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

PAIN ( 668 FDA reports)
MYOCARDIAL INFARCTION ( 543 FDA reports)
HYPERTENSION ( 531 FDA reports)
DYSPNOEA ( 522 FDA reports)
ANXIETY ( 491 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 459 FDA reports)
NAUSEA ( 453 FDA reports)
DIZZINESS ( 447 FDA reports)
OEDEMA PERIPHERAL ( 443 FDA reports)
DEPRESSION ( 420 FDA reports)
FATIGUE ( 409 FDA reports)
CHEST PAIN ( 403 FDA reports)
INJURY ( 402 FDA reports)
ASTHENIA ( 390 FDA reports)
CEREBROVASCULAR ACCIDENT ( 378 FDA reports)
DIARRHOEA ( 365 FDA reports)
PAIN IN EXTREMITY ( 355 FDA reports)
CORONARY ARTERY DISEASE ( 327 FDA reports)
HEADACHE ( 327 FDA reports)
ANAEMIA ( 326 FDA reports)
FALL ( 326 FDA reports)
PNEUMONIA ( 309 FDA reports)
ARTHRALGIA ( 304 FDA reports)
DRUG INEFFECTIVE ( 294 FDA reports)
BACK PAIN ( 289 FDA reports)
VOMITING ( 288 FDA reports)
DIABETES MELLITUS ( 268 FDA reports)
RENAL FAILURE ( 266 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 253 FDA reports)
BLOOD GLUCOSE INCREASED ( 249 FDA reports)
WEIGHT DECREASED ( 248 FDA reports)
EMOTIONAL DISTRESS ( 245 FDA reports)
INSOMNIA ( 235 FDA reports)
ATRIAL FIBRILLATION ( 233 FDA reports)
OSTEOARTHRITIS ( 230 FDA reports)
CONSTIPATION ( 218 FDA reports)
COUGH ( 215 FDA reports)
URINARY TRACT INFECTION ( 207 FDA reports)
MYALGIA ( 206 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 204 FDA reports)
BLOOD PRESSURE INCREASED ( 203 FDA reports)
CARDIAC DISORDER ( 202 FDA reports)
WEIGHT INCREASED ( 198 FDA reports)
HYPERLIPIDAEMIA ( 197 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 196 FDA reports)
HYPOAESTHESIA ( 195 FDA reports)
DEHYDRATION ( 191 FDA reports)
ANHEDONIA ( 187 FDA reports)
ABDOMINAL PAIN ( 185 FDA reports)
DEATH ( 184 FDA reports)
HYPOTENSION ( 174 FDA reports)
RENAL FAILURE ACUTE ( 171 FDA reports)
MALAISE ( 163 FDA reports)
CARDIOMEGALY ( 162 FDA reports)
MUSCLE SPASMS ( 161 FDA reports)
OSTEONECROSIS OF JAW ( 160 FDA reports)
ARTHRITIS ( 157 FDA reports)
CELLULITIS ( 154 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 153 FDA reports)
BRONCHITIS ( 151 FDA reports)
CONFUSIONAL STATE ( 151 FDA reports)
RASH ( 145 FDA reports)
ABDOMINAL PAIN UPPER ( 140 FDA reports)
CONDITION AGGRAVATED ( 140 FDA reports)
GAIT DISTURBANCE ( 138 FDA reports)
PALPITATIONS ( 134 FDA reports)
SINUSITIS ( 134 FDA reports)
SYNCOPE ( 134 FDA reports)
HAEMORRHOIDS ( 133 FDA reports)
PYREXIA ( 131 FDA reports)
FEELING ABNORMAL ( 129 FDA reports)
NECK PAIN ( 129 FDA reports)
OSTEOMYELITIS ( 129 FDA reports)
FEAR ( 128 FDA reports)
TREMOR ( 128 FDA reports)
HYPERHIDROSIS ( 126 FDA reports)
LOSS OF CONSCIOUSNESS ( 125 FDA reports)
ARRHYTHMIA ( 123 FDA reports)
DYSPEPSIA ( 122 FDA reports)
NEPHROLITHIASIS ( 122 FDA reports)
STRESS ( 122 FDA reports)
ANGINA PECTORIS ( 121 FDA reports)
DECREASED APPETITE ( 121 FDA reports)
ASTHMA ( 120 FDA reports)
GASTRITIS ( 120 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 118 FDA reports)
VISION BLURRED ( 118 FDA reports)
NEUROPATHY PERIPHERAL ( 117 FDA reports)
MITRAL VALVE INCOMPETENCE ( 116 FDA reports)
PARAESTHESIA ( 116 FDA reports)
CORONARY ARTERY OCCLUSION ( 114 FDA reports)
INFECTION ( 112 FDA reports)
PRURITUS ( 112 FDA reports)
SPINAL OSTEOARTHRITIS ( 112 FDA reports)
ARTERIOSCLEROSIS ( 111 FDA reports)
CHOLELITHIASIS ( 110 FDA reports)
DEEP VEIN THROMBOSIS ( 110 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 110 FDA reports)
PANCREATITIS ( 110 FDA reports)
UNEVALUABLE EVENT ( 110 FDA reports)
CATARACT ( 109 FDA reports)
CHEST DISCOMFORT ( 107 FDA reports)
HAEMATOMA ( 106 FDA reports)
BONE DISORDER ( 105 FDA reports)
CONTUSION ( 104 FDA reports)
PAIN IN JAW ( 104 FDA reports)
RENAL FAILURE CHRONIC ( 104 FDA reports)
SWELLING ( 104 FDA reports)
JOINT SWELLING ( 103 FDA reports)
OSTEOPOROSIS ( 102 FDA reports)
CARDIAC MURMUR ( 101 FDA reports)
OBESITY ( 101 FDA reports)
SOMNOLENCE ( 100 FDA reports)
RENAL IMPAIRMENT ( 99 FDA reports)
TYPE 2 DIABETES MELLITUS ( 99 FDA reports)
ATELECTASIS ( 97 FDA reports)
DYSPHAGIA ( 96 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 96 FDA reports)
DYSPNOEA EXERTIONAL ( 95 FDA reports)
HEART RATE INCREASED ( 94 FDA reports)
OSTEONECROSIS ( 94 FDA reports)
OEDEMA ( 93 FDA reports)
PLEURAL EFFUSION ( 91 FDA reports)
MYOCARDIAL ISCHAEMIA ( 89 FDA reports)
ERYTHEMA ( 88 FDA reports)
HYPOKALAEMIA ( 88 FDA reports)
CONVULSION ( 86 FDA reports)
ECONOMIC PROBLEM ( 86 FDA reports)
HYPOGLYCAEMIA ( 86 FDA reports)
OSTEOPENIA ( 86 FDA reports)
SLEEP APNOEA SYNDROME ( 86 FDA reports)
CAROTID ARTERY STENOSIS ( 85 FDA reports)
POLLAKIURIA ( 85 FDA reports)
HIATUS HERNIA ( 84 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 84 FDA reports)
TOOTH EXTRACTION ( 83 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 82 FDA reports)
BLOOD PRESSURE DECREASED ( 82 FDA reports)
TACHYCARDIA ( 82 FDA reports)
BRADYCARDIA ( 81 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 81 FDA reports)
RENAL INJURY ( 81 FDA reports)
HYPERSENSITIVITY ( 80 FDA reports)
RESPIRATORY FAILURE ( 80 FDA reports)
MUSCULAR WEAKNESS ( 79 FDA reports)
NEOPLASM MALIGNANT ( 79 FDA reports)
HYPERCHOLESTEROLAEMIA ( 78 FDA reports)
SINUS DISORDER ( 78 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 76 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 76 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 76 FDA reports)
SWELLING FACE ( 75 FDA reports)
CARDIOMYOPATHY ( 74 FDA reports)
DIABETIC NEUROPATHY ( 74 FDA reports)
DRY MOUTH ( 74 FDA reports)
TOOTH INFECTION ( 74 FDA reports)
NERVOUSNESS ( 73 FDA reports)
BONE LESION ( 72 FDA reports)
PULMONARY HYPERTENSION ( 72 FDA reports)
IMPAIRED HEALING ( 71 FDA reports)
MENTAL STATUS CHANGES ( 70 FDA reports)
ALOPECIA ( 69 FDA reports)
ANGINA UNSTABLE ( 69 FDA reports)
ARTHROPATHY ( 69 FDA reports)
CARDIAC ARREST ( 69 FDA reports)
DISABILITY ( 69 FDA reports)
GROIN PAIN ( 69 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 69 FDA reports)
PULMONARY EMBOLISM ( 69 FDA reports)
HAEMOGLOBIN DECREASED ( 68 FDA reports)
DRUG INTERACTION ( 67 FDA reports)
DYSURIA ( 67 FDA reports)
ROTATOR CUFF SYNDROME ( 67 FDA reports)
ABDOMINAL DISTENSION ( 66 FDA reports)
ERECTILE DYSFUNCTION ( 66 FDA reports)
HERPES ZOSTER ( 66 FDA reports)
METASTASES TO BONE ( 66 FDA reports)
TENDONITIS ( 66 FDA reports)
THROMBOSIS ( 66 FDA reports)
LETHARGY ( 65 FDA reports)
CARDIAC VALVE DISEASE ( 64 FDA reports)
CARPAL TUNNEL SYNDROME ( 64 FDA reports)
CHILLS ( 64 FDA reports)
SEPSIS ( 64 FDA reports)
EPISTAXIS ( 63 FDA reports)
FLUSHING ( 63 FDA reports)
STAPHYLOCOCCAL INFECTION ( 63 FDA reports)
URTICARIA ( 63 FDA reports)
AMNESIA ( 62 FDA reports)
IRRITABLE BOWEL SYNDROME ( 62 FDA reports)
PERICARDIAL EFFUSION ( 62 FDA reports)
VERTIGO ( 62 FDA reports)
BONE PAIN ( 61 FDA reports)
CARDIOVASCULAR DISORDER ( 61 FDA reports)
