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

DYSPNOEA ( 914 FDA reports)
NAUSEA ( 843 FDA reports)
FATIGUE ( 804 FDA reports)
PAIN ( 706 FDA reports)
DIZZINESS ( 670 FDA reports)
ASTHENIA ( 593 FDA reports)
DIARRHOEA ( 587 FDA reports)
VOMITING ( 544 FDA reports)
FALL ( 510 FDA reports)
ANAEMIA ( 499 FDA reports)
DRUG INEFFECTIVE ( 476 FDA reports)
ARTHRALGIA ( 471 FDA reports)
MALAISE ( 466 FDA reports)
PAIN IN EXTREMITY ( 458 FDA reports)
PYREXIA ( 456 FDA reports)
OEDEMA PERIPHERAL ( 450 FDA reports)
MYALGIA ( 449 FDA reports)
HEADACHE ( 437 FDA reports)
ANXIETY ( 428 FDA reports)
DRUG INTERACTION ( 428 FDA reports)
FLUSHING ( 419 FDA reports)
CHEST PAIN ( 406 FDA reports)
PRURITUS ( 397 FDA reports)
PNEUMONIA ( 390 FDA reports)
RENAL FAILURE ACUTE ( 384 FDA reports)
BACK PAIN ( 365 FDA reports)
MYOCARDIAL INFARCTION ( 356 FDA reports)
HYPOTENSION ( 352 FDA reports)
DEPRESSION ( 350 FDA reports)
HYPERTENSION ( 344 FDA reports)
WEIGHT DECREASED ( 333 FDA reports)
INSOMNIA ( 316 FDA reports)
GAIT DISTURBANCE ( 289 FDA reports)
PARAESTHESIA ( 287 FDA reports)
RENAL FAILURE ( 286 FDA reports)
WEIGHT INCREASED ( 281 FDA reports)
ATRIAL FIBRILLATION ( 280 FDA reports)
BLOOD GLUCOSE INCREASED ( 275 FDA reports)
COUGH ( 274 FDA reports)
CONFUSIONAL STATE ( 272 FDA reports)
DECREASED APPETITE ( 268 FDA reports)
DEHYDRATION ( 263 FDA reports)
RASH ( 262 FDA reports)
ABDOMINAL PAIN ( 255 FDA reports)
MUSCLE SPASMS ( 255 FDA reports)
PLEURAL EFFUSION ( 252 FDA reports)
SOMNOLENCE ( 251 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 243 FDA reports)
ERYTHEMA ( 239 FDA reports)
FEELING ABNORMAL ( 237 FDA reports)
INJURY ( 232 FDA reports)
MUSCULAR WEAKNESS ( 231 FDA reports)
HYPOAESTHESIA ( 230 FDA reports)
CEREBROVASCULAR ACCIDENT ( 220 FDA reports)
HAEMOGLOBIN DECREASED ( 218 FDA reports)
DEATH ( 215 FDA reports)
RECTAL HAEMORRHAGE ( 215 FDA reports)
ABDOMINAL PAIN UPPER ( 214 FDA reports)
BLOOD CREATININE INCREASED ( 203 FDA reports)
BRADYCARDIA ( 196 FDA reports)
HEPATIC ENZYME INCREASED ( 196 FDA reports)
URINARY TRACT INFECTION ( 196 FDA reports)
BLOOD PRESSURE INCREASED ( 190 FDA reports)
SYNCOPE ( 190 FDA reports)
CONDITION AGGRAVATED ( 186 FDA reports)
CONSTIPATION ( 185 FDA reports)
HYPERHIDROSIS ( 184 FDA reports)
LOSS OF CONSCIOUSNESS ( 184 FDA reports)
RESPIRATORY FAILURE ( 182 FDA reports)
RHABDOMYOLYSIS ( 181 FDA reports)
THROMBOCYTOPENIA ( 178 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 177 FDA reports)
PALPITATIONS ( 168 FDA reports)
DIABETES MELLITUS ( 163 FDA reports)
MEMORY IMPAIRMENT ( 162 FDA reports)
DYSPEPSIA ( 160 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 159 FDA reports)
CYSTITIS ( 159 FDA reports)
TREMOR ( 159 FDA reports)
CARDIAC FAILURE ( 157 FDA reports)
RENAL IMPAIRMENT ( 156 FDA reports)
CORONARY ARTERY DISEASE ( 155 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 154 FDA reports)
CONVULSION ( 152 FDA reports)
CHEST DISCOMFORT ( 150 FDA reports)
HYPONATRAEMIA ( 150 FDA reports)
ANGINA PECTORIS ( 149 FDA reports)
HAEMORRHOIDS ( 149 FDA reports)
MUSCULOSKELETAL PAIN ( 149 FDA reports)
NEUROPATHY PERIPHERAL ( 146 FDA reports)
CONTUSION ( 143 FDA reports)
VISION BLURRED ( 143 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 141 FDA reports)
INFECTION ( 140 FDA reports)
EMOTIONAL DISTRESS ( 139 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 137 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 135 FDA reports)
CARDIAC ARREST ( 135 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 135 FDA reports)
FEELING HOT ( 134 FDA reports)
NEUTROPENIA ( 134 FDA reports)
SEPSIS ( 134 FDA reports)
PANCYTOPENIA ( 133 FDA reports)
HEART RATE INCREASED ( 131 FDA reports)
URTICARIA ( 131 FDA reports)
DRUG DOSE OMISSION ( 130 FDA reports)
PLATELET COUNT DECREASED ( 128 FDA reports)
SINUSITIS ( 128 FDA reports)
DYSPHAGIA ( 126 FDA reports)
PULMONARY EMBOLISM ( 126 FDA reports)
BURNING SENSATION ( 124 FDA reports)
COLONIC POLYP ( 124 FDA reports)
BRONCHITIS ( 123 FDA reports)
HYPERSENSITIVITY ( 123 FDA reports)
OSTEOARTHRITIS ( 123 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 122 FDA reports)
APLASIA PURE RED CELL ( 120 FDA reports)
OVERDOSE ( 117 FDA reports)
CHILLS ( 116 FDA reports)
MUSCLE TWITCHING ( 116 FDA reports)
HYPOGLYCAEMIA ( 115 FDA reports)
INTERSTITIAL LUNG DISEASE ( 115 FDA reports)
ABDOMINAL DISCOMFORT ( 114 FDA reports)
GASTRITIS EROSIVE ( 114 FDA reports)
BALANCE DISORDER ( 111 FDA reports)
HAEMORRHAGE ( 111 FDA reports)
LEFT VENTRICULAR FAILURE ( 111 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 110 FDA reports)
BLOOD PRESSURE DECREASED ( 109 FDA reports)
TACHYCARDIA ( 109 FDA reports)
OFF LABEL USE ( 108 FDA reports)
VARICOSE VEIN ( 108 FDA reports)
ASTHMA ( 107 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 107 FDA reports)
HALLUCINATION ( 107 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 107 FDA reports)
ANAL FISSURE ( 106 FDA reports)
BONE PAIN ( 106 FDA reports)
RIGHT VENTRICULAR FAILURE ( 106 FDA reports)
HYPERKALAEMIA ( 105 FDA reports)
HYPOXIA ( 105 FDA reports)
SWELLING FACE ( 105 FDA reports)
DYSARTHRIA ( 104 FDA reports)
BLOOD UREA INCREASED ( 103 FDA reports)
CARDIAC DISORDER ( 102 FDA reports)
HYPOKALAEMIA ( 102 FDA reports)
OSTEONECROSIS OF JAW ( 102 FDA reports)
DYSPNOEA EXERTIONAL ( 101 FDA reports)
JOINT SWELLING ( 101 FDA reports)
HYPOPNOEA ( 99 FDA reports)
REFRACTORY ANAEMIA ( 99 FDA reports)
ECONOMIC PROBLEM ( 98 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 98 FDA reports)
NASOPHARYNGITIS ( 98 FDA reports)
VAGINAL ABSCESS ( 98 FDA reports)
ABDOMINAL DISTENSION ( 97 FDA reports)
OEDEMA ( 97 FDA reports)
SLEEP DISORDER ( 97 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 96 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 96 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 96 FDA reports)
INJECTION SITE PAIN ( 95 FDA reports)
MITRAL VALVE INCOMPETENCE ( 95 FDA reports)
DRY MOUTH ( 94 FDA reports)
EPISTAXIS ( 94 FDA reports)
HIATUS HERNIA ( 94 FDA reports)
MENTAL STATUS CHANGES ( 94 FDA reports)
HOT FLUSH ( 93 FDA reports)
PULMONARY OEDEMA ( 92 FDA reports)
ARTHRITIS ( 91 FDA reports)
CELLULITIS ( 91 FDA reports)
PRODUCT QUALITY ISSUE ( 91 FDA reports)
SUICIDAL IDEATION ( 91 FDA reports)
HYPERLIPIDAEMIA ( 90 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 90 FDA reports)
PANCREATITIS ( 90 FDA reports)
HYPERCHOLESTEROLAEMIA ( 89 FDA reports)
VISUAL IMPAIRMENT ( 89 FDA reports)
DRUG HYPERSENSITIVITY ( 87 FDA reports)
GASTRITIS ( 87 FDA reports)
WHEEZING ( 87 FDA reports)
AMNESIA ( 86 FDA reports)
COLITIS ( 86 FDA reports)
DYSURIA ( 86 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 85 FDA reports)
ALOPECIA ( 84 FDA reports)
BONE DISORDER ( 84 FDA reports)
RASH ERYTHEMATOUS ( 84 FDA reports)
ANHEDONIA ( 83 FDA reports)
VERTIGO ( 83 FDA reports)
NERVOUSNESS ( 82 FDA reports)
OSTEOMYELITIS ( 82 FDA reports)
DISORIENTATION ( 81 FDA reports)
ABNORMAL DREAMS ( 80 FDA reports)
LIVER DISORDER ( 80 FDA reports)
SLEEP APNOEA SYNDROME ( 80 FDA reports)
SWELLING ( 80 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 79 FDA reports)
CATARACT ( 79 FDA reports)
SKIN BURNING SENSATION ( 79 FDA reports)
RENAL FAILURE CHRONIC ( 78 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 77 FDA reports)
ARRHYTHMIA ( 76 FDA reports)
CARDIOMEGALY ( 76 FDA reports)
DEEP VEIN THROMBOSIS ( 75 FDA reports)
GASTRIC ULCER ( 75 FDA reports)
INFLAMMATION ( 75 FDA reports)
NEOPLASM MALIGNANT ( 75 FDA reports)
UNEVALUABLE EVENT ( 75 FDA reports)
ANOREXIA ( 74 FDA reports)
CORONARY ARTERY STENOSIS ( 74 FDA reports)
INCORRECT DOSE ADMINISTERED ( 74 FDA reports)
OXYGEN SATURATION DECREASED ( 74 FDA reports)
STRESS ( 74 FDA reports)
AGGRESSION ( 73 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 73 FDA reports)
CHOLELITHIASIS ( 73 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 73 FDA reports)
SEPTIC SHOCK ( 73 FDA reports)
INFLUENZA LIKE ILLNESS ( 72 FDA reports)
LUNG DISORDER ( 72 FDA reports)
MULTI-ORGAN FAILURE ( 72 FDA reports)
RASH PRURITIC ( 72 FDA reports)
HAEMATEMESIS ( 71 FDA reports)
HAEMATURIA ( 71 FDA reports)
HEPATIC STEATOSIS ( 71 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 71 FDA reports)
LYMPHADENOPATHY ( 71 FDA reports)
ABASIA ( 70 FDA reports)
ABNORMAL BEHAVIOUR ( 70 FDA reports)
AGITATION ( 70 FDA reports)
PRODUCTIVE COUGH ( 70 FDA reports)
LETHARGY ( 69 FDA reports)
MELAENA ( 69 FDA reports)
PAIN IN JAW ( 69 FDA reports)
PANCREATITIS ACUTE ( 69 FDA reports)
SCAR ( 69 FDA reports)
CORONARY ARTERY OCCLUSION ( 68 FDA reports)
DYSKINESIA ( 68 FDA reports)
FLATULENCE ( 68 FDA reports)
NECK PAIN ( 68 FDA reports)
DYSPHONIA ( 67 FDA reports)
HAEMATOMA ( 67 FDA reports)
HYPERGLYCAEMIA ( 67 FDA reports)
PALLOR ( 67 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 66 FDA reports)
FEBRILE NEUTROPENIA ( 65 FDA reports)
OSTEOPOROSIS ( 65 FDA reports)
SPINAL OSTEOARTHRITIS ( 65 FDA reports)
DISTURBANCE IN ATTENTION ( 64 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 64 FDA reports)
PULMONARY HYPERTENSION ( 64 FDA reports)
VENTRICULAR TACHYCARDIA ( 64 FDA reports)
BLOOD GLUCOSE DECREASED ( 63 FDA reports)
COMA ( 63 FDA reports)
DYSGEUSIA ( 63 FDA reports)
MYOCARDIAL ISCHAEMIA ( 63 FDA reports)
SKIN EXFOLIATION ( 63 FDA reports)
THROMBOSIS ( 63 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 63 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 63 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 62 FDA reports)
MOBILITY DECREASED ( 62 FDA reports)
