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

DYSPNOEA ( 881 FDA reports)
PAIN ( 840 FDA reports)
NAUSEA ( 744 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 725 FDA reports)
FATIGUE ( 684 FDA reports)
ASTHENIA ( 654 FDA reports)
ANXIETY ( 640 FDA reports)
DIZZINESS ( 605 FDA reports)
OEDEMA PERIPHERAL ( 601 FDA reports)
PNEUMONIA ( 596 FDA reports)
CHEST PAIN ( 565 FDA reports)
HYPERTENSION ( 554 FDA reports)
FALL ( 551 FDA reports)
ANAEMIA ( 522 FDA reports)
DIARRHOEA ( 522 FDA reports)
HEADACHE ( 484 FDA reports)
BACK PAIN ( 477 FDA reports)
DEPRESSION ( 477 FDA reports)
VOMITING ( 469 FDA reports)
INJURY ( 450 FDA reports)
ATRIAL FIBRILLATION ( 433 FDA reports)
ARTHRALGIA ( 374 FDA reports)
HYPOTENSION ( 373 FDA reports)
PAIN IN EXTREMITY ( 366 FDA reports)
DEHYDRATION ( 365 FDA reports)
RENAL FAILURE ( 364 FDA reports)
WEIGHT DECREASED ( 361 FDA reports)
CONSTIPATION ( 347 FDA reports)
MYOCARDIAL INFARCTION ( 344 FDA reports)
ABDOMINAL PAIN ( 324 FDA reports)
URINARY TRACT INFECTION ( 313 FDA reports)
OSTEOARTHRITIS ( 307 FDA reports)
OSTEONECROSIS OF JAW ( 303 FDA reports)
EMOTIONAL DISTRESS ( 297 FDA reports)
CEREBROVASCULAR ACCIDENT ( 294 FDA reports)
ECONOMIC PROBLEM ( 294 FDA reports)
INSOMNIA ( 294 FDA reports)
PYREXIA ( 290 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 289 FDA reports)
WEIGHT INCREASED ( 283 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 273 FDA reports)
DRUG INEFFECTIVE ( 273 FDA reports)
COUGH ( 272 FDA reports)
BLOOD GLUCOSE INCREASED ( 262 FDA reports)
MALAISE ( 259 FDA reports)
BONE DISORDER ( 255 FDA reports)
DEATH ( 254 FDA reports)
HYPOAESTHESIA ( 252 FDA reports)
RENAL FAILURE ACUTE ( 251 FDA reports)
GAIT DISTURBANCE ( 250 FDA reports)
CONFUSIONAL STATE ( 246 FDA reports)
CARDIOMEGALY ( 240 FDA reports)
HYPOKALAEMIA ( 240 FDA reports)
BRONCHITIS ( 238 FDA reports)
DYSPHAGIA ( 238 FDA reports)
DECREASED APPETITE ( 232 FDA reports)
PARAESTHESIA ( 230 FDA reports)
SYNCOPE ( 226 FDA reports)
SPINAL OSTEOARTHRITIS ( 222 FDA reports)
PLEURAL EFFUSION ( 220 FDA reports)
CORONARY ARTERY DISEASE ( 219 FDA reports)
INFECTION ( 219 FDA reports)
RASH ( 218 FDA reports)
ANHEDONIA ( 217 FDA reports)
DIABETES MELLITUS ( 217 FDA reports)
MUSCLE SPASMS ( 214 FDA reports)
NEUROPATHY PERIPHERAL ( 214 FDA reports)
MITRAL VALVE INCOMPETENCE ( 213 FDA reports)
PAIN IN JAW ( 209 FDA reports)
CONTUSION ( 206 FDA reports)
MUSCULOSKELETAL PAIN ( 206 FDA reports)
DEEP VEIN THROMBOSIS ( 200 FDA reports)
ATELECTASIS ( 195 FDA reports)
MULTIPLE INJURIES ( 195 FDA reports)
OEDEMA ( 194 FDA reports)
RESPIRATORY FAILURE ( 192 FDA reports)
OSTEOMYELITIS ( 191 FDA reports)
OSTEONECROSIS ( 190 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 186 FDA reports)
ARTHRITIS ( 185 FDA reports)
PULMONARY EMBOLISM ( 182 FDA reports)
MYALGIA ( 180 FDA reports)
ABDOMINAL PAIN UPPER ( 175 FDA reports)
SEPSIS ( 174 FDA reports)
BRADYCARDIA ( 173 FDA reports)
PALPITATIONS ( 173 FDA reports)
CELLULITIS ( 172 FDA reports)
CONDITION AGGRAVATED ( 172 FDA reports)
SOMNOLENCE ( 168 FDA reports)
CARDIOMYOPATHY ( 167 FDA reports)
HYPERLIPIDAEMIA ( 166 FDA reports)
ASTHMA ( 164 FDA reports)
DEFORMITY ( 163 FDA reports)
PULMONARY HYPERTENSION ( 162 FDA reports)
CHEST DISCOMFORT ( 161 FDA reports)
CHOLELITHIASIS ( 161 FDA reports)
DYSPNOEA EXERTIONAL ( 158 FDA reports)
PRURITUS ( 158 FDA reports)
FEELING ABNORMAL ( 156 FDA reports)
SINUSITIS ( 153 FDA reports)
TOOTH EXTRACTION ( 153 FDA reports)
ERYTHEMA ( 152 FDA reports)
SWELLING ( 152 FDA reports)
BALANCE DISORDER ( 149 FDA reports)
TREMOR ( 149 FDA reports)
HYPERHIDROSIS ( 148 FDA reports)
HYPOPHAGIA ( 146 FDA reports)
LOSS OF CONSCIOUSNESS ( 146 FDA reports)
CATARACT ( 145 FDA reports)
ARTERIOSCLEROSIS ( 142 FDA reports)
MUSCULAR WEAKNESS ( 142 FDA reports)
BONE PAIN ( 141 FDA reports)
CARDIAC DISORDER ( 141 FDA reports)
PANCYTOPENIA ( 141 FDA reports)
NECK PAIN ( 139 FDA reports)
SLEEP APNOEA SYNDROME ( 136 FDA reports)
SPINAL COLUMN STENOSIS ( 136 FDA reports)
CARDIAC FAILURE ( 135 FDA reports)
DENTAL CARIES ( 135 FDA reports)
BLOOD PRESSURE INCREASED ( 134 FDA reports)
HAEMOGLOBIN DECREASED ( 134 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 134 FDA reports)
JOINT SWELLING ( 133 FDA reports)
ABASIA ( 131 FDA reports)
ABDOMINAL DISTENSION ( 129 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 129 FDA reports)
RIB FRACTURE ( 129 FDA reports)
HEART RATE INCREASED ( 126 FDA reports)
ARRHYTHMIA ( 125 FDA reports)
RENAL FAILURE CHRONIC ( 124 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 123 FDA reports)
HIATUS HERNIA ( 122 FDA reports)
GASTRITIS ( 121 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 121 FDA reports)
VISION BLURRED ( 121 FDA reports)
THROMBOCYTOPENIA ( 120 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 120 FDA reports)
VERTIGO ( 120 FDA reports)
HAEMORRHOIDS ( 119 FDA reports)
METASTASES TO BONE ( 119 FDA reports)
MULTIPLE MYELOMA ( 118 FDA reports)
TACHYCARDIA ( 118 FDA reports)
HEART RATE IRREGULAR ( 116 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 116 FDA reports)
OSTEOPENIA ( 115 FDA reports)
EXOSTOSIS ( 114 FDA reports)
LUNG INFILTRATION ( 112 FDA reports)
CARDIAC MURMUR ( 111 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 111 FDA reports)
UNEVALUABLE EVENT ( 111 FDA reports)
DYSPEPSIA ( 109 FDA reports)
LUNG NEOPLASM ( 109 FDA reports)
OBESITY ( 109 FDA reports)
SURGERY ( 109 FDA reports)
THROMBOSIS ( 109 FDA reports)
BLOOD CREATININE INCREASED ( 107 FDA reports)
TYPE 2 DIABETES MELLITUS ( 107 FDA reports)
MEMORY IMPAIRMENT ( 105 FDA reports)
FLUID RETENTION ( 103 FDA reports)
BONE LESION ( 102 FDA reports)
CARDIAC ARREST ( 102 FDA reports)
DECREASED INTEREST ( 101 FDA reports)
HYPONATRAEMIA ( 100 FDA reports)
HYPERKALAEMIA ( 99 FDA reports)
MENTAL STATUS CHANGES ( 99 FDA reports)
NERVOUSNESS ( 99 FDA reports)
ARTHROPATHY ( 97 FDA reports)
BLOOD POTASSIUM DECREASED ( 97 FDA reports)
HYPOXIA ( 97 FDA reports)
OSTEOPOROSIS ( 97 FDA reports)
AMNESIA ( 95 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 95 FDA reports)
MOUTH ULCERATION ( 95 FDA reports)
SPINAL COMPRESSION FRACTURE ( 95 FDA reports)
ANGINA PECTORIS ( 94 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 94 FDA reports)
FLUSHING ( 93 FDA reports)
RENAL DISORDER ( 93 FDA reports)
CHILLS ( 92 FDA reports)
HAEMATOCHEZIA ( 91 FDA reports)
HERPES ZOSTER ( 91 FDA reports)
NEOPLASM MALIGNANT ( 91 FDA reports)
ABDOMINAL DISCOMFORT ( 90 FDA reports)
DIVERTICULUM INTESTINAL ( 90 FDA reports)
PRESYNCOPE ( 90 FDA reports)
TOOTHACHE ( 90 FDA reports)
DISCOMFORT ( 89 FDA reports)
SWELLING FACE ( 89 FDA reports)
VISUAL ACUITY REDUCED ( 89 FDA reports)
BLOOD UREA INCREASED ( 88 FDA reports)
HAEMORRHAGE ( 87 FDA reports)
LUMBAR SPINAL STENOSIS ( 86 FDA reports)
PRIMARY SEQUESTRUM ( 86 FDA reports)
LETHARGY ( 85 FDA reports)
OSTEOSCLEROSIS ( 85 FDA reports)
SCOLIOSIS ( 85 FDA reports)
DRUG INTERACTION ( 84 FDA reports)
RENAL CYST ( 84 FDA reports)
STOMATITIS ( 84 FDA reports)
CONVULSION ( 83 FDA reports)
IMPAIRED HEALING ( 83 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 83 FDA reports)
NEPHROLITHIASIS ( 82 FDA reports)
OVERDOSE ( 82 FDA reports)
PLATELET COUNT DECREASED ( 82 FDA reports)
WHEEZING ( 82 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 81 FDA reports)
OSTEITIS ( 81 FDA reports)
RADICULOPATHY ( 81 FDA reports)
URTICARIA ( 80 FDA reports)
EMPHYSEMA ( 79 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 79 FDA reports)
VENTRICULAR TACHYCARDIA ( 79 FDA reports)
HAEMATURIA ( 78 FDA reports)
PHYSICAL DISABILITY ( 78 FDA reports)
HYPOTHYROIDISM ( 77 FDA reports)
RECTAL HAEMORRHAGE ( 77 FDA reports)
BURSITIS ( 76 FDA reports)
DRY MOUTH ( 76 FDA reports)
STRESS ( 76 FDA reports)
SUICIDAL IDEATION ( 76 FDA reports)
EPISTAXIS ( 75 FDA reports)
HEAD INJURY ( 75 FDA reports)
HYPOGLYCAEMIA ( 75 FDA reports)
OROPHARYNGEAL PAIN ( 75 FDA reports)
SPEECH DISORDER ( 75 FDA reports)
EJECTION FRACTION DECREASED ( 74 FDA reports)
GOITRE ( 74 FDA reports)
TREATMENT NONCOMPLIANCE ( 74 FDA reports)
VISUAL IMPAIRMENT ( 74 FDA reports)
PULMONARY OEDEMA ( 73 FDA reports)
TOOTH LOSS ( 73 FDA reports)
AGITATION ( 72 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 72 FDA reports)
