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

FALL ( 873 FDA reports)
CONFUSIONAL STATE ( 741 FDA reports)
NAUSEA ( 636 FDA reports)
DIZZINESS ( 623 FDA reports)
ASTHENIA ( 571 FDA reports)
SOMNOLENCE ( 542 FDA reports)
DIARRHOEA ( 512 FDA reports)
CONVULSION ( 463 FDA reports)
VOMITING ( 463 FDA reports)
DRUG INTERACTION ( 437 FDA reports)
BRADYCARDIA ( 429 FDA reports)
GAIT DISTURBANCE ( 423 FDA reports)
FATIGUE ( 416 FDA reports)
LOSS OF CONSCIOUSNESS ( 411 FDA reports)
SYNCOPE ( 409 FDA reports)
DEMENTIA ( 399 FDA reports)
HYPOTENSION ( 390 FDA reports)
DEHYDRATION ( 388 FDA reports)
DYSPNOEA ( 373 FDA reports)
TREMOR ( 370 FDA reports)
URINARY TRACT INFECTION ( 368 FDA reports)
PNEUMONIA ( 364 FDA reports)
HALLUCINATION ( 343 FDA reports)
PAIN ( 343 FDA reports)
ANXIETY ( 335 FDA reports)
HEADACHE ( 334 FDA reports)
MALAISE ( 327 FDA reports)
DECREASED APPETITE ( 318 FDA reports)
AGITATION ( 314 FDA reports)
PYREXIA ( 311 FDA reports)
DEPRESSION ( 289 FDA reports)
ANAEMIA ( 283 FDA reports)
WEIGHT DECREASED ( 283 FDA reports)
ATRIAL FIBRILLATION ( 281 FDA reports)
CEREBROVASCULAR ACCIDENT ( 281 FDA reports)
DEATH ( 278 FDA reports)
RENAL FAILURE ACUTE ( 277 FDA reports)
DRUG INEFFECTIVE ( 276 FDA reports)
INSOMNIA ( 276 FDA reports)
OEDEMA PERIPHERAL ( 273 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 266 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 258 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 253 FDA reports)
CONDITION AGGRAVATED ( 233 FDA reports)
MYOCARDIAL INFARCTION ( 227 FDA reports)
RHABDOMYOLYSIS ( 224 FDA reports)
HYPERTENSION ( 222 FDA reports)
RENAL FAILURE ( 209 FDA reports)
MEMORY IMPAIRMENT ( 207 FDA reports)
BLOOD GLUCOSE INCREASED ( 206 FDA reports)
CHEST PAIN ( 203 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 199 FDA reports)
LETHARGY ( 198 FDA reports)
AGGRESSION ( 197 FDA reports)
BLOOD PRESSURE DECREASED ( 197 FDA reports)
BACK PAIN ( 196 FDA reports)
CONSTIPATION ( 195 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 192 FDA reports)
DYSPHAGIA ( 190 FDA reports)
MENTAL STATUS CHANGES ( 188 FDA reports)
OVERDOSE ( 183 FDA reports)
DELIRIUM ( 182 FDA reports)
ABNORMAL BEHAVIOUR ( 180 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 173 FDA reports)
DISORIENTATION ( 172 FDA reports)
URINARY INCONTINENCE ( 172 FDA reports)
BLOOD PRESSURE INCREASED ( 170 FDA reports)
HAEMOGLOBIN DECREASED ( 169 FDA reports)
FEELING ABNORMAL ( 168 FDA reports)
AMNESIA ( 167 FDA reports)
RASH ( 166 FDA reports)
ARRHYTHMIA ( 165 FDA reports)
CARDIAC ARREST ( 165 FDA reports)
INJURY ( 164 FDA reports)
PNEUMONIA ASPIRATION ( 157 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 156 FDA reports)
CARDIAC FAILURE ( 152 FDA reports)
PAIN IN EXTREMITY ( 152 FDA reports)
COGNITIVE DISORDER ( 151 FDA reports)
HYPERHIDROSIS ( 151 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 149 FDA reports)
MUSCULAR WEAKNESS ( 147 FDA reports)
COUGH ( 142 FDA reports)
ARTHRALGIA ( 140 FDA reports)
MUSCLE SPASMS ( 140 FDA reports)
BLOOD CREATININE INCREASED ( 136 FDA reports)
WEIGHT INCREASED ( 136 FDA reports)
ABASIA ( 135 FDA reports)
BALANCE DISORDER ( 135 FDA reports)
CONTUSION ( 135 FDA reports)
ANOREXIA ( 134 FDA reports)
RESPIRATORY FAILURE ( 134 FDA reports)
ABDOMINAL PAIN ( 133 FDA reports)
DYSKINESIA ( 128 FDA reports)
HYPONATRAEMIA ( 128 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 124 FDA reports)
CARDIOMEGALY ( 121 FDA reports)
SPEECH DISORDER ( 118 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 116 FDA reports)
ABDOMINAL PAIN UPPER ( 114 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 113 FDA reports)
BLOOD UREA INCREASED ( 112 FDA reports)
CARDIO-RESPIRATORY ARREST ( 111 FDA reports)
PLEURAL EFFUSION ( 111 FDA reports)
CORONARY ARTERY DISEASE ( 110 FDA reports)
CARDIAC DISORDER ( 109 FDA reports)
SEPSIS ( 109 FDA reports)
COMA ( 108 FDA reports)
ECONOMIC PROBLEM ( 107 FDA reports)
SINUS BRADYCARDIA ( 106 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 105 FDA reports)
ERYTHEMA ( 104 FDA reports)
HYPOGLYCAEMIA ( 103 FDA reports)
SUDDEN DEATH ( 103 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 103 FDA reports)
ABDOMINAL DISCOMFORT ( 101 FDA reports)
HALLUCINATION, VISUAL ( 101 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 100 FDA reports)
DIABETES MELLITUS ( 100 FDA reports)
PULMONARY EMBOLISM ( 100 FDA reports)
HYPERKALAEMIA ( 99 FDA reports)
PLATELET COUNT DECREASED ( 99 FDA reports)
RESTLESSNESS ( 98 FDA reports)
VISION BLURRED ( 97 FDA reports)
UNRESPONSIVE TO STIMULI ( 94 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 93 FDA reports)
DYSARTHRIA ( 92 FDA reports)
HYPOAESTHESIA ( 92 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 91 FDA reports)
HEART RATE DECREASED ( 91 FDA reports)
PARKINSONISM ( 91 FDA reports)
PSYCHOTIC DISORDER ( 91 FDA reports)
DYSSTASIA ( 90 FDA reports)
OFF LABEL USE ( 90 FDA reports)
DYSURIA ( 88 FDA reports)
HIP FRACTURE ( 88 FDA reports)
POLLAKIURIA ( 87 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 86 FDA reports)
THROMBOCYTOPENIA ( 86 FDA reports)
HYPERSOMNIA ( 85 FDA reports)
CEREBRAL HAEMORRHAGE ( 84 FDA reports)
PRURITUS ( 83 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 83 FDA reports)
CEREBRAL INFARCTION ( 82 FDA reports)
CATARACT ( 81 FDA reports)
SICK SINUS SYNDROME ( 81 FDA reports)
SUICIDAL IDEATION ( 81 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 80 FDA reports)
BRONCHITIS ( 80 FDA reports)
LIVER DISORDER ( 80 FDA reports)
OSTEOARTHRITIS ( 80 FDA reports)
ANHEDONIA ( 79 FDA reports)
APHASIA ( 79 FDA reports)
PARAESTHESIA ( 79 FDA reports)
RENAL IMPAIRMENT ( 79 FDA reports)
TACHYCARDIA ( 79 FDA reports)
MYALGIA ( 77 FDA reports)
NIGHTMARE ( 77 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 76 FDA reports)
NEUROPATHY PERIPHERAL ( 76 FDA reports)
FAECAL INCONTINENCE ( 75 FDA reports)
PULMONARY OEDEMA ( 75 FDA reports)
HYPOXIA ( 74 FDA reports)
INFECTION ( 74 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 73 FDA reports)
CHILLS ( 73 FDA reports)
VENTRICULAR TACHYCARDIA ( 73 FDA reports)
EPILEPSY ( 72 FDA reports)
ORTHOSTATIC HYPOTENSION ( 72 FDA reports)
HYPOKALAEMIA ( 71 FDA reports)
CHOLELITHIASIS ( 70 FDA reports)
HAEMORRHAGE ( 70 FDA reports)
HYPOPHAGIA ( 70 FDA reports)
PALPITATIONS ( 70 FDA reports)
RESPIRATORY ARREST ( 70 FDA reports)
URINARY RETENTION ( 70 FDA reports)
CIRCULATORY COLLAPSE ( 69 FDA reports)
INCONTINENCE ( 69 FDA reports)
RECTAL HAEMORRHAGE ( 69 FDA reports)
RENAL FAILURE CHRONIC ( 69 FDA reports)
CEREBRAL ATROPHY ( 68 FDA reports)
IRRITABILITY ( 68 FDA reports)
HEAD INJURY ( 67 FDA reports)
INTERSTITIAL LUNG DISEASE ( 67 FDA reports)
PARKINSON'S DISEASE ( 67 FDA reports)
SHOCK ( 67 FDA reports)
GASTRITIS ( 66 FDA reports)
THROMBOSIS ( 66 FDA reports)
DISEASE PROGRESSION ( 65 FDA reports)
