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

DEATH ( 729 FDA reports)
PYREXIA ( 628 FDA reports)
PAIN ( 458 FDA reports)
ARTHRALGIA ( 414 FDA reports)
FALL ( 383 FDA reports)
INFLUENZA LIKE ILLNESS ( 338 FDA reports)
HEADACHE ( 333 FDA reports)
MYALGIA ( 330 FDA reports)
NAUSEA ( 307 FDA reports)
PAIN IN EXTREMITY ( 289 FDA reports)
BONE PAIN ( 278 FDA reports)
MALAISE ( 261 FDA reports)
CHILLS ( 259 FDA reports)
FATIGUE ( 249 FDA reports)
VOMITING ( 241 FDA reports)
DYSPNOEA ( 213 FDA reports)
ASTHENIA ( 207 FDA reports)
DIZZINESS ( 206 FDA reports)
BACK PAIN ( 189 FDA reports)
DIARRHOEA ( 158 FDA reports)
OEDEMA PERIPHERAL ( 156 FDA reports)
GAIT DISTURBANCE ( 144 FDA reports)
SURGERY ( 143 FDA reports)
FEELING ABNORMAL ( 135 FDA reports)
PAIN IN JAW ( 122 FDA reports)
SYNCOPE ( 120 FDA reports)
CEREBROVASCULAR ACCIDENT ( 114 FDA reports)
CHEST PAIN ( 113 FDA reports)
PNEUMONIA ( 113 FDA reports)
HYPOCALCAEMIA ( 103 FDA reports)
TREMOR ( 102 FDA reports)
HYPOTENSION ( 100 FDA reports)
JOINT SWELLING ( 99 FDA reports)
LOSS OF CONSCIOUSNESS ( 90 FDA reports)
OSTEONECROSIS OF JAW ( 88 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 86 FDA reports)
MUSCLE SPASMS ( 84 FDA reports)
OSTEONECROSIS ( 84 FDA reports)
EYE PAIN ( 79 FDA reports)
ABDOMINAL PAIN ( 78 FDA reports)
ABDOMINAL PAIN UPPER ( 78 FDA reports)
BLOOD CREATININE INCREASED ( 76 FDA reports)
HIP FRACTURE ( 75 FDA reports)
INFLAMMATION ( 75 FDA reports)
DECREASED APPETITE ( 73 FDA reports)
INSOMNIA ( 73 FDA reports)
TOOTHACHE ( 71 FDA reports)
MYOCARDIAL INFARCTION ( 70 FDA reports)
OCULAR HYPERAEMIA ( 68 FDA reports)
MUSCULAR WEAKNESS ( 67 FDA reports)
NECK PAIN ( 66 FDA reports)
RASH ( 66 FDA reports)
WEIGHT DECREASED ( 66 FDA reports)
ARRHYTHMIA ( 65 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 65 FDA reports)
RENAL FAILURE ( 65 FDA reports)
ATRIAL FIBRILLATION ( 64 FDA reports)
CARDIAC DISORDER ( 64 FDA reports)
URINARY TRACT INFECTION ( 63 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 62 FDA reports)
TOOTH EXTRACTION ( 62 FDA reports)
ERYTHEMA ( 59 FDA reports)
FRACTURE ( 59 FDA reports)
HYPERTENSION ( 59 FDA reports)
DRUG INEFFECTIVE ( 58 FDA reports)
BLOOD PRESSURE INCREASED ( 57 FDA reports)
INFLUENZA ( 57 FDA reports)
PALPITATIONS ( 56 FDA reports)
ABASIA ( 55 FDA reports)
SPINAL FRACTURE ( 55 FDA reports)
HYPERHIDROSIS ( 53 FDA reports)
MUSCULOSKELETAL PAIN ( 53 FDA reports)
NEOPLASM MALIGNANT ( 53 FDA reports)
FEMUR FRACTURE ( 52 FDA reports)
MOVEMENT DISORDER ( 51 FDA reports)
SOMNOLENCE ( 51 FDA reports)
WRIST FRACTURE ( 51 FDA reports)
CONFUSIONAL STATE ( 50 FDA reports)
BEDRIDDEN ( 49 FDA reports)
HYPOAESTHESIA ( 49 FDA reports)
PARAESTHESIA ( 49 FDA reports)
DISCOMFORT ( 48 FDA reports)
PRURITUS ( 47 FDA reports)
UPPER LIMB FRACTURE ( 46 FDA reports)
DEPRESSION ( 45 FDA reports)
FOOT FRACTURE ( 45 FDA reports)
VISUAL ACUITY REDUCED ( 45 FDA reports)
ABDOMINAL DISCOMFORT ( 44 FDA reports)
BURNING SENSATION ( 44 FDA reports)
SWELLING FACE ( 44 FDA reports)
DEHYDRATION ( 43 FDA reports)
RIB FRACTURE ( 43 FDA reports)
TACHYCARDIA ( 43 FDA reports)
BLOOD CALCIUM DECREASED ( 42 FDA reports)
HAEMOGLOBIN DECREASED ( 42 FDA reports)
INFECTION ( 42 FDA reports)
VISION BLURRED ( 42 FDA reports)
COUGH ( 41 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 41 FDA reports)
BONE DISORDER ( 40 FDA reports)
CARDIAC FAILURE ( 39 FDA reports)
CONVULSION ( 39 FDA reports)
HEART RATE INCREASED ( 38 FDA reports)
MIGRAINE ( 38 FDA reports)
VERTIGO ( 38 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 37 FDA reports)
DYSSTASIA ( 37 FDA reports)
CHEST DISCOMFORT ( 36 FDA reports)
LUNG NEOPLASM MALIGNANT ( 36 FDA reports)
SWELLING ( 36 FDA reports)
VISUAL IMPAIRMENT ( 36 FDA reports)
BREAST CANCER ( 35 FDA reports)
EYE IRRITATION ( 34 FDA reports)
LACRIMATION INCREASED ( 34 FDA reports)
ARTHRITIS ( 33 FDA reports)
BLOOD PRESSURE DECREASED ( 33 FDA reports)
ANAEMIA ( 32 FDA reports)
ANXIETY ( 32 FDA reports)
OSTEOARTHRITIS ( 32 FDA reports)
RENAL FAILURE ACUTE ( 32 FDA reports)
SPEECH DISORDER ( 32 FDA reports)
BALANCE DISORDER ( 31 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 30 FDA reports)
COLON CANCER ( 30 FDA reports)
DRY MOUTH ( 30 FDA reports)
GINGIVAL DISORDER ( 30 FDA reports)
JAW DISORDER ( 30 FDA reports)
PELVIC FRACTURE ( 30 FDA reports)
