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

DYSPNOEA ( 825 FDA reports)
NAUSEA ( 797 FDA reports)
DIZZINESS ( 678 FDA reports)
ASTHENIA ( 611 FDA reports)
PAIN ( 602 FDA reports)
ATRIAL FIBRILLATION ( 582 FDA reports)
FATIGUE ( 554 FDA reports)
COMPLETED SUICIDE ( 537 FDA reports)
OEDEMA PERIPHERAL ( 513 FDA reports)
HYPOTENSION ( 510 FDA reports)
VOMITING ( 497 FDA reports)
DIARRHOEA ( 455 FDA reports)
PNEUMONIA ( 432 FDA reports)
ANXIETY ( 413 FDA reports)
DRUG INEFFECTIVE ( 399 FDA reports)
FALL ( 394 FDA reports)
CHEST PAIN ( 390 FDA reports)
HYPERTENSION ( 367 FDA reports)
BRADYCARDIA ( 365 FDA reports)
RENAL FAILURE ( 365 FDA reports)
RENAL FAILURE ACUTE ( 362 FDA reports)
DRUG INTERACTION ( 351 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 347 FDA reports)
PYREXIA ( 338 FDA reports)
HEADACHE ( 335 FDA reports)
CARDIAC ARREST ( 334 FDA reports)
ARTHRALGIA ( 320 FDA reports)
ANAEMIA ( 309 FDA reports)
BACK PAIN ( 309 FDA reports)
WEIGHT DECREASED ( 299 FDA reports)
MALAISE ( 297 FDA reports)
PAIN IN EXTREMITY ( 293 FDA reports)
INJURY ( 289 FDA reports)
MYOCARDIAL INFARCTION ( 274 FDA reports)
DEATH ( 254 FDA reports)
DEHYDRATION ( 252 FDA reports)
ABDOMINAL PAIN ( 250 FDA reports)
COUGH ( 247 FDA reports)
GAIT DISTURBANCE ( 246 FDA reports)
BLOOD GLUCOSE INCREASED ( 243 FDA reports)
SYNCOPE ( 232 FDA reports)
DEPRESSION ( 230 FDA reports)
INSOMNIA ( 229 FDA reports)
HEART RATE INCREASED ( 224 FDA reports)
PRURITUS ( 223 FDA reports)
CONFUSIONAL STATE ( 220 FDA reports)
CEREBROVASCULAR ACCIDENT ( 219 FDA reports)
PALPITATIONS ( 218 FDA reports)
CONSTIPATION ( 216 FDA reports)
BLOOD PRESSURE INCREASED ( 212 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 211 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 208 FDA reports)
WEIGHT INCREASED ( 205 FDA reports)
HAEMOGLOBIN DECREASED ( 199 FDA reports)
SOMNOLENCE ( 198 FDA reports)
RASH ( 190 FDA reports)
LOSS OF CONSCIOUSNESS ( 188 FDA reports)
MYALGIA ( 188 FDA reports)
ABDOMINAL PAIN UPPER ( 185 FDA reports)
DECREASED APPETITE ( 185 FDA reports)
CONDITION AGGRAVATED ( 183 FDA reports)
BLOOD CREATININE INCREASED ( 181 FDA reports)
FEELING ABNORMAL ( 180 FDA reports)
EMOTIONAL DISTRESS ( 179 FDA reports)
TREMOR ( 176 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 172 FDA reports)
URINARY TRACT INFECTION ( 172 FDA reports)
HYPERHIDROSIS ( 170 FDA reports)
ECONOMIC PROBLEM ( 165 FDA reports)
FLUSHING ( 163 FDA reports)
RESPIRATORY FAILURE ( 163 FDA reports)
MULTIPLE DRUG OVERDOSE ( 160 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 159 FDA reports)
VISION BLURRED ( 159 FDA reports)
RENAL IMPAIRMENT ( 158 FDA reports)
HYPOAESTHESIA ( 157 FDA reports)
PARAESTHESIA ( 157 FDA reports)
RHABDOMYOLYSIS ( 157 FDA reports)
PLEURAL EFFUSION ( 156 FDA reports)
ARRHYTHMIA ( 151 FDA reports)
SEPSIS ( 149 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 148 FDA reports)
PULMONARY OEDEMA ( 146 FDA reports)
TACHYCARDIA ( 146 FDA reports)
DYSPEPSIA ( 145 FDA reports)
MUSCLE SPASMS ( 142 FDA reports)
UNEVALUABLE EVENT ( 142 FDA reports)
CORONARY ARTERY DISEASE ( 141 FDA reports)
MUSCULAR WEAKNESS ( 140 FDA reports)
ANHEDONIA ( 139 FDA reports)
CHEST DISCOMFORT ( 139 FDA reports)
OVERDOSE ( 139 FDA reports)
BLOOD PRESSURE DECREASED ( 134 FDA reports)
ABDOMINAL DISTENSION ( 131 FDA reports)
ERYTHEMA ( 129 FDA reports)
RESPIRATORY ARREST ( 128 FDA reports)
ASTHMA ( 125 FDA reports)
CONTUSION ( 123 FDA reports)
CARDIO-RESPIRATORY ARREST ( 121 FDA reports)
DIABETES MELLITUS ( 120 FDA reports)
DRUG TOXICITY ( 118 FDA reports)
OEDEMA ( 118 FDA reports)
CARDIAC DISORDER ( 117 FDA reports)
CARDIAC FAILURE ( 117 FDA reports)
HEART RATE DECREASED ( 117 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 115 FDA reports)
BRONCHITIS ( 113 FDA reports)
HYPERKALAEMIA ( 113 FDA reports)
HYPONATRAEMIA ( 108 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 108 FDA reports)
BALANCE DISORDER ( 107 FDA reports)
HYPOKALAEMIA ( 107 FDA reports)
MENTAL STATUS CHANGES ( 106 FDA reports)
THROMBOCYTOPENIA ( 106 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 105 FDA reports)
FEAR ( 105 FDA reports)
DRY MOUTH ( 103 FDA reports)
MULTI-ORGAN FAILURE ( 103 FDA reports)
STRESS ( 103 FDA reports)
CHILLS ( 102 FDA reports)
CONVULSION ( 102 FDA reports)
HEART RATE IRREGULAR ( 101 FDA reports)
HYPOGLYCAEMIA ( 101 FDA reports)
RECTAL HAEMORRHAGE ( 101 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 100 FDA reports)
INFECTION ( 100 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 98 FDA reports)
MULTIPLE INJURIES ( 98 FDA reports)
DYSPHAGIA ( 97 FDA reports)
HYPOXIA ( 95 FDA reports)
PLATELET COUNT DECREASED ( 95 FDA reports)
JOINT SWELLING ( 94 FDA reports)
SINUSITIS ( 94 FDA reports)
SWELLING ( 94 FDA reports)
CELLULITIS ( 93 FDA reports)
HYPERGLYCAEMIA ( 93 FDA reports)
OSTEOARTHRITIS ( 93 FDA reports)
HAEMORRHAGE ( 92 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 92 FDA reports)
ANGINA PECTORIS ( 91 FDA reports)
PRODUCT QUALITY ISSUE ( 91 FDA reports)
ABDOMINAL DISCOMFORT ( 90 FDA reports)
RENAL FAILURE CHRONIC ( 89 FDA reports)
WHEEZING ( 89 FDA reports)
ALOPECIA ( 88 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 88 FDA reports)
COMA ( 88 FDA reports)
DYSURIA ( 88 FDA reports)
PULMONARY EMBOLISM ( 88 FDA reports)
ATELECTASIS ( 87 FDA reports)
BLOOD UREA INCREASED ( 87 FDA reports)
NEUROPATHY PERIPHERAL ( 86 FDA reports)
OSTEONECROSIS OF JAW ( 86 FDA reports)
AMNESIA ( 85 FDA reports)
INCORRECT DOSE ADMINISTERED ( 85 FDA reports)
INTENTIONAL DRUG MISUSE ( 84 FDA reports)
POISONING ( 83 FDA reports)
CARDIOMEGALY ( 82 FDA reports)
DEEP VEIN THROMBOSIS ( 82 FDA reports)
PRESYNCOPE ( 82 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 82 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 82 FDA reports)
LETHARGY ( 81 FDA reports)
METABOLIC ACIDOSIS ( 81 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 80 FDA reports)
NERVOUSNESS ( 80 FDA reports)
FEELING HOT ( 79 FDA reports)
MITRAL VALVE INCOMPETENCE ( 79 FDA reports)
RENAL INJURY ( 79 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 78 FDA reports)
SINUS BRADYCARDIA ( 78 FDA reports)
VISUAL IMPAIRMENT ( 78 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 77 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 77 FDA reports)
TREATMENT NONCOMPLIANCE ( 77 FDA reports)
CHOLELITHIASIS ( 76 FDA reports)
HAEMATOCRIT DECREASED ( 75 FDA reports)
VENTRICULAR TACHYCARDIA ( 75 FDA reports)
CARDIOGENIC SHOCK ( 74 FDA reports)
EPISTAXIS ( 74 FDA reports)
MOBILITY DECREASED ( 74 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 74 FDA reports)
FLATULENCE ( 73 FDA reports)
PROTHROMBIN TIME PROLONGED ( 73 FDA reports)
ABASIA ( 71 FDA reports)
DYSPNOEA EXERTIONAL ( 71 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 70 FDA reports)
OROPHARYNGEAL PAIN ( 70 FDA reports)
OSTEOMYELITIS ( 70 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 69 FDA reports)
VERTIGO ( 69 FDA reports)
CATARACT ( 67 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 67 FDA reports)
MEDICATION ERROR ( 67 FDA reports)
SPINAL OSTEOARTHRITIS ( 67 FDA reports)
UNRESPONSIVE TO STIMULI ( 67 FDA reports)
BONE DISORDER ( 66 FDA reports)
ATRIAL FLUTTER ( 65 FDA reports)
BONE PAIN ( 65 FDA reports)
HYPERSENSITIVITY ( 65 FDA reports)
LEUKOCYTOSIS ( 65 FDA reports)
MEMORY IMPAIRMENT ( 65 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 65 FDA reports)
PANCYTOPENIA ( 64 FDA reports)
FLUID OVERLOAD ( 63 FDA reports)
INTENTIONAL OVERDOSE ( 63 FDA reports)
URTICARIA ( 63 FDA reports)
LUNG NEOPLASM MALIGNANT ( 62 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 62 FDA reports)
NECK PAIN ( 62 FDA reports)
TYPE 2 DIABETES MELLITUS ( 62 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 62 FDA reports)
HYPERLIPIDAEMIA ( 61 FDA reports)
HYPOPHAGIA ( 61 FDA reports)
INJECTION SITE PAIN ( 61 FDA reports)
PANCREATITIS ( 61 FDA reports)
DISORIENTATION ( 60 FDA reports)
PAIN IN JAW ( 60 FDA reports)
SINUS TACHYCARDIA ( 60 FDA reports)