DENTAL CARIES ( 61 FDA reports)
MEMORY IMPAIRMENT ( 61 FDA reports)
PULMONARY OEDEMA ( 61 FDA reports)
RENAL DISORDER ( 61 FDA reports)
BLOOD CREATININE INCREASED ( 60 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 60 FDA reports)
BLOOD GLUCOSE DECREASED ( 59 FDA reports)
ROAD TRAFFIC ACCIDENT ( 59 FDA reports)
SKIN ULCER ( 59 FDA reports)
DIVERTICULUM INTESTINAL ( 58 FDA reports)
NASOPHARYNGITIS ( 58 FDA reports)
ABDOMINAL DISCOMFORT ( 57 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 57 FDA reports)
JOINT STIFFNESS ( 57 FDA reports)
MUSCULOSKELETAL PAIN ( 57 FDA reports)
SUICIDAL IDEATION ( 57 FDA reports)
TREATMENT NONCOMPLIANCE ( 57 FDA reports)
HYPOTHYROIDISM ( 56 FDA reports)
MOUTH ULCERATION ( 56 FDA reports)
DIVERTICULITIS ( 55 FDA reports)
DIVERTICULUM ( 55 FDA reports)
MULTI-ORGAN FAILURE ( 55 FDA reports)
SLEEP DISORDER ( 55 FDA reports)
SPEECH DISORDER ( 55 FDA reports)
HAEMORRHAGE ( 54 FDA reports)
HYPERGLYCAEMIA ( 54 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 54 FDA reports)
MENTAL DISORDER ( 54 FDA reports)
GOUT ( 53 FDA reports)
LEUKOCYTOSIS ( 53 FDA reports)
BREAST CANCER ( 52 FDA reports)
FISTULA ( 52 FDA reports)
HAEMATURIA ( 52 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 52 FDA reports)
VENTRICULAR TACHYCARDIA ( 52 FDA reports)
BALANCE DISORDER ( 51 FDA reports)
BLOOD POTASSIUM DECREASED ( 51 FDA reports)
BURSITIS ( 51 FDA reports)
GINGIVAL PAIN ( 51 FDA reports)
STOMACH DISCOMFORT ( 51 FDA reports)
CHRONIC SINUSITIS ( 50 FDA reports)
EXOSTOSIS ( 50 FDA reports)
GOITRE ( 50 FDA reports)
ORAL INFECTION ( 50 FDA reports)
OVERDOSE ( 50 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 50 FDA reports)
VISUAL ACUITY REDUCED ( 50 FDA reports)
AZOTAEMIA ( 49 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 49 FDA reports)
CANDIDIASIS ( 49 FDA reports)
DYSPHONIA ( 49 FDA reports)
HEART RATE IRREGULAR ( 49 FDA reports)
LUNG NEOPLASM ( 49 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 49 FDA reports)
OXYGEN SATURATION DECREASED ( 49 FDA reports)
SPINAL COLUMN STENOSIS ( 49 FDA reports)
WHEEZING ( 49 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 48 FDA reports)
BLOOD URINE PRESENT ( 48 FDA reports)
HEAD INJURY ( 48 FDA reports)
NECK INJURY ( 48 FDA reports)
RHINITIS ALLERGIC ( 48 FDA reports)
ANGIOPATHY ( 47 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 47 FDA reports)
OSTEITIS ( 47 FDA reports)
BACK DISORDER ( 46 FDA reports)
COLITIS ( 46 FDA reports)
COLONIC POLYP ( 46 FDA reports)
DRUG EFFECT DECREASED ( 46 FDA reports)
HEART RATE DECREASED ( 46 FDA reports)
HYDRONEPHROSIS ( 46 FDA reports)
JAW FRACTURE ( 46 FDA reports)
ABASIA ( 45 FDA reports)
BLOOD UREA INCREASED ( 45 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 45 FDA reports)
FLUID OVERLOAD ( 45 FDA reports)
GASTROINTESTINAL DISORDER ( 45 FDA reports)
INFLAMMATION ( 45 FDA reports)
SINUS TACHYCARDIA ( 45 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 45 FDA reports)
ADVERSE EVENT ( 44 FDA reports)
BACTERIAL INFECTION ( 44 FDA reports)
DRUG HYPERSENSITIVITY ( 44 FDA reports)
ENCEPHALOPATHY ( 44 FDA reports)
HAEMATOCHEZIA ( 44 FDA reports)
KIDNEY INFECTION ( 44 FDA reports)
PATHOLOGICAL FRACTURE ( 44 FDA reports)
RECTAL HAEMORRHAGE ( 44 FDA reports)
SEASONAL ALLERGY ( 44 FDA reports)
DEAFNESS ( 43 FDA reports)
GASTRIC DISORDER ( 43 FDA reports)
HEPATIC STEATOSIS ( 43 FDA reports)
LYMPHOEDEMA ( 43 FDA reports)
MULTIPLE INJURIES ( 43 FDA reports)
NEOPLASM PROGRESSION ( 43 FDA reports)
ABSCESS ( 42 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 42 FDA reports)
DYSGEUSIA ( 42 FDA reports)
FEMUR FRACTURE ( 42 FDA reports)
HYPOXIA ( 42 FDA reports)
RASH PRURITIC ( 42 FDA reports)
URINARY INCONTINENCE ( 42 FDA reports)
EJECTION FRACTION DECREASED ( 41 FDA reports)
FLUID RETENTION ( 41 FDA reports)
PANCYTOPENIA ( 41 FDA reports)
SKIN DISCOLOURATION ( 41 FDA reports)
SKIN DISORDER ( 41 FDA reports)
SKIN LESION ( 41 FDA reports)
CARDIAC FAILURE ( 40 FDA reports)
CYSTITIS ( 40 FDA reports)
HAEMATOCRIT DECREASED ( 40 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 40 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 40 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 40 FDA reports)
LYMPHADENOPATHY ( 40 FDA reports)
MULTIPLE MYELOMA ( 40 FDA reports)
ORTHOSTATIC HYPOTENSION ( 40 FDA reports)
PULMONARY CONGESTION ( 40 FDA reports)
RESTLESS LEGS SYNDROME ( 40 FDA reports)
AGITATION ( 39 FDA reports)
ATRIAL FLUTTER ( 39 FDA reports)
DEFORMITY ( 39 FDA reports)
FEELING HOT ( 39 FDA reports)
HYPONATRAEMIA ( 39 FDA reports)
PANCREATITIS ACUTE ( 39 FDA reports)
SCOLIOSIS ( 39 FDA reports)
TOOTHACHE ( 39 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 38 FDA reports)
BURNING SENSATION ( 38 FDA reports)
CORONARY ARTERY STENOSIS ( 38 FDA reports)
DIFFICULTY IN WALKING ( 38 FDA reports)
DYSLIPIDAEMIA ( 38 FDA reports)
EXPOSED BONE IN JAW ( 38 FDA reports)
MEDICATION ERROR ( 38 FDA reports)
RADICULOPATHY ( 38 FDA reports)
TYPE 1 DIABETES MELLITUS ( 38 FDA reports)
AORTIC VALVE INCOMPETENCE ( 37 FDA reports)
ASCITES ( 37 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 37 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 37 FDA reports)
MITRAL VALVE CALCIFICATION ( 37 FDA reports)
NERVE INJURY ( 37 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 37 FDA reports)
BLINDNESS ( 36 FDA reports)
BLOOD PRESSURE ABNORMAL ( 36 FDA reports)
BLOOD SODIUM DECREASED ( 36 FDA reports)
EXCORIATION ( 36 FDA reports)
LIMB INJURY ( 36 FDA reports)
LUMBAR SPINAL STENOSIS ( 36 FDA reports)
SKIN TIGHTNESS ( 36 FDA reports)
THROMBOCYTOPENIA ( 36 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 36 FDA reports)
ANKLE FRACTURE ( 35 FDA reports)
DILATATION VENTRICULAR ( 35 FDA reports)
DRY SKIN ( 35 FDA reports)
LACERATION ( 35 FDA reports)
LOBAR PNEUMONIA ( 35 FDA reports)
LUNG INFILTRATION ( 35 FDA reports)
PEPTIC ULCER ( 35 FDA reports)
CARDIO-RESPIRATORY ARREST ( 34 FDA reports)
FLATULENCE ( 34 FDA reports)
HALLUCINATION ( 34 FDA reports)
RENAL CYST ( 34 FDA reports)
RHABDOMYOLYSIS ( 34 FDA reports)
CYANOSIS ( 33 FDA reports)
CYST ( 33 FDA reports)
DILATATION ATRIAL ( 33 FDA reports)
DISORIENTATION ( 33 FDA reports)
EYE DISORDER ( 33 FDA reports)
FLANK PAIN ( 33 FDA reports)
IRON DEFICIENCY ANAEMIA ( 33 FDA reports)
PANIC ATTACK ( 33 FDA reports)
PHYSICAL DISABILITY ( 33 FDA reports)
SURGERY ( 33 FDA reports)
BACK INJURY ( 32 FDA reports)
CHEST WALL PAIN ( 32 FDA reports)
EMOTIONAL DISORDER ( 32 FDA reports)
HEPATIC ENZYME INCREASED ( 32 FDA reports)
ILL-DEFINED DISORDER ( 32 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 32 FDA reports)
MUSCLE STRAIN ( 32 FDA reports)
NODULE ( 32 FDA reports)
ORTHOPNOEA ( 32 FDA reports)
PLATELET COUNT DECREASED ( 32 FDA reports)
RECTAL POLYP ( 32 FDA reports)
RHINORRHOEA ( 32 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 32 FDA reports)