TOOTH DISORDER ( 30 FDA reports)
ASTHMA ( 29 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 29 FDA reports)
ANKLE FRACTURE ( 28 FDA reports)
CATARACT ( 28 FDA reports)
HAEMORRHAGE ( 28 FDA reports)
HIP SURGERY ( 28 FDA reports)
PHOTOPHOBIA ( 28 FDA reports)
SEPSIS ( 28 FDA reports)
TOOTH ABSCESS ( 28 FDA reports)
TOOTH LOSS ( 28 FDA reports)
ARTHROPATHY ( 27 FDA reports)
BODY TEMPERATURE INCREASED ( 27 FDA reports)
CIRCULATORY COLLAPSE ( 27 FDA reports)
EYE SWELLING ( 27 FDA reports)
FEELING COLD ( 27 FDA reports)
HYPOKINESIA ( 27 FDA reports)
LOOSE TOOTH ( 27 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 27 FDA reports)
RESPIRATORY FAILURE ( 27 FDA reports)
BLOOD UREA INCREASED ( 26 FDA reports)
CARDIAC ARREST ( 26 FDA reports)
CYSTITIS ( 26 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 26 FDA reports)
HERPES ZOSTER ( 26 FDA reports)
HIP ARTHROPLASTY ( 26 FDA reports)
NEPHROLITHIASIS ( 26 FDA reports)
OSTEOPOROSIS ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 25 FDA reports)
HEART RATE IRREGULAR ( 25 FDA reports)
HYPONATRAEMIA ( 25 FDA reports)
LOWER LIMB FRACTURE ( 25 FDA reports)
OEDEMA ( 25 FDA reports)
CATARACT OPERATION ( 24 FDA reports)
CONDITION AGGRAVATED ( 24 FDA reports)
HEAD INJURY ( 24 FDA reports)
ORAL PAIN ( 24 FDA reports)
URTICARIA ( 24 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 23 FDA reports)
BLOOD SODIUM DECREASED ( 23 FDA reports)
COMA ( 23 FDA reports)
HAEMATURIA ( 23 FDA reports)
HYPERSENSITIVITY ( 23 FDA reports)
LETHARGY ( 23 FDA reports)
PLEURAL EFFUSION ( 23 FDA reports)
PULMONARY EMBOLISM ( 23 FDA reports)
TINNITUS ( 23 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 23 FDA reports)
ACCIDENT ( 22 FDA reports)
APHASIA ( 22 FDA reports)
CONSTIPATION ( 22 FDA reports)
EYELID OEDEMA ( 22 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 22 FDA reports)
HAEMATOMA ( 22 FDA reports)
IMPAIRED HEALING ( 22 FDA reports)
LIMB DISCOMFORT ( 22 FDA reports)
LUNG DISORDER ( 22 FDA reports)
OSTEOMYELITIS ( 22 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 21 FDA reports)
CARDIO-RESPIRATORY ARREST ( 21 FDA reports)
EYE DISORDER ( 21 FDA reports)
GASTRITIS ( 21 FDA reports)
MUSCLE RIGIDITY ( 21 FDA reports)
RENAL PAIN ( 21 FDA reports)
RHEUMATOID ARTHRITIS ( 21 FDA reports)
THROMBOSIS ( 21 FDA reports)
VIRAL INFECTION ( 21 FDA reports)
BLISTER ( 20 FDA reports)
BONE DENSITY DECREASED ( 20 FDA reports)
DEAFNESS ( 20 FDA reports)
DYSURIA ( 20 FDA reports)
FEMORAL NECK FRACTURE ( 20 FDA reports)
GASTROINTESTINAL DISORDER ( 20 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 20 FDA reports)
HOT FLUSH ( 20 FDA reports)
INJURY ( 20 FDA reports)
SLEEP DISORDER ( 20 FDA reports)
SPINAL OPERATION ( 20 FDA reports)
CHROMATURIA ( 19 FDA reports)
DENTAL CARIES ( 19 FDA reports)
DISORIENTATION ( 19 FDA reports)
PARALYSIS ( 19 FDA reports)
POOR PERSONAL HYGIENE ( 19 FDA reports)
RENAL DISORDER ( 19 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
ROAD TRAFFIC ACCIDENT ( 19 FDA reports)
SPINAL COMPRESSION FRACTURE ( 19 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
BONE LESION ( 18 FDA reports)
CONJUNCTIVITIS ( 18 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 18 FDA reports)
DIPLOPIA ( 18 FDA reports)
DYSPEPSIA ( 18 FDA reports)
EAR PAIN ( 18 FDA reports)
FEELING HOT ( 18 FDA reports)
HALLUCINATION ( 18 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 18 FDA reports)
MOBILITY DECREASED ( 18 FDA reports)
NASOPHARYNGITIS ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 18 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 18 FDA reports)
ANGINA PECTORIS ( 17 FDA reports)
BLOOD POTASSIUM DECREASED ( 17 FDA reports)
BRADYCARDIA ( 17 FDA reports)
DEMENTIA ( 17 FDA reports)
DYSGEUSIA ( 17 FDA reports)
EYE INFLAMMATION ( 17 FDA reports)
KNEE ARTHROPLASTY ( 17 FDA reports)
OROPHARYNGEAL PAIN ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
URINARY INCONTINENCE ( 17 FDA reports)
WALKING AID USER ( 17 FDA reports)
WHEELCHAIR USER ( 17 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
CROHN'S DISEASE ( 16 FDA reports)
HYPOPHAGIA ( 16 FDA reports)
TETANY ( 16 FDA reports)
THROMBOCYTOPENIA ( 16 FDA reports)
ABNORMAL SENSATION IN EYE ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 15 FDA reports)
AMNESIA ( 15 FDA reports)
APHAGIA ( 15 FDA reports)
DELIRIUM ( 15 FDA reports)
