTURE ( 43 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 42 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 42 FDA reports)
FOOT DEFORMITY ( 42 FDA reports)
GASTROINTESTINAL DISORDER ( 42 FDA reports)
GOITRE ( 42 FDA reports)
HYPOACUSIS ( 42 FDA reports)
IRRITABILITY ( 42 FDA reports)
MASTICATION DISORDER ( 42 FDA reports)
NASAL CONGESTION ( 42 FDA reports)
ORAL INFECTION ( 42 FDA reports)
BRUXISM ( 41 FDA reports)
CANDIDIASIS ( 41 FDA reports)
COMPRESSION FRACTURE ( 41 FDA reports)
GENERALISED OEDEMA ( 41 FDA reports)
PROTHROMBIN TIME PROLONGED ( 41 FDA reports)
RESPIRATORY DISTRESS ( 41 FDA reports)
STEM CELL TRANSPLANT ( 41 FDA reports)
ASCITES ( 40 FDA reports)
DENTAL FISTULA ( 40 FDA reports)
DIFFICULTY IN WALKING ( 40 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 40 FDA reports)
INJECTION SITE PAIN ( 40 FDA reports)
LUMBAR RADICULOPATHY ( 40 FDA reports)
MULTI-ORGAN FAILURE ( 40 FDA reports)
ORAL CAVITY FISTULA ( 40 FDA reports)
PNEUMONITIS ( 40 FDA reports)
RADIOTHERAPY ( 40 FDA reports)
VISUAL DISTURBANCE ( 40 FDA reports)
DECUBITUS ULCER ( 39 FDA reports)
DRUG TOXICITY ( 39 FDA reports)
ECONOMIC PROBLEM ( 39 FDA reports)
GALLBLADDER DISORDER ( 39 FDA reports)
HYPERKALAEMIA ( 39 FDA reports)
HYPOAESTHESIA ORAL ( 39 FDA reports)
JOINT INJURY ( 39 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 39 FDA reports)
SURGERY ( 39 FDA reports)
VENTRICULAR HYPERTROPHY ( 39 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 38 FDA reports)
CARDIO-RESPIRATORY ARREST ( 38 FDA reports)
FUNGAL INFECTION ( 38 FDA reports)
HAEMOPTYSIS ( 38 FDA reports)
MASS ( 38 FDA reports)
ORAL CANDIDIASIS ( 38 FDA reports)
ORAL SURGERY ( 38 FDA reports)
PERICARDIAL EFFUSION ( 38 FDA reports)
SKIN DISCOLOURATION ( 38 FDA reports)
SPINAL DISORDER ( 38 FDA reports)
ABSCESS JAW ( 37 FDA reports)
AORTIC VALVE INCOMPETENCE ( 37 FDA reports)
ATHEROSCLEROSIS ( 37 FDA reports)
BIOPSY ( 37 FDA reports)
CARDIOVASCULAR DISORDER ( 37 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 37 FDA reports)
COMA ( 37 FDA reports)
DRY EYE ( 37 FDA reports)
INCONTINENCE ( 37 FDA reports)
NEURALGIA ( 37 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 36 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 36 FDA reports)
CATHETERISATION CARDIAC ( 36 FDA reports)
ENTEROCOCCAL INFECTION ( 36 FDA reports)
GASTROENTERITIS ( 36 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 36 FDA reports)
RHINITIS ( 36 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 36 FDA reports)
CHRONIC SINUSITIS ( 35 FDA reports)
CORONARY ARTERY OCCLUSION ( 35 FDA reports)
GLAUCOMA ( 35 FDA reports)
INFLUENZA ( 35 FDA reports)
PELVIC FRACTURE ( 35 FDA reports)
PNEUMONIA ASPIRATION ( 35 FDA reports)
PNEUMOTHORAX ( 35 FDA reports)
SEPTIC SHOCK ( 35 FDA reports)
SKIN LACERATION ( 35 FDA reports)
ABDOMINAL HERNIA ( 34 FDA reports)
ABDOMINAL PAIN LOWER ( 34 FDA reports)
ANOREXIA ( 34 FDA reports)
APPENDICECTOMY ( 34 FDA reports)
ATAXIA ( 34 FDA reports)
BONE FRAGMENTATION ( 34 FDA reports)
DEPRESSED MOOD ( 34 FDA reports)
DRUG DEPENDENCE ( 34 FDA reports)
FLUID OVERLOAD ( 34 FDA reports)
ILEUS ( 34 FDA reports)
INFLUENZA LIKE ILLNESS ( 34 FDA reports)
MEDICATION ERROR ( 34 FDA reports)
OTITIS MEDIA ( 34 FDA reports)
PEPTIC ULCER ( 34 FDA reports)
PLATELET COUNT INCREASED ( 34 FDA reports)
RASH PRURITIC ( 34 FDA reports)
TINNITUS ( 34 FDA reports)
VAGINAL HAEMORRHAGE ( 34 FDA reports)
VASCULITIS ( 34 FDA reports)
APHASIA ( 33 FDA reports)
BRONCHITIS ACUTE ( 33 FDA reports)
BRONCHOPNEUMONIA ( 33 FDA reports)
CEREBRAL ISCHAEMIA ( 33 FDA reports)
CERVICAL SPINAL STENOSIS ( 33 FDA reports)
LUNG NEOPLASM MALIGNANT ( 33 FDA reports)
OROPHARYNGEAL PAIN ( 33 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 33 FDA reports)
PULMONARY FIBROSIS ( 33 FDA reports)
VENTRICULAR TACHYCARDIA ( 33 FDA reports)
BLINDNESS ( 32 FDA reports)
BLOOD BILIRUBIN INCREASED ( 32 FDA reports)
BLOOD GLUCOSE DECREASED ( 32 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 32 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 32 FDA reports)
DUODENITIS ( 32 FDA reports)
FAILURE TO THRIVE ( 32 FDA reports)
FEAR ( 32 FDA reports)
HEPATITIS ( 32 FDA reports)
HYPERKERATOSIS ( 32 FDA reports)
INTERMITTENT CLAUDICATION ( 32 FDA reports)
JAW FRACTURE ( 32 FDA reports)
LIVER DISORDER ( 32 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 32 FDA reports)
METASTASES TO LIVER ( 32 FDA reports)
SINUS BRADYCARDIA ( 32 FDA reports)
ABSCESS DRAINAGE ( 31 FDA reports)
CHOLECYSTECTOMY ( 31 FDA reports)
DISEASE PROGRESSION ( 31 FDA reports)
EMOTIONAL DISORDER ( 31 FDA reports)
EXCORIATION ( 31 FDA reports)
FACIAL PAIN ( 31 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 31 FDA reports)
IRON DEFICIENCY ANAEMIA ( 31 FDA reports)
LIFE EXPECTANCY SHORTENED ( 31 FDA reports)
SUICIDE ATTEMPT ( 31 FDA reports)
TOOTH REPAIR ( 31 FDA reports)
UNEVALUABLE EVENT ( 31 FDA reports)
VERTIGO POSITIONAL ( 31 FDA reports)
WOUND DRAINAGE ( 31 FDA reports)
CORONARY ARTERY STENOSIS ( 30 FDA reports)
GANGRENE ( 30 FDA reports)
HEARING IMPAIRED ( 30 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 30 FDA reports)
KNEE ARTHROPLASTY ( 30 FDA reports)
MUSCLE CRAMP ( 30 FDA reports)
PRESYNCOPE ( 30 FDA reports)
BACK INJURY ( 29 FDA reports)
BACTERIAL INFECTION ( 29 FDA reports)
DILATATION ATRIAL ( 29 FDA reports)
EJECTION FRACTION DECREASED ( 29 FDA reports)
ELECTROLYTE IMBALANCE ( 29 FDA reports)
FEBRILE NEUTROPENIA ( 29 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 29 FDA reports)
FLUSHING ( 29 FDA reports)
HAEMANGIOMA ( 29 FDA reports)
HUMERUS FRACTURE ( 29 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 29 FDA reports)
INJECTION SITE HAEMORRHAGE ( 29 FDA reports)
METASTASES TO LUNG ( 29 FDA reports)
NERVOUS SYSTEM DISORDER ( 29 FDA reports)
NON-CARDIAC CHEST PAIN ( 29 FDA reports)
PANIC ATTACK ( 29 FDA reports)
POOR DENTAL CONDITION ( 29 FDA reports)
URINARY INCONTINENCE ( 29 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 28 FDA reports)
BILE DUCT STENOSIS ( 28 FDA reports)
CERUMEN IMPACTION ( 28 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 28 FDA reports)
CYSTITIS ( 28 FDA reports)
DRUG ABUSE ( 28 FDA reports)
GYNAECOMASTIA ( 28 FDA reports)
HEMIPARESIS ( 28 FDA reports)
HEPATIC LESION ( 28 FDA reports)
HYPOVOLAEMIA ( 28 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 28 FDA reports)
NASOPHARYNGITIS ( 28 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 28 FDA reports)
RASH MACULAR ( 28 FDA reports)
SHOULDER ARTHROPLASTY ( 28 FDA reports)
SKIN LESION ( 28 FDA reports)
SQUAMOUS CELL CARCINOMA ( 28 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 28 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 28 FDA reports)
AGGRESSION ( 27 FDA reports)
ATRIAL FLUTTER ( 27 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 27 FDA reports)
COGNITIVE DISORDER ( 27 FDA reports)
CRANIOTOMY ( 27 FDA reports)
DRY SKIN ( 27 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 27 FDA reports)