DIVERTICULUM ( 72 FDA reports)
LEUKOCYTOSIS ( 72 FDA reports)
ROTATOR CUFF SYNDROME ( 72 FDA reports)
TOOTH FRACTURE ( 71 FDA reports)
CORONARY ARTERY OCCLUSION ( 69 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 69 FDA reports)
HYPERCHOLESTEROLAEMIA ( 68 FDA reports)
HYPERGLYCAEMIA ( 68 FDA reports)
BLOOD GLUCOSE DECREASED ( 67 FDA reports)
BONE DEBRIDEMENT ( 67 FDA reports)
COLITIS ( 67 FDA reports)
DISEASE PROGRESSION ( 67 FDA reports)
HALLUCINATION ( 67 FDA reports)
IRRITABILITY ( 67 FDA reports)
PROTHROMBIN TIME PROLONGED ( 67 FDA reports)
SINUS TACHYCARDIA ( 67 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 66 FDA reports)
BONE DENSITY DECREASED ( 66 FDA reports)
ILL-DEFINED DISORDER ( 66 FDA reports)
NEUTROPENIA ( 66 FDA reports)
RESPIRATORY DISTRESS ( 66 FDA reports)
FLUID OVERLOAD ( 65 FDA reports)
NASOPHARYNGITIS ( 65 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 65 FDA reports)
POLLAKIURIA ( 65 FDA reports)
PURULENT DISCHARGE ( 65 FDA reports)
STAPHYLOCOCCAL INFECTION ( 65 FDA reports)
ACUTE SINUSITIS ( 64 FDA reports)
DRUG HYPERSENSITIVITY ( 64 FDA reports)
GINGIVAL PAIN ( 64 FDA reports)
HYPOMAGNESAEMIA ( 64 FDA reports)
OESOPHAGITIS ( 64 FDA reports)
RHINITIS ALLERGIC ( 64 FDA reports)
TENDERNESS ( 64 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 64 FDA reports)
HAEMATOCRIT DECREASED ( 63 FDA reports)
MASTICATION DISORDER ( 63 FDA reports)
DISORIENTATION ( 62 FDA reports)
GALLBLADDER DISORDER ( 62 FDA reports)
HAEMATOMA ( 62 FDA reports)
TENDONITIS ( 62 FDA reports)
URINARY INCONTINENCE ( 62 FDA reports)
BLOOD PRESSURE DECREASED ( 61 FDA reports)
BURNING SENSATION ( 61 FDA reports)
CYSTITIS ( 61 FDA reports)
HYPERKERATOSIS ( 61 FDA reports)
ATRIAL FLUTTER ( 60 FDA reports)
CAROTID ARTERY STENOSIS ( 60 FDA reports)
DYSARTHRIA ( 60 FDA reports)
ORTHOPNOEA ( 60 FDA reports)
ORTHOSTATIC HYPOTENSION ( 60 FDA reports)
PULMONARY CONGESTION ( 60 FDA reports)
SKIN ULCER ( 60 FDA reports)
UNRESPONSIVE TO STIMULI ( 60 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 59 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 59 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 59 FDA reports)
DYSURIA ( 59 FDA reports)
FLATULENCE ( 59 FDA reports)
HEPATIC ENZYME INCREASED ( 59 FDA reports)
ORAL PAIN ( 59 FDA reports)
BASAL CELL CARCINOMA ( 58 FDA reports)
CARPAL TUNNEL SYNDROME ( 58 FDA reports)
DYSKINESIA ( 57 FDA reports)
HOT FLUSH ( 57 FDA reports)
LIFE EXPECTANCY SHORTENED ( 57 FDA reports)
PANCREATITIS ( 57 FDA reports)
CEREBRAL ATROPHY ( 56 FDA reports)
DRUG DOSE OMISSION ( 56 FDA reports)
GLAUCOMA ( 56 FDA reports)
HEART RATE DECREASED ( 56 FDA reports)
INJECTION SITE PAIN ( 56 FDA reports)
CANDIDIASIS ( 55 FDA reports)
DEPRESSED MOOD ( 55 FDA reports)
EMOTIONAL DISORDER ( 55 FDA reports)
GENERALISED OEDEMA ( 55 FDA reports)
HAEMOPTYSIS ( 55 FDA reports)
HYPOCALCAEMIA ( 55 FDA reports)
HYPOVOLAEMIA ( 55 FDA reports)
LYMPHADENOPATHY ( 55 FDA reports)
AZOTAEMIA ( 54 FDA reports)
DYSPHONIA ( 54 FDA reports)
FEAR ( 54 FDA reports)
FEELING HOT ( 54 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 54 FDA reports)
LACUNAR INFARCTION ( 54 FDA reports)
MIGRAINE ( 54 FDA reports)
MYOCARDIAL ISCHAEMIA ( 54 FDA reports)
CYST ( 53 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 53 FDA reports)
GINGIVITIS ( 53 FDA reports)
GOUT ( 53 FDA reports)
HEPATIC STEATOSIS ( 53 FDA reports)
HIP FRACTURE ( 53 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 53 FDA reports)
PULMONARY MASS ( 53 FDA reports)
RESTLESS LEGS SYNDROME ( 53 FDA reports)
SINUS BRADYCARDIA ( 53 FDA reports)
CARDIO-RESPIRATORY ARREST ( 52 FDA reports)
DISTURBANCE IN ATTENTION ( 52 FDA reports)
PRODUCTIVE COUGH ( 52 FDA reports)
DECUBITUS ULCER ( 51 FDA reports)
FEMUR FRACTURE ( 51 FDA reports)
FOOT FRACTURE ( 51 FDA reports)
AORTIC VALVE INCOMPETENCE ( 50 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 50 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 50 FDA reports)
OXYGEN SATURATION DECREASED ( 50 FDA reports)
ROAD TRAFFIC ACCIDENT ( 50 FDA reports)
SKIN LESION ( 50 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 50 FDA reports)
VIRAL INFECTION ( 50 FDA reports)
ALOPECIA ( 49 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 49 FDA reports)
BREAST CANCER ( 49 FDA reports)
COLONIC POLYP ( 49 FDA reports)
DEAFNESS ( 49 FDA reports)
DISABILITY ( 49 FDA reports)
ENCEPHALOPATHY ( 49 FDA reports)
GINGIVAL INFECTION ( 49 FDA reports)
HYPERSENSITIVITY ( 49 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 49 FDA reports)
LIMB INJURY ( 49 FDA reports)
MASS ( 49 FDA reports)
NODULE ( 49 FDA reports)
SCIATICA ( 49 FDA reports)
ABSCESS ( 48 FDA reports)
BLINDNESS UNILATERAL ( 48 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 48 FDA reports)
DELIRIUM ( 48 FDA reports)
DIABETIC NEUROPATHY ( 48 FDA reports)
DIPLOPIA ( 48 FDA reports)
DRUG EFFECT DECREASED ( 48 FDA reports)
PRODUCT QUALITY ISSUE ( 48 FDA reports)
URINARY RETENTION ( 48 FDA reports)
DENTAL FISTULA ( 47 FDA reports)
FUNGAL INFECTION ( 47 FDA reports)
INTERSTITIAL LUNG DISEASE ( 47 FDA reports)
IRRITABLE BOWEL SYNDROME ( 47 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 47 FDA reports)
NASAL CONGESTION ( 47 FDA reports)
RHINORRHOEA ( 47 FDA reports)
SINUS CONGESTION ( 47 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 47 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 46 FDA reports)
DEMENTIA ( 46 FDA reports)
GASTROENTERITIS ( 46 FDA reports)
INFLAMMATION ( 46 FDA reports)
INTESTINAL OBSTRUCTION ( 46 FDA reports)
JAW DISORDER ( 46 FDA reports)
MOBILITY DECREASED ( 46 FDA reports)
OFF LABEL USE ( 46 FDA reports)
RALES ( 46 FDA reports)
RESTLESSNESS ( 46 FDA reports)
SINUS DISORDER ( 46 FDA reports)
SYNOVIAL CYST ( 46 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 46 FDA reports)
ENDODONTIC PROCEDURE ( 45 FDA reports)
FISTULA ( 45 FDA reports)
HERNIA ( 45 FDA reports)
INFLUENZA ( 45 FDA reports)
MALNUTRITION ( 45 FDA reports)
MYOPATHY ( 45 FDA reports)
RHEUMATOID ARTHRITIS ( 45 FDA reports)
DENTURE WEARER ( 44 FDA reports)
INCONTINENCE ( 44 FDA reports)
INFLUENZA LIKE ILLNESS ( 44 FDA reports)
LEUKOPENIA ( 44 FDA reports)
LOOSE TOOTH ( 44 FDA reports)
PERICARDIAL EFFUSION ( 44 FDA reports)
SICK SINUS SYNDROME ( 44 FDA reports)
SKIN CANCER ( 44 FDA reports)
SPINAL DISORDER ( 44 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 43 FDA reports)
CHRONIC SINUSITIS ( 43 FDA reports)
DIVERTICULITIS ( 43 FDA reports)
GASTROINTESTINAL DISORDER ( 43 FDA reports)
GROIN PAIN ( 43 FDA reports)
LUNG CONSOLIDATION ( 43 FDA reports)
MULTI-ORGAN FAILURE ( 43 FDA reports)
ANKLE FRACTURE ( 42 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 42 FDA reports)
CHOLECYSTITIS ( 42 FDA reports)
FLANK PAIN ( 42 FDA reports)
HEPATIC CYST ( 42 FDA reports)
HEPATITIS ( 42 FDA reports)
ILEUS ( 42 FDA reports)
KIDNEY INFECTION ( 42 FDA reports)
LUNG NEOPLASM MALIGNANT ( 42 FDA reports)
MENTAL DISORDER ( 42 FDA reports)
SPONDYLOLISTHESIS ( 42 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 42 FDA reports)
WOUND DEHISCENCE ( 42 FDA reports)
ACUTE RESPIRATORY FAILURE ( 41 FDA reports)
HYPERCALCAEMIA ( 41 FDA reports)
JAW FRACTURE ( 41 FDA reports)
LIVER DISORDER ( 41 FDA reports)
MYOSITIS ( 41 FDA reports)
CARDIAC PACEMAKER INSERTION ( 40 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 40 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 40 FDA reports)
ANGINA UNSTABLE ( 39 FDA reports)
BLADDER DISORDER ( 39 FDA reports)
BLOOD CALCIUM INCREASED ( 39 FDA reports)
BLOOD POTASSIUM INCREASED ( 39 FDA reports)
INCORRECT DOSE ADMINISTERED ( 39 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 39 FDA reports)
LUNG DISORDER ( 39 FDA reports)
METASTASES TO LUNG ( 39 FDA reports)
NEURALGIA ( 39 FDA reports)
PERIODONTAL DISEASE ( 39 FDA reports)
POLYP ( 39 FDA reports)
RENAL IMPAIRMENT ( 39 FDA reports)
SCAR ( 39 FDA reports)
SKIN DISCOLOURATION ( 39 FDA reports)
WOUND INFECTION ( 39 FDA reports)
CORONARY ARTERY STENOSIS ( 38 FDA reports)
EATING DISORDER ( 38 FDA reports)
ECCHYMOSIS ( 38 FDA reports)
EXPOSED BONE IN JAW ( 38 FDA reports)
FACET JOINT SYNDROME ( 38 FDA reports)
FACIAL PAIN ( 38 FDA reports)