OROPHARYNGEAL PAIN ( 62 FDA reports)
SUICIDE ATTEMPT ( 62 FDA reports)
DEFORMITY ( 61 FDA reports)
HERPES ZOSTER ( 61 FDA reports)
NEPHROLITHIASIS ( 61 FDA reports)
POLLAKIURIA ( 61 FDA reports)
CARDIO-RESPIRATORY ARREST ( 60 FDA reports)
DIPLOPIA ( 60 FDA reports)
HAEMOPTYSIS ( 60 FDA reports)
BLOOD POTASSIUM INCREASED ( 59 FDA reports)
DRY SKIN ( 59 FDA reports)
DYSSTASIA ( 59 FDA reports)
HAEMATOCHEZIA ( 59 FDA reports)
HYPOPHAGIA ( 59 FDA reports)
LEUKOPENIA ( 59 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 59 FDA reports)
SPEECH DISORDER ( 59 FDA reports)
ARTHROPATHY ( 58 FDA reports)
IRRITABILITY ( 58 FDA reports)
PSORIASIS ( 58 FDA reports)
RENAL DISORDER ( 58 FDA reports)
SWOLLEN TONGUE ( 58 FDA reports)
TREATMENT NONCOMPLIANCE ( 58 FDA reports)
VISUAL ACUITY REDUCED ( 58 FDA reports)
HEMIPLEGIA ( 57 FDA reports)
MULTIPLE MYELOMA ( 57 FDA reports)
SKIN LESION ( 57 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 57 FDA reports)
CEREBRAL INFARCTION ( 56 FDA reports)
STAPHYLOCOCCAL INFECTION ( 56 FDA reports)
STOMATITIS ( 56 FDA reports)
BLOOD BILIRUBIN INCREASED ( 55 FDA reports)
IMPAIRED HEALING ( 55 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 55 FDA reports)
MIGRAINE ( 55 FDA reports)
MULTIPLE INJURIES ( 55 FDA reports)
SURGERY ( 55 FDA reports)
TYPE 2 DIABETES MELLITUS ( 55 FDA reports)
CARDIOMYOPATHY ( 54 FDA reports)
EOSINOPHILIA ( 54 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 54 FDA reports)
MENTAL DISORDER ( 54 FDA reports)
SKIN ULCER ( 54 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 53 FDA reports)
ANGIOEDEMA ( 52 FDA reports)
ECZEMA ( 52 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 52 FDA reports)
METABOLIC ACIDOSIS ( 52 FDA reports)
MYOPATHY ( 52 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 52 FDA reports)
UNRESPONSIVE TO STIMULI ( 52 FDA reports)
CHOLESTASIS ( 51 FDA reports)
EMPHYSEMA ( 51 FDA reports)
HEAD INJURY ( 51 FDA reports)
HEART RATE IRREGULAR ( 51 FDA reports)
INFLUENZA ( 51 FDA reports)
PRURITUS GENERALISED ( 51 FDA reports)
RASH MACULAR ( 51 FDA reports)
DRUG EFFECT DECREASED ( 50 FDA reports)
HEMIPARESIS ( 50 FDA reports)
HEPATIC FAILURE ( 50 FDA reports)
HEPATITIS ( 50 FDA reports)
NEURALGIA ( 50 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 50 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 50 FDA reports)
ARTERIOSCLEROSIS ( 49 FDA reports)
ASCITES ( 49 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 49 FDA reports)
DISEASE PROGRESSION ( 49 FDA reports)
FLUID RETENTION ( 49 FDA reports)
HEART RATE DECREASED ( 49 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 49 FDA reports)
PANIC ATTACK ( 49 FDA reports)
ROAD TRAFFIC ACCIDENT ( 49 FDA reports)
BLISTER ( 48 FDA reports)
DISCOMFORT ( 48 FDA reports)
HIP FRACTURE ( 48 FDA reports)
ORTHOSTATIC HYPOTENSION ( 48 FDA reports)
SKIN DISCOLOURATION ( 48 FDA reports)
JAUNDICE ( 47 FDA reports)
LEUKOCYTOSIS ( 47 FDA reports)
POST PROCEDURAL COMPLICATION ( 47 FDA reports)
FEAR ( 46 FDA reports)
HYPOTHYROIDISM ( 46 FDA reports)
OSTEONECROSIS ( 46 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 46 FDA reports)
TENDON RUPTURE ( 46 FDA reports)
TOXIC SKIN ERUPTION ( 46 FDA reports)
JOINT STIFFNESS ( 45 FDA reports)
LUNG INFILTRATION ( 45 FDA reports)
PROSTATE CANCER ( 45 FDA reports)
VENTRICULAR FIBRILLATION ( 45 FDA reports)
ATELECTASIS ( 44 FDA reports)
BASAL CELL CARCINOMA ( 44 FDA reports)
INTENTIONAL DRUG MISUSE ( 44 FDA reports)
PULMONARY FIBROSIS ( 44 FDA reports)
RESTLESSNESS ( 44 FDA reports)
SEDATION ( 44 FDA reports)
CEREBRAL HAEMORRHAGE ( 43 FDA reports)
CYTOLYTIC HEPATITIS ( 43 FDA reports)
DIVERTICULUM ( 43 FDA reports)
PERICARDIAL EFFUSION ( 43 FDA reports)
RESTLESS LEGS SYNDROME ( 43 FDA reports)
TOOTHACHE ( 43 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 42 FDA reports)
EYE PAIN ( 42 FDA reports)
FACE OEDEMA ( 42 FDA reports)
GOUT ( 42 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 42 FDA reports)
NEUTROPHIL COUNT DECREASED ( 42 FDA reports)
RASH MACULO-PAPULAR ( 42 FDA reports)
RENAL PAIN ( 42 FDA reports)
SPINAL COLUMN STENOSIS ( 42 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 42 FDA reports)
URINARY INCONTINENCE ( 42 FDA reports)
AORTIC VALVE INCOMPETENCE ( 41 FDA reports)
CERVICAL DYSPLASIA ( 41 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 41 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 41 FDA reports)
MENTAL IMPAIRMENT ( 41 FDA reports)
PHYSICAL DISABILITY ( 41 FDA reports)
RASH GENERALISED ( 41 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 41 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 40 FDA reports)
LUNG NEOPLASM ( 40 FDA reports)
MANIA ( 40 FDA reports)
OESOPHAGITIS ( 40 FDA reports)
RHEUMATOID ARTHRITIS ( 40 FDA reports)
APHASIA ( 39 FDA reports)
BLOOD POTASSIUM DECREASED ( 39 FDA reports)
CYANOSIS ( 39 FDA reports)
EJECTION FRACTION DECREASED ( 39 FDA reports)
GASTROINTESTINAL DISORDER ( 39 FDA reports)
HAEMODIALYSIS ( 39 FDA reports)
LIP SWELLING ( 39 FDA reports)
MOOD SWINGS ( 39 FDA reports)
NIGHTMARE ( 39 FDA reports)
SHOCK ( 39 FDA reports)
TRANSAMINASES INCREASED ( 39 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 38 FDA reports)
DERMATITIS CONTACT ( 38 FDA reports)
DIVERTICULITIS ( 38 FDA reports)
DRUG INTOLERANCE ( 38 FDA reports)
DYSLIPIDAEMIA ( 38 FDA reports)
FAECES DISCOLOURED ( 38 FDA reports)
HAEMATOCRIT DECREASED ( 38 FDA reports)
PLATELET COUNT INCREASED ( 38 FDA reports)
PSYCHOTIC DISORDER ( 38 FDA reports)
SQUAMOUS CELL CARCINOMA ( 38 FDA reports)
BEDRIDDEN ( 37 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 37 FDA reports)
GASTROENTERITIS ( 37 FDA reports)
INJECTION SITE HAEMATOMA ( 37 FDA reports)
MOVEMENT DISORDER ( 37 FDA reports)
MUSCLE ATROPHY ( 37 FDA reports)
DELUSION ( 36 FDA reports)
FEELING COLD ( 36 FDA reports)
INJECTION SITE ERYTHEMA ( 36 FDA reports)
PNEUMONITIS ( 36 FDA reports)
PRESYNCOPE ( 36 FDA reports)
RALES ( 36 FDA reports)
SUDDEN DEATH ( 36 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 36 FDA reports)
THROAT IRRITATION ( 36 FDA reports)
VIITH NERVE PARALYSIS ( 36 FDA reports)
ACUTE RESPIRATORY FAILURE ( 35 FDA reports)
COMPLETED SUICIDE ( 35 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 35 FDA reports)
DELIRIUM ( 35 FDA reports)
DERMATITIS ( 35 FDA reports)
DRUG TOXICITY ( 35 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 35 FDA reports)
MUCOSAL INFLAMMATION ( 35 FDA reports)
MULTIPLE SCLEROSIS ( 35 FDA reports)
NERVOUS SYSTEM DISORDER ( 35 FDA reports)
PHARYNGEAL OEDEMA ( 35 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 35 FDA reports)
RESPIRATORY DEPRESSION ( 35 FDA reports)
SCIATICA ( 35 FDA reports)
URINARY RETENTION ( 35 FDA reports)
CHROMATURIA ( 34 FDA reports)
DEMENTIA ( 34 FDA reports)
EMOTIONAL DISORDER ( 34 FDA reports)
EYE DISORDER ( 34 FDA reports)
FACIAL PAIN ( 34 FDA reports)
GALLBLADDER DISORDER ( 34 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 34 FDA reports)
HORDEOLUM ( 34 FDA reports)
LUNG NEOPLASM MALIGNANT ( 34 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 34 FDA reports)
RENAL CYST ( 34 FDA reports)
RESPIRATORY DISTRESS ( 34 FDA reports)
RHINORRHOEA ( 34 FDA reports)
SPINAL COMPRESSION FRACTURE ( 34 FDA reports)
TOOTH EXTRACTION ( 34 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 33 FDA reports)
BLOOD SODIUM DECREASED ( 33 FDA reports)
BONE MARROW FAILURE ( 33 FDA reports)
DRY EYE ( 33 FDA reports)
EYE SWELLING ( 33 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 33 FDA reports)
HYPERSOMNIA ( 33 FDA reports)
ILL-DEFINED DISORDER ( 33 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 33 FDA reports)
OSTEOPENIA ( 33 FDA reports)
PURPURA ( 33 FDA reports)
SINUS TACHYCARDIA ( 33 FDA reports)
AGEUSIA ( 32 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 32 FDA reports)
BREAST CANCER ( 32 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 32 FDA reports)
ENCEPHALOPATHY ( 32 FDA reports)
ERECTILE DYSFUNCTION ( 32 FDA reports)
HALLUCINATION, VISUAL ( 32 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 32 FDA reports)
LUNG INFECTION ( 32 FDA reports)
MEDICATION ERROR ( 32 FDA reports)
METASTASES TO LIVER ( 32 FDA reports)
PERIPHERAL COLDNESS ( 32 FDA reports)
SKIN TIGHTNESS ( 32 FDA reports)
COGNITIVE DISORDER ( 31 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 31 FDA reports)
DUODENAL ULCER ( 31 FDA reports)
EATING DISORDER ( 31 FDA reports)
EPILEPSY ( 31 FDA reports)
HOSPITALISATION ( 31 FDA reports)
HYPOVOLAEMIA ( 31 FDA reports)
INFUSION RELATED REACTION ( 31 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 31 FDA reports)
NASAL CONGESTION ( 31 FDA reports)
PARANOIA ( 31 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 31 FDA reports)
RASH PAPULAR ( 31 FDA reports)
SPLENOMEGALY ( 31 FDA reports)
TINNITUS ( 31 FDA reports)
WALKING AID USER ( 31 FDA reports)
WITHDRAWAL SYNDROME ( 31 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 30 FDA reports)
BRONCHOSPASM ( 30 FDA reports)
CAROTID ARTERY STENOSIS ( 30 FDA reports)
CARPAL TUNNEL SYNDROME ( 30 FDA reports)
EXOSTOSIS ( 30 FDA reports)
FEMUR FRACTURE ( 30 FDA reports)
FIBROMYALGIA ( 30 FDA reports)
FUNGAL INFECTION ( 30 FDA reports)
HYPERNATRAEMIA ( 30 FDA reports)
HYPOALBUMINAEMIA ( 30 FDA reports)
HYPOKINESIA ( 30 FDA reports)
MACULAR DEGENERATION ( 30 FDA reports)
MOTOR DYSFUNCTION ( 30 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 30 FDA reports)
STENT PLACEMENT ( 30 FDA reports)
TORSADE DE POINTES ( 30 FDA reports)
TRISMUS ( 30 FDA reports)
