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

BLOOD GLUCOSE INCREASED ( 2338 FDA reports)
NAUSEA ( 2034 FDA reports)
WEIGHT DECREASED ( 1456 FDA reports)
HYPOGLYCAEMIA ( 1217 FDA reports)
DECREASED APPETITE ( 1011 FDA reports)
BLOOD GLUCOSE DECREASED ( 1005 FDA reports)
VOMITING ( 974 FDA reports)
MYOCARDIAL INFARCTION ( 952 FDA reports)
DIARRHOEA ( 885 FDA reports)
DIZZINESS ( 853 FDA reports)
DYSPNOEA ( 782 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 763 FDA reports)
ASTHENIA ( 689 FDA reports)
FATIGUE ( 651 FDA reports)
OEDEMA PERIPHERAL ( 625 FDA reports)
DRUG INEFFECTIVE ( 579 FDA reports)
PYREXIA ( 576 FDA reports)
HEADACHE ( 560 FDA reports)
FALL ( 552 FDA reports)
PAIN ( 528 FDA reports)
RENAL FAILURE ACUTE ( 515 FDA reports)
DIABETES MELLITUS ( 508 FDA reports)
MALAISE ( 507 FDA reports)
PNEUMONIA ( 504 FDA reports)
ANAEMIA ( 500 FDA reports)
HYPERTENSION ( 484 FDA reports)
CHEST PAIN ( 479 FDA reports)
CORONARY ARTERY DISEASE ( 478 FDA reports)
WEIGHT INCREASED ( 462 FDA reports)
CEREBROVASCULAR ACCIDENT ( 444 FDA reports)
TREMOR ( 433 FDA reports)
RENAL FAILURE ( 410 FDA reports)
ANXIETY ( 378 FDA reports)
ATRIAL FIBRILLATION ( 369 FDA reports)
ABDOMINAL PAIN ( 366 FDA reports)
FEELING ABNORMAL ( 364 FDA reports)
BACK PAIN ( 363 FDA reports)
CARDIAC FAILURE ( 363 FDA reports)
HYPERHIDROSIS ( 358 FDA reports)
DEHYDRATION ( 355 FDA reports)
LOSS OF CONSCIOUSNESS ( 355 FDA reports)
ABDOMINAL PAIN UPPER ( 351 FDA reports)
HYPERGLYCAEMIA ( 351 FDA reports)
DEPRESSION ( 349 FDA reports)
PLEURAL EFFUSION ( 348 FDA reports)
CONDITION AGGRAVATED ( 337 FDA reports)
ARTHRALGIA ( 327 FDA reports)
CONSTIPATION ( 327 FDA reports)
PAIN IN EXTREMITY ( 322 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 320 FDA reports)
RENAL IMPAIRMENT ( 314 FDA reports)
ABDOMINAL DISTENSION ( 307 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 305 FDA reports)
RASH ( 305 FDA reports)
PLATELET COUNT DECREASED ( 299 FDA reports)
INTERSTITIAL LUNG DISEASE ( 296 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 295 FDA reports)
URINARY TRACT INFECTION ( 293 FDA reports)
SOMNOLENCE ( 292 FDA reports)
BLOOD CREATININE INCREASED ( 284 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 284 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 283 FDA reports)
LIVER DISORDER ( 282 FDA reports)
INSOMNIA ( 278 FDA reports)
HYPOAESTHESIA ( 277 FDA reports)
PANCREATITIS ( 277 FDA reports)
BLOOD PRESSURE INCREASED ( 275 FDA reports)
COUGH ( 275 FDA reports)
DEATH ( 271 FDA reports)
DYSPEPSIA ( 270 FDA reports)
CONFUSIONAL STATE ( 268 FDA reports)
HYPOTENSION ( 260 FDA reports)
PRURITUS ( 250 FDA reports)
DRUG INTERACTION ( 249 FDA reports)
CARDIAC DISORDER ( 246 FDA reports)
SYNCOPE ( 239 FDA reports)
INJURY ( 231 FDA reports)
VISION BLURRED ( 229 FDA reports)
HYPERKALAEMIA ( 228 FDA reports)
GAIT DISTURBANCE ( 227 FDA reports)
HAEMOGLOBIN DECREASED ( 226 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 225 FDA reports)
ANOREXIA ( 223 FDA reports)
INJECTION SITE BRUISING ( 222 FDA reports)
INJECTION SITE PAIN ( 215 FDA reports)
OEDEMA ( 213 FDA reports)
DRUG EFFECT DECREASED ( 205 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 204 FDA reports)
MUSCLE SPASMS ( 202 FDA reports)
PALPITATIONS ( 201 FDA reports)
SEPSIS ( 199 FDA reports)
BLOOD UREA INCREASED ( 197 FDA reports)
CELLULITIS ( 197 FDA reports)
CARDIAC ARREST ( 195 FDA reports)
CEREBRAL INFARCTION ( 195 FDA reports)
TYPE 2 DIABETES MELLITUS ( 188 FDA reports)
EMOTIONAL DISTRESS ( 182 FDA reports)
HYPOGLYCAEMIC COMA ( 182 FDA reports)
ARRHYTHMIA ( 179 FDA reports)
ERYTHEMA ( 179 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 177 FDA reports)
MYALGIA ( 176 FDA reports)
INJECTION SITE HAEMORRHAGE ( 175 FDA reports)
CHOLELITHIASIS ( 174 FDA reports)
HYPERLIPIDAEMIA ( 174 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 172 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 171 FDA reports)
HEART RATE INCREASED ( 171 FDA reports)
RHABDOMYOLYSIS ( 171 FDA reports)
FEELING JITTERY ( 169 FDA reports)
NASOPHARYNGITIS ( 169 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 165 FDA reports)
CONVULSION ( 165 FDA reports)
MUSCULAR WEAKNESS ( 164 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 162 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 159 FDA reports)
BLOOD PRESSURE DECREASED ( 159 FDA reports)
CHEST DISCOMFORT ( 158 FDA reports)
HYPONATRAEMIA ( 158 FDA reports)
DYSGEUSIA ( 157 FDA reports)
RESPIRATORY FAILURE ( 157 FDA reports)
CONTUSION ( 155 FDA reports)
THROMBOCYTOPENIA ( 154 FDA reports)
CHILLS ( 152 FDA reports)
MYOCARDIAL ISCHAEMIA ( 152 FDA reports)
NERVOUSNESS ( 152 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 149 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 148 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 145 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 144 FDA reports)
NEUROPATHY PERIPHERAL ( 142 FDA reports)
PARAESTHESIA ( 137 FDA reports)
ABDOMINAL DISCOMFORT ( 136 FDA reports)
MEDICATION ERROR ( 135 FDA reports)
BRADYCARDIA ( 134 FDA reports)
BRONCHITIS ( 134 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 134 FDA reports)
CARDIO-RESPIRATORY ARREST ( 133 FDA reports)
ANGINA PECTORIS ( 132 FDA reports)
LACTIC ACIDOSIS ( 131 FDA reports)
PULMONARY OEDEMA ( 131 FDA reports)
RENAL DISORDER ( 131 FDA reports)
FLATULENCE ( 130 FDA reports)
INFECTION ( 130 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 129 FDA reports)
HAEMATURIA ( 129 FDA reports)
INCORRECT DOSE ADMINISTERED ( 129 FDA reports)
ASTHMA ( 127 FDA reports)
ARTERIOSCLEROSIS ( 126 FDA reports)
CARDIOMEGALY ( 125 FDA reports)
OSTEOARTHRITIS ( 125 FDA reports)
FLUID RETENTION ( 124 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 124 FDA reports)
HYPOKALAEMIA ( 123 FDA reports)
DYSPHAGIA ( 122 FDA reports)
RENAL FAILURE CHRONIC ( 119 FDA reports)
CATARACT ( 118 FDA reports)
DIABETIC NEUROPATHY ( 117 FDA reports)
VISUAL ACUITY REDUCED ( 117 FDA reports)
OVERDOSE ( 116 FDA reports)
STRESS ( 114 FDA reports)
ASCITES ( 113 FDA reports)
CARDIOMYOPATHY ( 113 FDA reports)
HEPATIC FAILURE ( 113 FDA reports)
COMA ( 112 FDA reports)
JAUNDICE ( 112 FDA reports)
THROMBOSIS ( 108 FDA reports)
AMNESIA ( 107 FDA reports)
COLD SWEAT ( 105 FDA reports)
TACHYCARDIA ( 104 FDA reports)
BLOOD BILIRUBIN INCREASED ( 102 FDA reports)
ERUCTATION ( 102 FDA reports)
HERPES ZOSTER ( 102 FDA reports)
ARTHRITIS ( 101 FDA reports)
DEEP VEIN THROMBOSIS ( 101 FDA reports)
SINUSITIS ( 101 FDA reports)
TREATMENT NONCOMPLIANCE ( 100 FDA reports)
HYPERSENSITIVITY ( 99 FDA reports)
NECK PAIN ( 99 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 98 FDA reports)
URTICARIA ( 98 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 97 FDA reports)
MITRAL VALVE INCOMPETENCE ( 97 FDA reports)
PANCYTOPENIA ( 97 FDA reports)
SLEEP APNOEA SYNDROME ( 97 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 96 FDA reports)
ANHEDONIA ( 95 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 95 FDA reports)
PANCREATITIS ACUTE ( 94 FDA reports)
HEART INJURY ( 93 FDA reports)
INJECTION SITE ERYTHEMA ( 93 FDA reports)
NEPHROLITHIASIS ( 93 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 93 FDA reports)
PULMONARY EMBOLISM ( 93 FDA reports)
HEPATIC STEATOSIS ( 92 FDA reports)
BLOOD POTASSIUM INCREASED ( 91 FDA reports)
CARDIOVASCULAR DISORDER ( 91 FDA reports)
MULTI-ORGAN FAILURE ( 91 FDA reports)
OSTEOMYELITIS ( 91 FDA reports)
OSTEONECROSIS OF JAW ( 91 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 91 FDA reports)
PULMONARY HYPERTENSION ( 91 FDA reports)
GASTRIC ULCER ( 90 FDA reports)
ATELECTASIS ( 89 FDA reports)
ECONOMIC PROBLEM ( 89 FDA reports)
IMPAIRED HEALING ( 89 FDA reports)
POLLAKIURIA ( 89 FDA reports)
BLADDER CANCER ( 88 FDA reports)
DISEASE PROGRESSION ( 88 FDA reports)
JOINT SWELLING ( 87 FDA reports)
LETHARGY ( 87 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 85 FDA reports)
BALANCE DISORDER ( 85 FDA reports)
FEELING COLD ( 84 FDA reports)
GASTRITIS ( 84 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 83 FDA reports)
DYSARTHRIA ( 83 FDA reports)
HAEMATOCRIT DECREASED ( 83 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 83 FDA reports)
DISORIENTATION ( 82 FDA reports)
DYSPNOEA EXERTIONAL ( 82 FDA reports)
HYPOXIA ( 82 FDA reports)
HALLUCINATION ( 81 FDA reports)
HEPATIC ENZYME INCREASED ( 81 FDA reports)
DIABETIC RETINOPATHY ( 80 FDA reports)
DRY MOUTH ( 80 FDA reports)
IRRITABILITY ( 80 FDA reports)
UNEVALUABLE EVENT ( 79 FDA reports)
VENTRICULAR TACHYCARDIA ( 79 FDA reports)
AGITATION ( 78 FDA reports)
CORONARY ARTERY OCCLUSION ( 78 FDA reports)
METABOLIC ACIDOSIS ( 78 FDA reports)
MUSCULOSKELETAL PAIN ( 78 FDA reports)
SPINAL OSTEOARTHRITIS ( 78 FDA reports)
MEMORY IMPAIRMENT ( 77 FDA reports)
ROAD TRAFFIC ACCIDENT ( 77 FDA reports)
CORONARY ARTERY STENOSIS ( 76 FDA reports)
LUNG DISORDER ( 76 FDA reports)
SHOCK ( 76 FDA reports)
SPEECH DISORDER ( 76 FDA reports)
RASH GENERALISED ( 75 FDA reports)
SWELLING ( 75 FDA reports)
GENERALISED OEDEMA ( 74 FDA reports)
HEPATIC CIRRHOSIS ( 74 FDA reports)
HYPOPHAGIA ( 74 FDA reports)
HAEMORRHAGE ( 73 FDA reports)
PAIN IN JAW ( 73 FDA reports)
PANCREATIC CARCINOMA ( 73 FDA reports)
STOMATITIS ( 73 FDA reports)
SWELLING FACE ( 73 FDA reports)
FLUSHING ( 72 FDA reports)
MENTAL STATUS CHANGES ( 72 FDA reports)
OFF LABEL USE ( 72 FDA reports)
OSTEONECROSIS ( 72 FDA reports)
EPISTAXIS ( 71 FDA reports)
ERECTILE DYSFUNCTION ( 71 FDA reports)
HEPATITIS ( 71 FDA reports)
ANGINA UNSTABLE ( 70 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 70 FDA reports)
FEELING HOT ( 70 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 70 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 70 FDA reports)
ACUTE CORONARY SYNDROME ( 69 FDA reports)
BLOOD POTASSIUM DECREASED ( 69 FDA reports)
BONE DISORDER ( 69 FDA reports)