OSTEONECROSIS OF JAW ( 65 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 65 FDA reports)
TORSADE DE POINTES ( 65 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 64 FDA reports)
ILL-DEFINED DISORDER ( 63 FDA reports)
OSTEOMYELITIS ( 63 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 63 FDA reports)
ABNORMAL DREAMS ( 62 FDA reports)
BLOOD POTASSIUM DECREASED ( 62 FDA reports)
DISTURBANCE IN ATTENTION ( 62 FDA reports)
EMOTIONAL DISTRESS ( 62 FDA reports)
MEDICATION ERROR ( 62 FDA reports)
MIOSIS ( 62 FDA reports)
PANCYTOPENIA ( 62 FDA reports)
PARANOIA ( 62 FDA reports)
DELUSION ( 61 FDA reports)
MITRAL VALVE INCOMPETENCE ( 61 FDA reports)
SWELLING ( 61 FDA reports)
ASTHMA ( 60 FDA reports)
ATRIOVENTRICULAR BLOCK ( 60 FDA reports)
HAEMATOCRIT DECREASED ( 60 FDA reports)
ROTATOR CUFF SYNDROME ( 60 FDA reports)
TARDIVE DYSKINESIA ( 60 FDA reports)
GASTRIC ULCER ( 59 FDA reports)
HYPERLIPIDAEMIA ( 59 FDA reports)
ANGER ( 58 FDA reports)
EYE IRRITATION ( 58 FDA reports)
OSTEOPENIA ( 58 FDA reports)
PANCREATITIS ( 58 FDA reports)
RESPIRATORY DISORDER ( 58 FDA reports)
STRESS ( 58 FDA reports)
FEMUR FRACTURE ( 57 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 57 FDA reports)
GRAND MAL CONVULSION ( 57 FDA reports)
NERVOUSNESS ( 57 FDA reports)
GASTROENTERITIS ( 56 FDA reports)
HYPERGLYCAEMIA ( 56 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 56 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 56 FDA reports)
WHEEZING ( 56 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 55 FDA reports)
DECUBITUS ULCER ( 55 FDA reports)
DEEP VEIN THROMBOSIS ( 54 FDA reports)
DYSPNOEA EXERTIONAL ( 54 FDA reports)
HAEMATOCHEZIA ( 54 FDA reports)
HAEMATOMA ( 54 FDA reports)
MULTI-ORGAN FAILURE ( 54 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 54 FDA reports)
SPINAL OSTEOARTHRITIS ( 54 FDA reports)
BLOOD SODIUM DECREASED ( 53 FDA reports)
CHEST DISCOMFORT ( 52 FDA reports)
HAEMATEMESIS ( 52 FDA reports)
MULTIPLE SCLEROSIS ( 52 FDA reports)
UNEVALUABLE EVENT ( 52 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 51 FDA reports)
MUSCULOSKELETAL PAIN ( 51 FDA reports)
PRESYNCOPE ( 51 FDA reports)
TREATMENT NONCOMPLIANCE ( 51 FDA reports)
HEART RATE INCREASED ( 50 FDA reports)
SEDATION ( 50 FDA reports)
COLD SWEAT ( 49 FDA reports)
JOINT SWELLING ( 49 FDA reports)
MELAENA ( 49 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 49 FDA reports)
ATELECTASIS ( 48 FDA reports)
HEART RATE IRREGULAR ( 48 FDA reports)
INCORRECT DOSE ADMINISTERED ( 48 FDA reports)
MALNUTRITION ( 48 FDA reports)
MENTAL DISORDER ( 48 FDA reports)
MULTIPLE INJURIES ( 48 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 48 FDA reports)
ARTHRITIS ( 47 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 47 FDA reports)
DRUG DOSE OMISSION ( 47 FDA reports)
HYPERNATRAEMIA ( 47 FDA reports)
OEDEMA ( 47 FDA reports)
OSTEONECROSIS ( 47 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 47 FDA reports)
TYPE 2 DIABETES MELLITUS ( 47 FDA reports)
BLOOD BILIRUBIN INCREASED ( 46 FDA reports)
HYPOTHYROIDISM ( 46 FDA reports)
INFLUENZA ( 46 FDA reports)
NASOPHARYNGITIS ( 46 FDA reports)
PALLOR ( 46 FDA reports)
RHINORRHOEA ( 46 FDA reports)
RIB FRACTURE ( 46 FDA reports)
SUBDURAL HAEMATOMA ( 46 FDA reports)
BONE DISORDER ( 45 FDA reports)
MENTAL IMPAIRMENT ( 45 FDA reports)
PULMONARY HYPERTENSION ( 45 FDA reports)
SLEEP DISORDER ( 45 FDA reports)
DRUG LEVEL INCREASED ( 44 FDA reports)
LUNG INFECTION ( 44 FDA reports)
NEUTROPENIA ( 44 FDA reports)
STAPHYLOCOCCAL INFECTION ( 44 FDA reports)
ASPIRATION ( 43 FDA reports)
CAROTID ARTERY STENOSIS ( 43 FDA reports)
CELLULITIS ( 43 FDA reports)
DUODENAL ULCER ( 43 FDA reports)
HERPES ZOSTER ( 43 FDA reports)
MOVEMENT DISORDER ( 43 FDA reports)
ABDOMINAL DISTENSION ( 42 FDA reports)
ACCIDENTAL OVERDOSE ( 42 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 42 FDA reports)
DIFFICULTY IN WALKING ( 42 FDA reports)
EMPHYSEMA ( 42 FDA reports)
METABOLIC ACIDOSIS ( 42 FDA reports)
OSTEOPOROSIS ( 42 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 41 FDA reports)
DRY MOUTH ( 41 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 41 FDA reports)
MOBILITY DECREASED ( 41 FDA reports)
MUSCLE RIGIDITY ( 41 FDA reports)
OXYGEN SATURATION DECREASED ( 41 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 41 FDA reports)
RENAL DISORDER ( 41 FDA reports)
SINUSITIS ( 41 FDA reports)
URINE FLOW DECREASED ( 41 FDA reports)
ANGINA PECTORIS ( 40 FDA reports)
CEREBRAL ISCHAEMIA ( 40 FDA reports)
CRYING ( 40 FDA reports)
DIVERTICULUM INTESTINAL ( 40 FDA reports)
FEELING HOT ( 40 FDA reports)
HEPATIC ENZYME INCREASED ( 40 FDA reports)
INTESTINAL OBSTRUCTION ( 40 FDA reports)
LUNG DISORDER ( 40 FDA reports)
PELVIC FRACTURE ( 40 FDA reports)
VERTIGO ( 40 FDA reports)
BLOOD GLUCOSE DECREASED ( 39 FDA reports)
BLOOD POTASSIUM INCREASED ( 39 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 39 FDA reports)
FAECES DISCOLOURED ( 39 FDA reports)
FLUSHING ( 39 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 39 FDA reports)
SINUS ARREST ( 39 FDA reports)
COORDINATION ABNORMAL ( 38 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 38 FDA reports)
GLAUCOMA ( 38 FDA reports)
HALLUCINATION, AUDITORY ( 38 FDA reports)
HYPOTHERMIA ( 38 FDA reports)
NEPHROLITHIASIS ( 38 FDA reports)
BLADDER DISCOMFORT ( 37 FDA reports)
DRUG TOXICITY ( 37 FDA reports)
FAILURE TO THRIVE ( 37 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 37 FDA reports)
SALIVARY HYPERSECRETION ( 37 FDA reports)
VITAMIN D DECREASED ( 37 FDA reports)
ARTERIOSCLEROSIS ( 36 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 36 FDA reports)
CHOKING ( 36 FDA reports)
DRUG EFFECT DECREASED ( 36 FDA reports)
FOOT FRACTURE ( 36 FDA reports)
INFLUENZA LIKE ILLNESS ( 36 FDA reports)
LEUKOPENIA ( 36 FDA reports)
MANIA ( 36 FDA reports)
RASH MACULO-PAPULAR ( 36 FDA reports)
RESPIRATORY DISTRESS ( 36 FDA reports)
SLEEP APNOEA SYNDROME ( 36 FDA reports)
SUICIDE ATTEMPT ( 36 FDA reports)
BLOOD ALBUMIN DECREASED ( 35 FDA reports)
COMPLETED SUICIDE ( 35 FDA reports)
MIGRAINE ( 35 FDA reports)
VENTRICULAR FIBRILLATION ( 35 FDA reports)
VISUAL IMPAIRMENT ( 35 FDA reports)
DROOLING ( 34 FDA reports)
FEAR ( 34 FDA reports)
HEMIPARESIS ( 34 FDA reports)
PNEUMONIA BACTERIAL ( 34 FDA reports)
SKIN ULCER ( 34 FDA reports)
SPINAL COLUMN STENOSIS ( 34 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 34 FDA reports)
ALOPECIA ( 33 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 33 FDA reports)
CEREBROVASCULAR DISORDER ( 33 FDA reports)
COAGULOPATHY ( 33 FDA reports)
COLITIS ( 33 FDA reports)
FEELING COLD ( 33 FDA reports)
FLATULENCE ( 33 FDA reports)
NECK PAIN ( 33 FDA reports)
NOCTURIA ( 33 FDA reports)
ORAL INTAKE REDUCED ( 33 FDA reports)
PROSTATE CANCER ( 33 FDA reports)
AZOTAEMIA ( 32 FDA reports)