VASCULITIS ( 30 FDA reports)
ACNE ( 29 FDA reports)
ANGIONEUROTIC OEDEMA ( 29 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 29 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 29 FDA reports)
CARDIAC MURMUR ( 29 FDA reports)
CORONARY ANGIOPLASTY ( 29 FDA reports)
DEPRESSED MOOD ( 29 FDA reports)
EAR PAIN ( 29 FDA reports)
JOINT EFFUSION ( 29 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 29 FDA reports)
NIGHT SWEATS ( 29 FDA reports)
RESPIRATORY ARREST ( 29 FDA reports)
SINUS BRADYCARDIA ( 29 FDA reports)
SKIN HYPERTROPHY ( 29 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 28 FDA reports)
APATHY ( 28 FDA reports)
BLINDNESS ( 28 FDA reports)
FLUID OVERLOAD ( 28 FDA reports)
FRACTURE ( 28 FDA reports)
GROIN PAIN ( 28 FDA reports)
HEPATOMEGALY ( 28 FDA reports)
IRON DEFICIENCY ANAEMIA ( 28 FDA reports)
ISCHAEMIA ( 28 FDA reports)
LIPASE INCREASED ( 28 FDA reports)
METASTASES TO BONE ( 28 FDA reports)
RIB FRACTURE ( 28 FDA reports)
TACHYPNOEA ( 28 FDA reports)
TROPONIN INCREASED ( 28 FDA reports)
ANGER ( 27 FDA reports)
AORTIC STENOSIS ( 27 FDA reports)
BARRETT'S OESOPHAGUS ( 27 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 27 FDA reports)
COAGULOPATHY ( 27 FDA reports)
GASTRIC HAEMORRHAGE ( 27 FDA reports)
GENERALISED ERYTHEMA ( 27 FDA reports)
GENERALISED OEDEMA ( 27 FDA reports)
GRAND MAL CONVULSION ( 27 FDA reports)
HYPERTHYROIDISM ( 27 FDA reports)
MIDDLE INSOMNIA ( 27 FDA reports)
PULMONARY CONGESTION ( 27 FDA reports)
RADICULOPATHY ( 27 FDA reports)
RESPIRATORY DISORDER ( 27 FDA reports)
TENDONITIS ( 27 FDA reports)
ABDOMINAL PAIN LOWER ( 26 FDA reports)
ANGINA UNSTABLE ( 26 FDA reports)
BRONCHOPNEUMONIA ( 26 FDA reports)
CARDIOGENIC SHOCK ( 26 FDA reports)
CARDIOVASCULAR DISORDER ( 26 FDA reports)
CEREBRAL ATROPHY ( 26 FDA reports)
CIRCULATORY COLLAPSE ( 26 FDA reports)
DRUG LEVEL INCREASED ( 26 FDA reports)
GLAUCOMA ( 26 FDA reports)
GRIP STRENGTH DECREASED ( 26 FDA reports)
INTRACARDIAC THROMBUS ( 26 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 26 FDA reports)
NOCTURIA ( 26 FDA reports)
ORAL PAIN ( 26 FDA reports)
PROTHROMBIN TIME PROLONGED ( 26 FDA reports)
RENAL TUBULAR NECROSIS ( 26 FDA reports)
SKIN INDURATION ( 26 FDA reports)
THINKING ABNORMAL ( 26 FDA reports)
VENTRICULAR HYPERTROPHY ( 26 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 25 FDA reports)
AGRANULOCYTOSIS ( 25 FDA reports)
ANAPHYLACTIC REACTION ( 25 FDA reports)
ANGIOPLASTY ( 25 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 25 FDA reports)
CERVIX CARCINOMA ( 25 FDA reports)
COLON CANCER ( 25 FDA reports)
CROHN'S DISEASE ( 25 FDA reports)
CRYING ( 25 FDA reports)
DENTAL CARIES ( 25 FDA reports)
DIALYSIS ( 25 FDA reports)
DRUG ERUPTION ( 25 FDA reports)
DYSTONIA ( 25 FDA reports)
HEPATIC CIRRHOSIS ( 25 FDA reports)
INCONTINENCE ( 25 FDA reports)
JOINT INJURY ( 25 FDA reports)
KIDNEY INFECTION ( 25 FDA reports)
NEPHROTIC SYNDROME ( 25 FDA reports)
OCULAR HYPERAEMIA ( 25 FDA reports)
ORAL CANDIDIASIS ( 25 FDA reports)
ORTHOPNOEA ( 25 FDA reports)
PERIPHERAL ISCHAEMIA ( 25 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 25 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 25 FDA reports)
UROSEPSIS ( 25 FDA reports)
ACUTE PULMONARY OEDEMA ( 24 FDA reports)
ANAPHYLACTIC SHOCK ( 24 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 24 FDA reports)
COMPRESSION FRACTURE ( 24 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 24 FDA reports)
COORDINATION ABNORMAL ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
DRUG ADMINISTRATION ERROR ( 24 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 24 FDA reports)
GASTRIC CANCER ( 24 FDA reports)
GLOSSODYNIA ( 24 FDA reports)
HYDRONEPHROSIS ( 24 FDA reports)
IMPLANT SITE INFECTION ( 24 FDA reports)
LUMBAR SPINAL STENOSIS ( 24 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 24 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 24 FDA reports)
PHOTOSENSITIVITY REACTION ( 24 FDA reports)
RADIATION ASSOCIATED PAIN ( 24 FDA reports)
RADICULAR PAIN ( 24 FDA reports)
RENAL INJURY ( 24 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 24 FDA reports)
SINUS CONGESTION ( 24 FDA reports)
VIRAL INFECTION ( 24 FDA reports)
ADVERSE EVENT ( 23 FDA reports)
APOLIPOPROTEIN A-I DECREASED ( 23 FDA reports)
BACTERIAL INFECTION ( 23 FDA reports)
BLOOD AMYLASE INCREASED ( 23 FDA reports)
BLOOD CREATINE INCREASED ( 23 FDA reports)
COLD SWEAT ( 23 FDA reports)
ECCHYMOSIS ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 23 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 23 FDA reports)
ISCHAEMIC STROKE ( 23 FDA reports)
LARGE INTESTINAL ULCER ( 23 FDA reports)
MUSCLE DISORDER ( 23 FDA reports)
NEOPLASM PROGRESSION ( 23 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 23 FDA reports)
PERITONITIS ( 23 FDA reports)
PLASMACYTOMA ( 23 FDA reports)
RHINITIS ALLERGIC ( 23 FDA reports)
SKIN DISORDER ( 23 FDA reports)
SPUTUM DISCOLOURED ( 23 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 23 FDA reports)
TOOTH INFECTION ( 23 FDA reports)
ULCER ( 23 FDA reports)
ABSCESS NECK ( 22 FDA reports)
ATRIAL FLUTTER ( 22 FDA reports)
BACTERAEMIA ( 22 FDA reports)
BLADDER CANCER ( 22 FDA reports)
BONE LESION ( 22 FDA reports)
CANDIDIASIS ( 22 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 22 FDA reports)
DILATATION VENTRICULAR ( 22 FDA reports)
INTENTIONAL OVERDOSE ( 22 FDA reports)
JOINT DISLOCATION ( 22 FDA reports)
LIMB DISCOMFORT ( 22 FDA reports)
MOOD ALTERED ( 22 FDA reports)
PROTEINURIA ( 22 FDA reports)
PYELONEPHRITIS ( 22 FDA reports)
REFLUX OESOPHAGITIS ( 22 FDA reports)
ACCIDENTAL OVERDOSE ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK ( 21 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 21 FDA reports)
BLOOD URINE PRESENT ( 21 FDA reports)
CEREBRAL ISCHAEMIA ( 21 FDA reports)
COLITIS ULCERATIVE ( 21 FDA reports)
DIFFICULTY IN WALKING ( 21 FDA reports)
DISEASE RECURRENCE ( 21 FDA reports)
FACIAL PALSY ( 21 FDA reports)
FAECAL INCONTINENCE ( 21 FDA reports)
FEELING JITTERY ( 21 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 21 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 21 FDA reports)
LACTIC ACIDOSIS ( 21 FDA reports)
MALNUTRITION ( 21 FDA reports)
MYELODYSPLASTIC SYNDROME ( 21 FDA reports)
NO ADVERSE EVENT ( 21 FDA reports)
OBESITY ( 21 FDA reports)
OCCULT BLOOD POSITIVE ( 21 FDA reports)
POOR QUALITY SLEEP ( 21 FDA reports)
SYNOVIAL CYST ( 21 FDA reports)
WRIST FRACTURE ( 21 FDA reports)
ANGIOPATHY ( 20 FDA reports)
ANOSMIA ( 20 FDA reports)
BLOOD ALBUMIN DECREASED ( 20 FDA reports)
CARDIAC VALVE DISEASE ( 20 FDA reports)
COLITIS ISCHAEMIC ( 20 FDA reports)
DIASTOLIC DYSFUNCTION ( 20 FDA reports)
DYSPLASIA ( 20 FDA reports)
FOOT FRACTURE ( 20 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 20 FDA reports)
HYPOACUSIS ( 20 FDA reports)
HYPOAESTHESIA ORAL ( 20 FDA reports)
INJECTION SITE REACTION ( 20 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 20 FDA reports)
LYMPHOCELE ( 20 FDA reports)
MUSCLE TIGHTNESS ( 20 FDA reports)
NECROSIS ( 20 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 20 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 20 FDA reports)
SNORING ( 20 FDA reports)
SPONDYLITIS ( 20 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 20 FDA reports)
WOUND INFECTION ( 20 FDA reports)
AKATHISIA ( 19 FDA reports)
ANKLE FRACTURE ( 19 FDA reports)
BLADDER DISORDER ( 19 FDA reports)
BLINDNESS UNILATERAL ( 19 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 19 FDA reports)
BRAIN OEDEMA ( 19 FDA reports)
CYST ( 19 FDA reports)
DIABETIC NEUROPATHY ( 19 FDA reports)
EOSINOPHIL COUNT INCREASED ( 19 FDA reports)
EXPOSED BONE IN JAW ( 19 FDA reports)
FLANK PAIN ( 19 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 19 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 19 FDA reports)
GUILLAIN-BARRE SYNDROME ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 19 FDA reports)
INGUINAL HERNIA ( 19 FDA reports)
INJECTION SITE HAEMORRHAGE ( 19 FDA reports)
IRRITABLE BOWEL SYNDROME ( 19 FDA reports)
LACRIMATION INCREASED ( 19 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 19 FDA reports)
NEUTROPHIL COUNT INCREASED ( 19 FDA reports)
PLEURAL FIBROSIS ( 19 FDA reports)
STRABISMUS ( 19 FDA reports)
SUBDURAL HAEMATOMA ( 19 FDA reports)
TRANSPLANT REJECTION ( 19 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 19 FDA reports)
UPPER LIMB FRACTURE ( 19 FDA reports)
ABSCESS ( 18 FDA reports)
ACUTE CORONARY SYNDROME ( 18 FDA reports)
ADVERSE DRUG REACTION ( 18 FDA reports)
ANURIA ( 18 FDA reports)
BACK DISORDER ( 18 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 18 FDA reports)
CARDIOPULMONARY FAILURE ( 18 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 18 FDA reports)
COMA SCALE ABNORMAL ( 18 FDA reports)
CORONARY ARTERY BYPASS ( 18 FDA reports)
DECUBITUS ULCER ( 18 FDA reports)
DRUG RESISTANCE ( 18 FDA reports)
EAR INFECTION ( 18 FDA reports)
EMBOLISM ( 18 FDA reports)
ESCHERICHIA INFECTION ( 18 FDA reports)
EYE IRRITATION ( 18 FDA reports)
EYE PRURITUS ( 18 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 18 FDA reports)
GINGIVAL BLEEDING ( 18 FDA reports)
HALLUCINATION, AUDITORY ( 18 FDA reports)
HEARING IMPAIRED ( 18 FDA reports)
HEPATIC MASS ( 18 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 18 FDA reports)
HYPERTENSIVE CRISIS ( 18 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 18 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 18 FDA reports)
ORAL DISORDER ( 18 FDA reports)
OVARIAN CYST ( 18 FDA reports)
PNEUMONIA ASPIRATION ( 18 FDA reports)