DYSURIA ( 69 FDA reports)
HAEMORRHOIDS ( 69 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 69 FDA reports)
PRESYNCOPE ( 69 FDA reports)
ALOPECIA ( 68 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 68 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 68 FDA reports)
PULMONARY CONGESTION ( 68 FDA reports)
RETINAL HAEMORRHAGE ( 68 FDA reports)
RIB FRACTURE ( 68 FDA reports)
VISUAL DISTURBANCE ( 68 FDA reports)
CARDIAC MURMUR ( 67 FDA reports)
HAEMATEMESIS ( 67 FDA reports)
INFLUENZA ( 67 FDA reports)
OXYGEN SATURATION DECREASED ( 67 FDA reports)
BURNING SENSATION ( 66 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 66 FDA reports)
TOOTH EXTRACTION ( 66 FDA reports)
VERTIGO ( 66 FDA reports)
DISTURBANCE IN ATTENTION ( 65 FDA reports)
LUNG INFILTRATION ( 65 FDA reports)
BLINDNESS ( 64 FDA reports)
FEAR ( 64 FDA reports)
HAEMOPTYSIS ( 63 FDA reports)
HEPATIC ENCEPHALOPATHY ( 63 FDA reports)
SKIN EXFOLIATION ( 63 FDA reports)
STOMACH DISCOMFORT ( 63 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 63 FDA reports)
CEREBRAL HAEMORRHAGE ( 62 FDA reports)
MELAENA ( 62 FDA reports)
FACE OEDEMA ( 61 FDA reports)
ADVERSE EVENT ( 60 FDA reports)
DEFORMITY ( 60 FDA reports)
DRUG ERUPTION ( 60 FDA reports)
EARLY SATIETY ( 60 FDA reports)
HYPOTHYROIDISM ( 60 FDA reports)
ORTHOSTATIC HYPOTENSION ( 60 FDA reports)
ILEUS ( 59 FDA reports)
INJECTION SITE IRRITATION ( 59 FDA reports)
TINNITUS ( 59 FDA reports)
URINARY RETENTION ( 59 FDA reports)
WHEEZING ( 59 FDA reports)
DELIRIUM ( 58 FDA reports)
DIABETIC KETOACIDOSIS ( 58 FDA reports)
GLAUCOMA ( 58 FDA reports)
PNEUMONIA ASPIRATION ( 58 FDA reports)
RECTAL HAEMORRHAGE ( 58 FDA reports)
RENAL CYST ( 58 FDA reports)
RESPIRATORY DISTRESS ( 58 FDA reports)
SUICIDE ATTEMPT ( 58 FDA reports)
GALLBLADDER DISORDER ( 57 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 57 FDA reports)
INJECTION SITE URTICARIA ( 57 FDA reports)
INTENTIONAL OVERDOSE ( 57 FDA reports)
MULTIPLE INJURIES ( 57 FDA reports)
NEOPLASM MALIGNANT ( 57 FDA reports)
PROTEIN URINE PRESENT ( 57 FDA reports)
INJECTION SITE PRURITUS ( 56 FDA reports)
NEUTROPENIA ( 56 FDA reports)
BLISTER ( 55 FDA reports)
CHOLECYSTITIS ( 55 FDA reports)
DEPRESSED MOOD ( 55 FDA reports)
DIALYSIS ( 55 FDA reports)
DYSPHONIA ( 55 FDA reports)
ECZEMA ( 55 FDA reports)
EXOSTOSIS ( 55 FDA reports)
RESTLESSNESS ( 55 FDA reports)
RHINORRHOEA ( 55 FDA reports)
STAPHYLOCOCCAL INFECTION ( 55 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 55 FDA reports)
HYPOVOLAEMIA ( 54 FDA reports)
INCREASED APPETITE ( 54 FDA reports)
OBESITY ( 54 FDA reports)
SUDDEN DEATH ( 54 FDA reports)
ACUTE RESPIRATORY FAILURE ( 53 FDA reports)
BLOOD SODIUM DECREASED ( 53 FDA reports)
HIATUS HERNIA ( 53 FDA reports)
HUNGER ( 53 FDA reports)
ARTHROPATHY ( 52 FDA reports)
FLUID OVERLOAD ( 52 FDA reports)
HAEMODIALYSIS ( 52 FDA reports)
INFLUENZA LIKE ILLNESS ( 52 FDA reports)
LIMB INJURY ( 52 FDA reports)
MACULAR OEDEMA ( 52 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 52 FDA reports)
DRUG HYPERSENSITIVITY ( 51 FDA reports)
LIPASE INCREASED ( 51 FDA reports)
PERICARDIAL EFFUSION ( 51 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 51 FDA reports)
RHEUMATOID ARTHRITIS ( 51 FDA reports)
ABASIA ( 50 FDA reports)
BACTERIAL INFECTION ( 50 FDA reports)
GASTROENTERITIS ( 50 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 50 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 50 FDA reports)
RASH PAPULAR ( 50 FDA reports)
SKIN ULCER ( 50 FDA reports)
VENTRICULAR FIBRILLATION ( 50 FDA reports)
DYSKINESIA ( 49 FDA reports)
FEBRILE NEUTROPENIA ( 49 FDA reports)
GOITRE ( 49 FDA reports)
HAEMATOMA ( 49 FDA reports)
URINARY INCONTINENCE ( 49 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 48 FDA reports)
HEART RATE IRREGULAR ( 48 FDA reports)
HEMIPARESIS ( 48 FDA reports)
MULTIPLE MYELOMA ( 48 FDA reports)
NASAL CONGESTION ( 48 FDA reports)
PRODUCTIVE COUGH ( 48 FDA reports)
SUICIDAL IDEATION ( 48 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 48 FDA reports)
AGRANULOCYTOSIS ( 47 FDA reports)
CAROTID ARTERY STENOSIS ( 47 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 46 FDA reports)
HYPERCHOLESTEROLAEMIA ( 46 FDA reports)
TENDONITIS ( 46 FDA reports)
TOOTHACHE ( 46 FDA reports)
APHASIA ( 45 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 45 FDA reports)
MENTAL DISORDER ( 45 FDA reports)
NEUTROPHIL COUNT DECREASED ( 45 FDA reports)
RETCHING ( 45 FDA reports)
ROTATOR CUFF SYNDROME ( 45 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 44 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 44 FDA reports)
INFLAMMATION ( 44 FDA reports)
LYMPHADENOPATHY ( 44 FDA reports)
METASTASES TO BONE ( 44 FDA reports)
MOBILITY DECREASED ( 44 FDA reports)
RASH PRURITIC ( 44 FDA reports)
SLEEP DISORDER ( 44 FDA reports)
AZOTAEMIA ( 43 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 43 FDA reports)
DIVERTICULITIS ( 43 FDA reports)
DIVERTICULUM INTESTINAL ( 43 FDA reports)
FOOT FRACTURE ( 43 FDA reports)
HIP FRACTURE ( 43 FDA reports)
LIGAMENT SPRAIN ( 43 FDA reports)
NEOPLASM PROGRESSION ( 43 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 43 FDA reports)
PROTHROMBIN TIME PROLONGED ( 43 FDA reports)
SEPTIC SHOCK ( 43 FDA reports)
SINUS TACHYCARDIA ( 43 FDA reports)
AORTIC VALVE INCOMPETENCE ( 42 FDA reports)
BONE MARROW FAILURE ( 42 FDA reports)
CARDIAC VALVE DISEASE ( 42 FDA reports)
EYE PAIN ( 42 FDA reports)
GASTROINTESTINAL DISORDER ( 42 FDA reports)
HOSPITALISATION ( 42 FDA reports)
OROPHARYNGEAL PAIN ( 42 FDA reports)
PRODUCT QUALITY ISSUE ( 42 FDA reports)
RESPIRATORY ARREST ( 42 FDA reports)
VIRAL INFECTION ( 42 FDA reports)
CARPAL TUNNEL SYNDROME ( 41 FDA reports)
DIVERTICULUM ( 41 FDA reports)
ILL-DEFINED DISORDER ( 41 FDA reports)
INJECTION SITE RASH ( 41 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 41 FDA reports)
BRAIN OEDEMA ( 40 FDA reports)
CARDIAC FAILURE ACUTE ( 40 FDA reports)
GASTRIC CANCER ( 40 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 40 FDA reports)
SKIN DISCOLOURATION ( 40 FDA reports)
ATRIOVENTRICULAR BLOCK ( 39 FDA reports)
CARDIOGENIC SHOCK ( 39 FDA reports)
CHROMATURIA ( 39 FDA reports)
DISCOMFORT ( 39 FDA reports)
EJECTION FRACTION DECREASED ( 39 FDA reports)
GASTRIC DISORDER ( 39 FDA reports)
HEAD INJURY ( 39 FDA reports)
HYPERSOMNIA ( 39 FDA reports)
HYPOMAGNESAEMIA ( 39 FDA reports)
JOINT INJURY ( 39 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 39 FDA reports)
ACCIDENTAL OVERDOSE ( 38 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 38 FDA reports)
ATRIAL FLUTTER ( 38 FDA reports)
HEMIPLEGIA ( 38 FDA reports)
LACUNAR INFARCTION ( 38 FDA reports)
LUNG NEOPLASM ( 38 FDA reports)
PSYCHOTIC DISORDER ( 38 FDA reports)
RENAL INJURY ( 38 FDA reports)
SICK SINUS SYNDROME ( 38 FDA reports)
STENT PLACEMENT ( 38 FDA reports)
STEVENS-JOHNSON SYNDROME ( 38 FDA reports)
UNRESPONSIVE TO STIMULI ( 38 FDA reports)
DEMENTIA ( 37 FDA reports)
FAECES DISCOLOURED ( 37 FDA reports)
FEMUR FRACTURE ( 37 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 37 FDA reports)
LEUKOPENIA ( 37 FDA reports)
MUSCLE TWITCHING ( 37 FDA reports)
OSTEOPOROSIS ( 37 FDA reports)
PALLOR ( 37 FDA reports)
POST PROCEDURAL COMPLICATION ( 37 FDA reports)
PURPURA ( 37 FDA reports)
TRANSAMINASES INCREASED ( 37 FDA reports)
VISUAL IMPAIRMENT ( 37 FDA reports)
ABNORMAL BEHAVIOUR ( 36 FDA reports)
BONE PAIN ( 36 FDA reports)
COLONIC POLYP ( 36 FDA reports)
DRY SKIN ( 36 FDA reports)
PANIC ATTACK ( 36 FDA reports)
PLEURISY ( 36 FDA reports)
ANURIA ( 35 FDA reports)
BLADDER DISORDER ( 35 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 35 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 35 FDA reports)
CYSTITIS ( 35 FDA reports)
DILATATION ATRIAL ( 35 FDA reports)
ELECTROLYTE IMBALANCE ( 35 FDA reports)
FRACTURE ( 35 FDA reports)
MENTAL IMPAIRMENT ( 35 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 35 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 35 FDA reports)
URINE OUTPUT DECREASED ( 35 FDA reports)
AGGRESSION ( 34 FDA reports)
COAGULOPATHY ( 34 FDA reports)
COGNITIVE DISORDER ( 34 FDA reports)
CORONARY ARTERY BYPASS ( 34 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 34 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 34 FDA reports)
HEART RATE DECREASED ( 34 FDA reports)
HEPATITIS FULMINANT ( 34 FDA reports)
MALNUTRITION ( 34 FDA reports)
ORAL DISORDER ( 34 FDA reports)
PULMONARY FIBROSIS ( 34 FDA reports)
SPLENOMEGALY ( 34 FDA reports)
THIRST ( 34 FDA reports)
THROAT IRRITATION ( 34 FDA reports)
VENTRICULAR HYPERTROPHY ( 34 FDA reports)
BLOOD AMYLASE INCREASED ( 33 FDA reports)
BLOOD URINE PRESENT ( 33 FDA reports)
CONJUNCTIVITIS ( 33 FDA reports)
DRUG TOXICITY ( 33 FDA reports)
ENERGY INCREASED ( 33 FDA reports)
EXCORIATION ( 33 FDA reports)
EYE HAEMORRHAGE ( 33 FDA reports)
HEPATITIS ACUTE ( 33 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 33 FDA reports)
MUCOSAL INFLAMMATION ( 33 FDA reports)
OSTEOPENIA ( 33 FDA reports)
PHARYNGEAL OEDEMA ( 33 FDA reports)
PROTEINURIA ( 33 FDA reports)
RETINOPATHY ( 33 FDA reports)
ABSCESS ( 32 FDA reports)
CANDIDIASIS ( 32 FDA reports)
DIABETIC NEPHROPATHY ( 32 FDA reports)
DIFFICULTY IN WALKING ( 32 FDA reports)
DRUG ADMINISTRATION ERROR ( 32 FDA reports)
DYSLIPIDAEMIA ( 32 FDA reports)
FLANK PAIN ( 32 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 32 FDA reports)
GASTROENTERITIS VIRAL ( 32 FDA reports)
HYPERURICAEMIA ( 32 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 32 FDA reports)
LYMPHOMA ( 32 FDA reports)
MOUTH HAEMORRHAGE ( 32 FDA reports)
OESOPHAGITIS ( 32 FDA reports)
SCIATICA ( 32 FDA reports)
SINUS BRADYCARDIA ( 32 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 32 FDA reports)
AORTIC STENOSIS ( 31 FDA reports)
BACK INJURY ( 31 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 31 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 31 FDA reports)