CYSTITIS ( 32 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 32 FDA reports)
EPISTAXIS ( 32 FDA reports)
HEPATIC FAILURE ( 32 FDA reports)
ISCHAEMIC STROKE ( 32 FDA reports)
JAUNDICE ( 32 FDA reports)
PERICARDIAL EFFUSION ( 32 FDA reports)
TOOTH DISORDER ( 32 FDA reports)
AGRANULOCYTOSIS ( 31 FDA reports)
BLOOD CALCIUM DECREASED ( 31 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 31 FDA reports)
BURSITIS ( 31 FDA reports)
DYSPEPSIA ( 31 FDA reports)
EATING DISORDER ( 31 FDA reports)
ENCEPHALOPATHY ( 31 FDA reports)
HOSPITALISATION ( 31 FDA reports)
HYPERPARATHYROIDISM ( 31 FDA reports)
HYPERSENSITIVITY ( 31 FDA reports)
INFLAMMATION ( 31 FDA reports)
MYOCLONUS ( 31 FDA reports)
NEOPLASM MALIGNANT ( 31 FDA reports)
PANCREATITIS ACUTE ( 31 FDA reports)
POSTURE ABNORMAL ( 31 FDA reports)
PULSE ABSENT ( 31 FDA reports)
RESPIRATORY RATE INCREASED ( 31 FDA reports)
RETCHING ( 31 FDA reports)
SURGERY ( 31 FDA reports)
THINKING ABNORMAL ( 31 FDA reports)
AORTIC ANEURYSM ( 30 FDA reports)
BLINDNESS ( 30 FDA reports)
BLISTER ( 30 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 30 FDA reports)
CATATONIA ( 30 FDA reports)
DEPRESSED MOOD ( 30 FDA reports)
DIALYSIS ( 30 FDA reports)
DIVERTICULUM ( 30 FDA reports)
DRUG HYPERSENSITIVITY ( 30 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 30 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 30 FDA reports)
HAEMATURIA ( 30 FDA reports)
IMPAIRED HEALING ( 30 FDA reports)
LACERATION ( 30 FDA reports)
LIPASE INCREASED ( 30 FDA reports)
MYOCARDIAL ISCHAEMIA ( 30 FDA reports)
SKIN DISCOLOURATION ( 30 FDA reports)
CARDIAC PACEMAKER INSERTION ( 29 FDA reports)
CHROMATURIA ( 29 FDA reports)
DEFORMITY ( 29 FDA reports)
LEUKOCYTOSIS ( 29 FDA reports)
NERVOUS SYSTEM DISORDER ( 29 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 29 FDA reports)
URTICARIA ( 29 FDA reports)
BRONCHOPNEUMONIA ( 28 FDA reports)
CARDIAC MURMUR ( 28 FDA reports)
CYTOLYTIC HEPATITIS ( 28 FDA reports)
EMOTIONAL DISORDER ( 28 FDA reports)
GASTROINTESTINAL DISORDER ( 28 FDA reports)
HICCUPS ( 28 FDA reports)
HYPOKINESIA ( 28 FDA reports)
LUNG NEOPLASM MALIGNANT ( 28 FDA reports)
PERSONALITY CHANGE ( 28 FDA reports)
PORIOMANIA ( 28 FDA reports)
PROTEINURIA ( 28 FDA reports)
COLONIC POLYP ( 27 FDA reports)
CYANOSIS ( 27 FDA reports)
ECZEMA ( 27 FDA reports)
FUNGAL INFECTION ( 27 FDA reports)
GASTRIC DISORDER ( 27 FDA reports)
HYPERCALCAEMIA ( 27 FDA reports)
ILEUS ( 27 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 27 FDA reports)
MOTOR DYSFUNCTION ( 27 FDA reports)
PANIC ATTACK ( 27 FDA reports)
PLEUROTHOTONUS ( 27 FDA reports)
TOOTH EXTRACTION ( 27 FDA reports)
UROSEPSIS ( 27 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 26 FDA reports)
ARTHROPATHY ( 26 FDA reports)
DIVERTICULITIS ( 26 FDA reports)
HYDROCEPHALUS ( 26 FDA reports)
HYPOTONIA ( 26 FDA reports)
LACUNAR INFARCTION ( 26 FDA reports)
LIMB INJURY ( 26 FDA reports)
MAJOR DEPRESSION ( 26 FDA reports)
MUSCLE TWITCHING ( 26 FDA reports)
RHINITIS ( 26 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 26 FDA reports)
TOOTH FRACTURE ( 26 FDA reports)
WITHDRAWAL SYNDROME ( 26 FDA reports)
BEDRIDDEN ( 25 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 25 FDA reports)
BLOOD URINE PRESENT ( 25 FDA reports)
BODY TEMPERATURE INCREASED ( 25 FDA reports)
BREAST CANCER ( 25 FDA reports)
CATARACT OPERATION ( 25 FDA reports)
DIPLOPIA ( 25 FDA reports)
DRUG ERUPTION ( 25 FDA reports)
DYSPHONIA ( 25 FDA reports)
FLUID RETENTION ( 25 FDA reports)
HAEMODIALYSIS ( 25 FDA reports)
HAEMORRHOIDS ( 25 FDA reports)
HYPOVOLAEMIA ( 25 FDA reports)
MOOD SWINGS ( 25 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 25 FDA reports)
SPINAL COMPRESSION FRACTURE ( 25 FDA reports)
VISUAL ACUITY REDUCED ( 25 FDA reports)
WRIST FRACTURE ( 25 FDA reports)
ANKLE FRACTURE ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 24 FDA reports)
BLOOD CHLORIDE DECREASED ( 24 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 24 FDA reports)
BODY TEMPERATURE DECREASED ( 24 FDA reports)
CARDIOMYOPATHY ( 24 FDA reports)
CYST ( 24 FDA reports)
DRUG ADMINISTRATION ERROR ( 24 FDA reports)
DYSTONIA ( 24 FDA reports)
EOSINOPHILIA ( 24 FDA reports)
FLUID OVERLOAD ( 24 FDA reports)
INCOHERENT ( 24 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 24 FDA reports)
MULTIPLE MYELOMA ( 24 FDA reports)
PRODUCT QUALITY ISSUE ( 24 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 24 FDA reports)
RADICULOPATHY ( 24 FDA reports)
RASH ERYTHEMATOUS ( 24 FDA reports)
SCREAMING ( 24 FDA reports)
STEVENS-JOHNSON SYNDROME ( 24 FDA reports)
ANGINA UNSTABLE ( 23 FDA reports)
APATHY ( 23 FDA reports)
APHAGIA ( 23 FDA reports)
ASCITES ( 23 FDA reports)
BURNING SENSATION ( 23 FDA reports)
COMPRESSION FRACTURE ( 23 FDA reports)
DIASTOLIC DYSFUNCTION ( 23 FDA reports)
HYPERCHOLESTEROLAEMIA ( 23 FDA reports)
HYPERTENSIVE CRISIS ( 23 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 23 FDA reports)
LUNG INFILTRATION ( 23 FDA reports)
PROTHROMBIN TIME PROLONGED ( 23 FDA reports)
RALES ( 23 FDA reports)
SINUS TACHYCARDIA ( 23 FDA reports)
SKIN EXFOLIATION ( 23 FDA reports)
SOCIAL PROBLEM ( 23 FDA reports)
TINNITUS ( 23 FDA reports)
VENTRICULAR HYPERTROPHY ( 23 FDA reports)
ACUTE RESPIRATORY FAILURE ( 22 FDA reports)
CERVICAL SPINAL STENOSIS ( 22 FDA reports)
COMMUNICATION DISORDER ( 22 FDA reports)
DECREASED ACTIVITY ( 22 FDA reports)
EYELID PTOSIS ( 22 FDA reports)
HYPERTONIA ( 22 FDA reports)
MIDDLE INSOMNIA ( 22 FDA reports)
PULMONARY FIBROSIS ( 22 FDA reports)
PURULENT DISCHARGE ( 22 FDA reports)
RESPIRATORY DEPRESSION ( 22 FDA reports)
RESTLESS LEGS SYNDROME ( 22 FDA reports)
ROAD TRAFFIC ACCIDENT ( 22 FDA reports)
SEPTIC SHOCK ( 22 FDA reports)
SPONDYLOLISTHESIS ( 22 FDA reports)
STOMACH DISCOMFORT ( 22 FDA reports)
TOOTHACHE ( 22 FDA reports)
VASCULAR DEMENTIA ( 22 FDA reports)
ABSCESS ( 21 FDA reports)
BILE DUCT STONE ( 21 FDA reports)
BLOOD AMYLASE INCREASED ( 21 FDA reports)
CARDIOGENIC SHOCK ( 21 FDA reports)
CARDIOVASCULAR DISORDER ( 21 FDA reports)
ERUCTATION ( 21 FDA reports)
EYE DISORDER ( 21 FDA reports)
JOINT INJURY ( 21 FDA reports)
LUMBAR SPINAL STENOSIS ( 21 FDA reports)
LYMPHADENOPATHY ( 21 FDA reports)
MOUTH ULCERATION ( 21 FDA reports)
OBESITY ( 21 FDA reports)
PARALYSIS ( 21 FDA reports)
POOR QUALITY SLEEP ( 21 FDA reports)
RASH PRURITIC ( 21 FDA reports)
SCHIZOPHRENIA ( 21 FDA reports)
SKIN LACERATION ( 21 FDA reports)
ABDOMINAL PAIN LOWER ( 20 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 20 FDA reports)
ATRIAL FLUTTER ( 20 FDA reports)
BONE PAIN ( 20 FDA reports)
DEAFNESS ( 20 FDA reports)
EXOSTOSIS ( 20 FDA reports)
FACE INJURY ( 20 FDA reports)
FRACTURE ( 20 FDA reports)
HEPATITIS ( 20 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 20 FDA reports)
MUSCLE CRAMP ( 20 FDA reports)
OESOPHAGITIS ( 20 FDA reports)
ONYCHOMYCOSIS ( 20 FDA reports)
