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

DYSPNOEA ( 684 FDA reports)
DIZZINESS ( 656 FDA reports)
NAUSEA ( 632 FDA reports)
OEDEMA PERIPHERAL ( 583 FDA reports)
PYREXIA ( 571 FDA reports)
RENAL FAILURE ACUTE ( 530 FDA reports)
DRUG INEFFECTIVE ( 518 FDA reports)
ANAEMIA ( 509 FDA reports)
HEADACHE ( 490 FDA reports)
MALAISE ( 485 FDA reports)
FALL ( 482 FDA reports)
DIARRHOEA ( 479 FDA reports)
FATIGUE ( 479 FDA reports)
DRUG INTERACTION ( 463 FDA reports)
ASTHENIA ( 461 FDA reports)
VOMITING ( 450 FDA reports)
HYPERTENSION ( 445 FDA reports)
HYPOTENSION ( 425 FDA reports)
PNEUMONIA ( 423 FDA reports)
ARTHRALGIA ( 391 FDA reports)
RENAL FAILURE ( 382 FDA reports)
BLOOD PRESSURE INCREASED ( 377 FDA reports)
PAIN ( 365 FDA reports)
CHEST PAIN ( 349 FDA reports)
RASH ( 328 FDA reports)
PAIN IN EXTREMITY ( 323 FDA reports)
PRURITUS ( 322 FDA reports)
CONDITION AGGRAVATED ( 312 FDA reports)
LOSS OF CONSCIOUSNESS ( 310 FDA reports)
ABDOMINAL PAIN ( 307 FDA reports)
HAEMOGLOBIN DECREASED ( 299 FDA reports)
BLOOD CREATININE INCREASED ( 295 FDA reports)
DEHYDRATION ( 287 FDA reports)
WEIGHT DECREASED ( 285 FDA reports)
RHABDOMYOLYSIS ( 279 FDA reports)
MYALGIA ( 274 FDA reports)
PLATELET COUNT DECREASED ( 270 FDA reports)
COUGH ( 260 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 252 FDA reports)
INSOMNIA ( 244 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 243 FDA reports)
FEELING ABNORMAL ( 238 FDA reports)
PLEURAL EFFUSION ( 237 FDA reports)
BACK PAIN ( 234 FDA reports)
DECREASED APPETITE ( 232 FDA reports)
DEATH ( 230 FDA reports)
INTERSTITIAL LUNG DISEASE ( 230 FDA reports)
CEREBROVASCULAR ACCIDENT ( 227 FDA reports)
SEPSIS ( 226 FDA reports)
CONFUSIONAL STATE ( 225 FDA reports)
MYOCARDIAL INFARCTION ( 220 FDA reports)
ATRIAL FIBRILLATION ( 214 FDA reports)
GAIT DISTURBANCE ( 214 FDA reports)
HYPOAESTHESIA ( 211 FDA reports)
PALPITATIONS ( 209 FDA reports)
RENAL IMPAIRMENT ( 206 FDA reports)
SYNCOPE ( 206 FDA reports)
BLOOD GLUCOSE INCREASED ( 205 FDA reports)
ANXIETY ( 204 FDA reports)
CONSTIPATION ( 202 FDA reports)
SOMNOLENCE ( 202 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 196 FDA reports)
HYPONATRAEMIA ( 195 FDA reports)
MUSCULAR WEAKNESS ( 192 FDA reports)
CARDIAC FAILURE ( 190 FDA reports)
THROMBOCYTOPENIA ( 187 FDA reports)
OVERDOSE ( 186 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 183 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 181 FDA reports)
URINARY TRACT INFECTION ( 181 FDA reports)
DEPRESSION ( 177 FDA reports)
MUSCLE SPASMS ( 176 FDA reports)
RESPIRATORY FAILURE ( 176 FDA reports)
BRADYCARDIA ( 174 FDA reports)
JOINT SWELLING ( 172 FDA reports)
CONVULSION ( 171 FDA reports)
BLOOD PRESSURE DECREASED ( 168 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 168 FDA reports)
HYPERKALAEMIA ( 168 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 161 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 160 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 159 FDA reports)
HYPERHIDROSIS ( 159 FDA reports)
ABDOMINAL DISTENSION ( 157 FDA reports)
ERYTHEMA ( 157 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 156 FDA reports)
HYPOKALAEMIA ( 155 FDA reports)
WEIGHT INCREASED ( 151 FDA reports)
ANOREXIA ( 150 FDA reports)
HYPOGLYCAEMIA ( 147 FDA reports)
LIVER DISORDER ( 147 FDA reports)
BLOOD UREA INCREASED ( 146 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 146 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 146 FDA reports)
COMPLETED SUICIDE ( 145 FDA reports)
CARDIAC ARREST ( 144 FDA reports)
VISION BLURRED ( 139 FDA reports)
HEART RATE INCREASED ( 137 FDA reports)
OEDEMA ( 135 FDA reports)
TREMOR ( 135 FDA reports)
ABDOMINAL PAIN UPPER ( 133 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 131 FDA reports)
DRY MOUTH ( 131 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 129 FDA reports)