PSYCHOMOTOR RETARDATION ( 18 FDA reports)
SALIVARY HYPERSECRETION ( 18 FDA reports)
SPINAL DISORDER ( 18 FDA reports)
TENDERNESS ( 18 FDA reports)
TENDON DISORDER ( 18 FDA reports)
APPLICATION SITE ERYTHEMA ( 17 FDA reports)
BLOOD CALCIUM INCREASED ( 17 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 17 FDA reports)
CARDIOVERSION ( 17 FDA reports)
ERYTHEMA MULTIFORME ( 17 FDA reports)
FEELING DRUNK ( 17 FDA reports)
FIBROSIS ( 17 FDA reports)
GANGRENE ( 17 FDA reports)
GYNAECOMASTIA ( 17 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 17 FDA reports)
HEART TRANSPLANT REJECTION ( 17 FDA reports)
HUMERUS FRACTURE ( 17 FDA reports)
LABORATORY TEST ABNORMAL ( 17 FDA reports)
LEFT ATRIAL DILATATION ( 17 FDA reports)
LIBIDO DECREASED ( 17 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 17 FDA reports)
METASTASES TO LYMPH NODES ( 17 FDA reports)
MIOSIS ( 17 FDA reports)
MYELITIS TRANSVERSE ( 17 FDA reports)
NEPHROPATHY ( 17 FDA reports)
NEPHROPATHY TOXIC ( 17 FDA reports)
POLYURIA ( 17 FDA reports)
PULMONARY HAEMORRHAGE ( 17 FDA reports)
RETCHING ( 17 FDA reports)
ROTATOR CUFF SYNDROME ( 17 FDA reports)
SINUS DISORDER ( 17 FDA reports)
TARDIVE DYSKINESIA ( 17 FDA reports)
THROAT TIGHTNESS ( 17 FDA reports)
ATAXIA ( 16 FDA reports)
BLEPHARITIS ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 16 FDA reports)
BODY HEIGHT DECREASED ( 16 FDA reports)
CHOLECYSTECTOMY ( 16 FDA reports)
CONJUNCTIVITIS ( 16 FDA reports)
DEAFNESS ( 16 FDA reports)
DECREASED INTEREST ( 16 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 16 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 16 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 16 FDA reports)
HYPERTHERMIA ( 16 FDA reports)
ILEUS ( 16 FDA reports)
IMPAIRED DRIVING ABILITY ( 16 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
INTESTINAL OBSTRUCTION ( 16 FDA reports)
LACERATION ( 16 FDA reports)
LARGE INTESTINE PERFORATION ( 16 FDA reports)
LOCAL SWELLING ( 16 FDA reports)
LOCALISED INFECTION ( 16 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 16 FDA reports)
MEDICAL DEVICE REMOVAL ( 16 FDA reports)
METASTASES TO SPINE ( 16 FDA reports)
MUSCLE HAEMORRHAGE ( 16 FDA reports)
NEUTROPENIC SEPSIS ( 16 FDA reports)
NO THERAPEUTIC RESPONSE ( 16 FDA reports)
NODULE ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
OESOPHAGEAL PAIN ( 16 FDA reports)
ONYCHOMYCOSIS ( 16 FDA reports)
PHOTOPHOBIA ( 16 FDA reports)
PHYSICAL ASSAULT ( 16 FDA reports)
PNEUMOTHORAX ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
RESPIRATORY TRACT INFECTION ( 16 FDA reports)
SENSORY DISTURBANCE ( 16 FDA reports)
SEROTONIN SYNDROME ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 16 FDA reports)
STEVENS-JOHNSON SYNDROME ( 16 FDA reports)
THIRST ( 16 FDA reports)
THYROID DISORDER ( 16 FDA reports)
TOOTH ABSCESS ( 16 FDA reports)
URINE OUTPUT DECREASED ( 16 FDA reports)
UTERINE LEIOMYOMA ( 16 FDA reports)
VENTRICULAR HYPOKINESIA ( 16 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 15 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 15 FDA reports)
APHTHOUS STOMATITIS ( 15 FDA reports)
AREFLEXIA ( 15 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 15 FDA reports)
BREAST PAIN ( 15 FDA reports)
CARDIAC PACEMAKER INSERTION ( 15 FDA reports)
CAROTID ARTERY OCCLUSION ( 15 FDA reports)
CATHETERISATION CARDIAC ( 15 FDA reports)
DECREASED ACTIVITY ( 15 FDA reports)
DIABETIC KETOACIDOSIS ( 15 FDA reports)
DIZZINESS POSTURAL ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 15 FDA reports)
ENTERITIS ( 15 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 15 FDA reports)
EXTRASYSTOLES ( 15 FDA reports)
FISTULA ( 15 FDA reports)
GASTROENTERITIS VIRAL ( 15 FDA reports)
HEART VALVE INCOMPETENCE ( 15 FDA reports)
HERNIA ( 15 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 15 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 15 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 15 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 15 FDA reports)
LYMPHOPENIA ( 15 FDA reports)
MICTURITION URGENCY ( 15 FDA reports)
MONOPLEGIA ( 15 FDA reports)
MUSCLE INJURY ( 15 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 15 FDA reports)
MYOCLONUS ( 15 FDA reports)
OSTEOLYSIS ( 15 FDA reports)
PERIODONTITIS ( 15 FDA reports)
POLYMYOSITIS ( 15 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 15 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 15 FDA reports)
RASH PUSTULAR ( 15 FDA reports)
TROPONIN T INCREASED ( 15 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
ACUTE PRERENAL FAILURE ( 14 FDA reports)
ACUTE SINUSITIS ( 14 FDA reports)
APLASTIC ANAEMIA ( 14 FDA reports)
BLOOD CALCIUM DECREASED ( 14 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 14 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 14 FDA reports)
BLOOD MAGNESIUM DECREASED ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
BURSITIS ( 14 FDA reports)
CARDIAC FAILURE ACUTE ( 14 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 14 FDA reports)
CERVICAL SPINAL STENOSIS ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
CHOLECYSTITIS CHRONIC ( 14 FDA reports)
DERMATITIS BULLOUS ( 14 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 14 FDA reports)
DUODENITIS ( 14 FDA reports)
EXCORIATION ( 14 FDA reports)
EYELID OEDEMA ( 14 FDA reports)
EYELID PTOSIS ( 14 FDA reports)
FACET JOINT SYNDROME ( 14 FDA reports)
GASTRIC DISORDER ( 14 FDA reports)
HAEMOLYTIC ANAEMIA ( 14 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 14 FDA reports)
HEPATOCELLULAR DAMAGE ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
HYPOPHOSPHATAEMIA ( 14 FDA reports)
ILEUS PARALYTIC ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 14 FDA reports)
JOINT CONTRACTURE ( 14 FDA reports)
LIFE EXPECTANCY SHORTENED ( 14 FDA reports)
LIPIDS INCREASED ( 14 FDA reports)
LIVER INJURY ( 14 FDA reports)
NAIL DISORDER ( 14 FDA reports)
NEURITIS ( 14 FDA reports)
OESOPHAGEAL ULCER ( 14 FDA reports)
ORAL INTAKE REDUCED ( 14 FDA reports)
OSTEOMYELITIS ACUTE ( 14 FDA reports)
PAIN OF SKIN ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
PARKINSON'S DISEASE ( 14 FDA reports)
PARKINSONISM ( 14 FDA reports)
PELVIC PAIN ( 14 FDA reports)
PHARYNGITIS ( 14 FDA reports)
PROTEIN TOTAL DECREASED ( 14 FDA reports)
RENAL TUBULAR DISORDER ( 14 FDA reports)
RESPIRATORY RATE INCREASED ( 14 FDA reports)
RESPIRATORY TRACT CONGESTION ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 14 FDA reports)
TRACHEOBRONCHITIS ( 14 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 14 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 14 FDA reports)
VULVITIS ( 14 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 13 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ANAL FISTULA ( 13 FDA reports)
AORTIC VALVE STENOSIS ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
BACK INJURY ( 13 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 13 FDA reports)
BLOOD CHLORIDE DECREASED ( 13 FDA reports)
BONE MARROW TRANSPLANT ( 13 FDA reports)
BREAST MASS ( 13 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 13 FDA reports)
CARDIAC TAMPONADE ( 13 FDA reports)
CHEST X-RAY ABNORMAL ( 13 FDA reports)
CHRONIC SINUSITIS ( 13 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 13 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
DRUG PRESCRIBING ERROR ( 13 FDA reports)
ERUCTATION ( 13 FDA reports)
FAILURE TO THRIVE ( 13 FDA reports)
HAEMODYNAMIC INSTABILITY ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
HYPERBILIRUBINAEMIA ( 13 FDA reports)
HYPERTENSIVE HEART DISEASE ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
ILIAC ARTERY STENOSIS ( 13 FDA reports)
INJECTION SITE RASH ( 13 FDA reports)
INJECTION SITE SWELLING ( 13 FDA reports)
IRITIS ( 13 FDA reports)
KNEE ARTHROPLASTY ( 13 FDA reports)
LYMPHOMA ( 13 FDA reports)
MENISCUS LESION ( 13 FDA reports)
MENORRHAGIA ( 13 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 13 FDA reports)
MUSCLE RIGIDITY ( 13 FDA reports)
MYASTHENIA GRAVIS ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 13 FDA reports)
POST LAMINECTOMY SYNDROME ( 13 FDA reports)
PROTEIN URINE PRESENT ( 13 FDA reports)
PULSE ABSENT ( 13 FDA reports)
PURULENT DISCHARGE ( 13 FDA reports)
RADIOTHERAPY ( 13 FDA reports)
RETINAL HAEMORRHAGE ( 13 FDA reports)
SKIN IRRITATION ( 13 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 13 FDA reports)
STATUS EPILEPTICUS ( 13 FDA reports)
THERAPY NON-RESPONDER ( 13 FDA reports)
TONGUE OEDEMA ( 13 FDA reports)
UMBILICAL HERNIA ( 13 FDA reports)
APHAGIA ( 12 FDA reports)
AUTONOMIC NEUROPATHY ( 12 FDA reports)
AZOTAEMIA ( 12 FDA reports)
BLOOD PRESSURE ABNORMAL ( 12 FDA reports)
BONE DENSITY DECREASED ( 12 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 12 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 12 FDA reports)
COMMUNICATION DISORDER ( 12 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 12 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 12 FDA reports)
DEAFNESS UNILATERAL ( 12 FDA reports)
DERMATITIS EXFOLIATIVE ( 12 FDA reports)
DEVICE RELATED INFECTION ( 12 FDA reports)
ENTEROCOCCAL INFECTION ( 12 FDA reports)
GASTROINTESTINAL INFECTION ( 12 FDA reports)
GASTROINTESTINAL PERFORATION ( 12 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 12 FDA reports)
HEPATIC ENCEPHALOPATHY ( 12 FDA reports)
HYPERKERATOSIS ( 12 FDA reports)
HYPOMAGNESAEMIA ( 12 FDA reports)
HYPOREFLEXIA ( 12 FDA reports)
INFARCTION ( 12 FDA reports)
LIMB INJURY ( 12 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 12 FDA reports)