DRUG INTERACTION ( 15 FDA reports)
EYE PRURITUS ( 15 FDA reports)
HEART RATE DECREASED ( 15 FDA reports)
ILEUS ( 15 FDA reports)
INFARCTION ( 15 FDA reports)
NERVOUS SYSTEM DISORDER ( 15 FDA reports)
PRESYNCOPE ( 15 FDA reports)
PURULENCE ( 15 FDA reports)
SALIVA ALTERED ( 15 FDA reports)
VITAMIN D DEFICIENCY ( 15 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 14 FDA reports)
DENTAL NECROSIS ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
ENDODONTIC PROCEDURE ( 14 FDA reports)
HAEMATEMESIS ( 14 FDA reports)
HAEMATOCRIT DECREASED ( 14 FDA reports)
IMMOBILE ( 14 FDA reports)
JOINT EFFUSION ( 14 FDA reports)
LIP SWELLING ( 14 FDA reports)
NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
POLLAKIURIA ( 14 FDA reports)
PROSTHESIS IMPLANTATION ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
RESPIRATORY DISORDER ( 14 FDA reports)
SPINAL DISORDER ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
URINARY RETENTION ( 14 FDA reports)
VEIN DISORDER ( 14 FDA reports)
BREAST MASS ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
CYST ( 13 FDA reports)
DYSARTHRIA ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
EXTRASYSTOLES ( 13 FDA reports)
HIATUS HERNIA ( 13 FDA reports)
JOINT STIFFNESS ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
NEURALGIA ( 13 FDA reports)
RADIUS FRACTURE ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
BLOOD URINE PRESENT ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
EYE OEDEMA ( 12 FDA reports)
FLANK PAIN ( 12 FDA reports)
HAEMORRHOIDS ( 12 FDA reports)
HEAD DISCOMFORT ( 12 FDA reports)
HYPOACUSIS ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
LEUKOCYTOSIS ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
POLYARTHRITIS ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
TENDERNESS ( 12 FDA reports)
THROAT TIGHTNESS ( 12 FDA reports)
VASCULITIS ( 12 FDA reports)
BLADDER DISORDER ( 11 FDA reports)
BLOOD PRESSURE ABNORMAL ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
COLD SWEAT ( 11 FDA reports)
COLECTOMY ( 11 FDA reports)
CONTUSION ( 11 FDA reports)
DRUG ADMINISTRATION ERROR ( 11 FDA reports)
EPILEPSY ( 11 FDA reports)
ERYSIPELAS ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
GLAUCOMA ( 11 FDA reports)
HAEMATOCHEZIA ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
INCOHERENT ( 11 FDA reports)
IRIDOCYCLITIS ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MENTAL DISORDER ( 11 FDA reports)
MONOPLEGIA ( 11 FDA reports)
MOUTH ULCERATION ( 11 FDA reports)
POLYMYALGIA RHEUMATICA ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
RHINITIS ( 11 FDA reports)
THYROID CANCER ( 11 FDA reports)
APPARENT DEATH ( 10 FDA reports)
CARDIAC FIBRILLATION ( 10 FDA reports)
CARDIAC PACEMAKER INSERTION ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
COMPRESSION FRACTURE ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 10 FDA reports)
DENTAL IMPLANTATION ( 10 FDA reports)
DEPRESSED MOOD ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
DISLOCATION OF VERTEBRA ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
FACIAL PALSY ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
GASTROENTERITIS ( 10 FDA reports)
GENERALISED ERYTHEMA ( 10 FDA reports)
GINGIVAL PAIN ( 10 FDA reports)
HYPERTHERMIA ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 10 FDA reports)
ORAL DISORDER ( 10 FDA reports)
PERICARDIAL EFFUSION ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
TRANSAMINASES INCREASED ( 10 FDA reports)
TUMOUR EXCISION ( 10 FDA reports)
URINE ANALYSIS ABNORMAL ( 10 FDA reports)
UVEITIS ( 10 FDA reports)
WHEEZING ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
BLOOD ALBUMIN DECREASED ( 9 FDA reports)
BLOOD ALBUMIN INCREASED ( 9 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 9 FDA reports)
BONE FISSURE ( 9 FDA reports)
BONE OPERATION ( 9 FDA reports)
BONE SWELLING ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
CHOLECYSTITIS ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
DEVICE FAILURE ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
DIVERTICULITIS ( 9 FDA reports)
HAND FRACTURE ( 9 FDA reports)
HEMIPLEGIA ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
HYPOAESTHESIA ORAL ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
INJECTION SITE SWELLING ( 9 FDA reports)
IRITIS ( 9 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