VENTRICULAR HYPERTROPHY ( 32 FDA reports)
VITAMIN D DECREASED ( 32 FDA reports)
ANGIONEUROTIC OEDEMA ( 31 FDA reports)
BLOOD CALCIUM DECREASED ( 31 FDA reports)
CHOLECYSTITIS ( 31 FDA reports)
DECUBITUS ULCER ( 31 FDA reports)
DISEASE PROGRESSION ( 31 FDA reports)
DYSARTHRIA ( 31 FDA reports)
FACET JOINT SYNDROME ( 31 FDA reports)
GLAUCOMA ( 31 FDA reports)
INFLUENZA LIKE ILLNESS ( 31 FDA reports)
LYMPHOMA ( 31 FDA reports)
MASTICATION DISORDER ( 31 FDA reports)
MUMPS ( 31 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 31 FDA reports)
RUBELLA ( 31 FDA reports)
SCARLET FEVER ( 31 FDA reports)
TINNITUS ( 31 FDA reports)
ACETABULUM FRACTURE ( 30 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 30 FDA reports)
DIABETIC KETOACIDOSIS ( 30 FDA reports)
EMPHYSEMA ( 30 FDA reports)
INGUINAL HERNIA ( 30 FDA reports)
RESPIRATORY DISTRESS ( 30 FDA reports)
SPINAL COMPRESSION FRACTURE ( 30 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 30 FDA reports)
ABDOMINAL PAIN LOWER ( 29 FDA reports)
COMA ( 29 FDA reports)
DRUG ABUSER ( 29 FDA reports)
DRUG DEPENDENCE ( 29 FDA reports)
GINGIVAL ERYTHEMA ( 29 FDA reports)
GINGIVAL SWELLING ( 29 FDA reports)
GINGIVAL ULCERATION ( 29 FDA reports)
JOINT EFFUSION ( 29 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 29 FDA reports)
MIGRAINE ( 29 FDA reports)
NERVOUS SYSTEM DISORDER ( 29 FDA reports)
RHEUMATOID ARTHRITIS ( 29 FDA reports)
SKIN HYPERTROPHY ( 29 FDA reports)
CARDIAC PACEMAKER INSERTION ( 28 FDA reports)
ECCHYMOSIS ( 28 FDA reports)
INTRACRANIAL ANEURYSM ( 28 FDA reports)
JOINT INJURY ( 28 FDA reports)
LOCALISED INFECTION ( 28 FDA reports)
LUNG DISORDER ( 28 FDA reports)
MITRAL VALVE PROLAPSE ( 28 FDA reports)
NASAL CONGESTION ( 28 FDA reports)
UMBILICAL HERNIA ( 28 FDA reports)
WOUND INFECTION ( 28 FDA reports)
ABSCESS DRAINAGE ( 27 FDA reports)
AORTIC ANEURYSM ( 27 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 27 FDA reports)
BODY HEIGHT DECREASED ( 27 FDA reports)
COAGULOPATHY ( 27 FDA reports)
DEVICE MALFUNCTION ( 27 FDA reports)
DIABETIC RETINOPATHY ( 27 FDA reports)
DUODENITIS ( 27 FDA reports)
FIBROMYALGIA ( 27 FDA reports)
LIGAMENT INJURY ( 27 FDA reports)
MOBILITY DECREASED ( 27 FDA reports)
MYOSITIS ( 27 FDA reports)
NEPHRITIS INTERSTITIAL ( 27 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 26 FDA reports)
CEREBROVASCULAR DISORDER ( 26 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 26 FDA reports)
DIABETIC GASTROPARESIS ( 26 FDA reports)
GENERALISED OEDEMA ( 26 FDA reports)
HOT FLUSH ( 26 FDA reports)
HYPERMETABOLISM ( 26 FDA reports)
LUNG ABSCESS ( 26 FDA reports)
NASAL SEPTUM DEVIATION ( 26 FDA reports)
NEURALGIA ( 26 FDA reports)
OSTEOLYSIS ( 26 FDA reports)
SYNOVIAL CYST ( 26 FDA reports)
ULCER ( 26 FDA reports)
ANOREXIA ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK ( 25 FDA reports)
BREAST CANCER FEMALE ( 25 FDA reports)
CEREBRAL ATROPHY ( 25 FDA reports)
EAR PAIN ( 25 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 25 FDA reports)
ESSENTIAL HYPERTENSION ( 25 FDA reports)
FUNGAL INFECTION ( 25 FDA reports)
GASTROINTESTINAL PAIN ( 25 FDA reports)
HAEMOPTYSIS ( 25 FDA reports)
HYPERKALAEMIA ( 25 FDA reports)
JOINT CONTRACTURE ( 25 FDA reports)
MUSCLE CRAMP ( 25 FDA reports)
PERIODONTITIS ( 25 FDA reports)
POLYP ( 25 FDA reports)
PROTEINURIA ( 25 FDA reports)
PYELONEPHRITIS ACUTE ( 25 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 25 FDA reports)
SKIN CANCER ( 25 FDA reports)
STRESS SYMPTOMS ( 25 FDA reports)
AORTIC VALVE CALCIFICATION ( 24 FDA reports)
BONE DEBRIDEMENT ( 24 FDA reports)
CEREBRAL ISCHAEMIA ( 24 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
CROHN'S DISEASE ( 24 FDA reports)
DRUG DOSE OMISSION ( 24 FDA reports)
DRUG TOXICITY ( 24 FDA reports)
ENDODONTIC PROCEDURE ( 24 FDA reports)
FACE OEDEMA ( 24 FDA reports)
HEARING IMPAIRED ( 24 FDA reports)
HEPATIC FAILURE ( 24 FDA reports)
INFLUENZA ( 24 FDA reports)
MENISCUS LESION ( 24 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 24 FDA reports)
RASH ERYTHEMATOUS ( 24 FDA reports)
RASH MACULO-PAPULAR ( 24 FDA reports)
SCAR ( 24 FDA reports)
SKIN BURNING SENSATION ( 24 FDA reports)
SPONDYLOLISTHESIS ( 24 FDA reports)
TOOTH ABSCESS ( 24 FDA reports)
ATHEROSCLEROSIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 23 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 23 FDA reports)
LEUKOPENIA ( 23 FDA reports)
METABOLIC ACIDOSIS ( 23 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 23 FDA reports)
OESOPHAGEAL SPASM ( 23 FDA reports)
OFF LABEL USE ( 23 FDA reports)
ORAL HERPES ( 23 FDA reports)
PROTHROMBIN TIME PROLONGED ( 23 FDA reports)
THYROID DISORDER ( 23 FDA reports)
TOOTH DISORDER ( 23 FDA reports)
TOOTH FRACTURE ( 23 FDA reports)
UNRESPONSIVE TO STIMULI ( 23 FDA reports)
URINARY RETENTION ( 23 FDA reports)
VISUAL DISTURBANCE ( 23 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 23 FDA reports)
WOUND ( 23 FDA reports)
ABNORMAL DREAMS ( 22 FDA reports)
BLOOD IRON DECREASED ( 22 FDA reports)
CEREBRAL INFARCTION ( 22 FDA reports)
COLON CANCER ( 22 FDA reports)
DEBRIDEMENT ( 22 FDA reports)
DEPRESSED MOOD ( 22 FDA reports)
EATING DISORDER ( 22 FDA reports)
JOINT SPRAIN ( 22 FDA reports)
LUNG NEOPLASM MALIGNANT ( 22 FDA reports)
MASS ( 22 FDA reports)
MELAENA ( 22 FDA reports)
PROTEIN URINE PRESENT ( 22 FDA reports)
SENSITIVITY OF TEETH ( 22 FDA reports)
SPINAL DISORDER ( 22 FDA reports)
SWOLLEN TONGUE ( 22 FDA reports)
TENOSYNOVITIS STENOSANS ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
AORTIC CALCIFICATION ( 21 FDA reports)
CAROTID ARTERY DISEASE ( 21 FDA reports)
CAROTID ARTERY OCCLUSION ( 21 FDA reports)
DELIRIUM ( 21 FDA reports)
FACIAL PAIN ( 21 FDA reports)
FEELING OF DESPAIR ( 21 FDA reports)
HYPERTHYROIDISM ( 21 FDA reports)
HYPOVOLAEMIA ( 21 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 21 FDA reports)
IRRITABILITY ( 21 FDA reports)
MACROCYTOSIS ( 21 FDA reports)
METASTASES TO LIVER ( 21 FDA reports)
PELVIC ABSCESS ( 21 FDA reports)
PERITONITIS ( 21 FDA reports)
RASH GENERALISED ( 21 FDA reports)
RESPIRATORY TRACT CONGESTION ( 21 FDA reports)
RESTLESSNESS ( 21 FDA reports)
SPLENOMEGALY ( 21 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 21 FDA reports)
VENTRICULAR FIBRILLATION ( 21 FDA reports)
DIALYSIS ( 20 FDA reports)
DIPLOPIA ( 20 FDA reports)
DISTURBANCE IN ATTENTION ( 20 FDA reports)
GINGIVAL INFECTION ( 20 FDA reports)
GINGIVITIS ( 20 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 20 FDA reports)
HEART INJURY ( 20 FDA reports)
HYPERCALCAEMIA ( 20 FDA reports)
HYPOVENTILATION ( 20 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 20 FDA reports)
NEUTROPENIA ( 20 FDA reports)
PRESCRIBED OVERDOSE ( 20 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 20 FDA reports)
SEPTIC SHOCK ( 20 FDA reports)