NASAL DISCOMFORT ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
OLIGURIA ( 12 FDA reports)
OPHTHALMOPLEGIA ( 12 FDA reports)
ORAL CAVITY FISTULA ( 12 FDA reports)
ORAL DISCOMFORT ( 12 FDA reports)
PARAESTHESIA ORAL ( 12 FDA reports)
PEPTIC ULCER ( 12 FDA reports)
RADICAL HYSTERECTOMY ( 12 FDA reports)
RENAL COLIC ( 12 FDA reports)
RESUSCITATION ( 12 FDA reports)
RHONCHI ( 12 FDA reports)
SELF-MEDICATION ( 12 FDA reports)
SENSORY LOSS ( 12 FDA reports)
SEPSIS SYNDROME ( 12 FDA reports)
SKIN SWELLING ( 12 FDA reports)
SPINAL FRACTURE ( 12 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 12 FDA reports)
STOMACH DISCOMFORT ( 12 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 12 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
VISUAL DISTURBANCE ( 12 FDA reports)
ACCIDENTAL EXPOSURE ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
ASPIRATION BONE MARROW ( 11 FDA reports)
BARTHOLIN'S CYST ( 11 FDA reports)
BLOOD CREATININE DECREASED ( 11 FDA reports)
BONE MARROW TOXICITY ( 11 FDA reports)
BREATH SOUNDS ABNORMAL ( 11 FDA reports)
CAECITIS ( 11 FDA reports)
CARDIAC ANEURYSM ( 11 FDA reports)
CAROTIDYNIA ( 11 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 11 FDA reports)
DEVICE BREAKAGE ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
DEVICE OCCLUSION ( 11 FDA reports)
DIABETIC RETINOPATHY ( 11 FDA reports)
DIARRHOEA INFECTIOUS ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
DRUG DISPENSING ERROR ( 11 FDA reports)
DRY THROAT ( 11 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 11 FDA reports)
ENDOCARDITIS ( 11 FDA reports)
ESSENTIAL HYPERTENSION ( 11 FDA reports)
EXERCISE TOLERANCE DECREASED ( 11 FDA reports)
FAECALOMA ( 11 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 11 FDA reports)
HAEMANGIOMA ( 11 FDA reports)
HAEMARTHROSIS ( 11 FDA reports)
HAEMOGLOBIN INCREASED ( 11 FDA reports)
HEPATOCELLULAR INJURY ( 11 FDA reports)
HYPERURICAEMIA ( 11 FDA reports)
INCREASED APPETITE ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
INTERMITTENT CLAUDICATION ( 11 FDA reports)
LIGAMENT INJURY ( 11 FDA reports)
LOBAR PNEUMONIA ( 11 FDA reports)
MACULAR OEDEMA ( 11 FDA reports)
MALIGNANT MELANOMA ( 11 FDA reports)
MASS ( 11 FDA reports)
MEDICAL DEVICE COMPLICATION ( 11 FDA reports)
METAPLASIA ( 11 FDA reports)
MOUTH ULCERATION ( 11 FDA reports)
MUSCLE RUPTURE ( 11 FDA reports)
MYOSITIS ( 11 FDA reports)
NERVE COMPRESSION ( 11 FDA reports)
NERVE INJURY ( 11 FDA reports)
NODAL RHYTHM ( 11 FDA reports)
NON-CARDIAC CHEST PAIN ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
POLYP ( 11 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 11 FDA reports)
RENAL ARTERY STENOSIS ( 11 FDA reports)
RETINOPATHY ( 11 FDA reports)
RHINITIS ( 11 FDA reports)
SCROTAL SWELLING ( 11 FDA reports)
SENSATION OF HEAVINESS ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SKIN WARM ( 11 FDA reports)
SPONDYLOLISTHESIS ( 11 FDA reports)
TONGUE DISORDER ( 11 FDA reports)
TRICUSPID VALVE DISEASE ( 11 FDA reports)
TUMOUR LYSIS SYNDROME ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VASCULAR OCCLUSION ( 11 FDA reports)
VITREOUS FLOATERS ( 11 FDA reports)
YELLOW SKIN ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
AORTIC ANEURYSM ( 10 FDA reports)
APHONIA ( 10 FDA reports)
ARTERIAL STENT INSERTION ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
ASTHENOPIA ( 10 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
BLOOD BICARBONATE DECREASED ( 10 FDA reports)
BLOOD BLISTER ( 10 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BONE NEOPLASM MALIGNANT ( 10 FDA reports)
BRAIN SCAN ABNORMAL ( 10 FDA reports)
CARDIAC OPERATION ( 10 FDA reports)
CAUDA EQUINA SYNDROME ( 10 FDA reports)
CEREBRAL HAEMATOMA ( 10 FDA reports)
CHOKING ( 10 FDA reports)
CHOKING SENSATION ( 10 FDA reports)
CHONDROPATHY ( 10 FDA reports)
CLOSTRIDIAL INFECTION ( 10 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 10 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
DEVICE FAILURE ( 10 FDA reports)
DILATATION ATRIAL ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 10 FDA reports)
ENDOCARDITIS BACTERIAL ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 10 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 10 FDA reports)
HEPATITIS B ( 10 FDA reports)
HYPERTONIA ( 10 FDA reports)
HYPOVOLAEMIC SHOCK ( 10 FDA reports)
INDURATION ( 10 FDA reports)
JAW OPERATION ( 10 FDA reports)
LUNG ADENOCARCINOMA ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
MEDICATION RESIDUE ( 10 FDA reports)
METABOLIC SYNDROME ( 10 FDA reports)
METASTASES TO EYE ( 10 FDA reports)
MUSCLE FATIGUE ( 10 FDA reports)
NEUTROPENIC COLITIS ( 10 FDA reports)
OEDEMA MOUTH ( 10 FDA reports)
PARTIAL SEIZURES ( 10 FDA reports)
PERINEAL PAIN ( 10 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PLEURISY ( 10 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 10 FDA reports)
PROCEDURAL COMPLICATION ( 10 FDA reports)
PRODUCT ADHESION ISSUE ( 10 FDA reports)
PSYCHIATRIC SYMPTOM ( 10 FDA reports)
PULMONARY GRANULOMA ( 10 FDA reports)
RENAL TRANSPLANT ( 10 FDA reports)
RESPIRATION ABNORMAL ( 10 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 10 FDA reports)
SCLERODACTYLIA ( 10 FDA reports)
SECRETION DISCHARGE ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 10 FDA reports)
TENOSYNOVITIS STENOSANS ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 10 FDA reports)
URETERIC STENOSIS ( 10 FDA reports)
VENOUS THROMBOSIS ( 10 FDA reports)
VITAMIN D DECREASED ( 10 FDA reports)
ABNORMAL FAECES ( 9 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
AFFECTIVE DISORDER ( 9 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 9 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 9 FDA reports)
AORTIC DILATATION ( 9 FDA reports)
APRAXIA ( 9 FDA reports)
ARTERIAL STENOSIS LIMB ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BONE LOSS ( 9 FDA reports)
CARDIAC FLUTTER ( 9 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
COLON CANCER METASTATIC ( 9 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 9 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 9 FDA reports)
DIVERTICULUM INTESTINAL ( 9 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 9 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 9 FDA reports)
ENDOTRACHEAL INTUBATION ( 9 FDA reports)
EXPIRED DRUG ADMINISTERED ( 9 FDA reports)
FACIAL BONES FRACTURE ( 9 FDA reports)
FOREIGN BODY ( 9 FDA reports)
GOITRE ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
HICCUPS ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HYPERPLASIA ( 9 FDA reports)
HYPOMANIA ( 9 FDA reports)
HYPOTHERMIA ( 9 FDA reports)
HYSTERECTOMY ( 9 FDA reports)
IMMUNOSUPPRESSION ( 9 FDA reports)
INJECTION SITE WARMTH ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 9 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 9 FDA reports)
LABILE BLOOD PRESSURE ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 9 FDA reports)
LIP OEDEMA ( 9 FDA reports)
LOCALISED OEDEMA ( 9 FDA reports)
LUNG CANCER METASTATIC ( 9 FDA reports)
LYMPHOEDEMA ( 9 FDA reports)
MEGACOLON ( 9 FDA reports)
METASTASES TO MENINGES ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
NEPHRITIS ( 9 FDA reports)
ONYCHALGIA ( 9 FDA reports)
OPEN WOUND ( 9 FDA reports)
ORAL SURGERY ( 9 FDA reports)
PANCREATIC ENZYMES INCREASED ( 9 FDA reports)
PANIC REACTION ( 9 FDA reports)
PERSONALITY CHANGE ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PLASMACYTOSIS ( 9 FDA reports)
PLEURITIC PAIN ( 9 FDA reports)
PROTHROMBIN TIME SHORTENED ( 9 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 9 FDA reports)
RHEUMATOID FACTOR INCREASED ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKIN PAPILLOMA ( 9 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 9 FDA reports)
STEM CELL TRANSPLANT ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
T-CELL LYMPHOMA ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
TYPE 1 DIABETES MELLITUS ( 9 FDA reports)
URINE ODOUR ABNORMAL ( 9 FDA reports)
VAGINAL HAEMORRHAGE ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
VENTRICULAR DYSFUNCTION ( 9 FDA reports)
VISUAL FIELD DEFECT ( 9 FDA reports)
WOUND ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
WRONG DRUG ADMINISTERED ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 8 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
APPLICATION SITE PAIN ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
APPLICATION SITE RASH ( 8 FDA reports)
ARTERIAL REPAIR ( 8 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 8 FDA reports)
ARTERIOSPASM CORONARY ( 8 FDA reports)
ATROPHY ( 8 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 8 FDA reports)
BONE FRAGMENTATION ( 8 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
BRONCHIECTASIS ( 8 FDA reports)
BRONCHIOLITIS ( 8 FDA reports)
CALCULUS URINARY ( 8 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 8 FDA reports)
DERMATITIS ALLERGIC ( 8 FDA reports)
DIABETIC MICROANGIOPATHY ( 8 FDA reports)
DRUG INTERACTION POTENTIATION ( 8 FDA reports)
DYSPHEMIA ( 8 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
ENDARTERECTOMY ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
EOSINOPHILIC PNEUMONIA ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
ESCHAR ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EXTREMITY CONTRACTURE ( 8 FDA reports)
FAMILY STRESS ( 8 FDA reports)
GRANULOMA ( 8 FDA reports)
HAEMOLYSIS ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HEART VALVE CALCIFICATION ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 8 FDA reports)