NEOPLASM MALIGNANT ( 27 FDA reports)
OTITIS MEDIA ACUTE ( 27 FDA reports)
POST PROCEDURAL COMPLICATION ( 27 FDA reports)
RHINORRHOEA ( 27 FDA reports)
STRESS FRACTURE ( 27 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 26 FDA reports)
BREATH ODOUR ( 26 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 26 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 26 FDA reports)
COMPLETED SUICIDE ( 26 FDA reports)
DIASTOLIC DYSFUNCTION ( 26 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 26 FDA reports)
GASTRIC DISORDER ( 26 FDA reports)
HEPATIC FAILURE ( 26 FDA reports)
HERNIA ( 26 FDA reports)
HYDRONEPHROSIS ( 26 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 26 FDA reports)
MENTAL DISORDER ( 26 FDA reports)
OTITIS EXTERNA ( 26 FDA reports)
PANCREATITIS ACUTE ( 26 FDA reports)
PULPITIS DENTAL ( 26 FDA reports)
SCLERODERMA ( 26 FDA reports)
SKELETAL INJURY ( 26 FDA reports)
THYROIDECTOMY ( 26 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 26 FDA reports)
AORTIC ANEURYSM ( 25 FDA reports)
APPENDICITIS ( 25 FDA reports)
BURNING SENSATION ( 25 FDA reports)
CHOLECYSTITIS ( 25 FDA reports)
DRUG ABUSER ( 25 FDA reports)
DRUG EFFECT DECREASED ( 25 FDA reports)
EYE SWELLING ( 25 FDA reports)
GINGIVAL DISORDER ( 25 FDA reports)
LOCALISED INFECTION ( 25 FDA reports)
MALOCCLUSION ( 25 FDA reports)
MOBILITY DECREASED ( 25 FDA reports)
ONYCHOMYCOSIS ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
ORTHOSIS USER ( 25 FDA reports)
RASH ERYTHEMATOUS ( 25 FDA reports)
RENAL ATROPHY ( 25 FDA reports)
SEBORRHOEIC KERATOSIS ( 25 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 25 FDA reports)
TIBIA FRACTURE ( 25 FDA reports)
TRISMUS ( 25 FDA reports)
ULCER ( 25 FDA reports)
ABNORMAL BEHAVIOUR ( 24 FDA reports)
BLOOD SODIUM DECREASED ( 24 FDA reports)
BREAST CANCER ( 24 FDA reports)
CEREBROVASCULAR DISORDER ( 24 FDA reports)
CERVICAL DYSPLASIA ( 24 FDA reports)
COLD SWEAT ( 24 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
DIALYSIS ( 24 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 24 FDA reports)
EYE LASER SURGERY ( 24 FDA reports)
GINGIVAL ERYTHEMA ( 24 FDA reports)
GRANULOMA ( 24 FDA reports)
ISCHAEMIA ( 24 FDA reports)
JAUNDICE ( 24 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 24 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 24 FDA reports)
MICTURITION URGENCY ( 24 FDA reports)
MYOSITIS ( 24 FDA reports)
OTORRHOEA ( 24 FDA reports)
REFLUX OESOPHAGITIS ( 24 FDA reports)
RENAL PAIN ( 24 FDA reports)
SEDATION ( 24 FDA reports)
SOFT TISSUE DISORDER ( 24 FDA reports)
SYNOVIAL CYST ( 24 FDA reports)
TOOTH DEPOSIT ( 24 FDA reports)
TOOTH INJURY ( 24 FDA reports)
WOUND DEHISCENCE ( 24 FDA reports)
ADVERSE DRUG REACTION ( 23 FDA reports)
ASPIRATION ( 23 FDA reports)
BONE SCAN ABNORMAL ( 23 FDA reports)
BREAST CALCIFICATIONS ( 23 FDA reports)
BREAST PAIN ( 23 FDA reports)
CHOLECYSTITIS CHRONIC ( 23 FDA reports)
CORONARY ARTERY BYPASS ( 23 FDA reports)
DELIRIUM ( 23 FDA reports)
DEVICE RELATED INFECTION ( 23 FDA reports)
DIABETIC NEPHROPATHY ( 23 FDA reports)
DRUG INTERACTION ( 23 FDA reports)
FEMUR FRACTURE ( 23 FDA reports)
GOUT ( 23 FDA reports)
HAEMANGIOMA OF LIVER ( 23 FDA reports)
HEPATIC CIRRHOSIS ( 23 FDA reports)
INTERSTITIAL LUNG DISEASE ( 23 FDA reports)
INTRAOCULAR LENS IMPLANT ( 23 FDA reports)
MENISCUS LESION ( 23 FDA reports)
MULTIPLE INJURIES ( 23 FDA reports)
OSTEITIS DEFORMANS ( 23 FDA reports)
OXYGEN SATURATION DECREASED ( 23 FDA reports)
PURULENCE ( 23 FDA reports)
RESPIRATORY DISORDER ( 23 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 23 FDA reports)
SKIN DISORDER ( 23 FDA reports)
TARDIVE DYSKINESIA ( 23 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 23 FDA reports)
WOUND INFECTION ( 23 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 22 FDA reports)
BLISTER ( 22 FDA reports)
BRAIN NEOPLASM ( 22 FDA reports)
DERMAL CYST ( 22 FDA reports)
EPICONDYLITIS ( 22 FDA reports)
FACIAL PALSY ( 22 FDA reports)
FIBROSIS ( 22 FDA reports)
HEMIPLEGIA ( 22 FDA reports)
INCREASED APPETITE ( 22 FDA reports)
INTESTINAL OBSTRUCTION ( 22 FDA reports)
LACERATION ( 22 FDA reports)
MENTAL IMPAIRMENT ( 22 FDA reports)
MOUTH HAEMORRHAGE ( 22 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 22 FDA reports)
OPEN REDUCTION OF FRACTURE ( 22 FDA reports)
PRURITUS GENERALISED ( 22 FDA reports)
PULMONARY MASS ( 22 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
SCAB ( 22 FDA reports)
SEQUESTRECTOMY ( 22 FDA reports)
SPINAL CORD COMPRESSION ( 22 FDA reports)
THROAT IRRITATION ( 22 FDA reports)
APHTHOUS STOMATITIS ( 21 FDA reports)
APTYALISM ( 21 FDA reports)
BIPOLAR I DISORDER ( 21 FDA reports)
BREAST CANCER METASTATIC ( 21 FDA reports)
CERVICOBRACHIAL SYNDROME ( 21 FDA reports)
CLOSTRIDIAL INFECTION ( 21 FDA reports)
DIABETIC RETINOPATHY ( 21 FDA reports)
FEELING HOT ( 21 FDA reports)
FRACTURE ( 21 FDA reports)
HALLUCINATION, VISUAL ( 21 FDA reports)
HYPERPLASIA ( 21 FDA reports)
INTENTIONAL OVERDOSE ( 21 FDA reports)
LOCAL SWELLING ( 21 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 21 FDA reports)
OLIGURIA ( 21 FDA reports)
SCIATICA ( 21 FDA reports)
THYROID DISORDER ( 21 FDA reports)
THYROID NEOPLASM ( 21 FDA reports)
TRANSFUSION ( 21 FDA reports)
WEGENER'S GRANULOMATOSIS ( 21 FDA reports)
AORTIC STENOSIS ( 20 FDA reports)
BONE EROSION ( 20 FDA reports)
BREAST MASS ( 20 FDA reports)
CONJUNCTIVITIS ( 20 FDA reports)
DEVICE FAILURE ( 20 FDA reports)
ENTERITIS ( 20 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 20 FDA reports)
EYE IRRITATION ( 20 FDA reports)
FACIAL NEURALGIA ( 20 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 20 FDA reports)
HEAD INJURY ( 20 FDA reports)
JOINT EFFUSION ( 20 FDA reports)
MELAENA ( 20 FDA reports)
METABOLIC ACIDOSIS ( 20 FDA reports)
MOOD SWINGS ( 20 FDA reports)
MOVEMENT DISORDER ( 20 FDA reports)
PAROTID GLAND ENLARGEMENT ( 20 FDA reports)
PROCEDURAL PAIN ( 20 FDA reports)
PYELONEPHRITIS ( 20 FDA reports)
SEASONAL ALLERGY ( 20 FDA reports)
SPINAL FRACTURE ( 20 FDA reports)
SPINAL FUSION SURGERY ( 20 FDA reports)
STRESS URINARY INCONTINENCE ( 20 FDA reports)
THROMBOCYTOSIS ( 20 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 20 FDA reports)
VAGINAL INFECTION ( 20 FDA reports)
VITREOUS DETACHMENT ( 20 FDA reports)
ANEURYSM ( 19 FDA reports)
BLOOD ALBUMIN DECREASED ( 19 FDA reports)
CHEST X-RAY ABNORMAL ( 19 FDA reports)
DEPENDENCE ( 19 FDA reports)
ESSENTIAL HYPERTENSION ( 19 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 19 FDA reports)
EYE PAIN ( 19 FDA reports)
FACE OEDEMA ( 19 FDA reports)
FAECALOMA ( 19 FDA reports)
GASTRITIS EROSIVE ( 19 FDA reports)
GINGIVAL RECESSION ( 19 FDA reports)
HEART RATE DECREASED ( 19 FDA reports)
HYPERCALCAEMIA ( 19 FDA reports)
HYPERTONIC BLADDER ( 19 FDA reports)
ILL-DEFINED DISORDER ( 19 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 19 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 19 FDA reports)