TOOTH REPAIR ( 20 FDA reports)
ABSCESS JAW ( 19 FDA reports)
AORTIC STENOSIS ( 19 FDA reports)
BRUXISM ( 19 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 19 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 19 FDA reports)
CONCUSSION ( 19 FDA reports)
DEAFNESS NEUROSENSORY ( 19 FDA reports)
DRUG INTOLERANCE ( 19 FDA reports)
GASTRIC ULCER ( 19 FDA reports)
HEPATOMEGALY ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
HYPOKINESIA ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
NON-CARDIAC CHEST PAIN ( 19 FDA reports)
ORAL DISCOMFORT ( 19 FDA reports)
OROPHARYNGEAL PAIN ( 19 FDA reports)
PALLOR ( 19 FDA reports)
PHARYNGITIS ( 19 FDA reports)
PNEUMOTHORAX ( 19 FDA reports)
POUCHITIS ( 19 FDA reports)
PSEUDOPOLYP ( 19 FDA reports)
SINUS BRADYCARDIA ( 19 FDA reports)
SKIN INDURATION ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
VASCULAR CALCIFICATION ( 19 FDA reports)
WOUND SECRETION ( 19 FDA reports)
ABNORMAL BEHAVIOUR ( 18 FDA reports)
BLADDER DISORDER ( 18 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 18 FDA reports)
CARDIOGENIC SHOCK ( 18 FDA reports)
CHOLECYSTECTOMY ( 18 FDA reports)
DECREASED INTEREST ( 18 FDA reports)
DEVICE FAILURE ( 18 FDA reports)
DUODENAL ULCER ( 18 FDA reports)
ENDOTRACHEAL INTUBATION ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
HAMARTOMA ( 18 FDA reports)
HIP FRACTURE ( 18 FDA reports)
HUMERUS FRACTURE ( 18 FDA reports)
HYPOPHAGIA ( 18 FDA reports)
INCREASED TENDENCY TO BRUISE ( 18 FDA reports)
ISCHAEMIA ( 18 FDA reports)
ISCHAEMIC STROKE ( 18 FDA reports)
JAW DISORDER ( 18 FDA reports)
LIVER DISORDER ( 18 FDA reports)
LOWER LIMB FRACTURE ( 18 FDA reports)
MALNUTRITION ( 18 FDA reports)
MULTIPLE SCLEROSIS ( 18 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 18 FDA reports)
OESOPHAGEAL STENOSIS ( 18 FDA reports)
RIGHT ATRIAL DILATATION ( 18 FDA reports)
SCIATICA ( 18 FDA reports)
THROAT IRRITATION ( 18 FDA reports)
TOOTH LOSS ( 18 FDA reports)
WHIPLASH INJURY ( 18 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 18 FDA reports)
ANGIOEDEMA ( 17 FDA reports)
ANXIETY DISORDER ( 17 FDA reports)
AORTIC VALVE STENOSIS ( 17 FDA reports)
BASAL CELL CARCINOMA ( 17 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 17 FDA reports)
BONE MARROW FAILURE ( 17 FDA reports)
COMPLETED SUICIDE ( 17 FDA reports)
DENTAL FISTULA ( 17 FDA reports)
DIABETIC FOOT ( 17 FDA reports)
ENDOCARDITIS ( 17 FDA reports)
FACE INJURY ( 17 FDA reports)
FOOT FRACTURE ( 17 FDA reports)
HAEMATEMESIS ( 17 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 17 FDA reports)
ILEUS ( 17 FDA reports)
IMPAIRED WORK ABILITY ( 17 FDA reports)
LACUNAR INFARCTION ( 17 FDA reports)
MICTURITION URGENCY ( 17 FDA reports)
MUCOSAL INFLAMMATION ( 17 FDA reports)
NEUROPATHY ( 17 FDA reports)
OEDEMA MOUTH ( 17 FDA reports)
PERIODONTAL DISEASE ( 17 FDA reports)
PERIPHERAL COLDNESS ( 17 FDA reports)
PHARYNGEAL OEDEMA ( 17 FDA reports)
POST PROCEDURAL COMPLICATION ( 17 FDA reports)
PROCEDURAL COMPLICATION ( 17 FDA reports)
RESPIRATORY DISORDER ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
RIB FRACTURE ( 17 FDA reports)
SEQUESTRECTOMY ( 17 FDA reports)
STOMATITIS ( 17 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 17 FDA reports)
TONGUE DISORDER ( 17 FDA reports)
ACUTE CORONARY SYNDROME ( 16 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 16 FDA reports)
BLISTER ( 16 FDA reports)
BONE NEOPLASM ( 16 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 16 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
CONJUNCTIVITIS ( 16 FDA reports)
DENTURE WEARER ( 16 FDA reports)
EAR NEOPLASM ( 16 FDA reports)
ELECTROLYTE IMBALANCE ( 16 FDA reports)
ERUCTATION ( 16 FDA reports)
FAECALOMA ( 16 FDA reports)
FAILURE TO THRIVE ( 16 FDA reports)
HEPATIC CIRRHOSIS ( 16 FDA reports)
HYPERTENSIVE HEART DISEASE ( 16 FDA reports)
HYPOALBUMINAEMIA ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
INDURATION ( 16 FDA reports)
JOINT DISLOCATION ( 16 FDA reports)
LABORATORY TEST ABNORMAL ( 16 FDA reports)
LICHEN PLANUS ( 16 FDA reports)
LIMB DISCOMFORT ( 16 FDA reports)
LIP DRY ( 16 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 16 FDA reports)
MACROGLOSSIA ( 16 FDA reports)
NIGHT SWEATS ( 16 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 16 FDA reports)
OESOPHAGITIS ( 16 FDA reports)
OSTEOMYELITIS CHRONIC ( 16 FDA reports)
OVERGROWTH BACTERIAL ( 16 FDA reports)
PRODUCT QUALITY ISSUE ( 16 FDA reports)
PRODUCTIVE COUGH ( 16 FDA reports)
RETCHING ( 16 FDA reports)
RETINOPATHY ( 16 FDA reports)
SHOULDER PAIN ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
SINUS CONGESTION ( 16 FDA reports)
SKIN HYPERPIGMENTATION ( 16 FDA reports)
VENTRICULAR DYSFUNCTION ( 16 FDA reports)
VITAMIN D DEFICIENCY ( 16 FDA reports)
ACUTE SINUSITIS ( 15 FDA reports)
AORTIC VALVE DISEASE ( 15 FDA reports)
BILE DUCT STONE ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
CERUMEN IMPACTION ( 15 FDA reports)
CERVICOBRACHIAL SYNDROME ( 15 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 15 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 15 FDA reports)
DIASTOLIC DYSFUNCTION ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
DYSKINESIA ( 15 FDA reports)
DYSSTASIA ( 15 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 15 FDA reports)
FEELING JITTERY ( 15 FDA reports)
FRACTURED SACRUM ( 15 FDA reports)
GASTROENTERITIS ( 15 FDA reports)
HAND FRACTURE ( 15 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 15 FDA reports)
HYPOTRICHOSIS ( 15 FDA reports)
IMPAIRED DRIVING ABILITY ( 15 FDA reports)
KNEE ARTHROPLASTY ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
PANIC DISORDER ( 15 FDA reports)
PELVIC INFECTION ( 15 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 15 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 15 FDA reports)
PROSTATOMEGALY ( 15 FDA reports)
PRURITUS GENERALISED ( 15 FDA reports)
PSORIASIS ( 15 FDA reports)
PURULENT DISCHARGE ( 15 FDA reports)
RENAL PAIN ( 15 FDA reports)
TIBIA FRACTURE ( 15 FDA reports)
UPPER LIMB FRACTURE ( 15 FDA reports)
VENTRICULAR HYPOKINESIA ( 15 FDA reports)
BEDRIDDEN ( 14 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 14 FDA reports)
BRONCHOPNEUMONIA ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 14 FDA reports)
CRYING ( 14 FDA reports)
DECREASED ACTIVITY ( 14 FDA reports)
DEMENTIA ( 14 FDA reports)
DERMOID CYST ( 14 FDA reports)
DIABETIC GASTROPATHY ( 14 FDA reports)
FACIAL PALSY ( 14 FDA reports)
FIBROMA ( 14 FDA reports)
FRACTURE ( 14 FDA reports)
GASTROENTERITIS VIRAL ( 14 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 14 FDA reports)
HYPERKERATOSIS ( 14 FDA reports)
INCONTINENCE ( 14 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 14 FDA reports)
JAW OPERATION ( 14 FDA reports)
KYPHOSIS ( 14 FDA reports)
LABILE HYPERTENSION ( 14 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 14 FDA reports)