BURSITIS ( 31 FDA reports)
CAROTID BRUIT ( 31 FDA reports)
DEAFNESS ( 31 FDA reports)
DISABILITY ( 31 FDA reports)
DUODENAL ULCER ( 31 FDA reports)
FACIAL PALSY ( 31 FDA reports)
KIDNEY INFECTION ( 31 FDA reports)
PANCREATITIS CHRONIC ( 31 FDA reports)
RENAL TUBULAR NECROSIS ( 31 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 31 FDA reports)
APATHY ( 30 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 30 FDA reports)
CYANOSIS ( 30 FDA reports)
DECUBITUS ULCER ( 30 FDA reports)
DIABETIC COMPLICATION ( 30 FDA reports)
HYDRONEPHROSIS ( 30 FDA reports)
LEUKOCYTOSIS ( 30 FDA reports)
LIMB DISCOMFORT ( 30 FDA reports)
NEPHROGENIC ANAEMIA ( 30 FDA reports)
NERVOUS SYSTEM DISORDER ( 30 FDA reports)
PIGMENTATION DISORDER ( 30 FDA reports)
SCAR ( 30 FDA reports)
SURGERY ( 30 FDA reports)
SWOLLEN TONGUE ( 30 FDA reports)
TYPE 1 DIABETES MELLITUS ( 30 FDA reports)
BLOOD ALBUMIN DECREASED ( 29 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 29 FDA reports)
BONE LESION ( 29 FDA reports)
CIRCULATORY COLLAPSE ( 29 FDA reports)
COLON CANCER ( 29 FDA reports)
HAEMATOCHEZIA ( 29 FDA reports)
HYPERKERATOSIS ( 29 FDA reports)
INTRACARDIAC THROMBUS ( 29 FDA reports)
IRON DEFICIENCY ANAEMIA ( 29 FDA reports)
MOUTH ULCERATION ( 29 FDA reports)
MYELODYSPLASTIC SYNDROME ( 29 FDA reports)
ORAL INTAKE REDUCED ( 29 FDA reports)
PNEUMONIA BACTERIAL ( 29 FDA reports)
POLYURIA ( 29 FDA reports)
RALES ( 29 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 29 FDA reports)
RESTLESS LEGS SYNDROME ( 29 FDA reports)
SKIN DISORDER ( 29 FDA reports)
SKIN LESION ( 29 FDA reports)
UTERINE LEIOMYOMA ( 29 FDA reports)
ANAPHYLACTIC SHOCK ( 28 FDA reports)
ANKLE FRACTURE ( 28 FDA reports)
BODY TEMPERATURE INCREASED ( 28 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 28 FDA reports)
EAR PAIN ( 28 FDA reports)
EOSINOPHILIA ( 28 FDA reports)
EYE DISORDER ( 28 FDA reports)
FUNGAL INFECTION ( 28 FDA reports)
INTESTINAL OBSTRUCTION ( 28 FDA reports)
LUNG NEOPLASM MALIGNANT ( 28 FDA reports)
METASTASES TO LIVER ( 28 FDA reports)
PULMONARY MASS ( 28 FDA reports)
RESPIRATORY DISORDER ( 28 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 28 FDA reports)
BLOOD IRON DECREASED ( 27 FDA reports)
CARDIAC PACEMAKER INSERTION ( 27 FDA reports)
CYTOLYTIC HEPATITIS ( 27 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 27 FDA reports)
EOSINOPHIL COUNT INCREASED ( 27 FDA reports)
FAECALOMA ( 27 FDA reports)
HOT FLUSH ( 27 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 27 FDA reports)
LOCALISED INFECTION ( 27 FDA reports)
MACULAR DEGENERATION ( 27 FDA reports)
METASTASES TO SPINE ( 27 FDA reports)
MIGRAINE ( 27 FDA reports)
MOVEMENT DISORDER ( 27 FDA reports)
MUSCLE STRAIN ( 27 FDA reports)
NEURALGIA ( 27 FDA reports)
ONYCHOMYCOSIS ( 27 FDA reports)
PATHOLOGICAL FRACTURE ( 27 FDA reports)
PROSTATE CANCER ( 27 FDA reports)
SERUM FERRITIN INCREASED ( 27 FDA reports)
THYROID NEOPLASM ( 27 FDA reports)
ULCER ( 27 FDA reports)
BONE DENSITY DECREASED ( 26 FDA reports)
CEREBRAL ATROPHY ( 26 FDA reports)
CHRONIC SINUSITIS ( 26 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 26 FDA reports)
EYE SWELLING ( 26 FDA reports)
GOUT ( 26 FDA reports)
HYPERCALCAEMIA ( 26 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 26 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 26 FDA reports)
NOCTURIA ( 26 FDA reports)
ORTHOPNOEA ( 26 FDA reports)
PHOTOPSIA ( 26 FDA reports)
POLYNEUROPATHY ( 26 FDA reports)
PURULENT DISCHARGE ( 26 FDA reports)
RESPIRATORY TRACT INFECTION ( 26 FDA reports)
TOOTH DISORDER ( 26 FDA reports)
VASODILATATION ( 26 FDA reports)
CATARACT OPERATION ( 25 FDA reports)
DECREASED ACTIVITY ( 25 FDA reports)
DECREASED INTEREST ( 25 FDA reports)
DRUG DOSE OMISSION ( 25 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 25 FDA reports)
EMOTIONAL DISORDER ( 25 FDA reports)
ENCEPHALOPATHY ( 25 FDA reports)
GINGIVAL PAIN ( 25 FDA reports)
HERNIA ( 25 FDA reports)
IRRITABLE BOWEL SYNDROME ( 25 FDA reports)
NEPHROTIC SYNDROME ( 25 FDA reports)
ORAL PAIN ( 25 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 25 FDA reports)
SNEEZING ( 25 FDA reports)
THERAPY NON-RESPONDER ( 25 FDA reports)
VITREOUS HAEMORRHAGE ( 25 FDA reports)
WRIST FRACTURE ( 25 FDA reports)
ABDOMINAL PAIN LOWER ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 24 FDA reports)
BREAST CANCER ( 24 FDA reports)
BRONCHITIS CHRONIC ( 24 FDA reports)
CEREBRAL ISCHAEMIA ( 24 FDA reports)
CRYING ( 24 FDA reports)
DILATATION VENTRICULAR ( 24 FDA reports)
DRUG DISPENSING ERROR ( 24 FDA reports)
DYSSTASIA ( 24 FDA reports)
EMPHYSEMA ( 24 FDA reports)
HALLUCINATION, VISUAL ( 24 FDA reports)
HEPATITIS CHOLESTATIC ( 24 FDA reports)
HEPATOMEGALY ( 24 FDA reports)
HYPOALBUMINAEMIA ( 24 FDA reports)
INJECTION SITE EXTRAVASATION ( 24 FDA reports)
INJECTION SITE REACTION ( 24 FDA reports)
MYOPATHY ( 24 FDA reports)
NIGHTMARE ( 24 FDA reports)
ONYCHOCLASIS ( 24 FDA reports)
TUMOUR LYSIS SYNDROME ( 24 FDA reports)
VISUAL FIELD DEFECT ( 24 FDA reports)
VITREOUS FLOATERS ( 24 FDA reports)
BRONCHITIS ACUTE ( 23 FDA reports)
DERMATITIS EXFOLIATIVE ( 23 FDA reports)
DIASTOLIC DYSFUNCTION ( 23 FDA reports)
DRUG DEPENDENCE ( 23 FDA reports)
EPILEPSY ( 23 FDA reports)
HEARING IMPAIRED ( 23 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 23 FDA reports)
LUNG CONSOLIDATION ( 23 FDA reports)
NODULE ( 23 FDA reports)
PRURITUS GENERALISED ( 23 FDA reports)
PULSE ABSENT ( 23 FDA reports)
SPINAL COLUMN INJURY ( 23 FDA reports)
SPINAL COMPRESSION FRACTURE ( 23 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 23 FDA reports)
VITAMIN D DEFICIENCY ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 22 FDA reports)
BLINDNESS UNILATERAL ( 22 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 22 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 22 FDA reports)
ERYTHEMA MULTIFORME ( 22 FDA reports)
HAEMOLYTIC ANAEMIA ( 22 FDA reports)
HEPATIC LESION ( 22 FDA reports)
HERPES SIMPLEX ( 22 FDA reports)
HYPOACUSIS ( 22 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 22 FDA reports)
ILEUS PARALYTIC ( 22 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 22 FDA reports)
LEFT ATRIAL DILATATION ( 22 FDA reports)
RECTAL POLYP ( 22 FDA reports)
SINUS DISORDER ( 22 FDA reports)
THROAT TIGHTNESS ( 22 FDA reports)
VARICOSE VEIN ( 22 FDA reports)
ACUTE PULMONARY OEDEMA ( 21 FDA reports)
ANAPHYLACTIC REACTION ( 21 FDA reports)
AORTIC ANEURYSM ( 21 FDA reports)
APNOEA ( 21 FDA reports)
BACK DISORDER ( 21 FDA reports)
BLOOD URIC ACID INCREASED ( 21 FDA reports)
CARDIAC FLUTTER ( 21 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 21 FDA reports)
COMPLETED SUICIDE ( 21 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 21 FDA reports)
DIPLOPIA ( 21 FDA reports)
DRUG ABUSER ( 21 FDA reports)
EYELID OEDEMA ( 21 FDA reports)
FAECAL INCONTINENCE ( 21 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 21 FDA reports)
GLUCOSE URINE PRESENT ( 21 FDA reports)
HEPATIC NECROSIS ( 21 FDA reports)
HYPOAESTHESIA ORAL ( 21 FDA reports)
JAW DISORDER ( 21 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 21 FDA reports)
PITTING OEDEMA ( 21 FDA reports)
PNEUMATOSIS INTESTINALIS ( 21 FDA reports)
SCOLIOSIS ( 21 FDA reports)
SINUS CONGESTION ( 21 FDA reports)
TOOTH LOSS ( 21 FDA reports)
VENTRICULAR DYSFUNCTION ( 21 FDA reports)
VITAMIN B12 DEFICIENCY ( 21 FDA reports)
ABSCESS JAW ( 20 FDA reports)
ANGIOPATHY ( 20 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 20 FDA reports)
BLOOD MAGNESIUM DECREASED ( 20 FDA reports)
BONE DEBRIDEMENT ( 20 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 20 FDA reports)
BREATH SOUNDS ABNORMAL ( 20 FDA reports)
COLITIS ( 20 FDA reports)
DENTAL OPERATION ( 20 FDA reports)
DRUG INTOLERANCE ( 20 FDA reports)
DRUG LEVEL INCREASED ( 20 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 20 FDA reports)
FIBROMYALGIA ( 20 FDA reports)
FIBULA FRACTURE ( 20 FDA reports)
GINGIVITIS ( 20 FDA reports)
LABORATORY TEST ABNORMAL ( 20 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 20 FDA reports)
LIFE EXPECTANCY SHORTENED ( 20 FDA reports)
MASS ( 20 FDA reports)
MONOPLEGIA ( 20 FDA reports)
NECK INJURY ( 20 FDA reports)
OCULAR HYPERAEMIA ( 20 FDA reports)
PHOTOSENSITIVITY REACTION ( 20 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 20 FDA reports)
PSORIASIS ( 20 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 20 FDA reports)
RASH MACULO-PAPULAR ( 20 FDA reports)
RENAL ARTERY STENOSIS ( 20 FDA reports)
RHINITIS ALLERGIC ( 20 FDA reports)
SEQUESTRECTOMY ( 20 FDA reports)
SPINAL COLUMN STENOSIS ( 20 FDA reports)
SUBDURAL HAEMATOMA ( 20 FDA reports)
TOOTH ABSCESS ( 20 FDA reports)
UMBILICAL HERNIA ( 20 FDA reports)
VENTRICULAR HYPOKINESIA ( 20 FDA reports)
ACUTE PRERENAL FAILURE ( 19 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
ANGIOEDEMA ( 19 FDA reports)
BRONCHOPNEUMONIA ( 19 FDA reports)
CEREBRAL HAEMATOMA ( 19 FDA reports)
CHEST X-RAY ABNORMAL ( 19 FDA reports)
DENTAL CARIES ( 19 FDA reports)
DEVICE MALFUNCTION ( 19 FDA reports)
GYNAECOMASTIA ( 19 FDA reports)
HICCUPS ( 19 FDA reports)
HYPERVENTILATION ( 19 FDA reports)
INFUSION RELATED REACTION ( 19 FDA reports)
JOINT SPRAIN ( 19 FDA reports)
KNEE ARTHROPLASTY ( 19 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 19 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
MUCOSAL ULCERATION ( 19 FDA reports)
MYOCLONUS ( 19 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 19 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 19 FDA reports)
TRACHEAL DEVIATION ( 19 FDA reports)
WEIGHT FLUCTUATION ( 19 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 19 FDA reports)
ACIDOSIS ( 18 FDA reports)
ANGIONEUROTIC OEDEMA ( 18 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 18 FDA reports)
AORTIC VALVE STENOSIS ( 18 FDA reports)
BEDRIDDEN ( 18 FDA reports)
BILE DUCT STENOSIS ( 18 FDA reports)