DIVERTICULITIS ( 59 FDA reports)
DYSGEUSIA ( 59 FDA reports)
HAEMORRHOIDS ( 59 FDA reports)
HALLUCINATION ( 59 FDA reports)
VENTRICULAR FIBRILLATION ( 59 FDA reports)
AGITATION ( 58 FDA reports)
HYPOTHYROIDISM ( 58 FDA reports)
ILL-DEFINED DISORDER ( 58 FDA reports)
PULMONARY HYPERTENSION ( 58 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 58 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 57 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 57 FDA reports)
HEPATIC ENZYME INCREASED ( 57 FDA reports)
BURNING SENSATION ( 56 FDA reports)
FLUID RETENTION ( 56 FDA reports)
MYOCARDIAL ISCHAEMIA ( 56 FDA reports)
POLLAKIURIA ( 56 FDA reports)
SURGERY ( 56 FDA reports)
BLOOD POTASSIUM DECREASED ( 55 FDA reports)
SLEEP APNOEA SYNDROME ( 55 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 55 FDA reports)
DYSPHONIA ( 54 FDA reports)
NEUTROPENIA ( 54 FDA reports)
POST PROCEDURAL COMPLICATION ( 54 FDA reports)
THROMBOSIS ( 54 FDA reports)
BLOOD GLUCOSE DECREASED ( 53 FDA reports)
DRUG HYPERSENSITIVITY ( 53 FDA reports)
RHINORRHOEA ( 53 FDA reports)
SKIN DISCOLOURATION ( 53 FDA reports)
BLOOD POTASSIUM INCREASED ( 52 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 52 FDA reports)
HAEMATOCHEZIA ( 52 FDA reports)
OXYGEN SATURATION DECREASED ( 52 FDA reports)
SEPTIC SHOCK ( 52 FDA reports)
BLOOD URINE PRESENT ( 51 FDA reports)
DIALYSIS ( 51 FDA reports)
DYSARTHRIA ( 51 FDA reports)
OFF LABEL USE ( 51 FDA reports)
SPEECH DISORDER ( 51 FDA reports)
GASTRITIS ( 50 FDA reports)
HAEMODIALYSIS ( 50 FDA reports)
ANGINA UNSTABLE ( 49 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 49 FDA reports)
HAEMATURIA ( 49 FDA reports)
HERPES ZOSTER ( 49 FDA reports)
NASOPHARYNGITIS ( 49 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 49 FDA reports)
CORONARY ARTERY OCCLUSION ( 48 FDA reports)
DYSSTASIA ( 48 FDA reports)
EJECTION FRACTION DECREASED ( 48 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 48 FDA reports)
HEPATIC STEATOSIS ( 48 FDA reports)
MYOPATHY ( 48 FDA reports)
NODAL RHYTHM ( 48 FDA reports)
PULMONARY CONGESTION ( 48 FDA reports)
RESPIRATORY DISTRESS ( 48 FDA reports)
TORSADE DE POINTES ( 48 FDA reports)
ANOREXIA ( 47 FDA reports)
BLOOD BILIRUBIN INCREASED ( 47 FDA reports)
COAGULOPATHY ( 47 FDA reports)
DISEASE PROGRESSION ( 47 FDA reports)
HAEMATEMESIS ( 47 FDA reports)
HYPOCALCAEMIA ( 47 FDA reports)
SKIN INDURATION ( 47 FDA reports)
SWOLLEN TONGUE ( 47 FDA reports)
URINARY INCONTINENCE ( 47 FDA reports)
ABNORMAL DREAMS ( 46 FDA reports)
ARTHRITIS ( 46 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 46 FDA reports)
MELAENA ( 46 FDA reports)
MUSCULOSKELETAL PAIN ( 46 FDA reports)
SUICIDE ATTEMPT ( 46 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 46 FDA reports)
ARTERIOSCLEROSIS ( 45 FDA reports)
HIP FRACTURE ( 45 FDA reports)
HOT FLUSH ( 45 FDA reports)
NEOPLASM MALIGNANT ( 45 FDA reports)
PULMONARY FIBROSIS ( 45 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 44 FDA reports)
EMPHYSEMA ( 44 FDA reports)
OSTEOPENIA ( 44 FDA reports)
RENAL CYST ( 44 FDA reports)
SKIN LESION ( 44 FDA reports)
BREAST CANCER ( 43 FDA reports)
CYSTITIS ( 43 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 43 FDA reports)
INTERSTITIAL LUNG DISEASE ( 43 FDA reports)
ORTHOSTATIC HYPOTENSION ( 43 FDA reports)
PRODUCTIVE COUGH ( 43 FDA reports)
SKIN ULCER ( 43 FDA reports)
TOOTH EXTRACTION ( 43 FDA reports)
ACUTE RESPIRATORY FAILURE ( 42 FDA reports)
GOUT ( 42 FDA reports)
HEAD INJURY ( 42 FDA reports)
OSTEOPOROSIS ( 42 FDA reports)
SUICIDAL IDEATION ( 42 FDA reports)
CANDIDIASIS ( 41 FDA reports)
CHROMATURIA ( 41 FDA reports)
DRUG EFFECT DECREASED ( 41 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 41 FDA reports)
PERICARDIAL EFFUSION ( 41 FDA reports)
BLISTER ( 40 FDA reports)
BLOOD SODIUM DECREASED ( 40 FDA reports)
DEFORMITY ( 40 FDA reports)
DEMENTIA ( 40 FDA reports)
ERECTILE DYSFUNCTION ( 40 FDA reports)
FEELING COLD ( 40 FDA reports)
GASTROENTERITIS ( 40 FDA reports)
INTESTINAL OBSTRUCTION ( 40 FDA reports)
LUNG DISORDER ( 40 FDA reports)
LUNG INFILTRATION ( 40 FDA reports)
RHEUMATOID ARTHRITIS ( 40 FDA reports)
SHOCK ( 40 FDA reports)
STAPHYLOCOCCAL INFECTION ( 40 FDA reports)
TINNITUS ( 40 FDA reports)
ANURIA ( 39 FDA reports)
ARTERIOSPASM CORONARY ( 39 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 39 FDA reports)
CIRCULATORY COLLAPSE ( 39 FDA reports)
LEFT ATRIAL DILATATION ( 39 FDA reports)
URINARY RETENTION ( 39 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 38 FDA reports)
DRUG DOSE OMISSION ( 38 FDA reports)
ECCHYMOSIS ( 38 FDA reports)
FEBRILE NEUTROPENIA ( 38 FDA reports)
GASTRIC ULCER ( 38 FDA reports)
HEPATIC FAILURE ( 38 FDA reports)
INFLUENZA LIKE ILLNESS ( 38 FDA reports)
MIGRAINE ( 38 FDA reports)
NO THERAPEUTIC RESPONSE ( 38 FDA reports)
RENAL DISORDER ( 38 FDA reports)
ATRIOVENTRICULAR BLOCK ( 37 FDA reports)
CARDIAC MURMUR ( 37 FDA reports)
DRY SKIN ( 37 FDA reports)
PANIC ATTACK ( 37 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 36 FDA reports)
DYSKINESIA ( 36 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 36 FDA reports)
LYMPHADENOPATHY ( 36 FDA reports)
MALNUTRITION ( 36 FDA reports)
MESOTHELIOMA ( 36 FDA reports)
MULTIPLE MYELOMA ( 36 FDA reports)
ORAL PAIN ( 36 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 36 FDA reports)
STOMATITIS ( 36 FDA reports)
ARTHROPATHY ( 35 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 35 FDA reports)
CEREBRAL INFARCTION ( 35 FDA reports)
DELIRIUM ( 35 FDA reports)
DIVERTICULUM ( 35 FDA reports)
HYPOVOLAEMIA ( 35 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 35 FDA reports)
NIGHTMARE ( 35 FDA reports)
ONYCHOMYCOSIS ( 35 FDA reports)
RASH PRURITIC ( 35 FDA reports)
SKIN EXFOLIATION ( 35 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 35 FDA reports)
VISUAL ACUITY REDUCED ( 35 FDA reports)
ASCITES ( 34 FDA reports)
DISCOMFORT ( 34 FDA reports)
EAR PAIN ( 34 FDA reports)
FAECES DISCOLOURED ( 34 FDA reports)
HAEMATOMA ( 34 FDA reports)
SKIN TIGHTNESS ( 34 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 33 FDA reports)
ADVERSE DRUG REACTION ( 33 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 33 FDA reports)
CONJUNCTIVITIS ( 33 FDA reports)
DECREASED INTEREST ( 33 FDA reports)
DRUG LEVEL INCREASED ( 33 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 33 FDA reports)
HAEMOPTYSIS ( 33 FDA reports)
INFLAMMATION ( 33 FDA reports)
PNEUMONIA ASPIRATION ( 33 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 33 FDA reports)
SWELLING FACE ( 33 FDA reports)
ANGIOEDEMA ( 32 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 32 FDA reports)
GASTRITIS EROSIVE ( 32 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 32 FDA reports)
NIGHT SWEATS ( 32 FDA reports)
PALLOR ( 32 FDA reports)
PRURITUS GENERALISED ( 32 FDA reports)
RASH GENERALISED ( 32 FDA reports)
RENAL TUBULAR NECROSIS ( 32 FDA reports)
RESPIRATORY RATE INCREASED ( 32 FDA reports)
SPINAL COMPRESSION FRACTURE ( 32 FDA reports)
CORONARY ARTERY STENOSIS ( 31 FDA reports)
CYANOSIS ( 31 FDA reports)
EMOTIONAL DISORDER ( 31 FDA reports)
GASTROINTESTINAL DISORDER ( 31 FDA reports)
RESPIRATORY DISORDER ( 31 FDA reports)
BODY HEIGHT DECREASED ( 30 FDA reports)
FACE OEDEMA ( 30 FDA reports)
PHARYNGEAL OEDEMA ( 30 FDA reports)
RALES ( 30 FDA reports)
SICK SINUS SYNDROME ( 30 FDA reports)
SKIN DISORDER ( 30 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 30 FDA reports)
BLOOD ALBUMIN DECREASED ( 29 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 29 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 29 FDA reports)
CARDIAC PACEMAKER INSERTION ( 29 FDA reports)
CEREBRAL HAEMORRHAGE ( 29 FDA reports)
CRYING ( 29 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 29 FDA reports)
HIATUS HERNIA ( 29 FDA reports)
JOINT STIFFNESS ( 29 FDA reports)
LACRIMATION INCREASED ( 29 FDA reports)
LEUKOPENIA ( 29 FDA reports)
MENTAL DISORDER ( 29 FDA reports)
MUSCLE TWITCHING ( 29 FDA reports)
MYOSITIS ( 29 FDA reports)
ORAL CANDIDIASIS ( 29 FDA reports)