OPEN WOUND ( 20 FDA reports)
PEMPHIGOID ( 20 FDA reports)
PETECHIAE ( 20 FDA reports)
PYELONEPHRITIS ( 20 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 20 FDA reports)
ACUTE PULMONARY OEDEMA ( 19 FDA reports)
AORTIC STENOSIS ( 19 FDA reports)
BLOOD CHLORIDE INCREASED ( 19 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 19 FDA reports)
CORONARY ARTERY STENOSIS ( 19 FDA reports)
DISEASE RECURRENCE ( 19 FDA reports)
EYE ROLLING ( 19 FDA reports)
FEMORAL NECK FRACTURE ( 19 FDA reports)
HEMIPLEGIA ( 19 FDA reports)
HYPERKERATOSIS ( 19 FDA reports)
IMPAIRED SELF-CARE ( 19 FDA reports)
INJECTION SITE PAIN ( 19 FDA reports)
IRON DEFICIENCY ANAEMIA ( 19 FDA reports)
LACRIMATION INCREASED ( 19 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 19 FDA reports)
OROPHARYNGEAL PAIN ( 19 FDA reports)
POST PROCEDURAL COMPLICATION ( 19 FDA reports)
STATUS EPILEPTICUS ( 19 FDA reports)
TOXIC SKIN ERUPTION ( 19 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
URINE OUTPUT DECREASED ( 19 FDA reports)
AORTIC VALVE INCOMPETENCE ( 18 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 18 FDA reports)
BODY HEIGHT DECREASED ( 18 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 18 FDA reports)
CONJUNCTIVITIS ( 18 FDA reports)
CORONARY ARTERY OCCLUSION ( 18 FDA reports)
DIABETIC NEUROPATHY ( 18 FDA reports)
EYE DISCHARGE ( 18 FDA reports)
FACIAL PALSY ( 18 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 18 FDA reports)
MASTICATION DISORDER ( 18 FDA reports)
MICTURITION URGENCY ( 18 FDA reports)
PEPTIC ULCER ( 18 FDA reports)
PERIPHERAL COLDNESS ( 18 FDA reports)
PNEUMOTHORAX ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
SCOLIOSIS ( 18 FDA reports)
SINUS CONGESTION ( 18 FDA reports)
SMALL INTESTINAL PERFORATION ( 18 FDA reports)
TORTICOLLIS ( 18 FDA reports)
URINE ODOUR ABNORMAL ( 18 FDA reports)
APNOEA ( 17 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 17 FDA reports)
CHOLESTASIS ( 17 FDA reports)
DIET REFUSAL ( 17 FDA reports)
EROSIVE OESOPHAGITIS ( 17 FDA reports)
FIBULA FRACTURE ( 17 FDA reports)
FLUID INTAKE REDUCED ( 17 FDA reports)
FOOT DEFORMITY ( 17 FDA reports)
GALLBLADDER DISORDER ( 17 FDA reports)
GINGIVAL BLEEDING ( 17 FDA reports)
HIATUS HERNIA ( 17 FDA reports)
HYPERTENSIVE HEART DISEASE ( 17 FDA reports)
LIP DISCOLOURATION ( 17 FDA reports)
NEPHROPATHY TOXIC ( 17 FDA reports)
NEPHROSCLEROSIS ( 17 FDA reports)
NEUTROPHIL COUNT DECREASED ( 17 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 17 FDA reports)
RENAL CYST ( 17 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 17 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 16 FDA reports)
BACTERIAL DISEASE CARRIER ( 16 FDA reports)
BLOOD SODIUM INCREASED ( 16 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 16 FDA reports)
BRONCHOPLEURAL FISTULA ( 16 FDA reports)
CANDIDIASIS ( 16 FDA reports)
CARDIAC FAILURE ACUTE ( 16 FDA reports)
CARPAL TUNNEL SYNDROME ( 16 FDA reports)
CHOLANGITIS ( 16 FDA reports)
CHOLECYSTITIS ( 16 FDA reports)
CORONARY ARTERY BYPASS ( 16 FDA reports)
DYSGEUSIA ( 16 FDA reports)
EMPYEMA ( 16 FDA reports)
EOSINOPHIL COUNT INCREASED ( 16 FDA reports)
EXTRASYSTOLES ( 16 FDA reports)
FAECALOMA ( 16 FDA reports)
GAZE PALSY ( 16 FDA reports)
HEPATIC CIRRHOSIS ( 16 FDA reports)
HEPATITIS C ( 16 FDA reports)
HYDRONEPHROSIS ( 16 FDA reports)
HYDROPNEUMOTHORAX ( 16 FDA reports)
HYPERAMMONAEMIA ( 16 FDA reports)
HYPOGLYCAEMIC COMA ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
INTENTIONAL DRUG MISUSE ( 16 FDA reports)
JOINT EFFUSION ( 16 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 16 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 16 FDA reports)
LOGORRHOEA ( 16 FDA reports)
MENOPAUSE ( 16 FDA reports)
NO ADVERSE EVENT ( 16 FDA reports)
NO THERAPEUTIC RESPONSE ( 16 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
OSTEORADIONECROSIS ( 16 FDA reports)
PAIN IN JAW ( 16 FDA reports)
POOR PERSONAL HYGIENE ( 16 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 16 FDA reports)
SCAR ( 16 FDA reports)
SEROTONIN SYNDROME ( 16 FDA reports)
SINOATRIAL BLOCK ( 16 FDA reports)
SPINAL CORD COMPRESSION ( 16 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 16 FDA reports)
TIBIA FRACTURE ( 16 FDA reports)
ABSCESS JAW ( 15 FDA reports)
ACUTE PRERENAL FAILURE ( 15 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 15 FDA reports)
AGEUSIA ( 15 FDA reports)
BENIGN COLONIC NEOPLASM ( 15 FDA reports)
BIPOLAR DISORDER ( 15 FDA reports)
BLADDER CANCER RECURRENT ( 15 FDA reports)
BLOOD CALCIUM INCREASED ( 15 FDA reports)
CHEST X-RAY ABNORMAL ( 15 FDA reports)
CHOLINERGIC SYNDROME ( 15 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 15 FDA reports)
CONCUSSION ( 15 FDA reports)
DILATATION ATRIAL ( 15 FDA reports)
GRANULOCYTOPENIA ( 15 FDA reports)
HAEMOPTYSIS ( 15 FDA reports)
HEPATIC ENCEPHALOPATHY ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
LABORATORY TEST ABNORMAL ( 15 FDA reports)
LARGE INTESTINE PERFORATION ( 15 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
MOOD ALTERED ( 15 FDA reports)
MUSCLE TIGHTNESS ( 15 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 15 FDA reports)
ORAL PAIN ( 15 FDA reports)
PETIT MAL EPILEPSY ( 15 FDA reports)
PHYSICAL DISABILITY ( 15 FDA reports)
READING DISORDER ( 15 FDA reports)
VIRAL INFECTION ( 15 FDA reports)
VISUAL DISTURBANCE ( 15 FDA reports)
WALKING AID USER ( 15 FDA reports)
WOUND INFECTION ( 15 FDA reports)
ABDOMINAL TENDERNESS ( 14 FDA reports)
ADVERSE EVENT ( 14 FDA reports)
ATRIAL TACHYCARDIA ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 14 FDA reports)
BLADDER DISORDER ( 14 FDA reports)
BLOOD MAGNESIUM DECREASED ( 14 FDA reports)
BRUXISM ( 14 FDA reports)
BUNDLE BRANCH BLOCK ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
DRUG PRESCRIBING ERROR ( 14 FDA reports)
DRY EYE ( 14 FDA reports)
EXCORIATION ( 14 FDA reports)
FAMILY STRESS ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
GASTRIC CANCER ( 14 FDA reports)
HEPATITIS FULMINANT ( 14 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 14 FDA reports)
INCREASED APPETITE ( 14 FDA reports)
INCREASED TENDENCY TO BRUISE ( 14 FDA reports)
INJECTION SITE HAEMATOMA ( 14 FDA reports)
INJECTION SITE HAEMORRHAGE ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
NEUROGENIC BLADDER ( 14 FDA reports)
OCCULT BLOOD POSITIVE ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
RED BLOOD CELL ABNORMALITY ( 14 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 14 FDA reports)
RENAL INJURY ( 14 FDA reports)
SENILE DEMENTIA ( 14 FDA reports)
SPINAL DISORDER ( 14 FDA reports)
SPINAL HAEMANGIOMA ( 14 FDA reports)
SUDDEN CARDIAC DEATH ( 14 FDA reports)
SWELLING FACE ( 14 FDA reports)
TYPE 1 DIABETES MELLITUS ( 14 FDA reports)
ACUTE PSYCHOSIS ( 13 FDA reports)
AKATHISIA ( 13 FDA reports)
ANURIA ( 13 FDA reports)