BLOOD CALCIUM DECREASED ( 18 FDA reports)
BUNDLE BRANCH BLOCK ( 18 FDA reports)
CHOLESTASIS ( 18 FDA reports)
DIABETIC COMA ( 18 FDA reports)
DISEASE RECURRENCE ( 18 FDA reports)
GASTRIC HAEMORRHAGE ( 18 FDA reports)
HEPATITIS C ( 18 FDA reports)
HUMERUS FRACTURE ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 18 FDA reports)
ISCHAEMIC STROKE ( 18 FDA reports)
JOINT EFFUSION ( 18 FDA reports)
MENINGITIS ( 18 FDA reports)
MITRAL VALVE PROLAPSE ( 18 FDA reports)
MUSCLE TIGHTNESS ( 18 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 18 FDA reports)
NEPHROPATHY ( 18 FDA reports)
OESOPHAGEAL STENOSIS ( 18 FDA reports)
PERICARDITIS ( 18 FDA reports)
PERIPHERAL COLDNESS ( 18 FDA reports)
PLATELET COUNT INCREASED ( 18 FDA reports)
POLYDIPSIA ( 18 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
PSEUDOMONAS INFECTION ( 18 FDA reports)
SALIVARY HYPERSECRETION ( 18 FDA reports)
SELF-MEDICATION ( 18 FDA reports)
SKIN ATROPHY ( 18 FDA reports)
SKIN BURNING SENSATION ( 18 FDA reports)
TACHYARRHYTHMIA ( 18 FDA reports)
TOXIC SKIN ERUPTION ( 18 FDA reports)
ACTINIC KERATOSIS ( 17 FDA reports)
AMMONIA INCREASED ( 17 FDA reports)
ANGER ( 17 FDA reports)
APHTHOUS STOMATITIS ( 17 FDA reports)
BRAIN STEM INFARCTION ( 17 FDA reports)
CATHETERISATION CARDIAC ( 17 FDA reports)
CHOKING ( 17 FDA reports)
COLON ADENOMA ( 17 FDA reports)
DELUSION ( 17 FDA reports)
DERMATITIS ( 17 FDA reports)
DRUG EFFECT DELAYED ( 17 FDA reports)
DRUG PRESCRIBING ERROR ( 17 FDA reports)
EATING DISORDER ( 17 FDA reports)
GENERALISED ERYTHEMA ( 17 FDA reports)
HAEMOLYSIS ( 17 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 17 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 17 FDA reports)
INITIAL INSOMNIA ( 17 FDA reports)
INJECTION SITE NODULE ( 17 FDA reports)
LIVER ABSCESS ( 17 FDA reports)
MEDICAL DEVICE COMPLICATION ( 17 FDA reports)
MUSCLE ATROPHY ( 17 FDA reports)
MYOSITIS ( 17 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 17 FDA reports)
NEUROPATHY ( 17 FDA reports)
ORAL CANDIDIASIS ( 17 FDA reports)
PARAESTHESIA ORAL ( 17 FDA reports)
PARONYCHIA ( 17 FDA reports)
PATHOLOGICAL GAMBLING ( 17 FDA reports)
PERIPHERAL ISCHAEMIA ( 17 FDA reports)
PHARYNGITIS ( 17 FDA reports)
PSYCHIATRIC SYMPTOM ( 17 FDA reports)
REFLUX OESOPHAGITIS ( 17 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 17 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 16 FDA reports)
BIPOLAR DISORDER ( 16 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 16 FDA reports)
BODY HEIGHT DECREASED ( 16 FDA reports)
BONE LOSS ( 16 FDA reports)
BONE SWELLING ( 16 FDA reports)
BREAST CANCER FEMALE ( 16 FDA reports)
CARDIAC OPERATION ( 16 FDA reports)
CEREBRAL DISORDER ( 16 FDA reports)
CHOLANGITIS ( 16 FDA reports)
CONCUSSION ( 16 FDA reports)
COR PULMONALE ( 16 FDA reports)
DEAFNESS NEUROSENSORY ( 16 FDA reports)
DERMATITIS ACNEIFORM ( 16 FDA reports)
DUODENAL ULCER PERFORATION ( 16 FDA reports)
EMBOLISM ( 16 FDA reports)
GASTRITIS EROSIVE ( 16 FDA reports)
HEPATOCELLULAR DAMAGE ( 16 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 16 FDA reports)
HYPERTHYROIDISM ( 16 FDA reports)
INJECTION SITE SWELLING ( 16 FDA reports)
JAUNDICE CHOLESTATIC ( 16 FDA reports)
LACRIMATION INCREASED ( 16 FDA reports)
LUNG ADENOCARCINOMA ( 16 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 16 FDA reports)
MANIA ( 16 FDA reports)
METASTASES TO LUNG ( 16 FDA reports)
NIGHT SWEATS ( 16 FDA reports)
OESOPHAGEAL ULCER ( 16 FDA reports)
PARALYSIS ( 16 FDA reports)
PARKINSON'S DISEASE ( 16 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 16 FDA reports)
PERITONITIS ( 16 FDA reports)
PETECHIAE ( 16 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 16 FDA reports)
RASH ERYTHEMATOUS ( 16 FDA reports)
RASH PUSTULAR ( 16 FDA reports)
RENAL CELL CARCINOMA ( 16 FDA reports)
RESPIRATORY RATE INCREASED ( 16 FDA reports)
RETINAL VEIN OCCLUSION ( 16 FDA reports)
SEBORRHOEIC KERATOSIS ( 16 FDA reports)
SHOULDER PAIN ( 16 FDA reports)
SKIN TIGHTNESS ( 16 FDA reports)
SYNOVIAL CYST ( 16 FDA reports)
THYROID CANCER ( 16 FDA reports)
TROPONIN INCREASED ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
WOUND ( 16 FDA reports)
AORTIC VALVE DISEASE ( 15 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 15 FDA reports)
BREAST PAIN ( 15 FDA reports)
CHOLECYSTECTOMY ( 15 FDA reports)
CHOLECYSTITIS CHRONIC ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
CYST ( 15 FDA reports)
DERMATITIS ALLERGIC ( 15 FDA reports)
DEVICE FAILURE ( 15 FDA reports)
DIABETIC GANGRENE ( 15 FDA reports)
ECCHYMOSIS ( 15 FDA reports)
EOSINOPHILIC PNEUMONIA ( 15 FDA reports)
FACE INJURY ( 15 FDA reports)
GINGIVAL ERYTHEMA ( 15 FDA reports)
GINGIVAL SWELLING ( 15 FDA reports)
GRAND MAL CONVULSION ( 15 FDA reports)
HALLUCINATION, AUDITORY ( 15 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 15 FDA reports)
INGUINAL HERNIA ( 15 FDA reports)
INJECTION SITE DISCOMFORT ( 15 FDA reports)
LACERATION ( 15 FDA reports)
LEUKAEMIA ( 15 FDA reports)
LOCAL SWELLING ( 15 FDA reports)
LYMPHOEDEMA ( 15 FDA reports)
NERVE INJURY ( 15 FDA reports)
PANIC REACTION ( 15 FDA reports)
PARKINSONISM ( 15 FDA reports)
PYELONEPHRITIS ( 15 FDA reports)
SENSORY LOSS ( 15 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 15 FDA reports)
TARDIVE DYSKINESIA ( 15 FDA reports)
THINKING ABNORMAL ( 15 FDA reports)
THYROID DISORDER ( 15 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
ADRENAL ADENOMA ( 14 FDA reports)
ASPIRATION ( 14 FDA reports)
BILE DUCT CANCER ( 14 FDA reports)
BLADDER NEOPLASM ( 14 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 14 FDA reports)
CALCULUS URETERIC ( 14 FDA reports)
CAROTID ARTERY OCCLUSION ( 14 FDA reports)
CEREBROVASCULAR DISORDER ( 14 FDA reports)
CHANGE OF BOWEL HABIT ( 14 FDA reports)
CHOLECYSTITIS ACUTE ( 14 FDA reports)
CHRONIC HEPATITIS ( 14 FDA reports)
DIABETIC FOOT ( 14 FDA reports)
EXTRASYSTOLES ( 14 FDA reports)
FAMILY STRESS ( 14 FDA reports)
FURUNCLE ( 14 FDA reports)
GROIN PAIN ( 14 FDA reports)
HAEMODYNAMIC INSTABILITY ( 14 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 14 FDA reports)
HEPATITIS B ( 14 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 14 FDA reports)
HYPERTHERMIA ( 14 FDA reports)
INCOHERENT ( 14 FDA reports)
INJECTION SITE HAEMATOMA ( 14 FDA reports)
LIP SWELLING ( 14 FDA reports)
LIVER INJURY ( 14 FDA reports)
MENISCUS LESION ( 14 FDA reports)
MIDDLE INSOMNIA ( 14 FDA reports)
PARANOIA ( 14 FDA reports)
PHYSICAL DISABILITY ( 14 FDA reports)
POLYP ( 14 FDA reports)
POST PROCEDURAL HAEMATOMA ( 14 FDA reports)
PULMONARY THROMBOSIS ( 14 FDA reports)
RENAL TUBULAR DISORDER ( 14 FDA reports)
RHINITIS ( 14 FDA reports)
SCAB ( 14 FDA reports)
SEDATION ( 14 FDA reports)
SUDDEN CARDIAC DEATH ( 14 FDA reports)
SUDDEN HEARING LOSS ( 14 FDA reports)
TENSION ( 14 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 14 FDA reports)
WRONG DRUG ADMINISTERED ( 14 FDA reports)
ABDOMINAL HERNIA ( 13 FDA reports)
ACETABULUM FRACTURE ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 13 FDA reports)
ALCOHOL ABUSE ( 13 FDA reports)
BASAL CELL CARCINOMA ( 13 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 13 FDA reports)
BIOPSY ( 13 FDA reports)
BLOOD CALCIUM INCREASED ( 13 FDA reports)
BLOOD PRESSURE ABNORMAL ( 13 FDA reports)
BLOOD SODIUM INCREASED ( 13 FDA reports)
BRADYARRHYTHMIA ( 13 FDA reports)
BREAST MASS ( 13 FDA reports)
CARDIAC TAMPONADE ( 13 FDA reports)
CAROTID ARTERY DISEASE ( 13 FDA reports)
CORONARY ARTERY RESTENOSIS ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
DIABETIC GASTROPARESIS ( 13 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 13 FDA reports)
EAR INFECTION ( 13 FDA reports)
ESSENTIAL HYPERTENSION ( 13 FDA reports)
EUPHORIC MOOD ( 13 FDA reports)
EYE IRRITATION ( 13 FDA reports)
FIBRIN D DIMER INCREASED ( 13 FDA reports)
GINGIVAL DISORDER ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
HYPERTENSIVE HEART DISEASE ( 13 FDA reports)
JAW FRACTURE ( 13 FDA reports)
KNEE OPERATION ( 13 FDA reports)
LIBIDO DECREASED ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
MOOD SWINGS ( 13 FDA reports)
MUSCLE CRAMP ( 13 FDA reports)
NO THERAPEUTIC RESPONSE ( 13 FDA reports)
NON-CARDIAC CHEST PAIN ( 13 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 13 FDA reports)
ORAL HERPES ( 13 FDA reports)
PANCREATIC DUCT STENOSIS ( 13 FDA reports)
PAROTITIS ( 13 FDA reports)
PEMPHIGOID ( 13 FDA reports)
PERSONALITY CHANGE ( 13 FDA reports)
PNEUMONITIS ( 13 FDA reports)
PROCEDURAL PAIN ( 13 FDA reports)
PROSTATITIS ( 13 FDA reports)
SKELETAL INJURY ( 13 FDA reports)
SKIN NECROSIS ( 13 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 13 FDA reports)
SPINAL CORD COMPRESSION ( 13 FDA reports)
TENDON RUPTURE ( 13 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
ADRENAL MASS ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
AGEUSIA ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
ARTERIOSPASM CORONARY ( 12 FDA reports)
ATAXIA ( 12 FDA reports)
AUTOIMMUNE HEPATITIS ( 12 FDA reports)
CARDIAC FAILURE CHRONIC ( 12 FDA reports)
CEREBELLAR INFARCTION ( 12 FDA reports)
CERVICAL SPINAL STENOSIS ( 12 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
DIZZINESS POSTURAL ( 12 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 12 FDA reports)
DYSLALIA ( 12 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 12 FDA reports)
FACET JOINT SYNDROME ( 12 FDA reports)
FISTULA ( 12 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 12 FDA reports)
HIP ARTHROPLASTY ( 12 FDA reports)
HYPERCAPNIA ( 12 FDA reports)
HYPERTENSIVE CRISIS ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 12 FDA reports)
INSULIN RESISTANCE ( 12 FDA reports)
INTENTIONAL DRUG MISUSE ( 12 FDA reports)
ISCHAEMIA ( 12 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 12 FDA reports)
JOINT STIFFNESS ( 12 FDA reports)
LISTLESS ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
MOOD ALTERED ( 12 FDA reports)