NOCTURIA ( 14 FDA reports)
NODAL RHYTHM ( 14 FDA reports)
RENAL ARTERY STENOSIS ( 14 FDA reports)
RENAL TUBULAR NECROSIS ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 14 FDA reports)
STEVENS-JOHNSON SYNDROME ( 14 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 14 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 14 FDA reports)
THROAT LESION ( 14 FDA reports)
TONGUE DISCOLOURATION ( 14 FDA reports)
VITAMIN B12 DEFICIENCY ( 14 FDA reports)
WALKING AID USER ( 14 FDA reports)
WOUND DRAINAGE ( 14 FDA reports)
ACROCHORDON ( 13 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
ANEURYSM ( 13 FDA reports)
BIPOLAR DISORDER ( 13 FDA reports)
BLOOD CHLORIDE DECREASED ( 13 FDA reports)
BRONCHITIS ACUTE ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
CLOSTRIDIAL INFECTION ( 13 FDA reports)
CLOSTRIDIUM COLITIS ( 13 FDA reports)
COLECTOMY ( 13 FDA reports)
EXTREMITY CONTRACTURE ( 13 FDA reports)
FAECAL INCONTINENCE ( 13 FDA reports)
GALLBLADDER DISORDER ( 13 FDA reports)
GASTROINTESTINAL PERFORATION ( 13 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 13 FDA reports)
HERPES SIMPLEX ( 13 FDA reports)
HYPOTONIA ( 13 FDA reports)
INADEQUATE ANALGESIA ( 13 FDA reports)
INJECTION SITE ERYTHEMA ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 13 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 13 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 13 FDA reports)
JAW CYST ( 13 FDA reports)
MACULAR DEGENERATION ( 13 FDA reports)
MICROCYTIC ANAEMIA ( 13 FDA reports)
MUSCLE INJURY ( 13 FDA reports)
ORAL PAIN ( 13 FDA reports)
PARONYCHIA ( 13 FDA reports)
PATELLA FRACTURE ( 13 FDA reports)
PLATELET COUNT INCREASED ( 13 FDA reports)
PNEUMONITIS ( 13 FDA reports)
POLYURIA ( 13 FDA reports)
PRESYNCOPE ( 13 FDA reports)
PRIMARY SEQUESTRUM ( 13 FDA reports)
RHINITIS ( 13 FDA reports)
SEDATION ( 13 FDA reports)
SKIN EXFOLIATION ( 13 FDA reports)
TESTICULAR PAIN ( 13 FDA reports)
THROAT TIGHTNESS ( 13 FDA reports)
VASCULAR OCCLUSION ( 13 FDA reports)
VISUAL FIELD DEFECT ( 13 FDA reports)
ACUTE RESPIRATORY FAILURE ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
BLEPHARITIS ( 12 FDA reports)
BLOOD ALBUMIN DECREASED ( 12 FDA reports)
BLOOD CALCIUM INCREASED ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
BONE EROSION ( 12 FDA reports)
BONE LOSS ( 12 FDA reports)
BREATH ODOUR ( 12 FDA reports)
CARDIAC FAILURE CHRONIC ( 12 FDA reports)
CAROTID BRUIT ( 12 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 12 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 12 FDA reports)
DIABETIC NEPHROPATHY ( 12 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 12 FDA reports)
FEAR OF DEATH ( 12 FDA reports)
GASTRIC HAEMORRHAGE ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
HERPES VIRUS INFECTION ( 12 FDA reports)
HYPERPHAGIA ( 12 FDA reports)
INGROWING NAIL ( 12 FDA reports)
LEG AMPUTATION ( 12 FDA reports)
LEUKOPLAKIA ORAL ( 12 FDA reports)
MITRAL VALVE STENOSIS ( 12 FDA reports)
MOVEMENT DISORDER ( 12 FDA reports)
NIGHTMARE ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PULMONARY FIBROSIS ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
SEBORRHOEIC KERATOSIS ( 12 FDA reports)
SINUS OPERATION ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
TRAUMATIC HAEMATOMA ( 12 FDA reports)
ABDOMINAL NEOPLASM ( 11 FDA reports)
AORTIC VALVE SCLEROSIS ( 11 FDA reports)
APHASIA ( 11 FDA reports)
BLADDER CANCER ( 11 FDA reports)
BLINDNESS UNILATERAL ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 11 FDA reports)
BONE MARROW TRANSPLANT ( 11 FDA reports)
BREAST CANCER METASTATIC ( 11 FDA reports)
BREATH SOUNDS ABNORMAL ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CARDIAC FIBRILLATION ( 11 FDA reports)
CHOKING ( 11 FDA reports)
CHONDROCALCINOSIS ( 11 FDA reports)
CORONARY ARTERY BYPASS ( 11 FDA reports)
DERMAL CYST ( 11 FDA reports)
DISEASE RECURRENCE ( 11 FDA reports)
EMPTY SELLA SYNDROME ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
EYE SWELLING ( 11 FDA reports)
FAECES DISCOLOURED ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
FEMORAL ARTERY OCCLUSION ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
GANGRENE ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
HEMIPARESIS ( 11 FDA reports)
HERNIA ( 11 FDA reports)
HIP ARTHROPLASTY ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
HYPERTENSIVE CRISIS ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
MITRAL VALVE DISEASE ( 11 FDA reports)
NO ADVERSE EVENT ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
OSTEOSCLEROSIS ( 11 FDA reports)
POLYDIPSIA ( 11 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 11 FDA reports)
PROSTATE CANCER ( 11 FDA reports)
RENAL COLIC ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
SNORING ( 11 FDA reports)
SPUTUM DISCOLOURED ( 11 FDA reports)
STENT PLACEMENT ( 11 FDA reports)
TENSION ( 11 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 11 FDA reports)
THYROID ADENOMA ( 11 FDA reports)
TOE AMPUTATION ( 11 FDA reports)
UROSEPSIS ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 11 FDA reports)
ACTINOMYCOSIS ( 10 FDA reports)
ANAEMIA POSTOPERATIVE ( 10 FDA reports)
APPENDIX DISORDER ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BLOOD CULTURE POSITIVE ( 10 FDA reports)
BLOOD GLUCOSE ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
BONE DENSITY DECREASED ( 10 FDA reports)
BRONCHITIS CHRONIC ( 10 FDA reports)
CARDIAC OUTPUT DECREASED ( 10 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 10 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
COLD SWEAT ( 10 FDA reports)
DIABETIC COMA ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
EYE IRRITATION ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
HEPATIC NEOPLASM ( 10 FDA reports)
HYPERSOMNIA ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INFUSION RELATED REACTION ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
INTERMITTENT CLAUDICATION ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 10 FDA reports)
INTRACARDIAC THROMBUS ( 10 FDA reports)
LACRIMATION INCREASED ( 10 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
METASTASES TO PANCREAS ( 10 FDA reports)
MOOD SWINGS ( 10 FDA reports)
MUSCLE TIGHTNESS ( 10 FDA reports)
MYELODYSPLASTIC SYNDROME ( 10 FDA reports)
MYOSCLEROSIS ( 10 FDA reports)
NAIL DISORDER ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
NON-SMALL CELL LUNG CANCER ( 10 FDA reports)
OPEN WOUND ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PANCREATIC CYST ( 10 FDA reports)
PARALYSIS ( 10 FDA reports)
PHYSICAL ASSAULT ( 10 FDA reports)
PLEURAL CALCIFICATION ( 10 FDA reports)
PROSTATE CANCER METASTATIC ( 10 FDA reports)
RETINAL TEAR ( 10 FDA reports)
SKIN LACERATION ( 10 FDA reports)
SOCIAL PROBLEM ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 10 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 10 FDA reports)