APPLICATION SITE ERYTHEMA ( 13 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 13 FDA reports)
BACK INJURY ( 13 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 13 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 13 FDA reports)
BLOOD URIC ACID INCREASED ( 13 FDA reports)
BRAIN OEDEMA ( 13 FDA reports)
BRONCHOSPASM ( 13 FDA reports)
CACHEXIA ( 13 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 13 FDA reports)
CHOREA ( 13 FDA reports)
CLOSTRIDIAL INFECTION ( 13 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 13 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 13 FDA reports)
DIABETIC NEPHROPATHY ( 13 FDA reports)
DRY SKIN ( 13 FDA reports)
EXPOSED BONE IN JAW ( 13 FDA reports)
FACIAL BONES FRACTURE ( 13 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 13 FDA reports)
HY'S LAW CASE ( 13 FDA reports)
HYPERBILIRUBINAEMIA ( 13 FDA reports)
HYPERSEXUALITY ( 13 FDA reports)
HYPOPROTEINAEMIA ( 13 FDA reports)
ILEUS PARALYTIC ( 13 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 13 FDA reports)
NEPHROPATHY ( 13 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 13 FDA reports)
OESOPHAGEAL ULCER ( 13 FDA reports)
PATHOLOGICAL GAMBLING ( 13 FDA reports)
PHARYNGEAL OEDEMA ( 13 FDA reports)
PLATELET COUNT INCREASED ( 13 FDA reports)
PLEURAL FIBROSIS ( 13 FDA reports)
PRESCRIBED OVERDOSE ( 13 FDA reports)
PRODUCTIVE COUGH ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
RASH MACULAR ( 13 FDA reports)
REFLUX OESOPHAGITIS ( 13 FDA reports)
RETINAL DETACHMENT ( 13 FDA reports)
ROSACEA ( 13 FDA reports)
SKIN LESION ( 13 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 13 FDA reports)
UPPER LIMB FRACTURE ( 13 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 13 FDA reports)
ANAPHYLACTIC SHOCK ( 12 FDA reports)
BLINDNESS UNILATERAL ( 12 FDA reports)
BREAST CANCER FEMALE ( 12 FDA reports)
CARDIAC VALVE DISEASE ( 12 FDA reports)
CARDIOPULMONARY FAILURE ( 12 FDA reports)
CENTRAL LINE INFECTION ( 12 FDA reports)
CERUMEN IMPACTION ( 12 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 12 FDA reports)
DEBRIDEMENT ( 12 FDA reports)
EAR PAIN ( 12 FDA reports)
ECCHYMOSIS ( 12 FDA reports)
EMBOLISM ( 12 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 12 FDA reports)
GRANULOCYTE COUNT DECREASED ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HYPERPHAGIA ( 12 FDA reports)
HYPERTHYROIDISM ( 12 FDA reports)
HYPOALBUMINAEMIA ( 12 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 12 FDA reports)
INTENTIONAL SELF-INJURY ( 12 FDA reports)
IRRITABLE BOWEL SYNDROME ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
LONG QT SYNDROME ( 12 FDA reports)
LOOSE STOOLS ( 12 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
MACULAR DEGENERATION ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
METASTASES TO LYMPH NODES ( 12 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 12 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 12 FDA reports)
NECROSIS ( 12 FDA reports)
NIGHT SWEATS ( 12 FDA reports)
NODAL RHYTHM ( 12 FDA reports)
PARTIAL SEIZURES ( 12 FDA reports)
PERICARDITIS ( 12 FDA reports)
PRIMARY SEQUESTRUM ( 12 FDA reports)
PURPURA ( 12 FDA reports)
RECTAL POLYP ( 12 FDA reports)
STUPOR ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
TENDERNESS ( 12 FDA reports)
TENDON RUPTURE ( 12 FDA reports)
UTERINE CANCER ( 12 FDA reports)
AFFECTIVE DISORDER ( 11 FDA reports)
APLASIA PURE RED CELL ( 11 FDA reports)
BACK DISORDER ( 11 FDA reports)
BRAIN HERNIATION ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
CARDIAC TAMPONADE ( 11 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 11 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 11 FDA reports)
COMPLEX PARTIAL SEIZURES ( 11 FDA reports)
CORONARY ARTERY RESTENOSIS ( 11 FDA reports)
CULTURE URINE POSITIVE ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DRESSLER'S SYNDROME ( 11 FDA reports)
DRUG DISPENSING ERROR ( 11 FDA reports)
EJECTION FRACTION DECREASED ( 11 FDA reports)
ENTEROCOLITIS ( 11 FDA reports)
ESSENTIAL HYPERTENSION ( 11 FDA reports)
EUPHORIC MOOD ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
GRIMACING ( 11 FDA reports)
HOT FLUSH ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
INTESTINAL ISCHAEMIA ( 11 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 11 FDA reports)
IRON DEFICIENCY ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
KIDNEY INFECTION ( 11 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
NEUTROPHIL COUNT INCREASED ( 11 FDA reports)
OLIGURIA ( 11 FDA reports)
PEMPHIGUS ( 11 FDA reports)
PERONEAL NERVE PALSY ( 11 FDA reports)
PHOTOSENSITIVITY REACTION ( 11 FDA reports)
PHYSICAL ASSAULT ( 11 FDA reports)
PULMONARY CONGESTION ( 11 FDA reports)
PULMONARY MASS ( 11 FDA reports)
RASH GENERALISED ( 11 FDA reports)
SEQUESTRECTOMY ( 11 FDA reports)
SKIN CANDIDA ( 11 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 11 FDA reports)
TENDONITIS ( 11 FDA reports)
THIRST ( 11 FDA reports)
ULCER HAEMORRHAGE ( 11 FDA reports)
VERBAL ABUSE ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 10 FDA reports)
AKINESIA ( 10 FDA reports)
AMMONIA INCREASED ( 10 FDA reports)
ANAPHYLACTIC REACTION ( 10 FDA reports)
ANGIOPATHY ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
BACTERIAL INFECTION ( 10 FDA reports)
BLOOD CREATINE INCREASED ( 10 FDA reports)
BLOOD PRESSURE ABNORMAL ( 10 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 10 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 10 FDA reports)
BRADYKINESIA ( 10 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 10 FDA reports)
BREAST CALCIFICATIONS ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
CAROTID ARTERY OCCLUSION ( 10 FDA reports)
CEREBRAL HAEMATOMA ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
CLAVICLE FRACTURE ( 10 FDA reports)
COLLAPSE OF LUNG ( 10 FDA reports)
DECREASED INTEREST ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DISSOCIATION ( 10 FDA reports)
DYSLIPIDAEMIA ( 10 FDA reports)
ELECTROLYTE IMBALANCE ( 10 FDA reports)
EMBOLIC STROKE ( 10 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FACE OEDEMA ( 10 FDA reports)
FISTULA ( 10 FDA reports)
FRUSTRATION ( 10 FDA reports)
GALLBLADDER CANCER ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
HAEMORRHAGIC ANAEMIA ( 10 FDA reports)
HALLUCINATION, OLFACTORY ( 10 FDA reports)
HEPATIC STEATOSIS ( 10 FDA reports)
HEPATOTOXICITY ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
IMPULSE-CONTROL DISORDER ( 10 FDA reports)
JOINT DISLOCATION ( 10 FDA reports)
LABYRINTHITIS ( 10 FDA reports)
LARGE INTESTINAL ULCER ( 10 FDA reports)
LOCAL SWELLING ( 10 FDA reports)
LOWER EXTREMITY MASS ( 10 FDA reports)
MUSCLE ATROPHY ( 10 FDA reports)
MUSCLE DISORDER ( 10 FDA reports)
MUSCLE HAEMORRHAGE ( 10 FDA reports)
MYDRIASIS ( 10 FDA reports)
NEPHRITIS ( 10 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 10 FDA reports)
ORGAN FAILURE ( 10 FDA reports)