METASTASES TO LIVER ( 9 FDA reports)
MULTIPLE FRACTURES ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
OROPHARYNGEAL BLISTERING ( 9 FDA reports)
PELVIC PAIN ( 9 FDA reports)
RENAL TUBULAR NECROSIS ( 9 FDA reports)
RETCHING ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
STRESS FRACTURE ( 9 FDA reports)
THIRST ( 9 FDA reports)
THYROID OPERATION ( 9 FDA reports)
TIBIA FRACTURE ( 9 FDA reports)
TRISMUS ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
VITREOUS DETACHMENT ( 9 FDA reports)
WOUND ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
BRAIN NEOPLASM ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
COLITIS ( 8 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 8 FDA reports)
DENTAL OPERATION ( 8 FDA reports)
EYE HAEMORRHAGE ( 8 FDA reports)
FACIAL PAIN ( 8 FDA reports)
FIBULA FRACTURE ( 8 FDA reports)
FLUID INTAKE REDUCED ( 8 FDA reports)
GINGIVAL INFECTION ( 8 FDA reports)
HYPERTHYROIDISM ( 8 FDA reports)
IMPAIRED WORK ABILITY ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
JOINT ARTHROPLASTY ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
LIMB OPERATION ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
LYMPHOPENIA ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
NEOPLASM ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PARAESTHESIA ORAL ( 8 FDA reports)
PERIODONTAL DISEASE ( 8 FDA reports)
PERIPHERAL NERVE LESION ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
PRURITUS GENERALISED ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SHOULDER OPERATION ( 8 FDA reports)
SKIN BURNING SENSATION ( 8 FDA reports)
SPINAL CORD COMPRESSION ( 8 FDA reports)
SPINAL OSTEOARTHRITIS ( 8 FDA reports)
SYNOVITIS ( 8 FDA reports)
TENDON PAIN ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
APHTHOUS STOMATITIS ( 7 FDA reports)
APTYALISM ( 7 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
BLOOD BICARBONATE DECREASED ( 7 FDA reports)
BLOOD CALCIUM INCREASED ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
FACE OEDEMA ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
GOUT ( 7 FDA reports)
GROIN PAIN ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
KIDNEY INFECTION ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
OSTEITIS ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PERIODONTITIS ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PO2 INCREASED ( 7 FDA reports)
POSTURE ABNORMAL ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
RENAL CYST ( 7 FDA reports)
RENAL INJURY ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SEQUESTRECTOMY ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VITAMIN D DECREASED ( 7 FDA reports)
VOLVULUS ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ACUTE PHASE REACTION ( 6 FDA reports)
AGITATION ( 6 FDA reports)
BED REST ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD CHLORIDE DECREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CAST APPLICATION ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CHONDROCALCINOSIS ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
FRACTURED SACRUM ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
GINGIVAL RECESSION ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
KNEE OPERATION ( 6 FDA reports)
LIP PAIN ( 6 FDA reports)
LYME DISEASE ( 6 FDA reports)
MASS ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OESOPHAGEAL DISORDER ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PARKINSON'S DISEASE ( 6 FDA reports)
PARKINSONISM ( 6 FDA reports)
PATHOLOGICAL FRACTURE ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL SURGERY ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SCLERODERMA ( 6 FDA reports)
SCOLIOSIS ( 6 FDA reports)
SENSITIVITY OF TEETH ( 6 FDA reports)
SKIN DISORDER ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
STRESS ( 6 FDA reports)
SYNOVIAL CYST ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
THROAT IRRITATION ( 6 FDA reports)
TOOTH INFECTION ( 6 FDA reports)
TUNNEL VISION ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
X-RAY DENTAL ( 6 FDA reports)
APATHY ( 5 FDA reports)
APHONIA ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD HEAVY METAL INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BONE ABSCESS ( 5 FDA reports)