INCREASED APPETITE ( 38 FDA reports)
RASH ERYTHEMATOUS ( 38 FDA reports)
ASCITES ( 37 FDA reports)
BLOOD SODIUM DECREASED ( 37 FDA reports)
BRONCHITIS CHRONIC ( 37 FDA reports)
CAROTID BRUIT ( 37 FDA reports)
METASTASES TO SPINE ( 37 FDA reports)
MUSCLE STRAIN ( 37 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 37 FDA reports)
RESPIRATORY ARREST ( 37 FDA reports)
ABNORMAL DREAMS ( 36 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 36 FDA reports)
CRYING ( 36 FDA reports)
DEVICE MALFUNCTION ( 36 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 36 FDA reports)
EYE DISORDER ( 36 FDA reports)
FAILURE TO THRIVE ( 36 FDA reports)
FIBROMYALGIA ( 36 FDA reports)
LEFT ATRIAL DILATATION ( 36 FDA reports)
MUCOSAL INFLAMMATION ( 36 FDA reports)
ORAL DISORDER ( 36 FDA reports)
RESPIRATORY DISORDER ( 36 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 36 FDA reports)
THYROID NEOPLASM ( 36 FDA reports)
TOOTH INFECTION ( 36 FDA reports)
BONE LOSS ( 35 FDA reports)
COMPRESSION FRACTURE ( 35 FDA reports)
DEBRIDEMENT ( 35 FDA reports)
DYSGEUSIA ( 35 FDA reports)
ENDOTRACHEAL INTUBATION ( 35 FDA reports)
HEPATIC LESION ( 35 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 35 FDA reports)
MITRAL VALVE PROLAPSE ( 35 FDA reports)
ONYCHOMYCOSIS ( 35 FDA reports)
SEBORRHOEIC KERATOSIS ( 35 FDA reports)
SEPTIC SHOCK ( 35 FDA reports)
BLINDNESS ( 34 FDA reports)
BREATH SOUNDS ABNORMAL ( 34 FDA reports)
CARDIOVASCULAR DISORDER ( 34 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 34 FDA reports)
INJECTION SITE HAEMATOMA ( 34 FDA reports)
ISCHAEMIC STROKE ( 34 FDA reports)
KNEE ARTHROPLASTY ( 34 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 34 FDA reports)
SLEEP DISORDER ( 34 FDA reports)
TARDIVE DYSKINESIA ( 34 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 34 FDA reports)
VENOUS INSUFFICIENCY ( 34 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 33 FDA reports)
RENAL INJURY ( 33 FDA reports)
RETINAL HAEMORRHAGE ( 33 FDA reports)
SHOULDER ARTHROPLASTY ( 33 FDA reports)
THYROID CANCER ( 33 FDA reports)
ALVEOLOPLASTY ( 32 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 32 FDA reports)
AORTIC ANEURYSM ( 32 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 32 FDA reports)
BACK DISORDER ( 32 FDA reports)
COGNITIVE DISORDER ( 32 FDA reports)
COMA ( 32 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 32 FDA reports)
DYSSTASIA ( 32 FDA reports)
HYPERSOMNIA ( 32 FDA reports)
HYPOACUSIS ( 32 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 32 FDA reports)
KYPHOSIS ( 32 FDA reports)
ONYCHOCLASIS ( 32 FDA reports)
ORAL INFECTION ( 32 FDA reports)
PANIC ATTACK ( 32 FDA reports)
PROSTATE CANCER ( 32 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 32 FDA reports)
SQUAMOUS CELL CARCINOMA ( 32 FDA reports)
VITAMIN D DEFICIENCY ( 32 FDA reports)
WALKING AID USER ( 32 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 31 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 31 FDA reports)
ANOREXIA ( 31 FDA reports)
BILE DUCT STENOSIS ( 31 FDA reports)
BLOOD URINE PRESENT ( 31 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 31 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 31 FDA reports)
FACE OEDEMA ( 31 FDA reports)
GYNAECOMASTIA ( 31 FDA reports)
INJECTION SITE HAEMORRHAGE ( 31 FDA reports)
IRON DEFICIENCY ANAEMIA ( 31 FDA reports)
LOBAR PNEUMONIA ( 31 FDA reports)
MUSCLE HAEMORRHAGE ( 31 FDA reports)
ORAL SURGERY ( 31 FDA reports)
PARKINSON'S DISEASE ( 31 FDA reports)
PHOTOPSIA ( 31 FDA reports)
PYELONEPHRITIS ( 31 FDA reports)
THYROID DISORDER ( 31 FDA reports)
VASCULAR CALCIFICATION ( 31 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 31 FDA reports)
ANAPHYLACTIC REACTION ( 30 FDA reports)
APNOEA ( 30 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
BLEPHARITIS ( 30 FDA reports)
BRUXISM ( 30 FDA reports)
CARDIAC VALVE DISEASE ( 30 FDA reports)
CERVICAL DYSPLASIA ( 30 FDA reports)
DILATATION ATRIAL ( 30 FDA reports)
FAECALOMA ( 30 FDA reports)
FAECES DISCOLOURED ( 30 FDA reports)
HEARING IMPAIRED ( 30 FDA reports)
HEMIPARESIS ( 30 FDA reports)
HUMERUS FRACTURE ( 30 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 30 FDA reports)
LABORATORY TEST ABNORMAL ( 30 FDA reports)
OTORRHOEA ( 30 FDA reports)
PLEURAL FIBROSIS ( 30 FDA reports)
PLEURITIC PAIN ( 30 FDA reports)
ADVERSE DRUG REACTION ( 29 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 29 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 29 FDA reports)
CEREBRAL ISCHAEMIA ( 29 FDA reports)
COLON CANCER ( 29 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 29 FDA reports)
DIASTOLIC DYSFUNCTION ( 29 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 29 FDA reports)
ERECTILE DYSFUNCTION ( 29 FDA reports)
FRACTURE ( 29 FDA reports)
MITRAL VALVE CALCIFICATION ( 29 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 29 FDA reports)
ULCER ( 29 FDA reports)
AORTIC STENOSIS ( 28 FDA reports)
ATAXIA ( 28 FDA reports)
BLOOD DISORDER ( 28 FDA reports)
BRAIN NEOPLASM ( 28 FDA reports)
DILATATION VENTRICULAR ( 28 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 28 FDA reports)
FEELING COLD ( 28 FDA reports)
FRACTURE NONUNION ( 28 FDA reports)
HYPERTENSIVE HEART DISEASE ( 28 FDA reports)
JOINT DISLOCATION ( 28 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 28 FDA reports)
MELAENA ( 28 FDA reports)
OESOPHAGEAL DISORDER ( 28 FDA reports)
PATHOLOGICAL FRACTURE ( 28 FDA reports)
SEQUESTRECTOMY ( 28 FDA reports)
SKIN DISORDER ( 28 FDA reports)
VARICOSE VEIN ( 28 FDA reports)
ADVERSE EVENT ( 27 FDA reports)
BLISTER ( 27 FDA reports)
DIABETIC RETINOPATHY ( 27 FDA reports)
GASTRIC ULCER ( 27 FDA reports)
GINGIVAL SWELLING ( 27 FDA reports)
HOSPITALISATION ( 27 FDA reports)
LOW TURNOVER OSTEOPATHY ( 27 FDA reports)
MYELODYSPLASTIC SYNDROME ( 27 FDA reports)
PHARYNGITIS ( 27 FDA reports)
PIGMENTATION DISORDER ( 27 FDA reports)
PNEUMONIA ASPIRATION ( 27 FDA reports)
RENAL PAIN ( 27 FDA reports)
TOOTH ABSCESS ( 27 FDA reports)
VITREOUS FLOATERS ( 27 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 26 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 26 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 26 FDA reports)
COLD SWEAT ( 26 FDA reports)
CRANIOTOMY ( 26 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 26 FDA reports)
DYSLIPIDAEMIA ( 26 FDA reports)
EXERCISE TOLERANCE DECREASED ( 26 FDA reports)
GRAND MAL CONVULSION ( 26 FDA reports)
INTERMITTENT CLAUDICATION ( 26 FDA reports)
JAW OPERATION ( 26 FDA reports)
LIGAMENT SPRAIN ( 26 FDA reports)
NIGHT SWEATS ( 26 FDA reports)
PHLEBITIS ( 26 FDA reports)
SUICIDE ATTEMPT ( 26 FDA reports)
TEMPERATURE INTOLERANCE ( 26 FDA reports)
THYROIDECTOMY ( 26 FDA reports)
TOOTH REPAIR ( 26 FDA reports)
VENTRICULAR HYPOKINESIA ( 26 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 26 FDA reports)
ATRIOVENTRICULAR BLOCK ( 25 FDA reports)
BLOOD CALCIUM DECREASED ( 25 FDA reports)
COAGULOPATHY ( 25 FDA reports)
DEVICE FAILURE ( 25 FDA reports)
EAR PAIN ( 25 FDA reports)
INTRACRANIAL ANEURYSM ( 25 FDA reports)
JOINT INJURY ( 25 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 25 FDA reports)
METABOLIC ACIDOSIS ( 25 FDA reports)
NOCTURIA ( 25 FDA reports)
PSORIASIS ( 25 FDA reports)
SPINAL FRACTURE ( 25 FDA reports)
SPLENOMEGALY ( 25 FDA reports)
VASODILATATION ( 25 FDA reports)
BLOOD IRON DECREASED ( 24 FDA reports)
BODY HEIGHT DECREASED ( 24 FDA reports)
BREATH ODOUR ( 24 FDA reports)
CATARACT OPERATION ( 24 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 24 FDA reports)
DRUG ADMINISTRATION ERROR ( 24 FDA reports)
HALLUCINATION, VISUAL ( 24 FDA reports)
INCREASED TENDENCY TO BRUISE ( 24 FDA reports)
LUMBAR RADICULOPATHY ( 24 FDA reports)
MOOD SWINGS ( 24 FDA reports)
NEURITIS ( 24 FDA reports)
PHARYNGEAL OEDEMA ( 24 FDA reports)
SKIN ATROPHY ( 24 FDA reports)
SPINAL COLUMN INJURY ( 24 FDA reports)
STOMATITIS NECROTISING ( 24 FDA reports)
VENOUS THROMBOSIS LIMB ( 24 FDA reports)
ADRENAL INSUFFICIENCY ( 23 FDA reports)
BIOPSY ( 23 FDA reports)
BODY TEMPERATURE INCREASED ( 23 FDA reports)
CARDIOGENIC SHOCK ( 23 FDA reports)
DERMATITIS CONTACT ( 23 FDA reports)
DEVICE RELATED INFECTION ( 23 FDA reports)
ECZEMA ( 23 FDA reports)