TARDIVE DYSKINESIA ( 10 FDA reports)
THROMBOPHLEBITIS ( 10 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
URINARY HESITATION ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 9 FDA reports)
ACIDOSIS ( 9 FDA reports)
ADJUSTMENT DISORDER ( 9 FDA reports)
AGEUSIA ( 9 FDA reports)
AGGRESSION ( 9 FDA reports)
ARTHRITIS INFECTIVE ( 9 FDA reports)
ASEPTIC NECROSIS BONE ( 9 FDA reports)
BLADDER PROLAPSE ( 9 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 9 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 9 FDA reports)
BRAIN NEOPLASM ( 9 FDA reports)
BREAST CALCIFICATIONS ( 9 FDA reports)
BRONCHOSPASM ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CACHEXIA ( 9 FDA reports)
CARDIAC TAMPONADE ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CHEST X-RAY ABNORMAL ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 9 FDA reports)
DEVICE RELATED INFECTION ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 9 FDA reports)
ENTEROCOCCAL INFECTION ( 9 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 9 FDA reports)
EXERCISE TOLERANCE DECREASED ( 9 FDA reports)
EXFOLIATIVE RASH ( 9 FDA reports)
EYE HAEMORRHAGE ( 9 FDA reports)
FEELING COLD ( 9 FDA reports)
FIBULA FRACTURE ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEAT EXHAUSTION ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
INTENTIONAL DRUG MISUSE ( 9 FDA reports)
LARYNGITIS ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
LOSS OF EMPLOYMENT ( 9 FDA reports)
MALIGNANT MELANOMA ( 9 FDA reports)
MENINGITIS VIRAL ( 9 FDA reports)
METASTASES TO KIDNEY ( 9 FDA reports)
NEUROENDOCRINE CARCINOMA ( 9 FDA reports)
NEUROGENIC BLADDER ( 9 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 9 FDA reports)
OCULAR HYPERAEMIA ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
OSTEOMYELITIS DRAINAGE ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERICARDIAL CYST ( 9 FDA reports)
PLATELET AGGREGATION INCREASED ( 9 FDA reports)
PLEURITIC PAIN ( 9 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 9 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 9 FDA reports)
POST POLIO SYNDROME ( 9 FDA reports)
PSYCHOTIC DISORDER ( 9 FDA reports)
RALES ( 9 FDA reports)
RASH MACULAR ( 9 FDA reports)
RHEUMATIC FEVER ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SINUS HEADACHE ( 9 FDA reports)
SKIN GRAFT ( 9 FDA reports)
STEM CELL TRANSPLANT ( 9 FDA reports)
SUBCUTANEOUS ABSCESS ( 9 FDA reports)
SUDDEN DEATH ( 9 FDA reports)
SYNOVITIS ( 9 FDA reports)
THERAPY NON-RESPONDER ( 9 FDA reports)
THIRST ( 9 FDA reports)
THYROID CYST ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
WHEELCHAIR USER ( 9 FDA reports)
ACUTE PRERENAL FAILURE ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ANIMAL BITE ( 8 FDA reports)
BILE DUCT OBSTRUCTION ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BONE MARROW OEDEMA ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CALCULUS URINARY ( 8 FDA reports)
CARDIAC FLUTTER ( 8 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 8 FDA reports)
CERVIX CARCINOMA ( 8 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
COORDINATION ABNORMAL ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DENTAL PLAQUE ( 8 FDA reports)
DIABETIC COMPLICATION ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
EMBOLISM ( 8 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 8 FDA reports)
GENERALISED ANXIETY DISORDER ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPERPARATHYROIDISM ( 8 FDA reports)
HYPERTENSIVE EMERGENCY ( 8 FDA reports)
HYPOAESTHESIA FACIAL ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
IMMUNE SYSTEM DISORDER ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INCREASED APPETITE ( 8 FDA reports)
INJECTION SITE HAEMORRHAGE ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LIFE EXPECTANCY SHORTENED ( 8 FDA reports)
LISTLESS ( 8 FDA reports)
MAJOR DEPRESSION ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
MIDDLE INSOMNIA ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MUSCLE ATROPHY ( 8 FDA reports)
MUSCLE SPASTICITY ( 8 FDA reports)
MUSCLE TWITCHING ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
NASAL POLYPS ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
ORTHOSIS USER ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PAPILLOEDEMA ( 8 FDA reports)
PATHOLOGICAL GAMBLING ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PERONEAL NERVE PALSY ( 8 FDA reports)
PERSONALITY CHANGE ( 8 FDA reports)
PIGMENTARY GLAUCOMA ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
PROSTATIC DISORDER ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
PULMONARY VALVE STENOSIS ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
PULSE ABSENT ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 8 FDA reports)
RETINAL DISORDER ( 8 FDA reports)
RETINAL VEIN OCCLUSION ( 8 FDA reports)
SENSORY LOSS ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SINUS POLYP ( 8 FDA reports)
SKIN FIBROSIS ( 8 FDA reports)
SKIN SWELLING ( 8 FDA reports)
TENDERNESS ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
UTERINE CANCER ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
ACCIDENT ( 7 FDA reports)
ACCIDENT AT WORK ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 7 FDA reports)
AORTIC DISORDER ( 7 FDA reports)
APATHY ( 7 FDA reports)
ARTERIAL DISORDER ( 7 FDA reports)
ARTERIAL INSUFFICIENCY ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
ASPIRATION PLEURAL CAVITY ( 7 FDA reports)
ASTERIXIS ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
ATROPHY ( 7 FDA reports)
BLOOD CALCIUM ABNORMAL ( 7 FDA reports)
BONE FRAGMENTATION ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
BREAST TENDERNESS ( 7 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 7 FDA reports)
BUNDLE BRANCH BLOCK ( 7 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 7 FDA reports)
CHRONIC FATIGUE SYNDROME ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 7 FDA reports)
COSTOCHONDRITIS ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
DIZZINESS POSTURAL ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG TOLERANCE ( 7 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENDARTERECTOMY ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
FEEDING DISORDER ( 7 FDA reports)
FLAT AFFECT ( 7 FDA reports)
GASTRIC POLYPS ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
GINGIVAL RECESSION ( 7 FDA reports)
HEART VALVE REPLACEMENT ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 7 FDA reports)
HOSPITALISATION ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPOMANIA ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
INCISION SITE COMPLICATION ( 7 FDA reports)
LIP SWELLING ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
LUNG LOBECTOMY ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MANIA ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