ISCHAEMIC STROKE ( 19 FDA reports)
LARYNGEAL OEDEMA ( 19 FDA reports)
LYMPHOEDEMA ( 19 FDA reports)
MASS EXCISION ( 19 FDA reports)
MULTIPLE SCLEROSIS ( 19 FDA reports)
NEOPLASM ( 19 FDA reports)
NERVE COMPRESSION ( 19 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 19 FDA reports)
OPEN WOUND ( 19 FDA reports)
PATHOLOGICAL GAMBLING ( 19 FDA reports)
PERONEAL NERVE PALSY ( 19 FDA reports)
PLEURITIC PAIN ( 19 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 19 FDA reports)
PRESBYOPIA ( 19 FDA reports)
PSEUDOMONAS INFECTION ( 19 FDA reports)
RESPIRATORY RATE INCREASED ( 19 FDA reports)
RHABDOMYOLYSIS ( 19 FDA reports)
ROSACEA ( 19 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 19 FDA reports)
THIRST ( 19 FDA reports)
UPPER LIMB FRACTURE ( 19 FDA reports)
VIITH NERVE PARALYSIS ( 19 FDA reports)
ACCIDENT AT WORK ( 18 FDA reports)
ANGIOPATHY ( 18 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 18 FDA reports)
BACK DISORDER ( 18 FDA reports)
BLADDER NECK OPERATION ( 18 FDA reports)
CARDIAC VALVE DISEASE ( 18 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 18 FDA reports)
DEMENTIA ( 18 FDA reports)
EAR HAEMORRHAGE ( 18 FDA reports)
FACET JOINT SYNDROME ( 18 FDA reports)
FACIAL BONES FRACTURE ( 18 FDA reports)
GRAND MAL CONVULSION ( 18 FDA reports)
HEART VALVE INCOMPETENCE ( 18 FDA reports)
HYPOKINESIA ( 18 FDA reports)
INCISIONAL DRAINAGE ( 18 FDA reports)
LIMB INJURY ( 18 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 18 FDA reports)
MUSCLE ATROPHY ( 18 FDA reports)
NERVE INJURY ( 18 FDA reports)
NEUROPATHY ( 18 FDA reports)
ODYNOPHAGIA ( 18 FDA reports)
OVARIAN CANCER ( 18 FDA reports)
PAPILLOMA ( 18 FDA reports)
PARANOIA ( 18 FDA reports)
PLASTIC SURGERY TO THE FACE ( 18 FDA reports)
RADIUS FRACTURE ( 18 FDA reports)
SKIN EXFOLIATION ( 18 FDA reports)
SPLENOMEGALY ( 18 FDA reports)
STOMATITIS NECROTISING ( 18 FDA reports)
SYNOVITIS ( 18 FDA reports)
VENTRICULAR HYPOKINESIA ( 18 FDA reports)
ACTINIC KERATOSIS ( 17 FDA reports)
ACUTE CORONARY SYNDROME ( 17 FDA reports)
BLOOD IRON DECREASED ( 17 FDA reports)
CAROTID ARTERY DISEASE ( 17 FDA reports)
CAROTID BRUIT ( 17 FDA reports)
COLONOSCOPY ABNORMAL ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
DYSPLASIA ( 17 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 17 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 17 FDA reports)
FAECES DISCOLOURED ( 17 FDA reports)
FLANK PAIN ( 17 FDA reports)
IMPAIRED DRIVING ABILITY ( 17 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 17 FDA reports)
LABYRINTHITIS ( 17 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 17 FDA reports)
NEURODERMATITIS ( 17 FDA reports)
NODULE ( 17 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 17 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 17 FDA reports)
ORAL DISORDER ( 17 FDA reports)
OVARIAN CYST ( 17 FDA reports)
PERIPHERAL COLDNESS ( 17 FDA reports)
PROTEINURIA ( 17 FDA reports)
QUADRIPLEGIA ( 17 FDA reports)
RASH GENERALISED ( 17 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 17 FDA reports)
THINKING ABNORMAL ( 17 FDA reports)
THYROID CANCER ( 17 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 16 FDA reports)
ACUTE RESPIRATORY FAILURE ( 16 FDA reports)
ADJUSTMENT DISORDER ( 16 FDA reports)
BREAST CANCER IN SITU ( 16 FDA reports)
CARDIAC OPERATION ( 16 FDA reports)
CARDIOGENIC SHOCK ( 16 FDA reports)
CERVIX CARCINOMA ( 16 FDA reports)
CORONARY ARTERY RESTENOSIS ( 16 FDA reports)
DYSSTASIA ( 16 FDA reports)
ECCHYMOSIS ( 16 FDA reports)
EYE DISORDER ( 16 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 16 FDA reports)
FLATULENCE ( 16 FDA reports)
GASTROENTERITIS VIRAL ( 16 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 16 FDA reports)
IMPAIRED WORK ABILITY ( 16 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 16 FDA reports)
LACRIMATION INCREASED ( 16 FDA reports)
MACROCYTOSIS ( 16 FDA reports)
METABOLIC ENCEPHALOPATHY ( 16 FDA reports)
NECK MASS ( 16 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 16 FDA reports)
PARAESTHESIA ORAL ( 16 FDA reports)
PARALYSIS ( 16 FDA reports)
POLYNEUROPATHY ( 16 FDA reports)
PROCTALGIA ( 16 FDA reports)
PROSTATOMEGALY ( 16 FDA reports)
RECTOCELE ( 16 FDA reports)
RESTLESSNESS ( 16 FDA reports)
RETCHING ( 16 FDA reports)
SOFT TISSUE INFLAMMATION ( 16 FDA reports)
TENSION ( 16 FDA reports)
UROSEPSIS ( 16 FDA reports)
VENTRICULAR DYSFUNCTION ( 16 FDA reports)
ACIDOSIS ( 15 FDA reports)
ANKLE FRACTURE ( 15 FDA reports)
AORTIC VALVE SCLEROSIS ( 15 FDA reports)
ARTHROSCOPY ( 15 FDA reports)
BLOOD CHLORIDE DECREASED ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 15 FDA reports)
CACHEXIA ( 15 FDA reports)
CARDIAC PACEMAKER INSERTION ( 15 FDA reports)
COLON POLYPECTOMY ( 15 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 15 FDA reports)
DEMYELINATION ( 15 FDA reports)
DERMATITIS ATOPIC ( 15 FDA reports)
DRUG INTOLERANCE ( 15 FDA reports)
DYSTONIA ( 15 FDA reports)
ENDOTRACHEAL INTUBATION ( 15 FDA reports)
FAECAL INCONTINENCE ( 15 FDA reports)
FOLLICULITIS ( 15 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 15 FDA reports)
HOMICIDAL IDEATION ( 15 FDA reports)
HYDROCEPHALUS ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
HYPOMAGNESAEMIA ( 15 FDA reports)
HYSTERECTOMY ( 15 FDA reports)
INCORRECT DOSE ADMINISTERED ( 15 FDA reports)
INFUSION RELATED REACTION ( 15 FDA reports)
LARGE INTESTINAL ULCER ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
LIPIDS INCREASED ( 15 FDA reports)
METAPLASIA ( 15 FDA reports)
PLEURAL FIBROSIS ( 15 FDA reports)
PROSTATE CANCER ( 15 FDA reports)
PSORIASIS ( 15 FDA reports)
PSYCHOTIC DISORDER ( 15 FDA reports)
PULMONARY INFARCTION ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 15 FDA reports)
SENSORY LOSS ( 15 FDA reports)
SOFT TISSUE INFECTION ( 15 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 15 FDA reports)
SPONDYLOSIS ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 15 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 15 FDA reports)
TRACHEITIS ( 15 FDA reports)
ABSCESS ORAL ( 14 FDA reports)
ADRENAL ADENOMA ( 14 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
APPENDICITIS PERFORATED ( 14 FDA reports)
BIPOLAR DISORDER ( 14 FDA reports)
BONE CALLUS EXCESSIVE ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
CLAUSTROPHOBIA ( 14 FDA reports)
CONCUSSION ( 14 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 14 FDA reports)
CRANIAL NERVE DISORDER ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
CYANOSIS ( 14 FDA reports)
EMBOLISM ( 14 FDA reports)
ERUCTATION ( 14 FDA reports)
FRACTURE NONUNION ( 14 FDA reports)
GASTROINTESTINAL PAIN ( 14 FDA reports)
HEPATITIS C ( 14 FDA reports)
HODGKIN'S DISEASE ( 14 FDA reports)
HORDEOLUM ( 14 FDA reports)
IMPLANT SITE INFECTION ( 14 FDA reports)
INCREASED TENDENCY TO BRUISE ( 14 FDA reports)
INFARCTION ( 14 FDA reports)
INJECTION SITE REACTION ( 14 FDA reports)
INJECTION SITE SWELLING ( 14 FDA reports)
LARGE INTESTINE PERFORATION ( 14 FDA reports)