MULTIPLE DRUG OVERDOSE ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
MYDRIASIS ( 12 FDA reports)
OSTEOMYELITIS ACUTE ( 12 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 12 FDA reports)
PHOTOPHOBIA ( 12 FDA reports)
POSTNASAL DRIP ( 12 FDA reports)
PRESCRIBED OVERDOSE ( 12 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
SENSATION OF HEAVINESS ( 12 FDA reports)
SERONEGATIVE ARTHRITIS ( 12 FDA reports)
SINUS ARREST ( 12 FDA reports)
SKIN HAEMORRHAGE ( 12 FDA reports)
SKIN HYPERPIGMENTATION ( 12 FDA reports)
SKIN LACERATION ( 12 FDA reports)
SUBCUTANEOUS ABSCESS ( 12 FDA reports)
TACHYPNOEA ( 12 FDA reports)
TIBIA FRACTURE ( 12 FDA reports)
TINEA PEDIS ( 12 FDA reports)
TOOTH INFECTION ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
TRANSFUSION ( 12 FDA reports)
VASCULAR PURPURA ( 12 FDA reports)
VITAMIN D DECREASED ( 12 FDA reports)
ABNORMAL SENSATION IN EYE ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
APHONIA ( 11 FDA reports)
ATRIAL TACHYCARDIA ( 11 FDA reports)
BODY TEMPERATURE DECREASED ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BONE MARROW TRANSPLANT ( 11 FDA reports)
BUTTOCK PAIN ( 11 FDA reports)
DUODENITIS ( 11 FDA reports)
DYSAESTHESIA ( 11 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 11 FDA reports)
FACIAL BONES FRACTURE ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GENERALISED ANXIETY DISORDER ( 11 FDA reports)
GENITAL CANDIDIASIS ( 11 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 11 FDA reports)
HELICOBACTER INFECTION ( 11 FDA reports)
HYPERBILIRUBINAEMIA ( 11 FDA reports)
HYPERCHLORHYDRIA ( 11 FDA reports)
HYPOPROTEINAEMIA ( 11 FDA reports)
IMPAIRED WORK ABILITY ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
INJECTION SITE INDURATION ( 11 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 11 FDA reports)
INTESTINAL ISCHAEMIA ( 11 FDA reports)
LIGAMENT INJURY ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MILD MENTAL RETARDATION ( 11 FDA reports)
MYELOPATHY ( 11 FDA reports)
OCCULT BLOOD POSITIVE ( 11 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 11 FDA reports)
OSTEITIS ( 11 FDA reports)
OVERWEIGHT ( 11 FDA reports)
PANCREATIC DISORDER ( 11 FDA reports)
PELVIC PAIN ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
PROCEDURAL COMPLICATION ( 11 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 11 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 11 FDA reports)
RADIUS FRACTURE ( 11 FDA reports)
RASH MACULAR ( 11 FDA reports)
RESPIRATORY ACIDOSIS ( 11 FDA reports)
SCROTAL ABSCESS ( 11 FDA reports)
SEASONAL ALLERGY ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
SHOCK HYPOGLYCAEMIC ( 11 FDA reports)
SINUS HEADACHE ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SLUGGISHNESS ( 11 FDA reports)
STRESS CARDIOMYOPATHY ( 11 FDA reports)
TOOTH FRACTURE ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 11 FDA reports)
UROSEPSIS ( 11 FDA reports)
VAGINAL INFECTION ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VIITH NERVE PARALYSIS ( 11 FDA reports)
WALKING AID USER ( 11 FDA reports)
WHIPLASH INJURY ( 11 FDA reports)
ACROCHORDON ( 10 FDA reports)
ACUTE PSYCHOSIS ( 10 FDA reports)
AFFECT LABILITY ( 10 FDA reports)
ALBUMIN URINE PRESENT ( 10 FDA reports)
ALCOHOL USE ( 10 FDA reports)
ATHEROSCLEROSIS ( 10 FDA reports)
BARRETT'S OESOPHAGUS ( 10 FDA reports)
BIOPSY GINGIVAL ( 10 FDA reports)
BLOOD CHLORIDE DECREASED ( 10 FDA reports)
BLOOD CREATININE DECREASED ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 10 FDA reports)
BRAIN MASS ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
CARDIAC HYPERTROPHY ( 10 FDA reports)
CHOLECYSTITIS INFECTIVE ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
COLITIS ISCHAEMIC ( 10 FDA reports)
COLORECTAL CANCER ( 10 FDA reports)
COMMINUTED FRACTURE ( 10 FDA reports)
CORONARY ANGIOPLASTY ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 10 FDA reports)
DERMATITIS CONTACT ( 10 FDA reports)
EMBOLIC STROKE ( 10 FDA reports)
ENTEROCOLITIS ( 10 FDA reports)
EPIDIDYMAL CYST ( 10 FDA reports)
ESCHERICHIA INFECTION ( 10 FDA reports)
FACIAL PAIN ( 10 FDA reports)
FAECES HARD ( 10 FDA reports)
FIBROSIS ( 10 FDA reports)
GALLBLADDER ENLARGEMENT ( 10 FDA reports)
GASTROINTESTINAL PERFORATION ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GINGIVAL INFECTION ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
GRAM STAIN POSITIVE ( 10 FDA reports)
GRANULOCYTOPENIA ( 10 FDA reports)
HAEMORRHAGIC DIATHESIS ( 10 FDA reports)
HEPATIC CONGESTION ( 10 FDA reports)
HYPERMETABOLISM ( 10 FDA reports)
HYPERPARATHYROIDISM ( 10 FDA reports)
HYPOCALCAEMIA ( 10 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 10 FDA reports)
LEFT VENTRICULAR FAILURE ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
MENINGIOMA ( 10 FDA reports)
METRORRHAGIA ( 10 FDA reports)
MICTURITION URGENCY ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MUSCLE DISORDER ( 10 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 10 FDA reports)
NECROSIS ( 10 FDA reports)
NOSOCOMIAL INFECTION ( 10 FDA reports)
OESOPHAGEAL CARCINOMA ( 10 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 10 FDA reports)
ORGAN FAILURE ( 10 FDA reports)
OTITIS MEDIA ( 10 FDA reports)
PANCREATITIS NECROTISING ( 10 FDA reports)
PERSONALITY DISORDER ( 10 FDA reports)
PROSTATE CANCER METASTATIC ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
QUADRIPLEGIA ( 10 FDA reports)
RENAL PAIN ( 10 FDA reports)
RIB DEFORMITY ( 10 FDA reports)
SCROTAL INFECTION ( 10 FDA reports)
SEBORRHOEIC DERMATITIS ( 10 FDA reports)
SKIN CANCER ( 10 FDA reports)
SKIN CANDIDA ( 10 FDA reports)
SPONDYLOLISTHESIS ( 10 FDA reports)
STASIS DERMATITIS ( 10 FDA reports)
STEM CELL TRANSPLANT ( 10 FDA reports)
STUPOR ( 10 FDA reports)
SUDDEN ONSET OF SLEEP ( 10 FDA reports)
TENOSYNOVITIS STENOSANS ( 10 FDA reports)
TONSILLITIS ( 10 FDA reports)
TRIGEMINAL NEURALGIA ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
UNDERDOSE ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
WEIGHT LOSS POOR ( 10 FDA reports)
WOUND INFECTION ( 10 FDA reports)
ABNORMAL FAECES ( 9 FDA reports)
ABSCESS LIMB ( 9 FDA reports)
ACCELERATED HYPERTENSION ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ANAEMIA POSTOPERATIVE ( 9 FDA reports)
ANASTOMOTIC STENOSIS ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANXIETY DISORDER ( 9 FDA reports)
BACTERAEMIA ( 9 FDA reports)
BLOOD DISORDER ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 9 FDA reports)
BONE MARROW DEPRESSION ( 9 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 9 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
COLLAPSE OF LUNG ( 9 FDA reports)
COMMUNICATION DISORDER ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
CYSTOCELE ( 9 FDA reports)
DEFAECATION URGENCY ( 9 FDA reports)
DENTURE WEARER ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 9 FDA reports)
DRY EYE ( 9 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 9 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 9 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 9 FDA reports)
EXERCISE TOLERANCE DECREASED ( 9 FDA reports)
FAILURE TO THRIVE ( 9 FDA reports)
FOOD AVERSION ( 9 FDA reports)
FOOD CRAVING ( 9 FDA reports)
GASTRIC ADENOMA ( 9 FDA reports)
GASTRIC OPERATION ( 9 FDA reports)
GASTRIC ULCER PERFORATION ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
GINGIVAL BLEEDING ( 9 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HAEMOTHORAX ( 9 FDA reports)
HODGKIN'S DISEASE ( 9 FDA reports)
HYDROCEPHALUS ( 9 FDA reports)
HYSTERECTOMY ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
INFARCTION ( 9 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 9 FDA reports)
JOINT CONTRACTURE ( 9 FDA reports)
KYPHOSCOLIOSIS ( 9 FDA reports)
LAZINESS ( 9 FDA reports)
LOWER LIMB FRACTURE ( 9 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 9 FDA reports)
METASTASES TO LYMPH NODES ( 9 FDA reports)
MITRAL VALVE DISEASE ( 9 FDA reports)
MUMPS ( 9 FDA reports)
NAIL DISORDER ( 9 FDA reports)
NEPHRITIS ( 9 FDA reports)
NEUROGENIC BLADDER ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
OESOPHAGEAL NEOPLASM ( 9 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
ORAL INFECTION ( 9 FDA reports)
OSTEITIS DEFORMANS ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PAROSMIA ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
PINGUECULA ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 9 FDA reports)
PRESBYOPIA ( 9 FDA reports)
PROCTALGIA ( 9 FDA reports)
PROTEIN TOTAL INCREASED ( 9 FDA reports)
PUBIS FRACTURE ( 9 FDA reports)
RADIOTHERAPY ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 9 FDA reports)
RETROGRADE EJACULATION ( 9 FDA reports)
RUBELLA ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SCARLET FEVER ( 9 FDA reports)
SCHIZOPHRENIA ( 9 FDA reports)
SCROTAL SWELLING ( 9 FDA reports)
SEXUAL DYSFUNCTION ( 9 FDA reports)
SHOULDER OPERATION ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
SPINAL DISORDER ( 9 FDA reports)
STEATORRHOEA ( 9 FDA reports)
STENT OCCLUSION ( 9 FDA reports)
STRESS URINARY INCONTINENCE ( 9 FDA reports)
TENDERNESS ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
URINE OUTPUT INCREASED ( 9 FDA reports)
VAGINAL HAEMORRHAGE ( 9 FDA reports)
VASCULAR OCCLUSION ( 9 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 9 FDA reports)
WOUND HAEMORRHAGE ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
ALCOHOL DETOXIFICATION ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANGIOPLASTY ( 8 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
APHAGIA ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
BALANOPOSTHITIS ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BLOOD CREATININE ABNORMAL ( 8 FDA reports)
BLOOD GLUCOSE ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BONE LESION EXCISION ( 8 FDA reports)