OSTEONECROSIS ( 29 FDA reports)
RESTLESSNESS ( 29 FDA reports)
BLINDNESS ( 28 FDA reports)
BLOOD PRESSURE ABNORMAL ( 28 FDA reports)
DISTURBANCE IN ATTENTION ( 28 FDA reports)
HEMIPARESIS ( 28 FDA reports)
IMPAIRED HEALING ( 28 FDA reports)
INCONTINENCE ( 28 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 28 FDA reports)
MACULAR DEGENERATION ( 28 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 28 FDA reports)
NASAL CONGESTION ( 28 FDA reports)
OLIGURIA ( 28 FDA reports)
PANCREATITIS ACUTE ( 28 FDA reports)
PERITONITIS ( 28 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 28 FDA reports)
AORTIC VALVE INCOMPETENCE ( 27 FDA reports)
APHASIA ( 27 FDA reports)
CARDIOMYOPATHY ( 27 FDA reports)
FUNGAL INFECTION ( 27 FDA reports)
HEPATITIS ( 27 FDA reports)
METASTASES TO BONE ( 27 FDA reports)
NEURALGIA ( 27 FDA reports)
SKIN HYPERTROPHY ( 27 FDA reports)
TENDON RUPTURE ( 27 FDA reports)
THROAT TIGHTNESS ( 27 FDA reports)
URINE FLOW DECREASED ( 27 FDA reports)
VIRAL INFECTION ( 27 FDA reports)
BRONCHOSPASM ( 26 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 26 FDA reports)
CARDIAC VALVE DISEASE ( 26 FDA reports)
CEREBRAL ISCHAEMIA ( 26 FDA reports)
FEMUR FRACTURE ( 26 FDA reports)
ILEUS ( 26 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 26 FDA reports)
IRRITABILITY ( 26 FDA reports)
MUCOSAL INFLAMMATION ( 26 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 26 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 26 FDA reports)
RENAL PAIN ( 26 FDA reports)
SINUS DISORDER ( 26 FDA reports)
THERAPY NON-RESPONDER ( 26 FDA reports)
AGGRESSION ( 25 FDA reports)
BLOOD MAGNESIUM DECREASED ( 25 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 25 FDA reports)
DEBRIDEMENT ( 25 FDA reports)
DRUG INTOLERANCE ( 25 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 25 FDA reports)
FAILURE TO THRIVE ( 25 FDA reports)
GASTRIC DISORDER ( 25 FDA reports)
JAUNDICE ( 25 FDA reports)
LIFE EXPECTANCY SHORTENED ( 25 FDA reports)
MEDICATION RESIDUE ( 25 FDA reports)
NEPHROLITHIASIS ( 25 FDA reports)
NODAL ARRHYTHMIA ( 25 FDA reports)
PERIPHERAL COLDNESS ( 25 FDA reports)
SCAR ( 25 FDA reports)
TACHYARRHYTHMIA ( 25 FDA reports)
ACUTE CORONARY SYNDROME ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 24 FDA reports)
AZOTAEMIA ( 24 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 24 FDA reports)
FAECAL INCONTINENCE ( 24 FDA reports)
FEAR OF EATING ( 24 FDA reports)
GENERALISED OEDEMA ( 24 FDA reports)
HYPERCALCAEMIA ( 24 FDA reports)
INTENTIONAL MISUSE ( 24 FDA reports)
LACERATION ( 24 FDA reports)
LIPASE INCREASED ( 24 FDA reports)
NOCTURIA ( 24 FDA reports)
OBESITY ( 24 FDA reports)
OESOPHAGITIS ( 24 FDA reports)
PROTEINURIA ( 24 FDA reports)
RIB FRACTURE ( 24 FDA reports)
SLEEP DISORDER ( 24 FDA reports)
TENDERNESS ( 24 FDA reports)
THYROID DISORDER ( 24 FDA reports)
VISUAL DISTURBANCE ( 24 FDA reports)
ABNORMAL BEHAVIOUR ( 23 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 23 FDA reports)
BURSITIS ( 23 FDA reports)
DEPRESSED MOOD ( 23 FDA reports)
DIFFICULTY IN WALKING ( 23 FDA reports)
EYE DISORDER ( 23 FDA reports)
EYE PAIN ( 23 FDA reports)
GLOSSODYNIA ( 23 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 23 FDA reports)
HYPOMAGNESAEMIA ( 23 FDA reports)
INFLUENZA ( 23 FDA reports)
INJECTION SITE ERYTHEMA ( 23 FDA reports)
KNEE ARTHROPLASTY ( 23 FDA reports)
LABORATORY TEST ABNORMAL ( 23 FDA reports)
MASS ( 23 FDA reports)
MOVEMENT DISORDER ( 23 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 23 FDA reports)
PNEUMONITIS ( 23 FDA reports)
SPINAL FRACTURE ( 23 FDA reports)
WALKING AID USER ( 23 FDA reports)
ATAXIA ( 22 FDA reports)
CAROTID ARTERY STENOSIS ( 22 FDA reports)
CHOLECYSTITIS ( 22 FDA reports)
DIASTOLIC DYSFUNCTION ( 22 FDA reports)
MASTICATION DISORDER ( 22 FDA reports)
MEDICAL DEVICE COMPLICATION ( 22 FDA reports)
MUSCLE TIGHTNESS ( 22 FDA reports)
MYOCLONUS ( 22 FDA reports)
ORTHOPNOEA ( 22 FDA reports)
PETECHIAE ( 22 FDA reports)
PHARYNGITIS ( 22 FDA reports)
PHLEBITIS ( 22 FDA reports)
RESTLESS LEGS SYNDROME ( 22 FDA reports)
STENT PLACEMENT ( 22 FDA reports)
URINE OUTPUT DECREASED ( 22 FDA reports)
ACCIDENTAL OVERDOSE ( 21 FDA reports)
ANGER ( 21 FDA reports)
AORTIC STENOSIS ( 21 FDA reports)
BODY TEMPERATURE INCREASED ( 21 FDA reports)
CARDIOVERSION ( 21 FDA reports)
DEAFNESS ( 21 FDA reports)
DENTAL CARIES ( 21 FDA reports)
DIABETIC NEUROPATHY ( 21 FDA reports)
EYE HAEMORRHAGE ( 21 FDA reports)
FEELING JITTERY ( 21 FDA reports)
HEPATIC CYST ( 21 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 21 FDA reports)
ILEUS PARALYTIC ( 21 FDA reports)
INJECTION SITE HAEMORRHAGE ( 21 FDA reports)
JAUNDICE CHOLESTATIC ( 21 FDA reports)
LOCAL SWELLING ( 21 FDA reports)
METASTASES TO SPINE ( 21 FDA reports)
MOUTH ULCERATION ( 21 FDA reports)
MUSCLE ATROPHY ( 21 FDA reports)
PSORIASIS ( 21 FDA reports)
SEDATION ( 21 FDA reports)
SENSORY DISTURBANCE ( 21 FDA reports)
SUBDURAL HAEMATOMA ( 21 FDA reports)
THIRST ( 21 FDA reports)
TOOTHACHE ( 21 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 20 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 20 FDA reports)
BACTERAEMIA ( 20 FDA reports)
CEREBRAL ATROPHY ( 20 FDA reports)
COLD SWEAT ( 20 FDA reports)
COLITIS ISCHAEMIC ( 20 FDA reports)
CYTOLYTIC HEPATITIS ( 20 FDA reports)
DERMATITIS EXFOLIATIVE ( 20 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 20 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 20 FDA reports)
ENCEPHALOPATHY ( 20 FDA reports)
EYE IRRITATION ( 20 FDA reports)
KYPHOSIS ( 20 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
LUNG INFECTION ( 20 FDA reports)
MIDDLE INSOMNIA ( 20 FDA reports)
QUALITY OF LIFE DECREASED ( 20 FDA reports)
RASH ERYTHEMATOUS ( 20 FDA reports)
RASH MACULO-PAPULAR ( 20 FDA reports)
RETCHING ( 20 FDA reports)
ROAD TRAFFIC ACCIDENT ( 20 FDA reports)
SCLERODERMA ( 20 FDA reports)
SKIN LACERATION ( 20 FDA reports)
THROAT IRRITATION ( 20 FDA reports)
AGEUSIA ( 19 FDA reports)
ANGIONEUROTIC OEDEMA ( 19 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 19 FDA reports)
CARDIOVASCULAR DISORDER ( 19 FDA reports)
CHOLESTASIS ( 19 FDA reports)
COGNITIVE DISORDER ( 19 FDA reports)
DERMATITIS ( 19 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 19 FDA reports)
DRUG ADMINISTRATION ERROR ( 19 FDA reports)
ERYTHEMA MULTIFORME ( 19 FDA reports)
GALLBLADDER DISORDER ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
HOSPITALISATION ( 19 FDA reports)
HYPERCHOLESTEROLAEMIA ( 19 FDA reports)
HYPOALBUMINAEMIA ( 19 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 19 FDA reports)
LACTIC ACIDOSIS ( 19 FDA reports)
LIVER DISORDER ( 19 FDA reports)
NEOPLASM PROGRESSION ( 19 FDA reports)
PNEUMOTHORAX ( 19 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 19 FDA reports)
RESPIRATORY ACIDOSIS ( 19 FDA reports)
RIGHT VENTRICULAR FAILURE ( 19 FDA reports)
ABSCESS ( 18 FDA reports)
ACIDOSIS ( 18 FDA reports)
ASPIRATION ( 18 FDA reports)
BLOOD CALCIUM DECREASED ( 18 FDA reports)
BONE LESION ( 18 FDA reports)
CHEST X-RAY ABNORMAL ( 18 FDA reports)
DEVICE RELATED INFECTION ( 18 FDA reports)
DIPLOPIA ( 18 FDA reports)
DISEASE RECURRENCE ( 18 FDA reports)
EOSINOPHILIA ( 18 FDA reports)
GYNAECOMASTIA ( 18 FDA reports)
HYPOACUSIS ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
INJECTION SITE HAEMATOMA ( 18 FDA reports)
INTESTINAL ISCHAEMIA ( 18 FDA reports)
ISCHAEMIC STROKE ( 18 FDA reports)
PLATELET COUNT INCREASED ( 18 FDA reports)
POISONING DELIBERATE ( 18 FDA reports)
PULSE ABSENT ( 18 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 18 FDA reports)
SCOLIOSIS ( 18 FDA reports)
TACHYPNOEA ( 18 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
UPPER LIMB FRACTURE ( 18 FDA reports)
ANAPHYLACTIC SHOCK ( 17 FDA reports)
APLASIA PURE RED CELL ( 17 FDA reports)
BLOOD CALCIUM INCREASED ( 17 FDA reports)
BREATH SOUNDS ABNORMAL ( 17 FDA reports)
CLOSTRIDIAL INFECTION ( 17 FDA reports)
DISABILITY ( 17 FDA reports)
DRY EYE ( 17 FDA reports)
DYSLIPIDAEMIA ( 17 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 17 FDA reports)