MENORRHAGIA ( 14 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 14 FDA reports)
MYELOPATHY ( 14 FDA reports)
NECROSIS ( 14 FDA reports)
NEUROENDOCRINE CARCINOMA ( 14 FDA reports)
ORAL INTAKE REDUCED ( 14 FDA reports)
OSTEORADIONECROSIS ( 14 FDA reports)
PELVIC PAIN ( 14 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 14 FDA reports)
PERSONALITY DISORDER ( 14 FDA reports)
POST PROCEDURAL FISTULA ( 14 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 14 FDA reports)
POST-TRAUMATIC PAIN ( 14 FDA reports)
RADIATION ASSOCIATED PAIN ( 14 FDA reports)
RESORPTION BONE INCREASED ( 14 FDA reports)
SCAN BONE MARROW ABNORMAL ( 14 FDA reports)
SKIN CANCER ( 14 FDA reports)
STOMACH DISCOMFORT ( 14 FDA reports)
STRESS SYMPTOMS ( 14 FDA reports)
VASCULAR CALCIFICATION ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 14 FDA reports)
ABDOMINAL ABSCESS ( 13 FDA reports)
ANGIOEDEMA ( 13 FDA reports)
APNOEA ( 13 FDA reports)
AUTONOMIC NEUROPATHY ( 13 FDA reports)
BLADDER DISORDER ( 13 FDA reports)
BLEPHARITIS ( 13 FDA reports)
BLOOD POTASSIUM INCREASED ( 13 FDA reports)
BODY HEIGHT DECREASED ( 13 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 13 FDA reports)
CRYING ( 13 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
ENCEPHALOMALACIA ( 13 FDA reports)
EXTRASKELETAL OSSIFICATION ( 13 FDA reports)
FEELING COLD ( 13 FDA reports)
FISTULA REPAIR ( 13 FDA reports)
GINGIVAL ULCERATION ( 13 FDA reports)
GRIP STRENGTH DECREASED ( 13 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
HYPERMETROPIA ( 13 FDA reports)
INGROWING NAIL ( 13 FDA reports)
INJECTION SITE PRURITUS ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
LYMPHADENECTOMY ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
MASTECTOMY ( 13 FDA reports)
MITRAL VALVE PROLAPSE ( 13 FDA reports)
MUSCLE INJURY ( 13 FDA reports)
MUSCLE TIGHTNESS ( 13 FDA reports)
MUSCLE TWITCHING ( 13 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 13 FDA reports)
PANIC DISORDER ( 13 FDA reports)
PERSONALITY CHANGE ( 13 FDA reports)
POST HERPETIC NEURALGIA ( 13 FDA reports)
PRESBYACUSIS ( 13 FDA reports)
PSORIATIC ARTHROPATHY ( 13 FDA reports)
RADICULAR PAIN ( 13 FDA reports)
RESPIRATORY DEPRESSION ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SINUS OPERATION ( 13 FDA reports)
STRESS INCONTINENCE ( 13 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
SWOLLEN TONGUE ( 13 FDA reports)
TIC ( 13 FDA reports)
TOE DEFORMITY ( 13 FDA reports)
TOOTH DISCOLOURATION ( 13 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
URINARY HESITATION ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
ABDOMINAL TENDERNESS ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 12 FDA reports)
ADRENAL MASS ( 12 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 12 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 12 FDA reports)
ANAL FISSURE ( 12 FDA reports)
APATHY ( 12 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
BILIARY DYSKINESIA ( 12 FDA reports)
BLOOD PRESSURE ABNORMAL ( 12 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 12 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 12 FDA reports)
CARDIAC ANEURYSM ( 12 FDA reports)
CATHETER SITE HAEMORRHAGE ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
COLLAPSE OF LUNG ( 12 FDA reports)
COLON CANCER ( 12 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 12 FDA reports)
CYSTOPEXY ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
DYSLIPIDAEMIA ( 12 FDA reports)
ECZEMA ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 12 FDA reports)
FAT NECROSIS ( 12 FDA reports)
FOOT OPERATION ( 12 FDA reports)
GROIN PAIN ( 12 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 12 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 12 FDA reports)
INCOHERENT ( 12 FDA reports)
INTENTIONAL DRUG MISUSE ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
MACULOPATHY ( 12 FDA reports)
MEDICAL DEVICE REMOVAL ( 12 FDA reports)
MENINGIOMA ( 12 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
MUSCULOSKELETAL DISORDER ( 12 FDA reports)
OCCULT BLOOD POSITIVE ( 12 FDA reports)
OEDEMA MUCOSAL ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
OSTEOMA ( 12 FDA reports)
PERIODONTAL OPERATION ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
POLYURIA ( 12 FDA reports)
POSTNASAL DRIP ( 12 FDA reports)
PROTEIN TOTAL DECREASED ( 12 FDA reports)
PSYCHIATRIC SYMPTOM ( 12 FDA reports)
RADICAL HYSTERECTOMY ( 12 FDA reports)
RASH PAPULAR ( 12 FDA reports)
SMEAR CERVIX ABNORMAL ( 12 FDA reports)
SOMNAMBULISM ( 12 FDA reports)
TACHYARRHYTHMIA ( 12 FDA reports)
TENDON INJURY ( 12 FDA reports)
TENOSYNOVITIS ( 12 FDA reports)
THORACOTOMY ( 12 FDA reports)
UTERINE ENLARGEMENT ( 12 FDA reports)
UTERINE HAEMORRHAGE ( 12 FDA reports)
VAGINAL PROLAPSE ( 12 FDA reports)
VERTEBROPLASTY ( 12 FDA reports)
WEIGHT FLUCTUATION ( 12 FDA reports)
ABDOMINAL MASS ( 11 FDA reports)
ACUTE PULMONARY OEDEMA ( 11 FDA reports)
ANOXIC ENCEPHALOPATHY ( 11 FDA reports)
BETA GLOBULIN INCREASED ( 11 FDA reports)
BONE FISSURE ( 11 FDA reports)
BONE GRAFT ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BONE MARROW TRANSPLANT ( 11 FDA reports)
BONE SWELLING ( 11 FDA reports)
BREAST NECROSIS ( 11 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 11 FDA reports)
CERVICAL CORD COMPRESSION ( 11 FDA reports)
COLPOCELE ( 11 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 11 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 11 FDA reports)
COR PULMONALE CHRONIC ( 11 FDA reports)
CROHN'S DISEASE ( 11 FDA reports)
CYSTOSCOPY ( 11 FDA reports)
DENTAL NECROSIS ( 11 FDA reports)
EAR INFECTION ( 11 FDA reports)
FACIAL OPERATION ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
GASTRODUODENITIS ( 11 FDA reports)
HAND DEFORMITY ( 11 FDA reports)
HEPATOCELLULAR DAMAGE ( 11 FDA reports)
HYPERTENSIVE HEART DISEASE ( 11 FDA reports)
IMMUNOSUPPRESSION ( 11 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 11 FDA reports)
INCISION SITE INFECTION ( 11 FDA reports)
INJECTION SITE IRRITATION ( 11 FDA reports)
JOINT LOCK ( 11 FDA reports)
KIDNEY SMALL ( 11 FDA reports)
LABORATORY TEST ABNORMAL ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 11 FDA reports)
MAXILLOFACIAL OPERATION ( 11 FDA reports)
MECHANICAL VENTILATION ( 11 FDA reports)
METASTASES TO LYMPH NODES ( 11 FDA reports)
METASTATIC PAIN ( 11 FDA reports)
MICROCYTIC ANAEMIA ( 11 FDA reports)
NASAL MUCOSAL DISORDER ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
OEDEMA MOUTH ( 11 FDA reports)
PARKINSON'S DISEASE ( 11 FDA reports)
PERIORBITAL HAEMATOMA ( 11 FDA reports)
PHOTOSENSITIVITY REACTION ( 11 FDA reports)
POOR PERIPHERAL CIRCULATION ( 11 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 11 FDA reports)
PROTEIN URINE ( 11 FDA reports)
RAYNAUD'S PHENOMENON ( 11 FDA reports)
REHABILITATION THERAPY ( 11 FDA reports)
RENAL INJURY ( 11 FDA reports)
SACROILIITIS ( 11 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 11 FDA reports)