HYPERAESTHESIA ( 8 FDA reports)
HYPOCAPNIA ( 8 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 8 FDA reports)
INCORRECT STORAGE OF DRUG ( 8 FDA reports)
INFECTED SKIN ULCER ( 8 FDA reports)
INGROWING NAIL ( 8 FDA reports)
INJECTION SITE INDURATION ( 8 FDA reports)
INNER EAR DISORDER ( 8 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 8 FDA reports)
INTESTINAL DILATATION ( 8 FDA reports)
JAW FRACTURE ( 8 FDA reports)
JAW LESION EXCISION ( 8 FDA reports)
LARYNGEAL OEDEMA ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LIPODYSTROPHY ACQUIRED ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LOSS OF LIBIDO ( 8 FDA reports)
LOWER LIMB FRACTURE ( 8 FDA reports)
LUNG CONSOLIDATION ( 8 FDA reports)
MENOPAUSAL SYMPTOMS ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
MICROALBUMINURIA ( 8 FDA reports)
MIXED LIVER INJURY ( 8 FDA reports)
MONOCYTE COUNT INCREASED ( 8 FDA reports)
MYELOMA RECURRENCE ( 8 FDA reports)
PALATAL DISORDER ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PERFORMANCE STATUS DECREASED ( 8 FDA reports)
PERIARTHRITIS ( 8 FDA reports)
PERICARDIAL HAEMORRHAGE ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 8 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
PRESBYOPIA ( 8 FDA reports)
PROCEDURAL PAIN ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 8 FDA reports)
PULMONARY THROMBOSIS ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RENAL ATROPHY ( 8 FDA reports)
RETROPERITONEAL HAEMATOMA ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SINUS HEADACHE ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
SYNCOPE VASOVAGAL ( 8 FDA reports)
TEMPERATURE INTOLERANCE ( 8 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 8 FDA reports)
TENDON PAIN ( 8 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 8 FDA reports)
TOE AMPUTATION ( 8 FDA reports)
TOOTH DISORDER ( 8 FDA reports)
TROPONIN I INCREASED ( 8 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 8 FDA reports)
URETERIC OBSTRUCTION ( 8 FDA reports)
WOUND DEHISCENCE ( 8 FDA reports)
ADRENOMEGALY ( 7 FDA reports)
ANORGASMIA ( 7 FDA reports)
ARTHROPOD BITE ( 7 FDA reports)
ASTIGMATISM ( 7 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
BLINDNESS TRANSIENT ( 7 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 7 FDA reports)
BODY TEMPERATURE DECREASED ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
CARDIAC ENZYMES INCREASED ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 7 FDA reports)
CEREBRAL THROMBOSIS ( 7 FDA reports)
CLEFT PALATE ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
DEPRESSIVE SYMPTOM ( 7 FDA reports)
DERMATITIS ACNEIFORM ( 7 FDA reports)
DIVERTICULAR PERFORATION ( 7 FDA reports)
DRUG SCREEN POSITIVE ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROLYTE IMBALANCE ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
ESCHERICHIA TEST POSITIVE ( 7 FDA reports)
EUPHORIC MOOD ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FOETAL GROWTH RESTRICTION ( 7 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 7 FDA reports)
GINGIVAL PAIN ( 7 FDA reports)
GINGIVAL SWELLING ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
GOUTY ARTHRITIS ( 7 FDA reports)
GRANULOCYTOPENIA ( 7 FDA reports)
HAIR COLOUR CHANGES ( 7 FDA reports)
HEPATIC CYST ( 7 FDA reports)
HEPATIC NECROSIS ( 7 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HYPOTONIA ( 7 FDA reports)
INJECTION SITE NODULE ( 7 FDA reports)
INTESTINAL ISCHAEMIA ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
INTRACRANIAL ANEURYSM ( 7 FDA reports)
JAW DISORDER ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
LIPIDS ABNORMAL ( 7 FDA reports)
LIVEDO RETICULARIS ( 7 FDA reports)
MAJOR DEPRESSION ( 7 FDA reports)
MELANOSIS COLI ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MICROPHTHALMOS ( 7 FDA reports)
MICROVASCULAR ANGINA ( 7 FDA reports)
MICTURITION DISORDER ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
MYELOPATHY ( 7 FDA reports)
MYOPIA ( 7 FDA reports)
NAIL DYSTROPHY ( 7 FDA reports)
NEPHRECTOMY ( 7 FDA reports)
NEPHROGENIC ANAEMIA ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 7 FDA reports)
OESOPHAGEAL SPASM ( 7 FDA reports)
OPTIC NEURITIS ( 7 FDA reports)
ORAL HERPES ( 7 FDA reports)
OROPHARYNGEAL BLISTERING ( 7 FDA reports)
PEAU D'ORANGE ( 7 FDA reports)
PENILE SWELLING ( 7 FDA reports)
PERSONALITY DISORDER ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
POLYPECTOMY ( 7 FDA reports)
POST PROCEDURAL HAEMATOMA ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
PRODUCT PHYSICAL ISSUE ( 7 FDA reports)
PROSTATECTOMY ( 7 FDA reports)
PYURIA ( 7 FDA reports)
RENAL CANCER ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 7 FDA reports)
SCOLIOSIS ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SHOCK HAEMORRHAGIC ( 7 FDA reports)
SIALOADENITIS ( 7 FDA reports)
SKIN FIBROSIS ( 7 FDA reports)
SKIN HYPERPIGMENTATION ( 7 FDA reports)
SKIN PLAQUE ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
SPINAL CORD COMPRESSION ( 7 FDA reports)
SPINAL FUSION SURGERY ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUICIDAL BEHAVIOUR ( 7 FDA reports)
SYSTOLIC DYSFUNCTION ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
TONGUE DISCOLOURATION ( 7 FDA reports)
TOXIC ENCEPHALOPATHY ( 7 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
ULCER HAEMORRHAGE ( 7 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 7 FDA reports)
URINE ABNORMALITY ( 7 FDA reports)
URINE OUTPUT INCREASED ( 7 FDA reports)
VENTRICULAR ARRHYTHMIA ( 7 FDA reports)
VITAMIN B12 DEFICIENCY ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ACCIDENT ( 6 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 6 FDA reports)
ANEURYSM ( 6 FDA reports)
ANOXIA ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 6 FDA reports)
BACTERIURIA ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLADDER INJURY ( 6 FDA reports)
BLOOD CORTISOL DECREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD LACTIC ACID INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BLOODY DISCHARGE ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 6 FDA reports)
CHOLESTATIC LIVER INJURY ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
CLEFT LIP ( 6 FDA reports)
COSTOCHONDRITIS ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
DYSHIDROSIS ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
EAR MALFORMATION ( 6 FDA reports)
EATING DISORDER SYMPTOM ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
EYE DISCHARGE ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GASTROENTERITIS SHIGELLA ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GINGIVAL DISORDER ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
GLOMERULONEPHRITIS ( 6 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HAIR GROWTH ABNORMAL ( 6 FDA reports)
HAND FRACTURE ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HYPERPHOSPHATAEMIA ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
HYPOVENTILATION ( 6 FDA reports)
ILEOSTOMY ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
INFECTIOUS PERITONITIS ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
INJECTION SITE IRRITATION ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
KYPHOSIS ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 6 FDA reports)
MELANOCYTIC NAEVUS ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
MUTISM ( 6 FDA reports)
NASAL POLYPS ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NEUTROPHILIA ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OCULAR HYPERTENSION ( 6 FDA reports)
OESOPHAGEAL STENOSIS ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
OPPORTUNISTIC INFECTION ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 6 FDA reports)
ORTHOSIS USER ( 6 FDA reports)
PATELLA FRACTURE ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PEMPHIGUS ( 6 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
POISONING ( 6 FDA reports)
POSTICTAL STATE ( 6 FDA reports)
POSTURE ABNORMAL ( 6 FDA reports)
PROSTATIC DISORDER ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 6 FDA reports)
PRURITUS GENITAL ( 6 FDA reports)
PSEUDOPOLYPOSIS ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RETINAL ARTERY OCCLUSION ( 6 FDA reports)
RETINAL DEGENERATION ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SERUM FERRITIN INCREASED ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
SOCIAL PROBLEM ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
STRESS URINARY INCONTINENCE ( 6 FDA reports)
SUBCUTANEOUS ABSCESS ( 6 FDA reports)
SUPERINFECTION ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
TENSION ( 6 FDA reports)
TETANY ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRANSFUSION ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VASCULAR GRAFT COMPLICATION ( 6 FDA reports)
VASCULAR PURPURA ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
WEIGHT LOSS POOR ( 6 FDA reports)
WOUND ABSCESS ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 5 FDA reports)
ABDOMINAL INJURY ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ABORTION ( 5 FDA reports)
ACANTHOSIS NIGRICANS ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ADNEXA UTERI CYST ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ALVEOLITIS FIBROSING ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANAL HAEMORRHAGE ( 5 FDA reports)
ANGIODYSPLASIA ( 5 FDA reports)
ANORECTAL DISCOMFORT ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
APALLIC SYNDROME ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