BREAST TENDERNESS ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHELATION THERAPY ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DEAFNESS NEUROSENSORY ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXTRAVASATION ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
GINGIVAL SWELLING ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HUMERUS FRACTURE ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
HYPOCHROMASIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
MASTECTOMY ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MONOPARESIS ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
NODULE ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
OSTEOSYNTHESIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
POLYCHROMASIA ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
POSTOPERATIVE ADHESION ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RESUSCITATION ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SALIVA ANALYSIS ABNORMAL ( 5 FDA reports)
SALIVARY GLAND DISORDER ( 5 FDA reports)
SCAR ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SPINAL DEFORMITY ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
THROMBOPHLEBITIS ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
YAWNING ( 5 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ANURIA ( 4 FDA reports)
AORTIC OCCLUSION ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 4 FDA reports)
ARTHRITIS REACTIVE ( 4 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 4 FDA reports)
BIOPSY BONE ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CALCIUM METABOLISM DISORDER ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CAROTID ARTERY BYPASS ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CATHETERISATION CARDIAC ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONJUNCTIVAL DISORDER ( 4 FDA reports)
DENTAL CLEANING ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFUSION SITE EXTRAVASATION ( 4 FDA reports)
INJECTION SITE EXTRAVASATION ( 4 FDA reports)
INJECTION SITE INJURY ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTESTINAL OPERATION ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MILIA ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NECROTISING ULCERATIVE PERIODONTITIS ( 4 FDA reports)
NEPHROSTOMY ( 4 FDA reports)
NERVE ROOT COMPRESSION ( 4 FDA reports)
NEUROGENIC SHOCK ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OPHTHALMOPLEGIA ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PAROPHTHALMIA ( 4 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SACROILIITIS ( 4 FDA reports)
SALIVARY GLAND MASS ( 4 FDA reports)
SCAB ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPLINTER ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SUTURE INSERTION ( 4 FDA reports)
TENSION ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TROPONIN T INCREASED ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VASODILATATION ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
WRIST SURGERY ( 4 FDA reports)
ABDOMINAL OPERATION ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACROCHORDON ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ALBUMIN URINE ( 3 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BENIGN BONE NEOPLASM ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CYTOKINE RELEASE SYNDROME ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EOSINOPHILIC FASCIITIS ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACIAL NERVE DISORDER ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEAD AND NECK CANCER ( 3 FDA reports)
HEAD DEFORMITY ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HERNIA HIATUS REPAIR ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPLANT SITE PAIN ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIMB IMMOBILISATION ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
OSTEOCHONDRITIS ( 3 FDA reports)
OTOSCLEROSIS ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARATHYROID TUMOUR MALIGNANT ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
RALES ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SPINAL SUPPORT ( 3 FDA reports)
SPLINT APPLICATION ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBDURAL EFFUSION ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
ULCER ( 3 FDA reports)
UTERINE OPERATION ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VERTIGO LABYRINTHINE ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIRAEMIA ( 3 FDA reports)