SERUM FERRITIN INCREASED ( 11 FDA reports)
SHOULDER PAIN ( 11 FDA reports)
SKIN HYPERPIGMENTATION ( 11 FDA reports)
SKIN REACTION ( 11 FDA reports)
SPINAL COLUMN INJURY ( 11 FDA reports)
SPINAL LAMINECTOMY ( 11 FDA reports)
STOMATOCYTES PRESENT ( 11 FDA reports)
TENDON DISORDER ( 11 FDA reports)
THROAT TIGHTNESS ( 11 FDA reports)
TINEA PEDIS ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
VERTEBRAL WEDGING ( 11 FDA reports)
WHEELCHAIR USER ( 11 FDA reports)
WOUND TREATMENT ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 10 FDA reports)
ANGER ( 10 FDA reports)
ANXIETY DISORDER ( 10 FDA reports)
ARTERIOSPASM CORONARY ( 10 FDA reports)
ARTHROSCOPIC SURGERY ( 10 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
BIOPSY BONE MARROW ( 10 FDA reports)
BLOOD AMYLASE INCREASED ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 10 FDA reports)
BLOOD OSMOLARITY DECREASED ( 10 FDA reports)
BLOOD URINE PRESENT ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
BREAST HAEMATOMA ( 10 FDA reports)
CALCULUS URETERIC ( 10 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 10 FDA reports)
CAROTID ARTERY OCCLUSION ( 10 FDA reports)
CATARACT NUCLEAR ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CHROMATURIA ( 10 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 10 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 10 FDA reports)
EAR DISCOMFORT ( 10 FDA reports)
EAR DISORDER ( 10 FDA reports)
EARLY SATIETY ( 10 FDA reports)
EDENTULOUS ( 10 FDA reports)
FIBROADENOMA OF BREAST ( 10 FDA reports)
FOOD POISONING ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
GENERALISED ANXIETY DISORDER ( 10 FDA reports)
GLIOSIS ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
GOUTY ARTHRITIS ( 10 FDA reports)
HEPATITIS B ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INCREASED BRONCHIAL SECRETION ( 10 FDA reports)
INJECTION SITE HAEMATOMA ( 10 FDA reports)
LIGAMENT RUPTURE ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
LUNG HYPERINFLATION ( 10 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
MACULAR DEGENERATION ( 10 FDA reports)
MITRAL VALVE STENOSIS ( 10 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 10 FDA reports)
MUSCLE DISORDER ( 10 FDA reports)
MYELODYSPLASTIC SYNDROME ( 10 FDA reports)
NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
ONYCHALGIA ( 10 FDA reports)
PATHOGEN RESISTANCE ( 10 FDA reports)
PERITONITIS ( 10 FDA reports)
POLYDIPSIA ( 10 FDA reports)
POST PROCEDURAL HAEMATOMA ( 10 FDA reports)
PURPURA ( 10 FDA reports)
RADIATION INJURY ( 10 FDA reports)
RADIATION OESOPHAGITIS ( 10 FDA reports)
SINUS CONGESTION ( 10 FDA reports)
SJOGREN'S SYNDROME ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
TACHYPNOEA ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
UTERINE DISORDER ( 10 FDA reports)
VITAMIN D DEFICIENCY ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
ACCIDENT ( 9 FDA reports)
ADRENAL INSUFFICIENCY ( 9 FDA reports)
ANAL FISTULA ( 9 FDA reports)
ANAPHYLACTIC REACTION ( 9 FDA reports)
BACTERIURIA ( 9 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 9 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 9 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 9 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 9 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 9 FDA reports)
BREAST HYPERPLASIA ( 9 FDA reports)
BURNS THIRD DEGREE ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
COLITIS ISCHAEMIC ( 9 FDA reports)
COLON ADENOMA ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DEMENTIA WITH LEWY BODIES ( 9 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 9 FDA reports)
DERMATOPHYTOSIS ( 9 FDA reports)
EAR TUBE INSERTION ( 9 FDA reports)
ENDOMETRIOSIS ( 9 FDA reports)
ENEMA ADMINISTRATION ( 9 FDA reports)
EXTREMITY NECROSIS ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 9 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 9 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 9 FDA reports)
HEARING DISABILITY ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPOGONADISM ( 9 FDA reports)
HYPOTONIA ( 9 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 9 FDA reports)
INFECTED SKIN ULCER ( 9 FDA reports)
INTENTIONAL SELF-INJURY ( 9 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 9 FDA reports)
JOINT CONTRACTURE ( 9 FDA reports)
JOINT STIFFNESS ( 9 FDA reports)
LAGOPHTHALMOS ( 9 FDA reports)
LIGAMENT SPRAIN ( 9 FDA reports)
LIPASE INCREASED ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
LOCALISED OSTEOARTHRITIS ( 9 FDA reports)
LUNG CONSOLIDATION ( 9 FDA reports)
MALIGNANT MELANOMA ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
MEDIASTINUM NEOPLASM ( 9 FDA reports)
MENINGITIS ASEPTIC ( 9 FDA reports)
METASTASES TO ADRENALS ( 9 FDA reports)
METASTASIS ( 9 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 9 FDA reports)
MONARTHRITIS ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MUCOSAL ULCERATION ( 9 FDA reports)
MULTIPLE ALLERGIES ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
NEUROMA ( 9 FDA reports)
NIGHTMARE ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER ( 9 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 9 FDA reports)
OLFACTORY NERVE DISORDER ( 9 FDA reports)
ORAL TORUS ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 9 FDA reports)
POLYP ( 9 FDA reports)
POSTOPERATIVE INFECTION ( 9 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RIGHT ATRIAL DILATATION ( 9 FDA reports)
SENSATION OF FOREIGN BODY ( 9 FDA reports)
SEPSIS SYNDROME ( 9 FDA reports)
SKIN INDURATION ( 9 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 9 FDA reports)
SPINAL CORPECTOMY ( 9 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 9 FDA reports)
THERAPY NON-RESPONDER ( 9 FDA reports)
TOOTH IMPACTED ( 9 FDA reports)
TOURETTE'S DISORDER ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TUBERCULOSIS ( 9 FDA reports)
UMBILICAL HERNIA ( 9 FDA reports)
ABDOMINAL ADHESIONS ( 8 FDA reports)
ACNE ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
ASPHYXIA ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 8 FDA reports)
BACTERIA URINE IDENTIFIED ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BLADDER CATHETERISATION ( 8 FDA reports)
BLOOD COUNT ABNORMAL ( 8 FDA reports)
BLOOD UREA DECREASED ( 8 FDA reports)
BOWEL SOUNDS ABNORMAL ( 8 FDA reports)
BRAIN HERNIATION ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 8 FDA reports)
CUSHINGOID ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DENTAL IMPLANTATION ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DIABETIC RETINAL OEDEMA ( 8 FDA reports)
DISEASE RECURRENCE ( 8 FDA reports)
DRUG TOLERANCE ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
FRACTURED COCCYX ( 8 FDA reports)
GALLBLADDER OPERATION ( 8 FDA reports)
GASTRIC ULCER PERFORATION ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
GINGIVAL EROSION ( 8 FDA reports)
GINGIVAL OEDEMA ( 8 FDA reports)