HYPERSOMNIA ( 17 FDA reports)
INFUSION RELATED REACTION ( 17 FDA reports)
INJECTION SITE REACTION ( 17 FDA reports)
IRRITABLE BOWEL SYNDROME ( 17 FDA reports)
JOINT INJURY ( 17 FDA reports)
LIBIDO DECREASED ( 17 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 17 FDA reports)
OCULAR HYPERAEMIA ( 17 FDA reports)
PROSTATE CANCER ( 17 FDA reports)
RASH PAPULAR ( 17 FDA reports)
SCAB ( 17 FDA reports)
SOCIAL PROBLEM ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA ( 17 FDA reports)
TOOTH INFECTION ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
VENTRICULAR HYPOKINESIA ( 17 FDA reports)
ABDOMINAL TENDERNESS ( 16 FDA reports)
ACCIDENTAL EXPOSURE ( 16 FDA reports)
AGRANULOCYTOSIS ( 16 FDA reports)
ANAPHYLACTIC REACTION ( 16 FDA reports)
ANKLE FRACTURE ( 16 FDA reports)
BLOOD CHLORIDE DECREASED ( 16 FDA reports)
BLOOD CREATINE INCREASED ( 16 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 16 FDA reports)
BLOOD CREATININE DECREASED ( 16 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 16 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 16 FDA reports)
DECREASED ACTIVITY ( 16 FDA reports)
DILATATION ATRIAL ( 16 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 16 FDA reports)
EATING DISORDER ( 16 FDA reports)
EPIDIDYMITIS ( 16 FDA reports)
ERUCTATION ( 16 FDA reports)
EXOSTOSIS ( 16 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 16 FDA reports)
HYPERKERATOSIS ( 16 FDA reports)
HYPERTENSIVE CRISIS ( 16 FDA reports)
IMPAIRED WORK ABILITY ( 16 FDA reports)
INITIAL INSOMNIA ( 16 FDA reports)
IRON DEFICIENCY ANAEMIA ( 16 FDA reports)
JAW DISORDER ( 16 FDA reports)
MARROW HYPERPLASIA ( 16 FDA reports)
MICTURITION URGENCY ( 16 FDA reports)
MOOD SWINGS ( 16 FDA reports)
MOUTH HAEMORRHAGE ( 16 FDA reports)
NEPHROPATHY TOXIC ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 16 FDA reports)
ORAL DISORDER ( 16 FDA reports)
ORAL INTAKE REDUCED ( 16 FDA reports)
PERIPHERAL EMBOLISM ( 16 FDA reports)
PHYSICAL DISABILITY ( 16 FDA reports)
PULMONARY MASS ( 16 FDA reports)
PURPURA ( 16 FDA reports)
RASH MACULAR ( 16 FDA reports)
RENAL CANCER ( 16 FDA reports)
RESPIRATORY DEPRESSION ( 16 FDA reports)
ROTATOR CUFF SYNDROME ( 16 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 16 FDA reports)
SUDDEN DEATH ( 16 FDA reports)
VENTRICULAR ARRHYTHMIA ( 16 FDA reports)
ACUTE PULMONARY OEDEMA ( 15 FDA reports)
ANAL HAEMORRHAGE ( 15 FDA reports)
APNOEA ( 15 FDA reports)
BLINDNESS UNILATERAL ( 15 FDA reports)
BLOOD TEST ABNORMAL ( 15 FDA reports)
CARDIAC VALVE ABSCESS ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 15 FDA reports)
DYSAESTHESIA ( 15 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 15 FDA reports)
ELECTROLYTE IMBALANCE ( 15 FDA reports)
GASTROENTERITIS VIRAL ( 15 FDA reports)
GLAUCOMA ( 15 FDA reports)
HEPATIC CIRRHOSIS ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
HEPATORENAL SYNDROME ( 15 FDA reports)
HYPERAESTHESIA ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
INTERMITTENT CLAUDICATION ( 15 FDA reports)
KIDNEY INFECTION ( 15 FDA reports)
LIMB INJURY ( 15 FDA reports)
LIP SWELLING ( 15 FDA reports)
LOBAR PNEUMONIA ( 15 FDA reports)
METABOLIC ENCEPHALOPATHY ( 15 FDA reports)
PCO2 DECREASED ( 15 FDA reports)
RENAL ARTERY STENOSIS ( 15 FDA reports)
RENAL ISCHAEMIA ( 15 FDA reports)
RHONCHI ( 15 FDA reports)
SINUS ARRHYTHMIA ( 15 FDA reports)
STOMACH DISCOMFORT ( 15 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 15 FDA reports)
TOOTH DISORDER ( 15 FDA reports)
VISUAL FIELD DEFECT ( 15 FDA reports)
VITAMIN D DECREASED ( 15 FDA reports)
WHEELCHAIR USER ( 15 FDA reports)
WRONG DRUG ADMINISTERED ( 15 FDA reports)
ANGIOPATHY ( 14 FDA reports)
BASAL CELL CARCINOMA ( 14 FDA reports)
BLOOD PH DECREASED ( 14 FDA reports)
BONE MARROW FAILURE ( 14 FDA reports)
CARDIAC OPERATION ( 14 FDA reports)
CARPAL TUNNEL SYNDROME ( 14 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 14 FDA reports)
COMPRESSION FRACTURE ( 14 FDA reports)
CREPITATIONS ( 14 FDA reports)
DILATATION VENTRICULAR ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
DRUG ERUPTION ( 14 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 14 FDA reports)
FAMILY STRESS ( 14 FDA reports)
FIBROSIS ( 14 FDA reports)
GROIN PAIN ( 14 FDA reports)
HAEMOLYTIC ANAEMIA ( 14 FDA reports)
HEPATIC CONGESTION ( 14 FDA reports)
HEPATOMEGALY ( 14 FDA reports)
HYDROCELE ( 14 FDA reports)
HYPOTONIA ( 14 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 14 FDA reports)
MENTAL IMPAIRMENT ( 14 FDA reports)
METASTASES TO LUNG ( 14 FDA reports)
MUSCLE CRAMP ( 14 FDA reports)
NERVE INJURY ( 14 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 14 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 14 FDA reports)
ORCHITIS ( 14 FDA reports)
PARANOIA ( 14 FDA reports)
PROCEDURAL COMPLICATION ( 14 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 14 FDA reports)
RHINITIS ALLERGIC ( 14 FDA reports)
SKIN TEST POSITIVE ( 14 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 14 FDA reports)
TENDONITIS ( 14 FDA reports)
THINKING ABNORMAL ( 14 FDA reports)
VAGINAL HAEMORRHAGE ( 14 FDA reports)
VIITH NERVE PARALYSIS ( 14 FDA reports)
WITHDRAWAL SYNDROME ( 14 FDA reports)
ALCOHOL USE ( 13 FDA reports)
ANOXIC ENCEPHALOPATHY ( 13 FDA reports)
APHAGIA ( 13 FDA reports)
BLADDER DISCOMFORT ( 13 FDA reports)
BLOOD BICARBONATE DECREASED ( 13 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 13 FDA reports)
CHRONIC SINUSITIS ( 13 FDA reports)
DIABETIC KETOACIDOSIS ( 13 FDA reports)
DRUG DEPENDENCE ( 13 FDA reports)
DRUG DISPENSING ERROR ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
DUODENAL ULCER ( 13 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 13 FDA reports)
FEAR OF DEATH ( 13 FDA reports)
GRAND MAL CONVULSION ( 13 FDA reports)
HAEMODYNAMIC INSTABILITY ( 13 FDA reports)
HEAD DISCOMFORT ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HEPATOCELLULAR DAMAGE ( 13 FDA reports)
HYPERBILIRUBINAEMIA ( 13 FDA reports)
HYPERTHYROIDISM ( 13 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 13 FDA reports)
HYPOKINESIA ( 13 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 13 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 13 FDA reports)
INJECTION SITE PRURITUS ( 13 FDA reports)
JOINT CONTRACTURE ( 13 FDA reports)
LOCALISED INFECTION ( 13 FDA reports)
MENISCUS LESION ( 13 FDA reports)
MULTIPLE SCLEROSIS ( 13 FDA reports)
NERVE COMPRESSION ( 13 FDA reports)
NEUROPATHY ( 13 FDA reports)
ODYNOPHAGIA ( 13 FDA reports)
PERIPHERAL ISCHAEMIA ( 13 FDA reports)
PHOTOSENSITIVITY REACTION ( 13 FDA reports)
PRIMARY SEQUESTRUM ( 13 FDA reports)
PSEUDOMONAS INFECTION ( 13 FDA reports)
PYELONEPHRITIS ( 13 FDA reports)
RESPIRATORY TRACT INFECTION ( 13 FDA reports)
SKIN BURNING SENSATION ( 13 FDA reports)
SKIN HAEMORRHAGE ( 13 FDA reports)
SNEEZING ( 13 FDA reports)
SPINAL COLUMN STENOSIS ( 13 FDA reports)
ULCER ( 13 FDA reports)
VASCULITIS ( 13 FDA reports)
VENTRICULAR HYPERTROPHY ( 13 FDA reports)
WOUND ( 13 FDA reports)
WOUND INFECTION ( 13 FDA reports)
BEDRIDDEN ( 12 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 12 FDA reports)
BLOOD MAGNESIUM INCREASED ( 12 FDA reports)
BODY TEMPERATURE DECREASED ( 12 FDA reports)
CARDIOPULMONARY FAILURE ( 12 FDA reports)
CATARACT OPERATION ( 12 FDA reports)
CATHETER RELATED COMPLICATION ( 12 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 12 FDA reports)
DECUBITUS ULCER ( 12 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 12 FDA reports)
DRUG ABUSER ( 12 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 12 FDA reports)
ENTEROCOCCAL INFECTION ( 12 FDA reports)
ENURESIS ( 12 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
EXTREMITY CONTRACTURE ( 12 FDA reports)
FIBRIN D DIMER INCREASED ( 12 FDA reports)
FISTULA ( 12 FDA reports)
GRANULOMA ( 12 FDA reports)
HALLUCINATION, VISUAL ( 12 FDA reports)
INCREASED TENDENCY TO BRUISE ( 12 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 12 FDA reports)
JOINT DISLOCATION ( 12 FDA reports)
LUNG NEOPLASM ( 12 FDA reports)
MELANOCYTIC NAEVUS ( 12 FDA reports)