BRAIN ABSCESS ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CLOSTRIDIAL INFECTION ( 8 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 8 FDA reports)
CORTICAL LAMINAR NECROSIS ( 8 FDA reports)
DEMYELINATION ( 8 FDA reports)
DENTAL CARE ( 8 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 8 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 8 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
ENTERITIS ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
EYE PRURITUS ( 8 FDA reports)
FEMORAL ARTERY OCCLUSION ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
GASTRIC NEOPLASM ( 8 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HAEMORRHAGIC INFARCTION ( 8 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 8 FDA reports)
HEPATOCELLULAR INJURY ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
HYPERTENSIVE EMERGENCY ( 8 FDA reports)
HYPOCHLORAEMIA ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
HYPOVOLAEMIC SHOCK ( 8 FDA reports)
INJECTION SITE DISCOLOURATION ( 8 FDA reports)
KETOACIDOSIS ( 8 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 8 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 8 FDA reports)
LIPOMA ( 8 FDA reports)
LUMBAR SPINAL STENOSIS ( 8 FDA reports)
MALIGNANT MELANOMA ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 8 FDA reports)
NEOPLASM ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
NEUROGLYCOPENIA ( 8 FDA reports)
NO ADVERSE EVENT ( 8 FDA reports)
NODAL RHYTHM ( 8 FDA reports)
OPEN WOUND ( 8 FDA reports)
OSTEOSARCOMA METASTATIC ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PANCREATIC CYST ( 8 FDA reports)
PANCREATIC NEOPLASM ( 8 FDA reports)
PANCREATIC PSEUDOCYST ( 8 FDA reports)
PHOTODERMATOSIS ( 8 FDA reports)
PHYSICAL ASSAULT ( 8 FDA reports)
PIGMENTARY GLAUCOMA ( 8 FDA reports)
PILOERECTION ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
POST HERPETIC NEURALGIA ( 8 FDA reports)
POSTRENAL FAILURE ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
QUADRIPARESIS ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
SNORING ( 8 FDA reports)
STILL'S DISEASE ADULT ONSET ( 8 FDA reports)
STRESS FRACTURE ( 8 FDA reports)
TOXIC ENCEPHALOPATHY ( 8 FDA reports)
URETERIC OBSTRUCTION ( 8 FDA reports)
VASOMOTOR RHINITIS ( 8 FDA reports)
VEIN DISORDER ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
XANTHOGRANULOMA ( 8 FDA reports)
ABDOMINAL NEOPLASM ( 7 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ALVEOLITIS ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
ASBESTOSIS ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BLADDER CYST ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BREAKTHROUGH PAIN ( 7 FDA reports)
CALCULUS BLADDER ( 7 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 7 FDA reports)
CATHETER PLACEMENT ( 7 FDA reports)
CEREBRAL CYST ( 7 FDA reports)
CEREBRAL THROMBOSIS ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CHRONIC FATIGUE SYNDROME ( 7 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 7 FDA reports)
DEVICE RELATED INFECTION ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
ENURESIS ( 7 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
EXPOSED BONE IN JAW ( 7 FDA reports)
EYELID PTOSIS ( 7 FDA reports)
FEELING DRUNK ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
FOETAL DEATH ( 7 FDA reports)
FOOD POISONING ( 7 FDA reports)
FRACTURE DELAYED UNION ( 7 FDA reports)
GALLBLADDER POLYP ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
GINGIVAL OEDEMA ( 7 FDA reports)
GRIP STRENGTH DECREASED ( 7 FDA reports)
HAND FRACTURE ( 7 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 7 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 7 FDA reports)
ILIUM FRACTURE ( 7 FDA reports)
IMMUNOSUPPRESSION ( 7 FDA reports)
INJECTION SITE WARMTH ( 7 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
INTESTINAL HAEMORRHAGE ( 7 FDA reports)
INTRACRANIAL ANEURYSM ( 7 FDA reports)
KETOSIS ( 7 FDA reports)
LEARNING DISORDER ( 7 FDA reports)
LEUKOENCEPHALOPATHY ( 7 FDA reports)
MALLORY-WEISS SYNDROME ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
MICROALBUMINURIA ( 7 FDA reports)
MITRAL VALVE SCLEROSIS ( 7 FDA reports)
MONOPARESIS ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
MUSCULOSKELETAL DISORDER ( 7 FDA reports)
MYOFASCIAL SPASM ( 7 FDA reports)
NAIL DISCOLOURATION ( 7 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
OSTEOMYELITIS CHRONIC ( 7 FDA reports)
OTITIS EXTERNA ( 7 FDA reports)
OVARIAN CYST ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
PERONEAL NERVE PALSY ( 7 FDA reports)
PICKWICKIAN SYNDROME ( 7 FDA reports)
PLEURAL DECORTICATION ( 7 FDA reports)
PLEURAL FIBROSIS ( 7 FDA reports)
PNEUMOMEDIASTINUM ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
POSTOPERATIVE FEVER ( 7 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 7 FDA reports)
PRINZMETAL ANGINA ( 7 FDA reports)
PROSTATOMEGALY ( 7 FDA reports)
RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
RETINAL DISORDER ( 7 FDA reports)
RETINAL OEDEMA ( 7 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 7 FDA reports)
RETROPERITONEAL FIBROSIS ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 7 FDA reports)
SCROTAL PAIN ( 7 FDA reports)
SKIN FIBROSIS ( 7 FDA reports)
SKIN OEDEMA ( 7 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
STRESS SYMPTOMS ( 7 FDA reports)
STRIDOR ( 7 FDA reports)
SYNCOPE VASOVAGAL ( 7 FDA reports)
THROMBOPHLEBITIS ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 7 FDA reports)
URINE ABNORMALITY ( 7 FDA reports)
URINE KETONE BODY PRESENT ( 7 FDA reports)
UTERINE POLYP ( 7 FDA reports)
VASCULAR PSEUDOANEURYSM ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
AKATHISIA ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANAEMIA MEGALOBLASTIC ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
ARTERIAL THROMBOSIS ( 6 FDA reports)
ARTHRITIS INFECTIVE ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
ATROPHY ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 6 FDA reports)
BACTERIA URINE IDENTIFIED ( 6 FDA reports)
BIOPSY LIVER ABNORMAL ( 6 FDA reports)
BIOPSY PROSTATE ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 6 FDA reports)
BLOOD TRYPSIN INCREASED ( 6 FDA reports)
BLOOD UREA DECREASED ( 6 FDA reports)
BLOOD URIC ACID ABNORMAL ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CLAUSTROPHOBIA ( 6 FDA reports)
COLITIS ULCERATIVE ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
DRUG-INDUCED LIVER INJURY ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ERYTHEMA OF EYELID ( 6 FDA reports)
FAT EMBOLISM ( 6 FDA reports)
FEELING OF DESPAIR ( 6 FDA reports)
FOAMING AT MOUTH ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 6 FDA reports)
GENITAL HAEMORRHAGE ( 6 FDA reports)
GLOSSODYNIA ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
GRANULOCYTE COUNT DECREASED ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HAEMOGLOBIN INCREASED ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HEPATIC CANCER METASTATIC ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HYDROURETER ( 6 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 6 FDA reports)
HYPERLACTACIDAEMIA ( 6 FDA reports)
HYPERPHAGIA ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INGROWING NAIL ( 6 FDA reports)
INTESTINAL MASS ( 6 FDA reports)
IRON DEFICIENCY ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LUMBAR RADICULOPATHY ( 6 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 6 FDA reports)
MEDIASTINAL DISORDER ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
MICROCYTIC ANAEMIA ( 6 FDA reports)
MITRAL VALVE CALCIFICATION ( 6 FDA reports)
MOANING ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
MUSCLE CONTRACTURE ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
NECK MASS ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NEUROSIS ( 6 FDA reports)
NO ADVERSE EFFECT ( 6 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 6 FDA reports)
OESOPHAGEAL SPASM ( 6 FDA reports)
ORCHIDECTOMY ( 6 FDA reports)
PANCREATIC ENZYMES INCREASED ( 6 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 6 FDA reports)
PCO2 DECREASED ( 6 FDA reports)
PERIODONTITIS ( 6 FDA reports)
PERIPHERAL EMBOLISM ( 6 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
PNEUMOCEPHALUS ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PULMONARY BULLA ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
PURULENCE ( 6 FDA reports)
RADICULITIS BRACHIAL ( 6 FDA reports)
RECTAL CANCER ( 6 FDA reports)
REFLUX GASTRITIS ( 6 FDA reports)
RENAL INFARCT ( 6 FDA reports)
SELF ESTEEM DECREASED ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 6 FDA reports)
SKIN INJURY ( 6 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 6 FDA reports)
SOFT TISSUE DISORDER ( 6 FDA reports)
SOLAR ELASTOSIS ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
SPINAL FRACTURE ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
THIRST DECREASED ( 6 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 6 FDA reports)
TOBACCO USER ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 6 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 6 FDA reports)
UMBILICAL CORD AROUND NECK ( 6 FDA reports)
URINE BILIRUBIN INCREASED ( 6 FDA reports)
VASCULAR CALCIFICATION ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VENTRICULAR FLUTTER ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
ACCIDENT ( 5 FDA reports)
ACTIVATION SYNDROME ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ALCOHOLISM ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 5 FDA reports)
ANAL SPHINCTER ATONY ( 5 FDA reports)
ANAPHYLACTOID SHOCK ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
AORTIC DILATATION ( 5 FDA reports)
AORTIC VALVE REPLACEMENT ( 5 FDA reports)
APNOEIC ATTACK ( 5 FDA reports)
ARTERIAL STENT INSERTION ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
ATRIAL THROMBOSIS ( 5 FDA reports)