VIRAL LABYRINTHITIS ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACUPUNCTURE ( 2 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ALOPECIA UNIVERSALIS ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANTERIOR CHAMBER DISORDER ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL BRUIT ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASPIRATION JOINT ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BONE CANCER METASTATIC ( 2 FDA reports)
BONE GRAFT LYSIS ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARTILAGE ATROPHY ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EVENTRATION PROCEDURE ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTRASKELETAL OSSIFICATION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FRACTURE TREATMENT ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GINGIVAL OPERATION ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILIAC ARTERY EMBOLISM ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLAMMATORY PAIN ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
LAPAROSCOPY ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIGAMENT OPERATION ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LUPUS VASCULITIS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHANGIOMA ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MACULAR FIBROSIS ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MANIA ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MASTOCYTOSIS ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MEDIAN NERVE INJURY ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
METASTASES TO LARGE INTESTINE ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASES TO STOMACH ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MOYAMOYA DISEASE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OSTEOMA ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHLEBITIS ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETROPERITONEAL CANCER ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SCIATIC NERVE NEUROPATHY ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL INTESTINAL RESECTION ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL CORD OPERATION ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUTURE REMOVAL ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TENDON SHEATH LESION EXCISION ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THERAPEUTIC ASPIRATION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROMBOEMBOLECTOMY ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TOOTH SOCKET SUTURE ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URETHRAL OPERATION ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VAGINAL PROLAPSE REPAIR ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY BONE MARROW ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURKHOLDERIA MALLEI INFECTION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CEMENTOBLASTOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CUPULOLITHIASIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR NEOPLASM ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOMETRIAL ABLATION ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR METAL TEST ABNORMAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRACRANIAL MENINGIOMA MALIGNANT ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY PERFORATION ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LATENT TETANY ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB PROSTHESIS USER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENISCUS OPERATION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MUIR-TORRE SYNDROME ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL CAVITY MASS ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PODAGRA ( 1 FDA reports)
PORCELAIN GALLBLADDER ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
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PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY LEVEL ABNORMAL ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
URETERIC CALCULUS REMOVAL ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE CALCIUM DECREASED ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE PHOSPHATE DECREASED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VERTEBRA DISLOCATION REDUCTION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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