MUSCULOSKELETAL DISORDER ( 12 FDA reports)
MYELODYSPLASTIC SYNDROME ( 12 FDA reports)
ORAL DISCOMFORT ( 12 FDA reports)
PANCREATIC CARCINOMA ( 12 FDA reports)
PARAESTHESIA ORAL ( 12 FDA reports)
PERIODONTITIS ( 12 FDA reports)
POLYP ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 12 FDA reports)
RESPIRATORY TRACT CONGESTION ( 12 FDA reports)
SINUS ARREST ( 12 FDA reports)
SKIN HYPERPIGMENTATION ( 12 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
TESTICULAR PAIN ( 12 FDA reports)
TOOTH FRACTURE ( 12 FDA reports)
URINE ABNORMALITY ( 12 FDA reports)
ABDOMINAL PAIN LOWER ( 11 FDA reports)
ADVERSE EVENT ( 11 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 11 FDA reports)
AORTIC ANEURYSM ( 11 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
ATRIAL TACHYCARDIA ( 11 FDA reports)
BACK DISORDER ( 11 FDA reports)
BLOOD LACTIC ACID INCREASED ( 11 FDA reports)
BREAST CANCER FEMALE ( 11 FDA reports)
BREAST MASS ( 11 FDA reports)
CARDIAC HYPERTROPHY ( 11 FDA reports)
CAROTID ARTERY DISEASE ( 11 FDA reports)
CATHETERISATION CARDIAC ( 11 FDA reports)
CHEILITIS ( 11 FDA reports)
COLITIS ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 11 FDA reports)
COR PULMONALE ( 11 FDA reports)
CYSTITIS HAEMORRHAGIC ( 11 FDA reports)
DRY THROAT ( 11 FDA reports)
ECZEMA ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 11 FDA reports)
EXPIRED DRUG ADMINISTERED ( 11 FDA reports)
FOOT FRACTURE ( 11 FDA reports)
FOREIGN BODY ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
GINGIVAL BLEEDING ( 11 FDA reports)
HEART RATE ABNORMAL ( 11 FDA reports)
HYDROCEPHALUS ( 11 FDA reports)
HYPOAESTHESIA FACIAL ( 11 FDA reports)
HYPOTHERMIA ( 11 FDA reports)
IMPAIRED DRIVING ABILITY ( 11 FDA reports)
INTRACARDIAC THROMBUS ( 11 FDA reports)
KLEBSIELLA INFECTION ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LOOSE TOOTH ( 11 FDA reports)
MENINGITIS ASEPTIC ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
NEUROGENIC BLADDER ( 11 FDA reports)
OCCULT BLOOD POSITIVE ( 11 FDA reports)
PEAU D'ORANGE ( 11 FDA reports)
PELVIC FRACTURE ( 11 FDA reports)
PHOTOPHOBIA ( 11 FDA reports)
PITTING OEDEMA ( 11 FDA reports)
PO2 DECREASED ( 11 FDA reports)
POLYNEUROPATHY ( 11 FDA reports)
PROSTATOMEGALY ( 11 FDA reports)
PROTEIN TOTAL DECREASED ( 11 FDA reports)
RADICULOPATHY ( 11 FDA reports)
RENAL TRANSPLANT ( 11 FDA reports)
RESUSCITATION ( 11 FDA reports)
SENSORY LOSS ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SKIN REACTION ( 11 FDA reports)
TARDIVE DYSKINESIA ( 11 FDA reports)
TESTICULAR SWELLING ( 11 FDA reports)
TROPONIN INCREASED ( 11 FDA reports)
UROSEPSIS ( 11 FDA reports)
WRIST FRACTURE ( 11 FDA reports)
ADVERSE REACTION ( 10 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 10 FDA reports)
AORTIC VALVE REPLACEMENT ( 10 FDA reports)
BACK INJURY ( 10 FDA reports)
BLADDER DISORDER ( 10 FDA reports)
BLOOD UREA DECREASED ( 10 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 10 FDA reports)
BLOOD URINE ( 10 FDA reports)
BRADYARRHYTHMIA ( 10 FDA reports)
BREAKTHROUGH PAIN ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
CHOKING ( 10 FDA reports)
CORONARY ARTERY BYPASS ( 10 FDA reports)
DELUSION ( 10 FDA reports)
DIABETIC NEPHROPATHY ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
EXFOLIATIVE RASH ( 10 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
FACIAL PAIN ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
FLANK PAIN ( 10 FDA reports)
GANGRENE ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HEARING IMPAIRED ( 10 FDA reports)
HEPATITIS ACUTE ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HIP ARTHROPLASTY ( 10 FDA reports)
HYPOAESTHESIA ORAL ( 10 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 10 FDA reports)
IRON DEFICIENCY ( 10 FDA reports)
ISCHAEMIA ( 10 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 10 FDA reports)
JAW FRACTURE ( 10 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
LUMBAR SPINAL STENOSIS ( 10 FDA reports)
METASTASES TO LIVER ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
NEPHROPATHY ( 10 FDA reports)
NEUROTOXICITY ( 10 FDA reports)
NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
OTITIS MEDIA ( 10 FDA reports)
PARKINSON'S DISEASE ( 10 FDA reports)
PEPTIC ULCER ( 10 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 10 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 10 FDA reports)
PLEURITIC PAIN ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
POST PROCEDURAL URINE LEAK ( 10 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 10 FDA reports)
PULMONARY HAEMORRHAGE ( 10 FDA reports)
PUPIL FIXED ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
SKIN FISSURES ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
STRESS URINARY INCONTINENCE ( 10 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 10 FDA reports)
THYROID CYST ( 10 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 10 FDA reports)
VASODILATATION ( 10 FDA reports)
ABNORMAL FAECES ( 9 FDA reports)
AORTIC VALVE SCLEROSIS ( 9 FDA reports)
APHONIA ( 9 FDA reports)
ARTERIAL HAEMORRHAGE ( 9 FDA reports)
ARTHRITIS BACTERIAL ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 9 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
CACHEXIA ( 9 FDA reports)
CAESAREAN SECTION ( 9 FDA reports)
CARDIAC FAILURE ACUTE ( 9 FDA reports)
CARDIAC FLUTTER ( 9 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 9 FDA reports)
CHAPPED LIPS ( 9 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
COLITIS ULCERATIVE ( 9 FDA reports)
DEVICE FAILURE ( 9 FDA reports)
DEVICE MALFUNCTION ( 9 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 9 FDA reports)
DIABETIC COMA ( 9 FDA reports)
DRUG ABUSE ( 9 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 9 FDA reports)
EXTERNAL EAR DISORDER ( 9 FDA reports)
EYE PRURITUS ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
FOAMING AT MOUTH ( 9 FDA reports)
GLOSSITIS ( 9 FDA reports)
HICCUPS ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 9 FDA reports)
INTESTINAL PERFORATION ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
LIVEDO RETICULARIS ( 9 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 9 FDA reports)
NON-CARDIAC CHEST PAIN ( 9 FDA reports)
OCULAR ICTERUS ( 9 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
ORGAN FAILURE ( 9 FDA reports)
OSTEOSCLEROSIS ( 9 FDA reports)
PERICARDITIS ( 9 FDA reports)
PNEUMOPERITONEUM ( 9 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 9 FDA reports)
PRINZMETAL ANGINA ( 9 FDA reports)
PROTEIN URINE PRESENT ( 9 FDA reports)
RADIUS FRACTURE ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RESPIRATORY RATE DECREASED ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SELF-MEDICATION ( 9 FDA reports)
SENSATION OF FOREIGN BODY ( 9 FDA reports)
SPLENOMEGALY ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 9 FDA reports)
THYROID NEOPLASM ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
UNEMPLOYMENT ( 9 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 9 FDA reports)
VAGINAL INFECTION ( 9 FDA reports)
VENOUS INSUFFICIENCY ( 9 FDA reports)
VENOUS THROMBOSIS ( 9 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 9 FDA reports)
YELLOW SKIN ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ACANTHOMA ( 8 FDA reports)
ACUTE PRERENAL FAILURE ( 8 FDA reports)
AMMONIA INCREASED ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
ANION GAP INCREASED ( 8 FDA reports)
ANOSMIA ( 8 FDA reports)
AORTIC VALVE DISEASE ( 8 FDA reports)
ARTERIAL SPASM ( 8 FDA reports)
BARRETT'S OESOPHAGUS ( 8 FDA reports)
BLADDER CANCER ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 8 FDA reports)
BLOOD SODIUM INCREASED ( 8 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
BRAIN DEATH ( 8 FDA reports)
BREAST CANCER RECURRENT ( 8 FDA reports)
BREAST CYST ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
CATHETER RELATED INFECTION ( 8 FDA reports)
CATHETER SEPSIS ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
CORNEAL ABRASION ( 8 FDA reports)
CULTURE URINE POSITIVE ( 8 FDA reports)