GUILLAIN-BARRE SYNDROME ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
ILIAC ARTERY STENOSIS ( 8 FDA reports)
INNER EAR DISORDER ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
JOINT CREPITATION ( 8 FDA reports)
KLEBSIELLA INFECTION ( 8 FDA reports)
LIMB DISCOMFORT ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
LIPOMA ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 8 FDA reports)
MEAN CELL VOLUME INCREASED ( 8 FDA reports)
MENISCUS REMOVAL ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
MITRAL VALVE CALCIFICATION ( 8 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 8 FDA reports)
NEURITIS ( 8 FDA reports)
NEUROPATHIC ULCER ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
ORTHOPNOEA ( 8 FDA reports)
OSTEOSARCOMA METASTATIC ( 8 FDA reports)
PAIN EXACERBATED ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PANCREATITIS CHRONIC ( 8 FDA reports)
PERITONEAL HAEMORRHAGE ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
PLASMACYTOMA ( 8 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 8 FDA reports)
PULSE ABSENT ( 8 FDA reports)
RADIATION SKIN INJURY ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
RENAL ABSCESS ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RENAL STONE REMOVAL ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RHONCHI ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
ROTATOR CUFF REPAIR ( 8 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SICK SINUS SYNDROME ( 8 FDA reports)
SIMPLE PARTIAL SEIZURES ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN OPERATION ( 8 FDA reports)
SOCIAL PROBLEM ( 8 FDA reports)
STASIS DERMATITIS ( 8 FDA reports)
STREPTOCOCCAL SEPSIS ( 8 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 8 FDA reports)
TEETH BRITTLE ( 8 FDA reports)
TEMPORAL ARTERITIS ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 8 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
TONGUE DISORDER ( 8 FDA reports)
TOOTH EROSION ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 8 FDA reports)
VENOUS INSUFFICIENCY ( 8 FDA reports)
VENOUS THROMBOSIS LIMB ( 8 FDA reports)
WEIGHT BEARING DIFFICULTY ( 8 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ADENOMA BENIGN ( 7 FDA reports)
AMYLOIDOSIS ( 7 FDA reports)
ANAL SPHINCTER ATONY ( 7 FDA reports)
ANORECTAL DISORDER ( 7 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 7 FDA reports)
AORTIC VALVE CALCIFICATION ( 7 FDA reports)
AORTIC VALVE REPLACEMENT ( 7 FDA reports)
ASPIRATION PLEURAL CAVITY ( 7 FDA reports)
ATROPHIC VULVOVAGINITIS ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BEDRIDDEN ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 7 FDA reports)
BRAIN DEATH ( 7 FDA reports)
BUNDLE BRANCH BLOCK ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CALCULUS URINARY ( 7 FDA reports)
CARDIAC FLUTTER ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CATHETER PLACEMENT ( 7 FDA reports)
CERVICITIS ( 7 FDA reports)
COARCTATION OF THE AORTA ( 7 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 7 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
DENTAL PROSTHESIS USER ( 7 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
EAR CONGESTION ( 7 FDA reports)
ECHOCARDIOGRAM ( 7 FDA reports)
EJECTION FRACTION ABNORMAL ( 7 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
EYELID PTOSIS ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
GASTROINTESTINAL SURGERY ( 7 FDA reports)
HAEMORRHAGIC ANAEMIA ( 7 FDA reports)
HEPATIC NEOPLASM ( 7 FDA reports)
HIP DEFORMITY ( 7 FDA reports)
HOSPITALISATION ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYPOGEUSIA ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INJECTION SITE RASH ( 7 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 7 FDA reports)
INTESTINAL PERFORATION ( 7 FDA reports)
INTESTINAL POLYP ( 7 FDA reports)
JUDGEMENT IMPAIRED ( 7 FDA reports)
KIDNEY INFECTION ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 7 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 7 FDA reports)
MALIGNANT TUMOUR EXCISION ( 7 FDA reports)
MENOPAUSAL SYMPTOMS ( 7 FDA reports)
METASTASES TO NECK ( 7 FDA reports)
MIDDLE INSOMNIA ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MYELOMA RECURRENCE ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
NASAL SEPTUM DEVIATION ( 7 FDA reports)
NASAL SINUS DRAINAGE ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
OPTIC NEURITIS ( 7 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 7 FDA reports)
OROANTRAL FISTULA ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
POST LAMINECTOMY SYNDROME ( 7 FDA reports)
POSTMENOPAUSE ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
QUADRIPARESIS ( 7 FDA reports)
RADIOTHERAPY TO BRAIN ( 7 FDA reports)
RALES ( 7 FDA reports)
RENAL TUBULAR NECROSIS ( 7 FDA reports)
SCAN ABNORMAL ( 7 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 7 FDA reports)
SEBORRHOEIC DERMATITIS ( 7 FDA reports)
SENSATION OF HEAVINESS ( 7 FDA reports)
SIALOADENITIS ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
SYNCOPE VASOVAGAL ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
THROMBOSIS IN DEVICE ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
ULNA FRACTURE ( 7 FDA reports)
URETHRAL DISORDER ( 7 FDA reports)
URINE FLOW DECREASED ( 7 FDA reports)
UTERINE PROLAPSE ( 7 FDA reports)
VASCULAR DEMENTIA ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ADENOMYOSIS ( 6 FDA reports)
ALVEOLAR OSTEITIS ( 6 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
ANIMAL BITE ( 6 FDA reports)
ANION GAP DECREASED ( 6 FDA reports)
APPENDIX DISORDER ( 6 FDA reports)
ASTIGMATISM ( 6 FDA reports)
ATROPHY ( 6 FDA reports)
AUTOIMMUNE HEPATITIS ( 6 FDA reports)
AXILLARY MASS ( 6 FDA reports)
BACTERIAL DISEASE CARRIER ( 6 FDA reports)
BACTERIAL TEST NEGATIVE ( 6 FDA reports)
BENIGN BONE NEOPLASM ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BIOPSY BONE ABNORMAL ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
BONE MARROW OEDEMA ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BREAST MICROCALCIFICATION ( 6 FDA reports)
BRONCHOPLEURAL FISTULA ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
CHEST TUBE INSERTION ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CHORIORETINAL DISORDER ( 6 FDA reports)
CHORIORETINOPATHY ( 6 FDA reports)
CHRONIC FATIGUE SYNDROME ( 6 FDA reports)
COR PULMONALE ( 6 FDA reports)
CORNEAL DYSTROPHY ( 6 FDA reports)
CYST REMOVAL ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DENTAL PLAQUE ( 6 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 6 FDA reports)
DIZZINESS POSTURAL ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DRY GANGRENE ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 6 FDA reports)
EPIDERMAL NAEVUS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EYELID MARGIN CRUSTING ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
FUNGAL RASH ( 6 FDA reports)
GAMMOPATHY ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GRANULOCYTOPENIA ( 6 FDA reports)