APPETITE DISORDER ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BILE DUCT OBSTRUCTION ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD DISORDER ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BONE FORMATION INCREASED ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
BREAST CANCER STAGE I ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CARCINOID TUMOUR PULMONARY ( 5 FDA reports)
CARDIAC FIBRILLATION ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CARDIORENAL SYNDROME ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
COLLAPSE OF LUNG ( 5 FDA reports)
COLON ADENOMA ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 5 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 5 FDA reports)
CONTRAST MEDIA REACTION ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DELIRIUM TREMENS ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DIABETIC COMPLICATION ( 5 FDA reports)
DIABETIC EYE DISEASE ( 5 FDA reports)
DIPLEGIA ( 5 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 5 FDA reports)
DUODENAL PERFORATION ( 5 FDA reports)
DUODENAL ULCER PERFORATION ( 5 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 5 FDA reports)
EPIDURITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
FRACTURED COCCYX ( 5 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
GRAFT INFECTION ( 5 FDA reports)
HAEMATOCRIT INCREASED ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HEMIANOPIA ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HEPATIC FIBROSIS ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOCOMPLEMENTAEMIA ( 5 FDA reports)
HYPOSIDERAEMIA ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFUSION SITE EXTRAVASATION ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
ITCHING SCAR ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KELOID SCAR ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
KNEE OPERATION ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
LYMPHOCYTIC INFILTRATION ( 5 FDA reports)
MASTITIS ( 5 FDA reports)
MEIBOMIANITIS ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
METHAEMOGLOBINAEMIA ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NECK INJURY ( 5 FDA reports)
NIPPLE PAIN ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
OESOPHAGEAL CARCINOMA ( 5 FDA reports)
OESOPHAGEAL MASS ( 5 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 5 FDA reports)
PAINFUL RESPIRATION ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PCO2 DECREASED ( 5 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 5 FDA reports)
PERIANAL ABSCESS ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PERONEAL NERVE PALSY ( 5 FDA reports)
PERSECUTORY DELUSION ( 5 FDA reports)
PO2 DECREASED ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POOR PERIPHERAL CIRCULATION ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
PROTEUS INFECTION ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
RETINAL ARTERY EMBOLISM ( 5 FDA reports)
RETINAL DETACHMENT ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SEPTIC EMBOLUS ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
SYNOVITIS ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
THROMBOCYTOSIS ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
TONGUE COATED ( 5 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
TRACHEITIS ( 5 FDA reports)
ULNA FRACTURE ( 5 FDA reports)
UNDERWEIGHT ( 5 FDA reports)
UPPER EXTREMITY MASS ( 5 FDA reports)
URETHRAL STENOSIS ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
UTERINE ENLARGEMENT ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VARICOSE ULCERATION ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VASCULITIC RASH ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
VOLUME BLOOD DECREASED ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
WHITE BLOOD CELL DISORDER ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ACCELERATED HYPERTENSION ( 4 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAL PRURITUS ( 4 FDA reports)
ANAPHYLACTOID SHOCK ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANXIETY DISORDER ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BACTERIAL PYELONEPHRITIS ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLADDER PROLAPSE ( 4 FDA reports)
BLEEDING VARICOSE VEIN ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 4 FDA reports)
BLOOD LACTIC ACID DECREASED ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BONE EROSION ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRONCHOPNEUMOPATHY ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CALCIUM METABOLISM DISORDER ( 4 FDA reports)
CALCULUS BLADDER ( 4 FDA reports)
CARDIAC DEATH ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CERUMEN IMPACTION ( 4 FDA reports)
CHEILOSIS ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CITROBACTER INFECTION ( 4 FDA reports)
CLAUSTROPHOBIA ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLONIC STENOSIS ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DEREALISATION ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC NEPHROPATHY ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DIZZINESS EXERTIONAL ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
DYSPHORIA ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOOD INTERACTION ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
FRACTURE NONUNION ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GASTRODUODENITIS ( 4 FDA reports)
GASTROENTERITIS NOROVIRUS ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INFUSION SITE PAIN ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LACRIMATION DECREASED ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LIMB MALFORMATION ( 4 FDA reports)
LITHOTRIPSY ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
LYMPHORRHOEA ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENSTRUAL DISORDER ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METAMORPHOPSIA ( 4 FDA reports)
METASTASES TO ADRENALS ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NEOVASCULARISATION ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PAPILLOEDEMA ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 4 FDA reports)
PHYSIOTHERAPY ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POLYCYTHAEMIA VERA ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PRE-EXISTING DISEASE ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PRODUCT TASTE ABNORMAL ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PSEUDOPOLYP ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RASH PAPULOSQUAMOUS ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
REGURGITATION ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RHEUMATOID LUNG ( 4 FDA reports)
RHEUMATOID NODULE ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SELF-INJURIOUS IDEATION ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SLEEP TALKING ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPINAL CORPECTOMY ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
STUPOR ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
THORACIC OPERATION ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONSIL CANCER ( 4 FDA reports)
TRAUMATIC HAEMATOMA ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
URINE SODIUM INCREASED ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VIITH NERVE INJURY ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
VULVOVAGINAL DRYNESS ( 4 FDA reports)
VULVOVAGINAL PRURITUS ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
ZINC DEFICIENCY ( 4 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ACCOMMODATION DISORDER ( 3 FDA reports)
ACROCHORDON ( 3 FDA reports)
ACTIVATION SYNDROME ( 3 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
AIR EMBOLISM ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANOMALY OF MIDDLE EAR CONGENITAL ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BIOPSY HEART ( 3 FDA reports)
BLADDER DILATATION ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST DISCOMFORT ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRONCHITIS PNEUMOCOCCAL ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BURN OESOPHAGEAL ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CALCIUM IONISED INCREASED ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 3 FDA reports)
CASTLEMAN'S DISEASE ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHORIORETINAL ATROPHY ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON CANCER STAGE IV ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL STRIAE ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
CYST RUPTURE ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DEFORMITY THORAX ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DEVICE INTERACTION ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ECZEMA WEEPING ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
ERECTION INCREASED ( 3 FDA reports)
ERYTHRODERMIC PSORIASIS ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYELID EXFOLIATION ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FIXED ERUPTION ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE VESICLES ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
JOINT INJECTION ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIPID METABOLISM DISORDER ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENISCUS OPERATION ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MITOCHONDRIAL MYOPATHY ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MUSCLE HYPERTROPHY ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OPTIC NERVE DISORDER ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