PROSTATE CANCER METASTATIC ( 10 FDA reports)
PSYCHOMOTOR RETARDATION ( 10 FDA reports)
PULMONARY THROMBOSIS ( 10 FDA reports)
QUADRIPLEGIA ( 10 FDA reports)
RENAL ATROPHY ( 10 FDA reports)
RESUSCITATION ( 10 FDA reports)
RIGHT ATRIAL DILATATION ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 10 FDA reports)
TONGUE BITING ( 10 FDA reports)
TONGUE DISORDER ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 10 FDA reports)
ABSCESS DRAINAGE ( 9 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
AORTIC VALVE STENOSIS ( 9 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
ASPHYXIA ( 9 FDA reports)
ASTHENOPIA ( 9 FDA reports)
BASAL CELL CARCINOMA ( 9 FDA reports)
BLOOD MAGNESIUM INCREASED ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BONE DEBRIDEMENT ( 9 FDA reports)
CAROTID ARTERY DISEASE ( 9 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 9 FDA reports)
DENTURE WEARER ( 9 FDA reports)
DERMATITIS CONTACT ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
ENDODONTIC PROCEDURE ( 9 FDA reports)
ENERGY INCREASED ( 9 FDA reports)
ERYTHEMA MULTIFORME ( 9 FDA reports)
EYE MOVEMENT DISORDER ( 9 FDA reports)
EYE PAIN ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GASTROINTESTINAL ULCER ( 9 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 9 FDA reports)
GENERALISED OEDEMA ( 9 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 9 FDA reports)
GOUT ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HIP ARTHROPLASTY ( 9 FDA reports)
HOSTILITY ( 9 FDA reports)
HYPERTONIC BLADDER ( 9 FDA reports)
HYPOMANIA ( 9 FDA reports)
IMMOBILE ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
INGROWING NAIL ( 9 FDA reports)
INITIAL INSOMNIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
KNEE ARTHROPLASTY ( 9 FDA reports)
LIMB DISCOMFORT ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
LISTLESS ( 9 FDA reports)
LOWER LIMB FRACTURE ( 9 FDA reports)
LUMBAR RADICULOPATHY ( 9 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 9 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 9 FDA reports)
MONOPLEGIA ( 9 FDA reports)
MUSCLE SPASTICITY ( 9 FDA reports)
NON-CARDIAC CHEST PAIN ( 9 FDA reports)
OCULAR HYPERAEMIA ( 9 FDA reports)
OPTIC NEURITIS ( 9 FDA reports)
ORTHOPNOEA ( 9 FDA reports)
PANCREATIC PSEUDOCYST ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PCO2 DECREASED ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 9 FDA reports)
PROSTATIC DISORDER ( 9 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 9 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 9 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 9 FDA reports)
SENSORY LOSS ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
SKIN PAPILLOMA ( 9 FDA reports)
SKIN WARM ( 9 FDA reports)
SLUGGISHNESS ( 9 FDA reports)
SNORING ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
TACHYARRHYTHMIA ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
THERAPY NON-RESPONDER ( 9 FDA reports)
THYROID DISORDER ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
URGE INCONTINENCE ( 9 FDA reports)
VESTIBULAR DISORDER ( 9 FDA reports)
ADAMS-STOKES SYNDROME ( 8 FDA reports)
AFFECT LABILITY ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 8 FDA reports)
BARRETT'S OESOPHAGUS ( 8 FDA reports)
BLADDER CATHETERISATION ( 8 FDA reports)
BLOOD OSMOLARITY INCREASED ( 8 FDA reports)
BRADYARRHYTHMIA ( 8 FDA reports)
CARDIAC FLUTTER ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 8 FDA reports)
COGNITIVE DETERIORATION ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 8 FDA reports)
DEMENTIA WITH LEWY BODIES ( 8 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 8 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
ERECTILE DYSFUNCTION ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HALLUCINATIONS, MIXED ( 8 FDA reports)
HEPATITIS CHOLESTATIC ( 8 FDA reports)
HOMOCYSTINAEMIA ( 8 FDA reports)
HYPERKINESIA ( 8 FDA reports)
HYPERVIGILANCE ( 8 FDA reports)
IMPAIRED WORK ABILITY ( 8 FDA reports)
INTRACARDIAC THROMBUS ( 8 FDA reports)
ISCHAEMIA ( 8 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
LIVER ABSCESS ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
MITRAL VALVE CALCIFICATION ( 8 FDA reports)
MITRAL VALVE DISEASE ( 8 FDA reports)
MONOCYTE COUNT INCREASED ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
PROCEDURAL COMPLICATION ( 8 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
RHEUMATOID ARTHRITIS ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
TIC ( 8 FDA reports)
VIITH NERVE PARALYSIS ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
ALVEOLOPLASTY ( 7 FDA reports)
ANAEMIA MACROCYTIC ( 7 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 7 FDA reports)
BIPOLAR I DISORDER ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 7 FDA reports)
BLOOD LACTIC ACID INCREASED ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
BONE OPERATION ( 7 FDA reports)
BREAST CANCER IN SITU ( 7 FDA reports)
BREAST LUMP REMOVAL ( 7 FDA reports)
BREAST OEDEMA ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CEREBRAL THROMBOSIS ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
DIABETIC COMPLICATION ( 7 FDA reports)
DIABETIC RETINOPATHY ( 7 FDA reports)
DIZZINESS POSTURAL ( 7 FDA reports)
DRUG DEPENDENCE ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
DUODENAL PERFORATION ( 7 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
FACIAL PAIN ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
GASTRIC ULCER HELICOBACTER ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 7 FDA reports)
GLOSSITIS ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HYPERTHERMIA MALIGNANT ( 7 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
LIBIDO INCREASED ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
MAMMOPLASTY ( 7 FDA reports)
MASTOIDITIS ( 7 FDA reports)
MICROANGIOPATHY ( 7 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 7 FDA reports)
MYOCLONIC EPILEPSY ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
PANCREATIC ENZYMES INCREASED ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PERITONEAL EFFUSION ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 7 FDA reports)
PROCEDURAL PAIN ( 7 FDA reports)
PULSE PRESSURE DECREASED ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ROTATOR CUFF REPAIR ( 7 FDA reports)
SENSORY DISTURBANCE ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SINUS HEADACHE ( 7 FDA reports)
STARING ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
TEMPORAL ARTERITIS ( 7 FDA reports)
THORACOTOMY ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
TRIGEMINAL NEURALGIA ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
VITREOUS FLOATERS ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
ABDOMINAL SEPSIS ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLOOD BICARBONATE DECREASED ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BREAST DISORDER ( 6 FDA reports)