ELECTROLYTE IMBALANCE ( 23 FDA reports)
FAECAL INCONTINENCE ( 23 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 23 FDA reports)
HEPATIC CIRRHOSIS ( 23 FDA reports)
HYPOKINESIA ( 23 FDA reports)
INJECTION SITE ERYTHEMA ( 23 FDA reports)
JOINT EFFUSION ( 23 FDA reports)
LACERATION ( 23 FDA reports)
LARYNGEAL OEDEMA ( 23 FDA reports)
LYMPHOMA ( 23 FDA reports)
MALIGNANT MELANOMA ( 23 FDA reports)
MECHANICAL VENTILATION ( 23 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 23 FDA reports)
PULMONARY FIBROSIS ( 23 FDA reports)
RASH PRURITIC ( 23 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
SENSATION OF HEAVINESS ( 23 FDA reports)
SOCIAL PROBLEM ( 23 FDA reports)
THROAT IRRITATION ( 23 FDA reports)
VENOUS THROMBOSIS ( 23 FDA reports)
ABDOMINAL PAIN LOWER ( 22 FDA reports)
ANGER ( 22 FDA reports)
BLOOD ALBUMIN DECREASED ( 22 FDA reports)
CATHETERISATION CARDIAC ( 22 FDA reports)
CEREBRAL INFARCTION ( 22 FDA reports)
CHOLECYSTITIS CHRONIC ( 22 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 22 FDA reports)
FEBRILE NEUTROPENIA ( 22 FDA reports)
HYPERCOAGULATION ( 22 FDA reports)
LYMPHOEDEMA ( 22 FDA reports)
MEDICATION ERROR ( 22 FDA reports)
MENINGIOMA ( 22 FDA reports)
MUSCLE ATROPHY ( 22 FDA reports)
NEPHROGENIC ANAEMIA ( 22 FDA reports)
PANCREATITIS ACUTE ( 22 FDA reports)
PARANOIA ( 22 FDA reports)
PROTEIN URINE PRESENT ( 22 FDA reports)
RETCHING ( 22 FDA reports)
SEASONAL ALLERGY ( 22 FDA reports)
SENSORY LOSS ( 22 FDA reports)
SHOCK ( 22 FDA reports)
SPINAL CORD COMPRESSION ( 22 FDA reports)
THINKING ABNORMAL ( 22 FDA reports)
THROAT TIGHTNESS ( 22 FDA reports)
VIITH NERVE PARALYSIS ( 22 FDA reports)
COLITIS ISCHAEMIC ( 21 FDA reports)
DRY EYE ( 21 FDA reports)
DYSTONIA ( 21 FDA reports)
EAR CONGESTION ( 21 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 21 FDA reports)
EPICONDYLITIS ( 21 FDA reports)
HEART INJURY ( 21 FDA reports)
HEPATOMEGALY ( 21 FDA reports)
HYPOAESTHESIA ORAL ( 21 FDA reports)
IMPAIRED WORK ABILITY ( 21 FDA reports)
INTRACARDIAC THROMBUS ( 21 FDA reports)
LOWER LIMB FRACTURE ( 21 FDA reports)
MIDDLE INSOMNIA ( 21 FDA reports)
MUCOSAL ULCERATION ( 21 FDA reports)
MULTIPLE SCLEROSIS ( 21 FDA reports)
NEOPLASM PROGRESSION ( 21 FDA reports)
PLEURISY ( 21 FDA reports)
POLYNEUROPATHY ( 21 FDA reports)
RETINAL VEIN OCCLUSION ( 21 FDA reports)
RHINITIS ( 21 FDA reports)
SERUM FERRITIN INCREASED ( 21 FDA reports)
SPUTUM DISCOLOURED ( 21 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 21 FDA reports)
TEMPORAL ARTERITIS ( 21 FDA reports)
TOOTH DISORDER ( 21 FDA reports)
TRACHEAL DEVIATION ( 21 FDA reports)
TROPONIN INCREASED ( 21 FDA reports)
UPPER LIMB FRACTURE ( 21 FDA reports)
VENTRICULAR HYPERTROPHY ( 21 FDA reports)
VISUAL FIELD DEFECT ( 21 FDA reports)
X-RAY ABNORMAL ( 21 FDA reports)
ANGIOEDEMA ( 20 FDA reports)
APPLICATION SITE PRURITUS ( 20 FDA reports)
AUTONOMIC NEUROPATHY ( 20 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
BONE MARROW TRANSPLANT ( 20 FDA reports)
BREAST HYPERPLASIA ( 20 FDA reports)
BRONCHIECTASIS ( 20 FDA reports)
BRONCHOSPASM ( 20 FDA reports)
CAROTID ARTERY OCCLUSION ( 20 FDA reports)
COLON ADENOMA ( 20 FDA reports)
CROHN'S DISEASE ( 20 FDA reports)
DEAFNESS NEUROSENSORY ( 20 FDA reports)
DEMENTIA WITH LEWY BODIES ( 20 FDA reports)
DENTAL OPERATION ( 20 FDA reports)
DERMATOPHYTOSIS ( 20 FDA reports)
FIBROMA ( 20 FDA reports)
GASTRIC DISORDER ( 20 FDA reports)
GASTROENTERITIS VIRAL ( 20 FDA reports)
HEARING DISABILITY ( 20 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 20 FDA reports)
JOINT STIFFNESS ( 20 FDA reports)
JUGULAR VEIN DISTENSION ( 20 FDA reports)
MICTURITION URGENCY ( 20 FDA reports)
MOVEMENT DISORDER ( 20 FDA reports)
NECK INJURY ( 20 FDA reports)
NEUTROPENIC SEPSIS ( 20 FDA reports)
OCCULT BLOOD POSITIVE ( 20 FDA reports)
OEDEMA MOUTH ( 20 FDA reports)
OLFACTORY NERVE DISORDER ( 20 FDA reports)
OSTEOLYSIS ( 20 FDA reports)
PERIPHERAL COLDNESS ( 20 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 20 FDA reports)
PNEUMOTHORAX ( 20 FDA reports)
POOR DENTAL CONDITION ( 20 FDA reports)
POST PROCEDURAL COMPLICATION ( 20 FDA reports)
SEDATION ( 20 FDA reports)
SENSITIVITY OF TEETH ( 20 FDA reports)
SKELETAL INJURY ( 20 FDA reports)
SUBDURAL HAEMATOMA ( 20 FDA reports)
TOURETTE'S DISORDER ( 20 FDA reports)
UMBILICAL HERNIA ( 20 FDA reports)
VITAMIN D DECREASED ( 20 FDA reports)
BACTERIAL INFECTION ( 19 FDA reports)
BONE OPERATION ( 19 FDA reports)
CERVICAL CORD COMPRESSION ( 19 FDA reports)
CHOKING ( 19 FDA reports)
CONDUCTION DISORDER ( 19 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 19 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 19 FDA reports)
GENITAL HERPES ( 19 FDA reports)
HISTOPLASMOSIS ( 19 FDA reports)
HYPOPHOSPHATAEMIA ( 19 FDA reports)
HYPOTONIA ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
ISCHAEMIA ( 19 FDA reports)
MENTAL IMPAIRMENT ( 19 FDA reports)
METASTASES TO LIVER ( 19 FDA reports)
NON-CARDIAC CHEST PAIN ( 19 FDA reports)
PELVIC PAIN ( 19 FDA reports)
RASH GENERALISED ( 19 FDA reports)
RASH MACULAR ( 19 FDA reports)
RESPIRATORY TRACT INFECTION ( 19 FDA reports)
RHONCHI ( 19 FDA reports)
SPINAL LAMINECTOMY ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
UTERINE LEIOMYOMA ( 19 FDA reports)
VENTRICULAR FIBRILLATION ( 19 FDA reports)
WOUND ( 19 FDA reports)
WRIST FRACTURE ( 19 FDA reports)
AFFECTIVE DISORDER ( 18 FDA reports)
BLOOD MAGNESIUM DECREASED ( 18 FDA reports)
BREAST CANCER FEMALE ( 18 FDA reports)
CIRCULATORY COLLAPSE ( 18 FDA reports)
COLON POLYPECTOMY ( 18 FDA reports)
EXCORIATION ( 18 FDA reports)
GASTRIC POLYPS ( 18 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 18 FDA reports)
HIP ARTHROPLASTY ( 18 FDA reports)
HYPOGONADISM ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
LUNG INFECTION ( 18 FDA reports)
MENISCUS LESION ( 18 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 18 FDA reports)
PATHOLOGICAL GAMBLING ( 18 FDA reports)
RECTAL POLYP ( 18 FDA reports)
RIGHT ATRIAL DILATATION ( 18 FDA reports)
SNORING ( 18 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 18 FDA reports)
VAGINAL HAEMORRHAGE ( 18 FDA reports)
VISUAL DISTURBANCE ( 18 FDA reports)
ABDOMINAL HERNIA ( 17 FDA reports)
ABNORMAL BEHAVIOUR ( 17 FDA reports)
ACUTE CORONARY SYNDROME ( 17 FDA reports)
BIOPSY BONE ABNORMAL ( 17 FDA reports)
CARDIAC FAILURE CHRONIC ( 17 FDA reports)
DERMAL CYST ( 17 FDA reports)
DERMATITIS ( 17 FDA reports)
FAMILY STRESS ( 17 FDA reports)
FIBROSIS ( 17 FDA reports)
FOOT DEFORMITY ( 17 FDA reports)
GLOSSODYNIA ( 17 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 17 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 17 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 17 FDA reports)
MAJOR DEPRESSION ( 17 FDA reports)
NERVOUS SYSTEM DISORDER ( 17 FDA reports)
NON-SMALL CELL LUNG CANCER ( 17 FDA reports)
OPEN WOUND ( 17 FDA reports)
OVERWEIGHT ( 17 FDA reports)
PALLOR ( 17 FDA reports)
RIGHT VENTRICULAR FAILURE ( 17 FDA reports)
SKIN LACERATION ( 17 FDA reports)
SUBCUTANEOUS ABSCESS ( 17 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
THIRST ( 17 FDA reports)
TRISMUS ( 17 FDA reports)
ABSCESS JAW ( 16 FDA reports)
ACETABULUM FRACTURE ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
AORTIC CALCIFICATION ( 16 FDA reports)
APHONIA ( 16 FDA reports)
BLOOD BILIRUBIN INCREASED ( 16 FDA reports)
BULLOUS LUNG DISEASE ( 16 FDA reports)
CAROTID ARTERY DISEASE ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
CYANOSIS ( 16 FDA reports)
EAR NEOPLASM ( 16 FDA reports)
EYE PAIN ( 16 FDA reports)
GINGIVAL ERYTHEMA ( 16 FDA reports)
GINGIVAL ULCERATION ( 16 FDA reports)
HEMIPLEGIA ( 16 FDA reports)
HOMICIDAL IDEATION ( 16 FDA reports)
HYPERAESTHESIA ( 16 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 16 FDA reports)
LIMB DISCOMFORT ( 16 FDA reports)
MACROGLOSSIA ( 16 FDA reports)
MACULAR DEGENERATION ( 16 FDA reports)
MUMPS ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
ORAL CANDIDIASIS ( 16 FDA reports)
PEPTIC ULCER ( 16 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 16 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 16 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 16 FDA reports)
PROCEDURAL PAIN ( 16 FDA reports)