CYST ( 8 FDA reports)
CYSTOCELE ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 8 FDA reports)
DRUG PRESCRIBING ERROR ( 8 FDA reports)
DYSPNOEA EXACERBATED ( 8 FDA reports)
EAR INFECTION ( 8 FDA reports)
EOSINOPHIL COUNT INCREASED ( 8 FDA reports)
ESCHERICHIA INFECTION ( 8 FDA reports)
EUPHORIC MOOD ( 8 FDA reports)
EYE INFLAMMATION ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FEMORAL NECK FRACTURE ( 8 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GASTROINTESTINAL ULCER ( 8 FDA reports)
GOITRE ( 8 FDA reports)
HEPATIC INFARCTION ( 8 FDA reports)
HEPATIC NECROSIS ( 8 FDA reports)
HUMERUS FRACTURE ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERNATRAEMIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
INFECTIOUS PERITONITIS ( 8 FDA reports)
LISTLESS ( 8 FDA reports)
LIVER INJURY ( 8 FDA reports)
LUNG HYPERINFLATION ( 8 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
MAJOR DEPRESSION ( 8 FDA reports)
MALIGNANT MELANOMA IN SITU ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
MENINGITIS ( 8 FDA reports)
MENSTRUATION IRREGULAR ( 8 FDA reports)
METASTATIC NEOPLASM ( 8 FDA reports)
MITRAL VALVE CALCIFICATION ( 8 FDA reports)
MUSCLE RIGIDITY ( 8 FDA reports)
MYOGLOBINURIA ( 8 FDA reports)
NASAL ULCER ( 8 FDA reports)
NO ADVERSE EVENT ( 8 FDA reports)
NONSPECIFIC REACTION ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
OESOPHAGEAL DISORDER ( 8 FDA reports)
ONYCHOMADESIS ( 8 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PANCREATIC CYST ( 8 FDA reports)
PLEURAL FIBROSIS ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
POOR PERIPHERAL CIRCULATION ( 8 FDA reports)
PROCTALGIA ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SCRATCH ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
SINOATRIAL BLOCK ( 8 FDA reports)
SKIN FIBROSIS ( 8 FDA reports)
SOFT TISSUE DISORDER ( 8 FDA reports)
SPLENIC CYST ( 8 FDA reports)
SUDDEN ONSET OF SLEEP ( 8 FDA reports)
TOXIC ENCEPHALOPATHY ( 8 FDA reports)
TRANSPLANT REJECTION ( 8 FDA reports)
TROPONIN I INCREASED ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 8 FDA reports)
VOCAL CORD PARALYSIS ( 8 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
ABSCESS LIMB ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ACNE ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 7 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
AORTIC DILATATION ( 7 FDA reports)
AORTIC VALVE STENOSIS ( 7 FDA reports)
ATRIAL THROMBOSIS ( 7 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BILIARY TRACT DISORDER ( 7 FDA reports)
BLOODY DISCHARGE ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BREAST CANCER IN SITU ( 7 FDA reports)
CARDIAC ENZYMES INCREASED ( 7 FDA reports)
CAROTID ARTERY OCCLUSION ( 7 FDA reports)
CATHETER SITE HAEMATOMA ( 7 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 7 FDA reports)
CEREBELLAR SYNDROME ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
CHYLOTHORAX ( 7 FDA reports)
COLON CANCER ( 7 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 7 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 7 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
DRUG EFFECT INCREASED ( 7 FDA reports)
DRUG LEVEL DECREASED ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
EMPYEMA ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
ESSENTIAL HYPERTENSION ( 7 FDA reports)
EXPOSED BONE IN JAW ( 7 FDA reports)
EYELID PTOSIS ( 7 FDA reports)
FEELING DRUNK ( 7 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 7 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 7 FDA reports)
FINGER DEFORMITY ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
GENERALISED ERYTHEMA ( 7 FDA reports)
GINGIVAL PAIN ( 7 FDA reports)
GINGIVAL RECESSION ( 7 FDA reports)
HAEMANGIOMA ( 7 FDA reports)
HAEMARTHROSIS ( 7 FDA reports)
HAEMOLYSIS ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HEPATIC HAEMATOMA ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
HERNIA ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INJECTION SITE MASS ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
LOSS OF EMPLOYMENT ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
LYMPHOEDEMA ( 7 FDA reports)
MACULE ( 7 FDA reports)
METASTASIS ( 7 FDA reports)
MOTOR DYSFUNCTION ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NEPHRECTOMY ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
OBSTRUCTIVE UROPATHY ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PAROTID GLAND ENLARGEMENT ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
PLATELET COUNT ABNORMAL ( 7 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
POTENTIATING DRUG INTERACTION ( 7 FDA reports)
PREGNANCY ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 7 FDA reports)
REFRACTORY ANAEMIA ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RHINITIS ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SINUS HEADACHE ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
SKIN WRINKLING ( 7 FDA reports)
SOMNAMBULISM ( 7 FDA reports)
SPINAL CORD COMPRESSION ( 7 FDA reports)
SPINAL DISORDER ( 7 FDA reports)
SPIROMETRY ABNORMAL ( 7 FDA reports)
SPLENIC GRANULOMA ( 7 FDA reports)
STASIS DERMATITIS ( 7 FDA reports)
STENT OCCLUSION ( 7 FDA reports)
SUBMANDIBULAR MASS ( 7 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 7 FDA reports)
TETANY ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
URINARY TRACT OBSTRUCTION ( 7 FDA reports)
URINE ANALYSIS ABNORMAL ( 7 FDA reports)
UTERINE CANCER ( 7 FDA reports)
VASCULAR INJURY ( 7 FDA reports)
VITAMIN D DEFICIENCY ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ACTINOMYCOSIS ( 6 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
AMPUTATION ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 6 FDA reports)
ANAL SPHINCTER ATONY ( 6 FDA reports)
ANORECTAL DISORDER ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
APATHY ( 6 FDA reports)
ASPIRATION JOINT ( 6 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
BLADDER OBSTRUCTION ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BONE MARROW DISORDER ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BREAST HYPERPLASIA ( 6 FDA reports)
BREAST OEDEMA ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CERVICAL SPINAL STENOSIS ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CLOSTRIDIUM COLITIS ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CORONARY ARTERY SURGERY ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DIARRHOEA INFECTIOUS ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
FAILED INDUCTION OF LABOUR ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
FULL BLOOD COUNT DECREASED ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
FUSOBACTERIUM INFECTION ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GINGIVAL SWELLING ( 6 FDA reports)
HAEMATOMA INFECTION ( 6 FDA reports)
HAEMOGLOBIN INCREASED ( 6 FDA reports)
HAIR GROWTH ABNORMAL ( 6 FDA reports)
HEART INJURY ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERCAPNIA ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
HYPOCHLORAEMIA ( 6 FDA reports)
HYPOGLYCAEMIC COMA ( 6 FDA reports)
HYPOPERFUSION ( 6 FDA reports)
IMPETIGO ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
INJECTION SITE SCAR ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
JOINT INSTABILITY ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
KERATOACANTHOMA ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LICHENOID KERATOSIS ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MANIA ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
METASTASES TO LYMPH NODES ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MICROCYTIC ANAEMIA ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
MITRAL VALVE REPAIR ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
MUSCLE FIBROSIS ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NIGHT BLINDNESS ( 6 FDA reports)
NODULE ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
OESOPHAGEAL PAIN ( 6 FDA reports)
OESOPHAGEAL SPASM ( 6 FDA reports)
OESOPHAGEAL STENOSIS ( 6 FDA reports)