BREAST MASS ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARBON DIOXIDE DECREASED ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DEPRESSIVE SYMPTOM ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DEVICE FAILURE ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ENDOMETRIAL CANCER ( 6 FDA reports)
ENTEROCOCCAL SEPSIS ( 6 FDA reports)
ENURESIS ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GOODPASTURE'S SYNDROME ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HAEMORRHAGIC DIATHESIS ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEPATIC CANCER METASTATIC ( 6 FDA reports)
HOMICIDAL IDEATION ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
IATROGENIC INJURY ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTESTINAL DILATATION ( 6 FDA reports)
INTRACRANIAL ANEURYSM ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 6 FDA reports)
LARGE INTESTINE CARCINOMA ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LEUKOENCEPHALOPATHY ( 6 FDA reports)
LIP HAEMORRHAGE ( 6 FDA reports)
LUNG OPERATION ( 6 FDA reports)
MALLORY-WEISS SYNDROME ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
MYOSITIS ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEOPLASM PROGRESSION ( 6 FDA reports)
NEURODEGENERATIVE DISORDER ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 6 FDA reports)
OESOPHAGEAL STENOSIS ( 6 FDA reports)
OPEN ANGLE GLAUCOMA ( 6 FDA reports)
ORAL CANDIDIASIS ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PANCREATIC NECROSIS ( 6 FDA reports)
PATHOGEN RESISTANCE ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
POSTNASAL DRIP ( 6 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 6 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RETINAL HAEMORRHAGE ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SINUS OPERATION ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SLEEP TALKING ( 6 FDA reports)
SMALL INTESTINE CARCINOMA ( 6 FDA reports)
SPUTUM ABNORMAL ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 6 FDA reports)
STOMATITIS HAEMORRHAGIC ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
TOOTH LOSS ( 6 FDA reports)
UTERINE HAEMORRHAGE ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VITAMIN B1 DEFICIENCY ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
WOUND DEHISCENCE ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ABULIA ( 5 FDA reports)
ACARODERMATITIS ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 5 FDA reports)
ANEURYSM ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APHONIA ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
APRAXIA ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BELLIGERENCE ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD DISORDER ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BONE MARROW TRANSPLANT ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CEREBRAL DISORDER ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHLAMYDIAL INFECTION ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
CONFABULATION ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
DAYDREAMING ( 5 FDA reports)
DECEREBRATION ( 5 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG LEVEL FLUCTUATING ( 5 FDA reports)
DRUG SCREEN POSITIVE ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENDARTERECTOMY ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 5 FDA reports)
ENTEROCOCCAL INFECTION ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXERCISE TOLERANCE DECREASED ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FOOD AVERSION ( 5 FDA reports)
FOOD CRAVING ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HORDEOLUM ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERTENSIVE EMERGENCY ( 5 FDA reports)
HYPNAGOGIC HALLUCINATION ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
HYSTEROSCOPY ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
INCISIONAL HERNIA ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTERMITTENT CLAUDICATION ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 5 FDA reports)
INTUSSUSCEPTION ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LACTOSE INTOLERANCE ( 5 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
MASKED FACIES ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MOANING ( 5 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
MUTISM ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PELVIC FLUID COLLECTION ( 5 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 5 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 5 FDA reports)
PERIRECTAL ABSCESS ( 5 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 5 FDA reports)
PICA ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POLYP ( 5 FDA reports)
POST PROCEDURAL PNEUMONIA ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
SCAB ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
THERAPY CESSATION ( 5 FDA reports)
THROMBOPHLEBITIS ( 5 FDA reports)
TONGUE DRY ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
ULCER ( 5 FDA reports)
URETHRAL STENOSIS ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
UTERINE LEIOMYOMA ( 5 FDA reports)
VAGINAL CANCER ( 5 FDA reports)
VAGINAL NEOPLASM ( 5 FDA reports)
VENTRICULAR FLUTTER ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AORTIC EMBOLUS ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CAROTID ARTERY ATHEROMA ( 4 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FREEZING PHENOMENON ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
GASTRIC NEOPLASM ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEAT STROKE ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERLIPASAEMIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INFESTATION ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INTERTRIGO ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LIP OEDEMA ( 4 FDA reports)
LOW TURNOVER OSTEOPATHY ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MARASMUS ( 4 FDA reports)
MASS ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MENINGORRHAGIA ( 4 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NEAR DROWNING ( 4 FDA reports)
NECK DEFORMITY ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEOPLASM RECURRENCE ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORAL TORUS ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHLEBITIS SUPERFICIAL ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
PSEUDOLYMPHOMA ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
PULPITIS DENTAL ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
RADIAL NERVE PALSY ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RASH PAPULOSQUAMOUS ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SCRATCH ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SKIN INJURY ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SLEEP WALKING ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPLENIC HAEMORRHAGE ( 4 FDA reports)