PULSE ABSENT ( 16 FDA reports)
RADIATION ASSOCIATED PAIN ( 16 FDA reports)
RUBELLA ( 16 FDA reports)
SARCOIDOSIS ( 16 FDA reports)
SCARLET FEVER ( 16 FDA reports)
SLEEP TERROR ( 16 FDA reports)
TINNITUS ( 16 FDA reports)
TONGUE INJURY ( 16 FDA reports)
TYPE 1 DIABETES MELLITUS ( 16 FDA reports)
UROSEPSIS ( 16 FDA reports)
WEIGHT FLUCTUATION ( 16 FDA reports)
WOUND DRAINAGE ( 16 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 15 FDA reports)
AGGRESSION ( 15 FDA reports)
BLADDER CYST ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 15 FDA reports)
BRAIN OEDEMA ( 15 FDA reports)
BREAST CANCER METASTATIC ( 15 FDA reports)
CARDIOVERSION ( 15 FDA reports)
CEREBRAL HAEMORRHAGE ( 15 FDA reports)
CERUMEN IMPACTION ( 15 FDA reports)
CHOLECYSTITIS ACUTE ( 15 FDA reports)
COLONOSCOPY ABNORMAL ( 15 FDA reports)
CYSTOCELE ( 15 FDA reports)
DELUSION ( 15 FDA reports)
DRUG DEPENDENCE ( 15 FDA reports)
DRUG INTOLERANCE ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
ERUCTATION ( 15 FDA reports)
FEELING JITTERY ( 15 FDA reports)
FURUNCLE ( 15 FDA reports)
GINGIVAL DISORDER ( 15 FDA reports)
HUNGER ( 15 FDA reports)
HYPERMETABOLISM ( 15 FDA reports)
HYPOALBUMINAEMIA ( 15 FDA reports)
INJECTION SITE PRURITUS ( 15 FDA reports)
INTESTINAL MASS ( 15 FDA reports)
MUSCLE INJURY ( 15 FDA reports)
ORAL HERPES ( 15 FDA reports)
ORTHOSIS USER ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
PLATELET COUNT INCREASED ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
POLYURIA ( 15 FDA reports)
SKIN EXFOLIATION ( 15 FDA reports)
SPINAL FUSION SURGERY ( 15 FDA reports)
STOMACH DISCOMFORT ( 15 FDA reports)
SWOLLEN TONGUE ( 15 FDA reports)
THROMBOSIS IN DEVICE ( 15 FDA reports)
TRIGGER FINGER ( 15 FDA reports)
UTERINE HAEMORRHAGE ( 15 FDA reports)
VASCULITIS ( 15 FDA reports)
ABDOMINAL TENDERNESS ( 14 FDA reports)
ABSCESS ORAL ( 14 FDA reports)
APHASIA ( 14 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 14 FDA reports)
BIPOLAR DISORDER ( 14 FDA reports)
BLOOD CHLORIDE DECREASED ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 14 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 14 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 14 FDA reports)
CATHETER PLACEMENT ( 14 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
COLECTOMY ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
DRUG TOXICITY ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 14 FDA reports)
GANGRENE ( 14 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 14 FDA reports)
HAEMATEMESIS ( 14 FDA reports)
HAEMOPHILUS INFECTION ( 14 FDA reports)
HAEMORRHAGIC DIATHESIS ( 14 FDA reports)
HILAR LYMPHADENOPATHY ( 14 FDA reports)
HORDEOLUM ( 14 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 14 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 14 FDA reports)
INTESTINAL ULCER ( 14 FDA reports)
LARYNGITIS ( 14 FDA reports)
LIGAMENT INJURY ( 14 FDA reports)
LOCAL SWELLING ( 14 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 14 FDA reports)
METASTASES TO LARGE INTESTINE ( 14 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 14 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 14 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 14 FDA reports)
ORAL NEOPLASM BENIGN ( 14 FDA reports)
OTITIS EXTERNA ( 14 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 14 FDA reports)
PLANTAR FASCIITIS ( 14 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 14 FDA reports)
PROSTATE CANCER METASTATIC ( 14 FDA reports)
PSEUDOMONAS INFECTION ( 14 FDA reports)
RENAL ARTERY STENOSIS ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SPINAL CORD DISORDER ( 14 FDA reports)
TENDON RUPTURE ( 14 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 14 FDA reports)
VITAMIN B12 DEFICIENCY ( 14 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 13 FDA reports)
ACUTE PRERENAL FAILURE ( 13 FDA reports)
ANAEMIA POSTOPERATIVE ( 13 FDA reports)
APPLICATION SITE ERYTHEMA ( 13 FDA reports)
ARTERIOSPASM CORONARY ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 13 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 13 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 13 FDA reports)
CERVIX CARCINOMA ( 13 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 13 FDA reports)
CHEST X-RAY ABNORMAL ( 13 FDA reports)
CHRONIC FATIGUE SYNDROME ( 13 FDA reports)
DECREASED ACTIVITY ( 13 FDA reports)
DENTAL DISCOMFORT ( 13 FDA reports)
DRY SKIN ( 13 FDA reports)
ENCEPHALOMALACIA ( 13 FDA reports)
EXTRASYSTOLES ( 13 FDA reports)
FEELING GUILTY ( 13 FDA reports)
FOREIGN BODY ( 13 FDA reports)
FRUSTRATION ( 13 FDA reports)
HALLUCINATION, AUDITORY ( 13 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 13 FDA reports)
HERPES SIMPLEX ( 13 FDA reports)
HYPERTROPHY ( 13 FDA reports)
INFUSION RELATED REACTION ( 13 FDA reports)
INTESTINAL DILATATION ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
KLEBSIELLA TEST POSITIVE ( 13 FDA reports)
LIP DRY ( 13 FDA reports)
LOCALISED INFECTION ( 13 FDA reports)
MEDICATION RESIDUE ( 13 FDA reports)
MENSTRUATION IRREGULAR ( 13 FDA reports)
MUSCLE TWITCHING ( 13 FDA reports)
MYASTHENIA GRAVIS ( 13 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 13 FDA reports)
OCULAR HYPERAEMIA ( 13 FDA reports)
ORGAN FAILURE ( 13 FDA reports)
OSTEITIS DEFORMANS ( 13 FDA reports)
PARATHYROID TUMOUR BENIGN ( 13 FDA reports)
POOR PERSONAL HYGIENE ( 13 FDA reports)
POSTNASAL DRIP ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
RESPIRATORY RATE INCREASED ( 13 FDA reports)
RESPIRATORY TRACT CONGESTION ( 13 FDA reports)
SENSORY DISTURBANCE ( 13 FDA reports)
SNEEZING ( 13 FDA reports)
STEM CELL TRANSPLANT ( 13 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 13 FDA reports)
TENSION ( 13 FDA reports)
URINE OUTPUT DECREASED ( 13 FDA reports)
UTERINE CANCER ( 13 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 13 FDA reports)
ANISOCYTOSIS ( 12 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BACTERIAL TEST POSITIVE ( 12 FDA reports)
BONE CYST ( 12 FDA reports)
BREAST TENDERNESS ( 12 FDA reports)
BRONCHIAL SECRETION RETENTION ( 12 FDA reports)
CARDIAC FLUTTER ( 12 FDA reports)
CARDIAC SEPTAL DEFECT ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
CERVICAL SPINAL STENOSIS ( 12 FDA reports)
CHOLECYSTECTOMY ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CONNECTIVE TISSUE DISORDER ( 12 FDA reports)
DENTAL PULP DISORDER ( 12 FDA reports)
DIFFUSE VASCULITIS ( 12 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
EYE INJURY ( 12 FDA reports)
EYELID PTOSIS ( 12 FDA reports)
FEELING DRUNK ( 12 FDA reports)
HAEMANGIOMA OF LIVER ( 12 FDA reports)
HYPOVENTILATION ( 12 FDA reports)
HYSTERECTOMY ( 12 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 12 FDA reports)
LUDWIG ANGINA ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
NEPHROPATHY ( 12 FDA reports)
NO THERAPEUTIC RESPONSE ( 12 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 12 FDA reports)
OESOPHAGEAL STENOSIS ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
POLYCYSTIC OVARIES ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 12 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
RESPIRATORY DEPRESSION ( 12 FDA reports)
SINUS HEADACHE ( 12 FDA reports)
SINUS OPERATION ( 12 FDA reports)
SPINAL FUSION ACQUIRED ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
TENDON DISORDER ( 12 FDA reports)
TENOSYNOVITIS STENOSANS ( 12 FDA reports)
TONGUE ULCERATION ( 12 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 12 FDA reports)
VOCAL CORD PARALYSIS ( 12 FDA reports)
WITHDRAWAL SYNDROME ( 12 FDA reports)
ACUTE PULMONARY OEDEMA ( 11 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 11 FDA reports)
BREAST PAIN ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
BUNDLE BRANCH BLOCK ( 11 FDA reports)
CALCULUS URINARY ( 11 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
EAR INFECTION ( 11 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 11 FDA reports)
EYE HAEMORRHAGE ( 11 FDA reports)
EYE PRURITUS ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
FULL BLOOD COUNT DECREASED ( 11 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 11 FDA reports)
GLOSSITIS ( 11 FDA reports)
HAEMORRHAGIC ANAEMIA ( 11 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 11 FDA reports)