ONYCHALGIA ( 6 FDA reports)
OPEN WOUND ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PATHOLOGICAL FRACTURE ( 6 FDA reports)
PNEUMOMEDIASTINUM ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
POLYMYALGIA RHEUMATICA ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 6 FDA reports)
PSYCHIATRIC SYMPTOM ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
PULMONARY TOXICITY ( 6 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 6 FDA reports)
RAYNAUD'S PHENOMENON ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RENAL TUBULAR ATROPHY ( 6 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SIALOADENITIS ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN NODULE ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SPUTUM CULTURE POSITIVE ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
STERNAL FRACTURE ( 6 FDA reports)
T-CELL LYMPHOMA ( 6 FDA reports)
TENDON DISORDER ( 6 FDA reports)
THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 6 FDA reports)
VASCULITIC RASH ( 6 FDA reports)
VENOOCCLUSIVE DISEASE ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ANAL FISSURE ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 5 FDA reports)
ASTIGMATISM ( 5 FDA reports)
ATROPHY ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD AMYLASE DECREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD PRESSURE ( 5 FDA reports)
BONE DEBRIDEMENT ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BUNDLE BRANCH BLOCK ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CARCINOID TUMOUR ( 5 FDA reports)
CARDIAC FIBRILLATION ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 5 FDA reports)
CERVICOBRACHIAL SYNDROME ( 5 FDA reports)
COLOUR BLINDNESS ( 5 FDA reports)
COMA SCALE ABNORMAL ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 5 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FACET JOINT SYNDROME ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
GALLBLADDER POLYP ( 5 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
GRIP STRENGTH DECREASED ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPERREFLEXIA ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INGUINAL HERNIA ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 5 FDA reports)
INTESTINAL HAEMORRHAGE ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
IRITIS ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LIVER TRANSPLANT REJECTION ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
LUNG CONSOLIDATION ( 5 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 5 FDA reports)
METASTASES TO CHEST WALL ( 5 FDA reports)
MICROALBUMINURIA ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MITRAL VALVE PROLAPSE ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MUCOSAL HAEMORRHAGE ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MUSCLE STRAIN ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NEOPLASM ( 5 FDA reports)
NEURITIS ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PANCREATITIS NECROTISING ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PELVIC FLUID COLLECTION ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
POST THROMBOTIC SYNDROME ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
PRE-ECLAMPSIA ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROCEDURAL VOMITING ( 5 FDA reports)
PRODUCT TASTE ABNORMAL ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SKIN FRAGILITY ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SLEEP TERROR ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SNORING ( 5 FDA reports)
SPINAL HAEMANGIOMA ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SYNCOPE VASOVAGAL ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
THERAPY REGIMEN CHANGED ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URGE INCONTINENCE ( 5 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 5 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VENTRICULAR ASYSTOLE ( 5 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACTINIC ELASTOSIS ( 4 FDA reports)
ACUTE PHASE REACTION ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ANAESTHETIC COMPLICATION ( 4 FDA reports)
ANORECTAL OPERATION ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC CALCIFICATION ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APPARENT DEATH ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
BAROTRAUMA ( 4 FDA reports)
BASAL GANGLIA INFARCTION ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BONE NEOPLASM ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
CARBON DIOXIDE DECREASED ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CAROTID ARTERY ATHEROMA ( 4 FDA reports)
CATHETER PLACEMENT ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CEREBELLAR HAEMATOMA ( 4 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHORIORETINOPATHY ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
COLLAGEN DISORDER ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
CREATININE URINE DECREASED ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CUTANEOUS VASCULITIS ( 4 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 4 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DRUG INTERACTION INHIBITION ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
EMBOLISM VENOUS ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EXTRAVASATION ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FEELINGS OF WORTHLESSNESS ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GENITAL CANDIDIASIS ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GRAFT LOSS ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMOGLOBIN ABNORMAL ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HEART RATE ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERCHLORHYDRIA ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 4 FDA reports)
IRIS ADHESIONS ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LARYNGEAL ULCERATION ( 4 FDA reports)
LEUKAEMOID REACTION ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTATIC CARCINOID TUMOUR ( 4 FDA reports)
MITRAL VALVE SCLEROSIS ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OPTIC DISC DISORDER ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGEAL HAEMATOMA ( 4 FDA reports)
PHLEBOLITH ( 4 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PRODUCT CONTAMINATION ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 4 FDA reports)
PULMONARY HILUM MASS ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
PUSTULAR PSORIASIS ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RECTAL PROLAPSE ( 4 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
RHYTHM IDIOVENTRICULAR ( 4 FDA reports)
RIB DEFORMITY ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SCROTAL ERYTHEMA ( 4 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN WARM ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
SPONDYLOLYSIS ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SYSTOLIC HYPERTENSION ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TONGUE DISCOLOURATION ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TROPONIN T INCREASED ( 4 FDA reports)
TUMOUR MARKER INCREASED ( 4 FDA reports)
TYPE I HYPERSENSITIVITY ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VENTRICULAR DYSKINESIA ( 4 FDA reports)
VIRAL PERICARDITIS ( 4 FDA reports)
VITRITIS ( 4 FDA reports)
WISDOM TEETH REMOVAL ( 4 FDA reports)
WOUND DRAINAGE ( 4 FDA reports)
ABDOMINAL OPERATION ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ADENOIDITIS ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALLERGIC COUGH ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AURA ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
BALANOPOSTHITIS ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLADDER SPHINCTER ATONY ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD FOLATE ABNORMAL ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CD8 LYMPHOCYTES ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CHOROIDITIS ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COLON POLYPECTOMY ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