HAEMOLYSIS ( 6 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPOCHROMIC ANAEMIA ( 6 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
INJURY CORNEAL ( 6 FDA reports)
JAW LESION EXCISION ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 6 FDA reports)
LIP DISCOLOURATION ( 6 FDA reports)
LIVEDO RETICULARIS ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MAMMOGRAM ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MELANOCYTIC NAEVUS ( 6 FDA reports)
MENINGITIS CHEMICAL ( 6 FDA reports)
MENINGITIS VIRAL ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
MESOTHELIOMA ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
MITRAL VALVE REPAIR ( 6 FDA reports)
NASAL ODOUR ( 6 FDA reports)
NECROSIS ISCHAEMIC ( 6 FDA reports)
NO ADVERSE EVENT ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
ONYCHOCLASIS ( 6 FDA reports)
ORGAN FAILURE ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OVARIAN DISORDER ( 6 FDA reports)
PANCOAST'S TUMOUR ( 6 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 6 FDA reports)
PAROTITIS ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PERIODONTAL INFECTION ( 6 FDA reports)
PHOTOPSIA ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PLASMACYTOSIS ( 6 FDA reports)
PLEURAL DISORDER ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
PROCEDURAL HYPERTENSION ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
RED BLOOD CELLS URINE ( 6 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
RETINAL DISORDER ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SALIVARY GLAND ADENOMA ( 6 FDA reports)
SALIVARY GLAND CANCER ( 6 FDA reports)
SALIVARY GLAND PAIN ( 6 FDA reports)
SERRATIA BACTERAEMIA ( 6 FDA reports)
SHOCK ( 6 FDA reports)
SHOULDER OPERATION ( 6 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SLEEP TALKING ( 6 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 6 FDA reports)
SPUTUM CULTURE POSITIVE ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
THERMAL BURN ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
TRIGEMINAL NEURALGIA ( 6 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 6 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 6 FDA reports)
URINE ANALYSIS ( 6 FDA reports)
VAGINAL ULCERATION ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT ( 6 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AMINO ACID LEVEL INCREASED ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLADDER PROLAPSE ( 5 FDA reports)
BLINDNESS UNILATERAL ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN CONTUSION ( 5 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
BREAST DISORDER ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CAUDA EQUINA SYNDROME ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CEREBELLAR ISCHAEMIA ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CERVICAL MYELOPATHY ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
CLOSED FRACTURE MANIPULATION ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CORONARY ARTERY SURGERY ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
CYSTOCELE ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DIABETIC COMA ( 5 FDA reports)
DROWNING ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOMETRIAL DISORDER ( 5 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GALLBLADDER POLYP ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAND FRACTURE ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HIDRADENITIS ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
ISCHAEMIC HEPATITIS ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
KYPHOSCOLIOSIS ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MAMMOPLASTY ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MERALGIA PARAESTHETICA ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MUSCLE FLAP OPERATION ( 5 FDA reports)
NASAL SINUS CANCER ( 5 FDA reports)
NECK INJURY ( 5 FDA reports)
NEPHROSCLEROSIS ( 5 FDA reports)
NERVE BLOCK ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PERIRECTAL ABSCESS ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
POLYSUBSTANCE ABUSE ( 5 FDA reports)
POOR PERSONAL HYGIENE ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
POST PROCEDURAL PAIN ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PSEUDOMONAL SEPSIS ( 5 FDA reports)
PULSE PRESSURE DECREASED ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
RECTAL POLYP ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RENAL TUBULAR ACIDOSIS ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 5 FDA reports)
SCHIZOPHRENIA ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SELF ESTEEM DECREASED ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SNORING ( 5 FDA reports)
SPINAL CLAUDICATION ( 5 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
STILL'S DISEASE ADULT ONSET ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
TARSAL TUNNEL SYNDROME ( 5 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
URETHRAL DILATATION ( 5 FDA reports)
URETHRAL FISTULA ( 5 FDA reports)
URINARY TRACT OPERATION ( 5 FDA reports)
URINE ABNORMALITY ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VAGINITIS ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 5 FDA reports)
VITAMIN B12 DECREASED ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
VOCAL CORD POLYP ( 5 FDA reports)
WOUND ( 5 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAL ULCER ( 4 FDA reports)
ANOREXIA NERVOSA ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC CALCIFICATION ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD MERCURY ABNORMAL ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BLUE TOE SYNDROME ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
BRAIN OPERATION ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 4 FDA reports)
CARDIAC HYPERTROPHY ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 4 FDA reports)
CHLORACNE ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 4 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DUODENAL ULCER PERFORATION ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ENDOMETRIAL CANCER ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
GALLBLADDER CANCER ( 4 FDA reports)
GASTRIC INFECTION ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INJECTION SITE STINGING ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LABILE HYPERTENSION ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MAMMOGRAM ABNORMAL ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENTAL DISABILITY ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MICTURITION DISORDER ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OCULAR HYPERTENSION ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OSTEOMYELITIS FUNGAL ( 4 FDA reports)
OVARIAN NEOPLASM ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PANCREATOLITHIASIS ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERFORATED ULCER ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PICKWICKIAN SYNDROME ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PLEURAL ADHESION ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYCYTHAEMIA ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