HAIR GROWTH ABNORMAL ( 11 FDA reports)
HEPATOJUGULAR REFLUX ( 11 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPERTHYROIDISM ( 11 FDA reports)
IMPLANT SITE INFECTION ( 11 FDA reports)
INJECTION SITE SWELLING ( 11 FDA reports)
LIGHT CHAIN ANALYSIS ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 11 FDA reports)
MANIA ( 11 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 11 FDA reports)
NEUROPATHY ( 11 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 11 FDA reports)
OBSTRUCTIVE UROPATHY ( 11 FDA reports)
OPEN REDUCTION OF FRACTURE ( 11 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 11 FDA reports)
OSTEOMALACIA ( 11 FDA reports)
PERIORBITAL OEDEMA ( 11 FDA reports)
PLASMACYTOSIS ( 11 FDA reports)
PROTEIN URINE ABSENT ( 11 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 11 FDA reports)
PULMONARY THROMBOSIS ( 11 FDA reports)
RADICAL MASTECTOMY ( 11 FDA reports)
RADICULAR PAIN ( 11 FDA reports)
RECTAL ULCER ( 11 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 11 FDA reports)
SCREAMING ( 11 FDA reports)
SKIN TIGHTNESS ( 11 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
ACTINOMYCES TEST POSITIVE ( 10 FDA reports)
ACUTE PSYCHOSIS ( 10 FDA reports)
AGEUSIA ( 10 FDA reports)
ANGIOPATHY ( 10 FDA reports)
AORTIC VALVE CALCIFICATION ( 10 FDA reports)
BLOOD FOLATE INCREASED ( 10 FDA reports)
BLOOD TEST ABNORMAL ( 10 FDA reports)
BONE MARROW OEDEMA ( 10 FDA reports)
BREAST CANCER IN SITU ( 10 FDA reports)
CARDIAC OPERATION ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
COELIAC DISEASE ( 10 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 10 FDA reports)
DIABETIC NEPHROPATHY ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 10 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 10 FDA reports)
ENTEROCOCCAL INFECTION ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FAT NECROSIS ( 10 FDA reports)
FIBULA FRACTURE ( 10 FDA reports)
GASTRIC BYPASS ( 10 FDA reports)
GASTROENTERITIS RADIATION ( 10 FDA reports)
GOUTY ARTHRITIS ( 10 FDA reports)
HYPERPHAGIA ( 10 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 10 FDA reports)
INCISIONAL DRAINAGE ( 10 FDA reports)
INGUINAL HERNIA ( 10 FDA reports)
INJECTION SITE REACTION ( 10 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 10 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 10 FDA reports)
JAUNDICE ( 10 FDA reports)
MENIERE'S DISEASE ( 10 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 10 FDA reports)
NEOPLASM ( 10 FDA reports)
OCCULT BLOOD ( 10 FDA reports)
ORAL INTAKE REDUCED ( 10 FDA reports)
POLYCYTHAEMIA ( 10 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 10 FDA reports)
PROCEDURAL COMPLICATION ( 10 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 10 FDA reports)
PYELOCALIECTASIS ( 10 FDA reports)
QRS AXIS ABNORMAL ( 10 FDA reports)
RADICULITIS LUMBOSACRAL ( 10 FDA reports)
RIB DEFORMITY ( 10 FDA reports)
SACROILIITIS ( 10 FDA reports)
SINUS ARRHYTHMIA ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
STRESS URINARY INCONTINENCE ( 10 FDA reports)
THORACOTOMY ( 10 FDA reports)
TUBERCULIN TEST POSITIVE ( 10 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 10 FDA reports)
VITAMIN B12 INCREASED ( 10 FDA reports)
ABDOMINAL ADHESIONS ( 9 FDA reports)
ACTINOMYCOSIS ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ADVERSE REACTION ( 9 FDA reports)
AMYLOIDOSIS ( 9 FDA reports)
ANAESTHETIC COMPLICATION ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANXIETY DISORDER ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BASEDOW'S DISEASE ( 9 FDA reports)
BEDRIDDEN ( 9 FDA reports)
BLOOD COUNT ABNORMAL ( 9 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 9 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 9 FDA reports)
BODY TEMPERATURE DECREASED ( 9 FDA reports)
BREAST MASS ( 9 FDA reports)
CHONDROCALCINOSIS ( 9 FDA reports)
CHROMATURIA ( 9 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 9 FDA reports)
COLLAPSE OF LUNG ( 9 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
DIABETIC COMPLICATION ( 9 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 9 FDA reports)
DIFFICULTY IN WALKING ( 9 FDA reports)
DISEASE RECURRENCE ( 9 FDA reports)
DRUG DISPENSING ERROR ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
EXCESSIVE EYE BLINKING ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
FACIAL PALSY ( 9 FDA reports)
FACTOR V LEIDEN MUTATION ( 9 FDA reports)
GALLBLADDER OPERATION ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
GRANULOMA ( 9 FDA reports)
HEART RATE ABNORMAL ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
HYPERVENTILATION ( 9 FDA reports)
INCISION SITE HAEMATOMA ( 9 FDA reports)
INJECTION SITE BRUISING ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 9 FDA reports)
LEG AMPUTATION ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
LOSS OF EMPLOYMENT ( 9 FDA reports)
LYMPHANGITIS ( 9 FDA reports)
MICROCYTIC ANAEMIA ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NEPHROSCLEROSIS ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
NO ADVERSE EVENT ( 9 FDA reports)
OESOPHAGEAL PAIN ( 9 FDA reports)
PANCREATIC CARCINOMA ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PARTNER STRESS ( 9 FDA reports)
PICKWICKIAN SYNDROME ( 9 FDA reports)
PITTING OEDEMA ( 9 FDA reports)
PROCTITIS ( 9 FDA reports)
PULMONARY GRANULOMA ( 9 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 9 FDA reports)
RADIUS FRACTURE ( 9 FDA reports)
RASH PAPULAR ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RENAL CANCER ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 9 FDA reports)
STENT PLACEMENT ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
SUBDURAL HAEMORRHAGE ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
TIC ( 9 FDA reports)
TUMOUR NECROSIS ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
URINARY TRACT DISORDER ( 9 FDA reports)
VASCULAR INSUFFICIENCY ( 9 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 9 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 9 FDA reports)
ABDOMINAL MASS ( 8 FDA reports)
ABDOMINAL WALL DISORDER ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
ANGIOPLASTY ( 8 FDA reports)
AORTIC VALVE STENOSIS ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
APPLICATION SITE RASH ( 8 FDA reports)
BILIARY DILATATION ( 8 FDA reports)
BLADDER CANCER ( 8 FDA reports)
BLADDER SPASM ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 8 FDA reports)
BLOODY DISCHARGE ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BRONCHOPNEUMONIA ( 8 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 8 FDA reports)
CEREBRAL PALSY ( 8 FDA reports)
CHOLECYSTITIS INFECTIVE ( 8 FDA reports)
COR PULMONALE ( 8 FDA reports)
CORNEAL DISORDER ( 8 FDA reports)
COSTOCHONDRITIS ( 8 FDA reports)
CUSHING'S SYNDROME ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DIABETIC KETOACIDOSIS ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
ENDOCARDITIS BACTERIAL ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
EPIGASTRIC DISCOMFORT ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
EXOPHTHALMOS ( 8 FDA reports)
FIBRIN D DIMER INCREASED ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
GINGIVAL BLEEDING ( 8 FDA reports)
HAND DEFORMITY ( 8 FDA reports)
HYDROPNEUMOTHORAX ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 8 FDA reports)
INFERTILITY ( 8 FDA reports)
INITIAL INSOMNIA ( 8 FDA reports)
INJECTION SITE MASS ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LARYNGITIS ALLERGIC ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
MALIGNANT HYPERTENSION ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
NECK MASS ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OPEN FRACTURE ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PATELLA FRACTURE ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PLATELET COUNT ABNORMAL ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
POLYMYALGIA RHEUMATICA ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
RECTOCELE ( 8 FDA reports)
REFLUX GASTRITIS ( 8 FDA reports)
RESPIRATION ABNORMAL ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
SEROMA ( 8 FDA reports)
SHOULDER PAIN ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