PANCREAS DIVISUM ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANCREATOLITHIASIS ( 3 FDA reports)
PANEL-REACTIVE ANTIBODY ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PAROTID GLAND INFLAMMATION ( 3 FDA reports)
PELVIC NEOPLASM ( 3 FDA reports)
PERICARDIAL EXCISION ( 3 FDA reports)
PERIODONTAL DISEASE ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHARYNX DISCOMFORT ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POST PROCEDURAL OEDEMA ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PULMONARY SEQUESTRATION ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 3 FDA reports)
RETINAL SCAR ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCAR PAIN ( 3 FDA reports)
SEBORRHOEA ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SERONEGATIVE ARTHRITIS ( 3 FDA reports)
SHIGELLA TEST POSITIVE ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SKIN ULCER HAEMORRHAGE ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOLILOQUY ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TALIPES ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THROMBOLYSIS ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRAUMATIC HAEMORRHAGE ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
URINE POTASSIUM INCREASED ( 3 FDA reports)
VAGUS NERVE DISORDER ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENOUS OCCLUSION ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VIROLOGIC FAILURE ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APOLIPOPROTEIN DECREASED ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE CELLULITIS ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTERITIS OBLITERANS ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BED REST ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BILIARY CYST ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BIOPSY STOMACH ABNORMAL ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD HIV RNA INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CANCER STAGE IV ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC MONITORING ABNORMAL ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARNITINE PALMITOYLTRANSFERASE DEFICIENCY ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHOLESTEATOMA ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 2 FDA reports)
COAGULATION TIME SHORTENED ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
CONJUNCTIVAL CYST ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONJUNCTIVAL PALLOR ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
CSF GLUCOSE INCREASED ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DAWN PHENOMENON ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG NAME CONFUSION ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMERGENCY CARE ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENTEROBACTER SEPSIS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXCHANGE BLOOD TRANSFUSION ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTERNAL EAR DISORDER ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE DEGENERATIVE DISORDER ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FATTY LIVER ALCOHOLIC ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID INTAKE RESTRICTION ( 2 FDA reports)
FOETAL ARRHYTHMIA ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOETAL MOVEMENTS DECREASED ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS RADIATION ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 2 FDA reports)
GLOMUS TYMPANICUM TUMOUR ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOTYMPANUM ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPNAGOGIC HALLUCINATION ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
ICHTHYOSIS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE HYPOAESTHESIA ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTIVE SPONDYLITIS ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL DYSPNOEA ( 2 FDA reports)
LARYNGEAL POLYP ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGAMENT CALCIFICATION ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS CHEMICAL ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYOCARDIAL CALCIFICATION ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL NEOPLASM BENIGN ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERIPROSTHETIC OSTEOLYSIS ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PHARYNGEAL HAEMATOMA ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POLYMERASE CHAIN REACTION ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PREPYLORIC STENOSIS ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROMINENT EPICANTHAL FOLDS ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 2 FDA reports)
RECTAL LESION ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL BURR CELLS PRESENT ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL GRAFT LOSS ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOMATIC DELUSION ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STICKY SKIN ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SUPERINFECTION VIRAL ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROXINE ABNORMAL ( 2 FDA reports)
TIC ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTH DECALCIFICATION ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TREPONEMA TEST POSITIVE ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINOMA ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR STENT INSERTION ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WHITE BLOOD CELL AGGLUTINATION PRESENT ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABDOMINAL WALL NEOPLASM ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACRODYNIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA SCARRING ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYLASE DECREASED ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-INSULIN ANTIBODY ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-B ANTIBODY POSITIVE ( 1 FDA reports)
ANTIACETYLCHOLINE RECEPTOR ANTIBODY POSITIVE ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIRETROVIRAL THERAPY ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHRITIS ALLERGIC ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATROPHIC GLOSSITIS ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT CANCER STAGE III ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER LESION EXCISION ( 1 FDA reports)
BLADDER NECK SCLEROSIS ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEPHARAL PIGMENTATION ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PRESSURE DIFFERENCE OF EXTREMITIES ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREAST SARCOMA ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCIUM IONISED ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MALARIA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLANGITIS CHRONIC ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY OF INNER EAR ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE NEGATIVE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DERMOID CYST ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXOMPHALOS ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELASH DISCOLOURATION ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLUTEN FREE DIET ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HIV INFECTION CDC CATEGORY A1 ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPOCALCIURIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNISATION ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE FIBROSIS ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KIDNEY ANASTOMOSIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACULAR FIBROSIS ( 1 FDA reports)
MACULE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALE GENITAL TRACT OPERATION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO BILIARY TRACT ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL CYST REMOVAL ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NASOPHARYNGEAL CANCER RECURRENT ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLYSIS SURGICAL ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODULAR VASCULITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-CONSUMMATION ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NOSOPHOBIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE PROSTHESIS INSERTION ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYNEUROPATHY CHRONIC ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROMYELOCYTE COUNT DECREASED ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION INTERACTION ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPEXY ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SALPINGO-OOPHORITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SCROTAL CYST ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBACEOUS GLAND DISORDER ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOMATIC HALLUCINATION ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC INFECTION BACTERIAL ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
STARING ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STROKE IN EVOLUTION ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SURGICAL VASCULAR SHUNT ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TICK-BORNE FEVER ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH AVULSION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
UBIQUINONE DECREASED ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URAEMIC PRURITUS ( 1 FDA reports)
URETERECTOMY ( 1 FDA reports)
URETERIC REPAIR ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
ZINC SULPHATE TURBIDITY INCREASED ( 1 FDA reports)