B-CELL LYMPHOMA STAGE I ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BACTERIURIA ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BILIARY SEPSIS ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BRONCHITIS VIRAL ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 5 FDA reports)
CARCINOID TUMOUR ( 5 FDA reports)
CARDIAC DEATH ( 5 FDA reports)
CARTILAGE HYPERTROPHY ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHOKING SENSATION ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CONJUNCTIVAL ABRASION ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
COSTOCHONDRITIS ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DRESSLER'S SYNDROME ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
EJACULATION DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
GASTRIC MUCOSAL LESION ( 5 FDA reports)
GASTROINTESTINAL PAIN ( 5 FDA reports)
GINGIVAL HYPERTROPHY ( 5 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 5 FDA reports)
GRANULOMA ( 5 FDA reports)
GRANULOMA ANNULARE ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATIC ARTERY OCCLUSION ( 5 FDA reports)
HEPATIC MASS ( 5 FDA reports)
HEPATITIS A ( 5 FDA reports)
HERNIA REPAIR ( 5 FDA reports)
HORNER'S SYNDROME ( 5 FDA reports)
HOSTILITY ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPHAEMA ( 5 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INTERMITTENT CLAUDICATION ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
JAW OPERATION ( 5 FDA reports)
KLEBSIELLA INFECTION ( 5 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LOSS OF LIBIDO ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYMPHADENECTOMY ( 5 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MASTITIS ( 5 FDA reports)
MELANODERMIA ( 5 FDA reports)
MENSTRUAL DISORDER ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
METASTASIS ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
METATARSALGIA ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
NASAL DISORDER ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
ORAL MUCOSA EROSION ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 5 FDA reports)
PARTIAL SEIZURES ( 5 FDA reports)
PENILE OEDEMA ( 5 FDA reports)
PERICARDIAL RUB ( 5 FDA reports)
PERTUSSIS ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
POLYTRAUMATISM ( 5 FDA reports)
POOR PERIPHERAL CIRCULATION ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULSE PRESSURE DECREASED ( 5 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
RENAL VESSEL DISORDER ( 5 FDA reports)
RETINAL EXUDATES ( 5 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 5 FDA reports)
SENSATION OF PRESSURE ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
THORACOSTOMY ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
THYROIDITIS ( 5 FDA reports)
TOE AMPUTATION ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TUMOUR HAEMORRHAGE ( 5 FDA reports)
UNINTENDED PREGNANCY ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
URETERIC CANCER ( 5 FDA reports)
URINE AMYLASE INCREASED ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
UVULECTOMY ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
VOCAL CORD PARALYSIS ( 5 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 5 FDA reports)
VULVOVAGINAL PAIN ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ANDROPAUSE ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APPLICATION SITE DERMATITIS ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
APPLICATION SITE PRURITUS ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BENIGN BREAST NEOPLASM ( 4 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 4 FDA reports)
BILE DUCT NECROSIS ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD URINE ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC STRESS TEST ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CHONDROMALACIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
CLOSED HEAD INJURY ( 4 FDA reports)
COAGULATION TEST ABNORMAL ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
DIABETIC VASCULAR DISORDER ( 4 FDA reports)
DROWNING ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
EAR PRURITUS ( 4 FDA reports)
ECZEMA INFECTED ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EXTRADURAL ABSCESS ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
FRACTURE NONUNION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 4 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GLIOBLASTOMA MULTIFORME ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEAT ILLNESS ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFUSION SITE PAIN ( 4 FDA reports)
INJECTION SITE CELLULITIS ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
MAGNESIUM DEFICIENCY ( 4 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 4 FDA reports)
MARASMUS ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASAL SINUS DRAINAGE ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEONATAL ASPHYXIA ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OBSTRUCTION GASTRIC ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
OLIGODENDROGLIOMA ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
ORAL FUNGAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PANCREAS LIPOMATOSIS ( 4 FDA reports)
PANCREATIC ABSCESS ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PENILE ERYTHEMA ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PENIS DISORDER ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PERICARDIAL DRAINAGE ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERIRECTAL ABSCESS ( 4 FDA reports)
PERITONEAL TUBERCULOSIS ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROSTATIC OBSTRUCTION ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY HYPOPLASIA ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
PUS IN STOOL ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RECTAL PERFORATION ( 4 FDA reports)
RECTAL PROLAPSE ( 4 FDA reports)
RECTOCELE ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
RENAL HAEMORRHAGE ( 4 FDA reports)
RESIDUAL URINE VOLUME ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETINAL VASCULAR DISORDER ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 4 FDA reports)
SCROTAL ERYTHEMA ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SUBCUTANEOUS NODULE ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
TENSION HEADACHE ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYROID CYST ( 4 FDA reports)
TOBACCO ABUSE ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRACHEAL FISTULA ( 4 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 4 FDA reports)
ULNAR NEURITIS ( 4 FDA reports)
URINARY HESITATION ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
VOLVULUS OF BOWEL ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 4 FDA reports)
WOUND DRAINAGE ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL INJURY ( 3 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ABDOMINAL WALL INFECTION ( 3 FDA reports)
ABSCESS MANAGEMENT ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ALLERGIC SINUSITIS ( 3 FDA reports)
ANAL EROSION ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANTI-GAD ANTIBODY POSITIVE ( 3 FDA reports)
ANTI-INSULIN ANTIBODY ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
ARTERIAL REPAIR ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ASPERGILLOSIS ORAL ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BALANITIS ( 3 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 3 FDA reports)
BLADDER MASS ( 3 FDA reports)
BLADDER TAMPONADE ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD GASTRIN INCREASED ( 3 FDA reports)
BLOOD INSULIN DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BLOOD URIC ACID ( 3 FDA reports)
BLOOD ZINC ABNORMAL ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BREAST HAEMATOMA ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CRANIOCEREBRAL INJURY ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DELUSIONAL PERCEPTION ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DEVICE CAPTURING ISSUE ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DISSOCIATIVE FUGUE ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DIVORCED ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DYSACUSIS ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
EPIGLOTTITIS ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FATTY LIVER ALCOHOLIC ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FLUID IMBALANCE ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOETOR HEPATICUS ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTRIC ILEUS ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 3 FDA reports)
GLUCOSE URINE ( 3 FDA reports)
GUN SHOT WOUND ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERLIPASAEMIA ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPAIRED INSULIN SECRETION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTESTINAL GANGRENE ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INTRASPINAL ABSCESS ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LARYNGEAL ULCERATION ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
MADAROSIS ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MASTECTOMY ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTASES TO BONE MARROW ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEAR DROWNING ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
NIPPLE SWELLING ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIA ( 3 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PERIODONTAL DISEASE ( 3 FDA reports)
PERIPHERAL PULSE DECREASED ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA CHLAMYDIAL ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLIOMYELITIS ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POLYSEROSITIS ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PROSTATE CANCER STAGE IV ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROSTATIC HAEMORRHAGE ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