MYOFASCIAL SPASM ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
OCCULT BLOOD ( 7 FDA reports)
OPTIC ATROPHY ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
PERIORBITAL HAEMATOMA ( 7 FDA reports)
PERIORBITAL OEDEMA ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
PROSTATITIS ( 7 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SEPSIS SYNDROME ( 7 FDA reports)
SKIN PLAQUE ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
THINKING ABNORMAL ( 7 FDA reports)
THYROXINE DECREASED ( 7 FDA reports)
TOE DEFORMITY ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
URETERIC OBSTRUCTION ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
UTERINE LEIOMYOMA ( 7 FDA reports)
VASODILATATION ( 7 FDA reports)
WEIGHT FLUCTUATION ( 7 FDA reports)
WEIGHT LOSS POOR ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ABSCESS ORAL ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
ALCOHOLIC LIVER DISEASE ( 6 FDA reports)
ALKALOSIS ( 6 FDA reports)
ALOPECIA TOTALIS ( 6 FDA reports)
ALOPECIA UNIVERSALIS ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ALVEOLAR OSTEITIS ( 6 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
ANURIA ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
APPLICATION SITE PRURITUS ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BLOOD CHOLESTEROL ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BONE CYST ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CATARACT NUCLEAR ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
CHOKING SENSATION ( 6 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
COMPRESSION FRACTURE ( 6 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 6 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 6 FDA reports)
CONGENITAL TRACHEOMALACIA ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CORONARY ARTERY SURGERY ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
EBSTEIN'S ANOMALY ( 6 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
FALLOT'S TETRALOGY ( 6 FDA reports)
FOETAL HEART RATE ABNORMAL ( 6 FDA reports)
FRUSTRATION ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GIANT CELL EPULIS ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
GRAM STAIN POSITIVE ( 6 FDA reports)
GRIMACING ( 6 FDA reports)
HAIR DISORDER ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HELICOBACTER TEST POSITIVE ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HUNGER ( 6 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
KETOACIDOSIS ( 6 FDA reports)
LARGE FOR DATES BABY ( 6 FDA reports)
LARGE INTESTINE PERFORATION ( 6 FDA reports)
LIGAMENT SPRAIN ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MANDIBULECTOMY ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
MIXED INCONTINENCE ( 6 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 6 FDA reports)
MUSCLE FIBROSIS ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
NEONATAL ASPIRATION ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NONSPECIFIC REACTION ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OPERATIVE HAEMORRHAGE ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PARANASAL CYST ( 6 FDA reports)
PARANOIA ( 6 FDA reports)
PARAPROTEINAEMIA ( 6 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 6 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PLEURAL FIBROSIS ( 6 FDA reports)
POST PROCEDURAL PAIN ( 6 FDA reports)
POST THROMBOTIC SYNDROME ( 6 FDA reports)
POSTNASAL DRIP ( 6 FDA reports)
POSTURE ABNORMAL ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PROSTHESIS IMPLANTATION ( 6 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 6 FDA reports)
PULMONARY MALFORMATION ( 6 FDA reports)
PYURIA ( 6 FDA reports)
QUADRIPARESIS ( 6 FDA reports)
RED MAN SYNDROME ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
RETINAL OEDEMA ( 6 FDA reports)
SCAB ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SKULL FRACTURE ( 6 FDA reports)
SNEEZING ( 6 FDA reports)
SOFT TISSUE MASS ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 6 FDA reports)
TRICUSPID VALVE DISEASE ( 6 FDA reports)
TRICUSPID VALVE PROLAPSE ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
TUBERCULIN TEST POSITIVE ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
URETERAL DISORDER ( 6 FDA reports)
UTERINE HAEMORRHAGE ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
VOCAL CORD PARALYSIS ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
WOUND DEBRIDEMENT ( 6 FDA reports)
WOUND DEHISCENCE ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 5 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANGER ( 5 FDA reports)
ANOSMIA ( 5 FDA reports)
APNOEA ( 5 FDA reports)
ARTHRODESIS ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BACTERIA URINE IDENTIFIED ( 5 FDA reports)
BARRETT'S OESOPHAGUS ( 5 FDA reports)
BEREAVEMENT REACTION ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD VISCOSITY INCREASED ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
CALCULUS BLADDER ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 5 FDA reports)
CSF PROTEIN INCREASED ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DYSAESTHESIA ( 5 FDA reports)
EJACULATION DISORDER ( 5 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAIR GROWTH ABNORMAL ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HEPATIC MASS ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
ILIAC ARTERY STENOSIS ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
IRIS ADHESIONS ( 5 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MASTECTOMY ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
MENOPAUSAL SYMPTOMS ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
METABOLIC SYNDROME ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MICROALBUMINURIA ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
OVARIAN DISORDER ( 5 FDA reports)
PAINFUL DEFAECATION ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PERIARTHRITIS ( 5 FDA reports)
PLANTAR FASCIITIS ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
PULPITIS DENTAL ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
SENSATION OF PRESSURE ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TOOTH CROWDING ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BREAST CYST ( 4 FDA reports)
BREAST INDURATION ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 4 FDA reports)
CATHETER SITE HAEMATOMA ( 4 FDA reports)
CELLS IN URINE ( 4 FDA reports)
CENTRAL LINE INFECTION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
COLON ADENOMA ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CORONARY OSTIAL STENOSIS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DROOLING ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EYE LASER SURGERY ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
FRACTURE NONUNION ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GAMMA RADIATION THERAPY ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