CYTOTOXIC OEDEMA ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DELAYED SLEEP PHASE ( 3 FDA reports)
DENGUE FEVER ( 3 FDA reports)
DENTAL PULP DISORDER ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
EATON-LAMBERT SYNDROME ( 3 FDA reports)
ECLAMPSIA ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOSCOPY ABNORMAL ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EPIDIDYMAL CYST ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HAEMORRHAGIC CYST ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEART TRANSPLANT ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOBLASTOMA ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HEREDITARY ANGIOEDEMA ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INHALATION THERAPY ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 3 FDA reports)
INTESTINAL HYPOMOTILITY ( 3 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
NAIL DYSTROPHY ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OEDEMATOUS PANCREATITIS ( 3 FDA reports)
OESOPHAGEAL IRRITATION ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
OSTEITIS DEFORMANS ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
PACEMAKER GENERATED RHYTHM ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATIC ATROPHY ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PAROTID GLAND INFLAMMATION ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PERIODONTAL DESTRUCTION ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLEURAL HAEMORRHAGE ( 3 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PRECOCIOUS PUBERTY ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PSEUDOMONAS BRONCHITIS ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
READING DISORDER ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RENAL CORTICAL NECROSIS ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
RETINAL ANOMALY CONGENITAL ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
RETINITIS PIGMENTOSA ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ROTAVIRUS INFECTION ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCEDOSPORIUM INFECTION ( 3 FDA reports)
SCROTAL ABSCESS ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SIGMOIDITIS ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SINUS TARSI SYNDROME ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SMOKER ( 3 FDA reports)
SOFT TISSUE INJURY ( 3 FDA reports)
SPEECH REHABILITATION ( 3 FDA reports)
SPIDER VEIN ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TACHYPHYLAXIS ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TEMPERATURE INTOLERANCE ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TESTICULAR ATROPHY ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
URINE OSMOLARITY DECREASED ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
URINE URIC ACID DECREASED ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ACUTE POLYNEUROPATHY ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC BYPASS ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC VALVE DISEASE MIXED ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTERIAL TEST ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC FUNCTION TEST ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CAST APPLICATION ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHLAMYDIA TEST POSITIVE ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY DISSECTION ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG THERAPY ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELEPHANTIASIS NOSTRAS VERRUCOSA ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENDOMETRIAL ATROPHY ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTERNAL EAR CELLULITIS ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMORRHAGIC HEPATIC CYST ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HISTONE ANTIBODY POSITIVE ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILEOSTOMY CLOSURE ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIGAMENT CALCIFICATION ( 2 FDA reports)
LIGAMENT LAXITY ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT HEPATOBILIARY NEOPLASM ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENISCAL DEGENERATION ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MICROVASCULAR ANGINA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MYCOPLASMA TEST POSITIVE ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPTIC DISC HAEMORRHAGE ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIORBITAL DISORDER ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURAL MESOTHELIOMA ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
REITER'S SYNDROME ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL HYPERTENSION ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENSION ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TILT TABLE TEST ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRICHORRHEXIS ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR DISSECTION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VESSEL PERFORATION ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL ERYTHEMA ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMNIOTIC CAVITY INFECTION ( 1 FDA reports)
AMPUTATION REVISION ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BREAST NORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING TIME ( 1 FDA reports)
BLINDNESS DAY ( 1 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BORRELIA BURGDORFERI SEROLOGY POSITIVE ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRANCHIAL CYST ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY INCREASED ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CAROTID ANEURYSM RUPTURE ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL DECOMPRESSION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CERVIX NEOPLASM ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONFUSIONAL AROUSAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE CAPTURING ISSUE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYSIPELOID ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILED TRIAL OF LABOUR ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR OF CROWDED PLACES ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRUCTOSAMINE INCREASED ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CYST ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE, OBSTRUCTIVE ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAMARTOMA VASCULAR ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE POSTOPERATIVE ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS NON-A NON-B NON-C ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
JUVENILE MELANOMA BENIGN ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL RIDGING ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NICOTINAMIDE DECREASED ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORF ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN ABNORMAL ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL MIGRAINE ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID NODULE REMOVAL ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SEPSIS PASTEURELLA ( 1 FDA reports)
SEPTIC RASH ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STARING ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST DECREASED ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROMBASTHENIA ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBIN TIME SHORTENED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TROPICAL SPRUE ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TRYPTASE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASONIC ANGIOGRAM ABNORMAL ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERIC REPAIR ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL OPERATION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR FRAGILITY ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS OXYGEN SATURATION DECREASED ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VITAMIN A DECREASED ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD CYST ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)