PYONEPHROSIS ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RED BLOOD CELL ABNORMALITY ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL ANEURYSM ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL CANCER ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RETINAL ANEURYSM ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RETROGRADE AMNESIA ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
ROTATOR CUFF REPAIR ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SEMEN VOLUME DECREASED ( 3 FDA reports)
SENILE DEMENTIA ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SERRATIA BACTERAEMIA ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPINAL CORD INJURY CERVICAL ( 3 FDA reports)
SPINAL CORD NEOPLASM ( 3 FDA reports)
SPLENIC ABSCESS ( 3 FDA reports)
SPLENIC ARTERY ANEURYSM ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 3 FDA reports)
STARING ( 3 FDA reports)
STENT MALFUNCTION ( 3 FDA reports)
SUPERINFECTION LUNG ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THALAMIC INFARCTION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TONIC CONVULSION ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRANSAMINASES DECREASED ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TUMOUR ASSOCIATED FEVER ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
URETHRAL STENOSIS ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
UROBILIN URINE PRESENT ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VALVULOPLASTY CARDIAC ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VERBAL ABUSE ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACANTHOSIS NIGRICANS ( 2 FDA reports)
ACCESSORY NAVICULAR SYNDROME ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAL SPASM ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC SURGERY ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AUTOMATIC BLADDER ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY DRAINAGE ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BILIRUBIN CONJUGATED ( 2 FDA reports)
BIOPSY STOMACH ABNORMAL ( 2 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER TRABECULATION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD CALCITONIN DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST DISORDER MALE ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CELLULITIS PHARYNGEAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CERVICOGENIC HEADACHE ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHOROIDAL HAEMORRHAGE ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COAGULATION FACTOR INCREASED ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR DECREASED ( 2 FDA reports)
CONGENITAL ABSENCE OF CRANIAL VAULT ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONVULSIONS LOCAL ( 2 FDA reports)
CORTISOL FREE URINE DECREASED ( 2 FDA reports)
CRANIOPHARYNGIOMA ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CSF GLUCOSE DECREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CYSTOURETHROCELE ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC RETINAL OEDEMA ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISUSE SYNDROME ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ECZEMA VESICULAR ( 2 FDA reports)
ECZEMA WEEPING ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID EROSION ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEMORAL NERVE INJURY ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FUNGUS CULTURE POSITIVE ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRINOMA ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL CANCER ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GENERAL NUTRITION DISORDER ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMATOCRIT ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMODILUTION ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A POSITIVE ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HUMORAL IMMUNE DEFECT ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERINSULINISM ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPLANT SITE DISCHARGE ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INJECTION SITE LACERATION ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 2 FDA reports)
INSULINOMA ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTERNAL HERNIA ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEDICAL INDUCTION OF COMA ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO BILIARY TRACT ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
MICROSOMIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NASAL VESTIBULITIS ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NOROVIRUS TEST POSITIVE ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OBTURATOR HERNIA ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OVARIAN ABSCESS ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC ISLETS HYPERPLASIA ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 2 FDA reports)
PERIANAL ERYTHEMA ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PERTUSSIS SEROLOGY POSITIVE ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHOTOSENSITIVE RASH ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PRESENILE DEMENTIA ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC CALCIFICATION ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHOSEXUAL DISORDER ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIATION MYELOPATHY ( 2 FDA reports)
RADIATION PERICARDITIS ( 2 FDA reports)
RECTAL OBSTRUCTION ( 2 FDA reports)
RECTAL SPASM ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL FAILURE NEONATAL ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL VASCULITIS ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 2 FDA reports)
RETROPERITONEAL INFECTION ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCIATIC NERVE NEUROPATHY ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SEXUAL ACTIVITY INCREASED ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TIC ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 2 FDA reports)
TOXIC DILATATION OF COLON ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL ULCER ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
VAGINAL ABSCESS ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VARICOSE VEIN RUPTURED ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICLE RUPTURE ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL NEOPLASM ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED HAEMOPHILIA WITH ANTI FVIII, XI, OR XIII ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM RETINA ABNORMAL ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BASE EXCESS ABNORMAL ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BERYLLIOSIS ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER IRRIGATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHOLINESTERASE ABNORMAL ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERULOPLASMIN INCREASED ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGIOADENOMA ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONTACT LENS COMPLICATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIOPHARYNGIOMA BENIGN ( 1 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DERMOID CYST ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG CLEARANCE INCREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
DYSPONESIS ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECTOPIA CORDIS ( 1 FDA reports)
ECTOPIC ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
ENDOCRINE TEST ( 1 FDA reports)
ENDOCRINE TEST ABNORMAL ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROCOLITIS FUNGAL ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR XI DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FRONTAL SINUS OPERATIONS ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HEPATITIS B DNA INCREASED ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLUENZA B VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL T-CELL LYMPHOMA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRANASAL PARAESTHESIA ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JAW OSTEITIS ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MISCARRIAGE OF PARTNER ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MORAXELLA TEST POSITIVE ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYRINGITIS ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE II ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSLER'S NODES ( 1 FDA reports)
OSTEOARTHROPATHY ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLASMINOGEN INCREASED ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE INDURATION ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
REMOVAL OF FOREIGN BODY ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM THROAT ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL MICROANEURYSMS ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 1 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC PHLEBITIS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE ABNORMAL ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL MYELOGRAM ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT EMBOLISATION ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TANNING ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON NECROSIS ( 1 FDA reports)
TENSILON TEST ABNORMAL ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROMBIN TIME ABNORMAL ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM BENIGN ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC ULCER ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UMBILICAL HAEMORRHAGE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC PERFORATION ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE POTASSIUM ABNORMAL ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
URTICARIA CONTACT ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS PRESSURE JUGULAR DECREASED ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)

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