ILEAL ULCER ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTESTINAL POLYP ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENSTRUAL DISORDER ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METAPLASIA ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
NASAL SINUS DRAINAGE ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORAL FUNGAL INFECTION ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARATHYROID TUMOUR BENIGN ( 4 FDA reports)
PARESIS CRANIAL NERVE ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
RECTAL PERFORATION ( 4 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
REGURGITATION OF FOOD ( 4 FDA reports)
RENAL TUMOUR EXCISION ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SKIN CANDIDA ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN GRAFT FAILURE ( 4 FDA reports)
SKIN HAEMORRHAGE ( 4 FDA reports)
SKIN INFECTION ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SPINAL LAMINECTOMY ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
TOBACCO ABUSE ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 4 FDA reports)
VISUAL BRIGHTNESS ( 4 FDA reports)
WALLENBERG SYNDROME ( 4 FDA reports)
WOUND CLOSURE ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ADAMS-STOKES SYNDROME ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTHROPOD STING ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BILIARY NEOPLASM ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMMINUTED FRACTURE ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 3 FDA reports)
DIABETIC FOOT INFECTION ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
FEMORAL BRUIT ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTRIC CANCER RECURRENT ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GLOBAL AMNESIA ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRIEF REACTION ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
GUN SHOT WOUND ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMOBILIA ( 3 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 3 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERPES OPHTHALMIC ( 3 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOMELESS ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HORDEOLUM ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCISION SITE HAEMATOMA ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LENS IMPLANT ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOW TURNOVER OSTEOPATHY ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 3 FDA reports)
MALOCCLUSION ( 3 FDA reports)
MAMMOPLASTY ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHARYNX DISCOMFORT ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RADIOISOTOPE SCAN ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RED BLOOD CELL ABNORMALITY ( 3 FDA reports)
REHABILITATION THERAPY ( 3 FDA reports)
RENAL CANCER ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RIGHT AORTIC ARCH ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SCROTAL CYST ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPONDYLOSIS ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
STRESS INCONTINENCE ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
THALAMIC INFARCTION ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
THYROXINE FREE DECREASED ( 3 FDA reports)
TINEA CAPITIS ( 3 FDA reports)
TOOTH MALFORMATION ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACANTHOSIS NIGRICANS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTIBIOTIC THERAPY ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BONE OPERATION ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BORRELIA TEST POSITIVE ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST CYST EXCISION ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CAROTID ARTERY STENT INSERTION ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST WALL CYST ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHOREA ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
CONGENITAL EYE NAEVUS ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS VIRAL ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXTERNAL EAR CELLULITIS ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATITIS D ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOACTIVE SEXUAL DESIRE DISORDER ( 2 FDA reports)
HYPOCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
IRIDOCELE ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT LIGAMENT RUPTURE ( 2 FDA reports)
KIDNEY RUPTURE ( 2 FDA reports)
KNEE MENISCECTOMY ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MILIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSTEOGENESIS IMPERFECTA ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PLATELET AGGREGATION ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSITTACOSIS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL OPERATION ( 2 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL DECOMPRESSION ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STARVATION ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
URETERIC OPERATION ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL PROLAPSE ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOCAL CORD ATROPHY ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
AURA ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT PRESSURE ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CATHETER PERMANENT ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CAFFEINE ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL OPERATION ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
EISENMENGER'S SYNDROME ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOCARDITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HYPERMOTILITY ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DERMATITIS ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CANCER STAGE IV ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION RELATED REACTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL FISTULA REPAIR ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRIS INJURY ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAW OSTEITIS ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PAPILLOMA ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET ADHESIVENESS ABNORMAL ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESENILE DEMENTIA ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY SIGHS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL PALLOR ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINITIS VIRAL ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERIC CANCER LOCAL ( 1 FDA reports)
URETHRAL CANCER LOCAL ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VAGOTOMY ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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