SPLENIC INJURY ( 4 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STATUS ASTHMATICUS ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
THYROXINE INCREASED ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONIC CLONIC MOVEMENTS ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 4 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
TYPHOID FEVER ( 4 FDA reports)
UMBILICAL HERNIA ( 4 FDA reports)
URINARY TRACT DISORDER ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VENTRICULAR ARRHYTHMIA ( 4 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ATHETOSIS ( 3 FDA reports)
ATONIC SEIZURES ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BLOOD ZINC DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRAIN STEM STROKE ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLONIC HAEMORRHAGE ( 3 FDA reports)
COLONIC OBSTRUCTION ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CRANIOPHARYNGIOMA ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DISTRACTIBILITY ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EAR NEOPLASM MALIGNANT ( 3 FDA reports)
EARLY MORNING AWAKENING ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
GALLBLADDER CANCER METASTATIC ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GUN SHOT WOUND ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
LEUKAEMIA PLASMACYTIC ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MUSCLE GRAFT ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 3 FDA reports)
NEUROPATHIC PAIN ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
OPISTHOTONUS ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PARASYSTOLE ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PNEUMOCONIOSIS ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST PROCEDURAL HAEMATURIA ( 3 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PSYCHOMOTOR AGITATION ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
REGRESSIVE BEHAVIOUR ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SOFT TISSUE DISORDER ( 3 FDA reports)
SOLILOQUY ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TONSILLAR HAEMORRHAGE ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH IMPACTED ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
TROUSSEAU'S SYNDROME ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
UHTHOFF'S PHENOMENON ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
UROBILINOGEN URINE INCREASED ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VITAMIN B6 DEFICIENCY ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
VOLVULUS OF BOWEL ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANOSOGNOSIA ( 2 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-INSULIN RECEPTOR ANTIBODY POSITIVE ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BASAL GANGLION DEGENERATION ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
BUNION ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVOCHALASIS ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ECZEMA WEEPING ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACTOR XIII DEFICIENCY ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HUNTINGTON'S CHOREA ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERCHROMIC ANAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
JEALOUS DELUSION ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KYPHOSCOLIOSIS ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LIP PRURITUS ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOTONIA CONGENITA ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEOLOGISM ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODULE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OPEN REDUCTION OF FRACTURE ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERIPHERAL NERVE PALSY ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 2 FDA reports)
POSTURING ( 2 FDA reports)
POVERTY OF THOUGHT CONTENT ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PUTAMEN HAEMORRHAGE ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYURIA ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL SCAR ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCHAMBERG'S DISEASE ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL X-RAY ABNORMAL ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPOUSAL ABUSE ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STUBBORNNESS ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBDURAL EFFUSION ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUPERINFECTION VIRAL ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THYROGLOBULIN DECREASED ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 1 FDA reports)
ACRODYNIA ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANKLE DEFORMITY ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC TELEMETRY ABNORMAL ( 1 FDA reports)
CARDIAC VALVE RUPTURE ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLONY STIMULATING FACTOR THERAPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL NEGATIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERAILMENT ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUODENAL ULCER REPAIR ( 1 FDA reports)
DUODENAL ULCER, OBSTRUCTIVE ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ECZEMA INFANTILE ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMOTIONAL POVERTY ( 1 FDA reports)
ENDOCRINE TEST ABNORMAL ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMODYNAMIC REBOUND ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
IRIDECTOMY ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPOEDEMA ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULAR RUPTURE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAGICAL THINKING ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOKERATITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PIGMENT NEPHROPATHY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SELF ESTEEM INFLATED ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
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TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TRACHEAL OPERATION ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROBILINOGEN URINE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
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VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
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VENOUS STASIS ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
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VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
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WATER INTOXICATION ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
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WOUND COMPLICATION ( 1 FDA reports)

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