TIBIA FRACTURE ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 8 FDA reports)
VERTEBROPLASTY ( 8 FDA reports)
VOMITING PROJECTILE ( 8 FDA reports)
WHEELCHAIR USER ( 8 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 7 FDA reports)
ABDOMINAL PANNICULECTOMY ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ACNE ( 7 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
APHAGIA ( 7 FDA reports)
APPLICATION SITE VESICLES ( 7 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 7 FDA reports)
AUTOIMMUNE HEPATITIS ( 7 FDA reports)
BIPOLAR I DISORDER ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
BRAIN HERNIATION ( 7 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 7 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
COORDINATION ABNORMAL ( 7 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 7 FDA reports)
ENDOCARDITIS ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
EXTREMITY CONTRACTURE ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 7 FDA reports)
GRAVITATIONAL OEDEMA ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HAEMORRHAGIC STROKE ( 7 FDA reports)
HEPATIC CONGESTION ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HYPERKINESIA ( 7 FDA reports)
HYPERMAGNESAEMIA ( 7 FDA reports)
IMMUNE SYSTEM DISORDER ( 7 FDA reports)
INADEQUATE ANALGESIA ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
INTERTRIGO ( 7 FDA reports)
KERATITIS ( 7 FDA reports)
LACTOSE INTOLERANCE ( 7 FDA reports)
LAZINESS ( 7 FDA reports)
LIGAMENT DISORDER ( 7 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
MALIGNANT MELANOMA IN SITU ( 7 FDA reports)
MEDIASTINAL MASS ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
NAIL DISCOLOURATION ( 7 FDA reports)
NAIL DISORDER ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
OESOPHAGEAL SPASM ( 7 FDA reports)
OESOPHAGITIS ULCERATIVE ( 7 FDA reports)
ORAL DISCOMFORT ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PATHOGEN RESISTANCE ( 7 FDA reports)
PERIANAL ABSCESS ( 7 FDA reports)
PERIODONTAL INFECTION ( 7 FDA reports)
PERIODONTITIS ( 7 FDA reports)
POSTMENOPAUSE ( 7 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
RADIOTHERAPY ( 7 FDA reports)
RESPIRATORY ACIDOSIS ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
TENDON INJURY ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
TONGUE DISCOLOURATION ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 7 FDA reports)
URGE INCONTINENCE ( 7 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
UTERINE POLYP ( 7 FDA reports)
VERTEBRAL WEDGING ( 7 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 6 FDA reports)
ABDOMINAL WALL INFECTION ( 6 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ACCIDENT ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ADNEXA UTERI MASS ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ALCOHOL ABUSE ( 6 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 6 FDA reports)
ANURIA ( 6 FDA reports)
ARM AMPUTATION ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ARTHRITIS INFECTIVE ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
BIOPSY LIVER ABNORMAL ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BLOOD PRESSURE ABNORMAL ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 6 FDA reports)
BODY TINEA ( 6 FDA reports)
BREAST CANCER RECURRENT ( 6 FDA reports)
BRONCHITIS ACUTE ( 6 FDA reports)
BRONCHOPLEURAL FISTULA ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARBON DIOXIDE INCREASED ( 6 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 6 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 6 FDA reports)
CHRONIC HEPATITIS ( 6 FDA reports)
CHRONIC TONSILLITIS ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
CUSHINGOID ( 6 FDA reports)
DEVICE OCCLUSION ( 6 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 6 FDA reports)
EXTRASKELETAL OSSIFICATION ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
EYE INFLAMMATION ( 6 FDA reports)
EYE IRRITATION ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FEEDING TUBE COMPLICATION ( 6 FDA reports)
FEMORAL NECK FRACTURE ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
GASTRIC CANCER RECURRENT ( 6 FDA reports)
GASTRIC HAEMORRHAGE ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 6 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
HAEMANGIOMA ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HOSPICE CARE ( 6 FDA reports)
HYPERCAPNIA ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
IMPAIRED DRIVING ABILITY ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 6 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
METASTASES TO PELVIS ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MUSCULOSKELETAL DISORDER ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 6 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 6 FDA reports)
OEDEMA GENITAL ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
ORAL TORUS ( 6 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PANCREATIC DUCT STENOSIS ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PERIPHERAL NERVE INJURY ( 6 FDA reports)
PERITONSILLAR ABSCESS ( 6 FDA reports)
PLASMACYTOMA ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
POST LAMINECTOMY SYNDROME ( 6 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 6 FDA reports)
PROTHROMBIN TIME SHORTENED ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RENAL TUBULAR ACIDOSIS ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
RETINAL ARTERY THROMBOSIS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SCROTAL CYST ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
STRESS FRACTURE ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SWEAT GLAND DISORDER ( 6 FDA reports)
TONGUE BLACK HAIRY ( 6 FDA reports)
URINE FLOW DECREASED ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
VENTRICULAR DYSFUNCTION ( 6 FDA reports)
VENTRICULAR FAILURE ( 6 FDA reports)
ABDOMINAL INJURY ( 5 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 5 FDA reports)
ACUTE LEUKAEMIA ( 5 FDA reports)
ADRENAL DISORDER ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
AMENORRHOEA ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANOSMIA ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
AORTIC DISORDER ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
ARTERIAL DISORDER ( 5 FDA reports)
ARTERIOGRAM CORONARY ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 5 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 5 FDA reports)
BENIGN NEOPLASM OF SKIN ( 5 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD UREA ABNORMAL ( 5 FDA reports)
BONE GRAFT ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BRAIN OPERATION ( 5 FDA reports)
BREAST CANCER STAGE I ( 5 FDA reports)
BREAST INFECTION ( 5 FDA reports)
BRONCHIAL IRRITATION ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CENTRAL LINE INFECTION ( 5 FDA reports)
CEREBROVASCULAR DISORDER ( 5 FDA reports)
CHANGE OF BOWEL HABIT ( 5 FDA reports)
COLON CANCER STAGE I ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DEVICE INEFFECTIVE ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
DYSPAREUNIA ( 5 FDA reports)
DYSPLASIA ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
EMBOLISM ARTERIAL ( 5 FDA reports)
ENDOMETRIAL CANCER ( 5 FDA reports)
EPILEPSY ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
FAT EMBOLISM ( 5 FDA reports)
FEAR OF DEATH ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GASTRECTOMY ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HEMIANOPIA HOMONYMOUS ( 5 FDA reports)
HORMONE LEVEL ABNORMAL ( 5 FDA reports)
HYPERINSULINAEMIA ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INFUSION SITE PRURITUS ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
INTESTINAL ISCHAEMIA ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
INTRAOCULAR LENS IMPLANT ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MUSCLE CONTRACTURE ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NEOPLASM SKIN ( 5 FDA reports)
NEUROFIBROMATOSIS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
ORAL SOFT TISSUE DISORDER ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
OSTEOCHONDROSIS ( 5 FDA reports)
OSTEOMYELITIS CHRONIC ( 5 FDA reports)
OTITIS MEDIA ( 5 FDA reports)