RADICULITIS BRACHIAL ( 4 FDA reports)
RECTAL FISSURE ( 4 FDA reports)
RECTAL FISTULA REPAIR ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCROTAL ABSCESS ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SERUM SEROTONIN DECREASED ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
TENSION HEADACHE ( 4 FDA reports)
TESTICULAR PAIN ( 4 FDA reports)
THROMBOANGIITIS OBLITERANS ( 4 FDA reports)
TINEA INFECTION ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
UTERINE ATONY ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACETABULUM FRACTURE ( 3 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 3 FDA reports)
ACUTE STRESS DISORDER ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANAEMIA POSTOPERATIVE ( 3 FDA reports)
ANAL DISCOMFORT ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BIOPSY COLON ( 3 FDA reports)
BIOPSY COLON ABNORMAL ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BREAST RECONSTRUCTION ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHIAL NEOPLASM ( 3 FDA reports)
BUNION ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHOREA ( 3 FDA reports)
COMPLICATED MIGRAINE ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CUBITAL TUNNEL SYNDROME ( 3 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 3 FDA reports)
CYSTITIS KLEBSIELLA ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIABETIC FOOT INFECTION ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG ADDICT ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
EMPTY SELLA SYNDROME ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
EYELID PTOSIS CONGENITAL ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 3 FDA reports)
GRIMACING ( 3 FDA reports)
GROIN ABSCESS ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HEAD AND NECK CANCER ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEREDITARY ANGIOEDEMA ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
IRIS ADHESIONS ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
MANIA ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MIXED HYPERLIPIDAEMIA ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN ADHESION ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC ENLARGEMENT ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC ADHESIONS ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PHARYNX DISCOMFORT ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PLEURAL CALCIFICATION ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POLYHYDRAMNIOS ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROCTITIS HERPES ( 3 FDA reports)
PROLONGED LABOUR ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PYOGENIC GRANULOMA ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
REPERFUSION ARRHYTHMIA ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETINAL PIGMENTATION ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SINOBRONCHITIS ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SOCIAL PHOBIA ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SPINAL HAEMANGIOMA ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBECTOMY ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THYROID GLAND CANCER ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
URETHRAL DISCHARGE ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL BRUIT ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABDOMINAL WALL CYST ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACOUSTIC NEURITIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
AEROPHAGIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BALANOPOSTHITIS ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY ARTERY ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER SUSPENSION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FEMORAL BRUIT ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GAMMA RADIATION THERAPY ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENITAL CANDIDIASIS ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS B VIRUS TEST ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HOFFMANN'S SIGN ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE DERMATITIS ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE DRYNESS ( 2 FDA reports)
INJECTION SITE EXFOLIATION ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LENTIGO ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO BLADDER ( 2 FDA reports)
METASTASES TO THORAX ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTOCELE REPAIR ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RHINITIS SEASONAL ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCROTAL INFECTION ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSATION OF BLOCK IN EAR ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STARING ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEROID THERAPY ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
THORACIC HAEMORRHAGE ( 2 FDA reports)
THROMBOSED VARICOSE VEIN ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE CANCER METASTATIC ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRAUMATIC RENAL INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 2 FDA reports)
UNEQUAL LIMB LENGTH ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL LABYRINTHITIS ( 2 FDA reports)
VIRAL RHINITIS ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS MOENCKEBERG-TYPE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION BREAST ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLINDNESS HYSTERICAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CARNITINE PALMITOYLTRANSFERASE DEFICIENCY ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS PHARYNGEAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL SPASM ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC ARTERY COMPRESSION SYNDROME ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
FACIAL LESION EXCISION ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRONECTIN INCREASED ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL WARFARIN SYNDROME ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OCCULT BLOOD POSITIVE ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCAL ANAESTHESIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE FIBROSIS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAEVUS CELL NAEVUS ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO DUST ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PLASMINOGEN INCREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VALVE SCLEROSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHUNT ANEURYSM ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, MIXED TYPE ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINOPLASTY ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B6 INCREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOCAL CORDECTOMY ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)