OTITIS MEDIA ACUTE ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
OXYGEN SUPPLEMENTATION ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PAPULE ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PERITONEAL HAEMORRHAGE ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
POLYDIPSIA ( 5 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY VASCULAR DISORDER ( 5 FDA reports)
PYOGENIC GRANULOMA ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SALPINGITIS ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SINUS ARREST ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SPLENIC INFARCTION ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STEROID THERAPY ( 5 FDA reports)
SUPERINFECTION ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
URINE ABNORMALITY ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VASCULAR PSEUDOANEURYSM ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
ADNEXA UTERI CYST ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
APATHY ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
APPLICATION SITE PAIN ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTHROSCOPIC SURGERY ( 4 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BRAIN CANCER METASTATIC ( 4 FDA reports)
BRAIN DEATH ( 4 FDA reports)
BREAST ENLARGEMENT ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CALCULUS BLADDER ( 4 FDA reports)
CARCINOID TUMOUR PULMONARY ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CHLORACNE ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CHOREA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DIAPHRAGMATIC DISORDER ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DROOLING ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INFUSION SITE PAIN ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INJECTION SITE SCAB ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
JAW CYST ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEDIASTINAL DISORDER ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MOUTH INJURY ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
ORAL CAVITY FISTULA ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POSTICTAL STATE ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PSYCHOLOGICAL TRAUMA ( 4 FDA reports)
PULSE PRESSURE DECREASED ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
RETINAL VASCULAR OCCLUSION ( 4 FDA reports)
RETROPERITONEAL CANCER ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
SALIVA ALTERED ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SCROTAL ABSCESS ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SOLAR ELASTOSIS ( 4 FDA reports)
SPINAL DECOMPRESSION ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
SPUTUM PURULENT ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STERNAL FRACTURE ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRANSFUSION ( 4 FDA reports)
URETERIC OBSTRUCTION ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
VAGOTOMY ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
WEANING FAILURE ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACHLORHYDRIA ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALLOIMMUNISATION ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APPLICATION SITE DISCHARGE ( 3 FDA reports)
APPLICATION SITE SCAB ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTHROPOD STING ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
BALANOPOSTHITIS ( 3 FDA reports)
BIOPSY COLON ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIAC ABLATION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CLEFT PALATE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
DARK CIRCLES UNDER EYES ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DEVICE CONNECTION ISSUE ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC ULCER ( 3 FDA reports)
DISINHIBITION ( 3 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
ELECTROCARDIOGRAM ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
EPIDIDYMAL CYST ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRACTURE DISPLACEMENT ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GENITAL CANDIDIASIS ( 3 FDA reports)
GLOBULIN ABNORMAL ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
ILEAL STENOSIS ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INJECTION SITE CELLULITIS ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MASTITIS ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MENOPAUSE ( 3 FDA reports)
METASTASES TO OVARY ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MITRAL VALVE REPAIR ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NERVE BLOCK ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OVARIAN CANCER STAGE IV ( 3 FDA reports)
OXYGEN SATURATION ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PANCREAS LIPOMATOSIS ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRODUCT FORMULATION ISSUE ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROSTATIC OBSTRUCTION ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RADIATION PNEUMONITIS ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 3 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RENAL LIPOMATOSIS ( 3 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKULL X-RAY ABNORMAL ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SPINAL CORPECTOMY ( 3 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
THALASSAEMIA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THYROID CYST ( 3 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URETHRAL CANCER ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
UTERINE DISORDER ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VAGINAL LESION ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VEIN DISCOLOURATION ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE DESQUAMATION ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BONE DEFORMITY ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCIUM IONISED ABNORMAL ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
EISENMENGER'S SYNDROME ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPIPLOIC APPENDAGITIS ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
FIBROUS HISTIOCYTOMA ( 2 FDA reports)
FOETOR HEPATICUS ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ICHTHYOSIS ACQUIRED ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTED VARICOSE VEIN ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER OPERATION ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NAIL AVULSION ( 2 FDA reports)
NASAL ABSCESS ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL TURBINATE ABNORMALITY ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORCHIDECTOMY ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIDIVERTICULITIS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SCAN BRAIN ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SINOBRONCHITIS ( 2 FDA reports)
SINUS ANTROSTOMY ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE ARSENIC INCREASED ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
WEIGHT LOSS DIET ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACALCULIA ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL PAP SMEAR ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANDROGENS DECREASED ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM RENAL ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTIFICIAL URINARY SPHINCTER IMPLANT ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN MUSCLE NEOPLASM ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COELIAC ARTERY COMPRESSION SYNDROME ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE PSYCHOGENIC COMPLICATION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIURETIC THERAPY ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLECTOMY ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRANEURAL CYST ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYPHILIS TEST POSITIVE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON TRANSFER ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UNEVALUABLE INVESTIGATION ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE VISCOSITY INCREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO LABYRINTHINE ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)