PARAESTHESIA ( 129 FDA reports)
PULMONARY OEDEMA ( 127 FDA reports)
DYSPHAGIA ( 122 FDA reports)
CEREBRAL INFARCTION ( 120 FDA reports)
DIABETES MELLITUS ( 120 FDA reports)
DRUG HYPERSENSITIVITY ( 119 FDA reports)
PULMONARY EMBOLISM ( 119 FDA reports)
PANCYTOPENIA ( 118 FDA reports)
BRONCHITIS ( 116 FDA reports)
INFECTION ( 115 FDA reports)
RENAL FAILURE CHRONIC ( 115 FDA reports)
URTICARIA ( 112 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 111 FDA reports)
CHEST DISCOMFORT ( 109 FDA reports)
CHILLS ( 109 FDA reports)
BURNING SENSATION ( 108 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 108 FDA reports)
HAEMODIALYSIS ( 107 FDA reports)
ARRHYTHMIA ( 106 FDA reports)
CELLULITIS ( 106 FDA reports)
HYPERSENSITIVITY ( 106 FDA reports)
NASOPHARYNGITIS ( 106 FDA reports)
CARDIAC DISORDER ( 104 FDA reports)
CYSTITIS ( 100 FDA reports)
HERPES ZOSTER ( 100 FDA reports)
CONTUSION ( 98 FDA reports)
NEUTROPENIA ( 98 FDA reports)
TACHYCARDIA ( 98 FDA reports)
CARDIOMEGALY ( 97 FDA reports)
CARDIO-RESPIRATORY ARREST ( 96 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 96 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 94 FDA reports)
RENAL DISORDER ( 93 FDA reports)
CORONARY ARTERY DISEASE ( 92 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 92 FDA reports)
DISORIENTATION ( 91 FDA reports)
GENERALISED OEDEMA ( 91 FDA reports)
METABOLIC ACIDOSIS ( 91 FDA reports)
RECTAL HAEMORRHAGE ( 89 FDA reports)
MEMORY IMPAIRMENT ( 88 FDA reports)
BLOOD POTASSIUM DECREASED ( 87 FDA reports)
FEBRILE NEUTROPENIA ( 86 FDA reports)
GASTRIC DISORDER ( 86 FDA reports)
HYPOXIA ( 86 FDA reports)
INJURY ( 86 FDA reports)
COMA ( 85 FDA reports)
HAEMATOCRIT DECREASED ( 85 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 85 FDA reports)
SHOCK ( 84 FDA reports)
BONE PAIN ( 83 FDA reports)
JAUNDICE ( 83 FDA reports)
NERVOUSNESS ( 83 FDA reports)
ANGINA PECTORIS ( 82 FDA reports)
ARTHRITIS ( 82 FDA reports)
HAEMORRHAGE ( 82 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 82 FDA reports)
HYPERGLYCAEMIA ( 81 FDA reports)
SUICIDE ATTEMPT ( 81 FDA reports)
CEREBRAL HAEMORRHAGE ( 80 FDA reports)
DEEP VEIN THROMBOSIS ( 80 FDA reports)
DRUG ERUPTION ( 80 FDA reports)
ANGIOEDEMA ( 78 FDA reports)
ASTHMA ( 78 FDA reports)
DYSARTHRIA ( 78 FDA reports)
EPISTAXIS ( 78 FDA reports)
GASTRIC ULCER ( 78 FDA reports)
FACE OEDEMA ( 77 FDA reports)
MULTI-ORGAN FAILURE ( 77 FDA reports)
OFF LABEL USE ( 77 FDA reports)
DRUG EFFECT DECREASED ( 76 FDA reports)
HALLUCINATION ( 76 FDA reports)
LETHARGY ( 76 FDA reports)
INFLAMMATION ( 74 FDA reports)
NEUTROPHIL COUNT DECREASED ( 74 FDA reports)
SWELLING ( 74 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 73 FDA reports)
DISEASE PROGRESSION ( 73 FDA reports)
STAPHYLOCOCCAL INFECTION ( 73 FDA reports)
AMNESIA ( 72 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 72 FDA reports)
DYSPEPSIA ( 72 FDA reports)
VERTIGO ( 72 FDA reports)
VISUAL IMPAIRMENT ( 72 FDA reports)
HAEMATURIA ( 71 FDA reports)
INGROWING NAIL ( 71 FDA reports)
ABDOMINAL DISCOMFORT ( 70 FDA reports)
DIALYSIS ( 70 FDA reports)
LUNG DISORDER ( 70 FDA reports)
ABASIA ( 69 FDA reports)
ASCITES ( 69 FDA reports)
DYSPNOEA EXERTIONAL ( 69 FDA reports)
MOVEMENT DISORDER ( 69 FDA reports)
RHEUMATOID ARTHRITIS ( 69 FDA reports)
ALOPECIA ( 68 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 68 FDA reports)
CHOLECYSTECTOMY ( 68 FDA reports)
DYSGEUSIA ( 68 FDA reports)
PERICARDIAL EFFUSION ( 68 FDA reports)
SPEECH DISORDER ( 68 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 67 FDA reports)
BLOOD COUNT ABNORMAL ( 67 FDA reports)
BLOOD POTASSIUM INCREASED ( 67 FDA reports)
CHOLELITHIASIS ( 67 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 67 FDA reports)
SEPTIC SHOCK ( 67 FDA reports)
URINARY INCONTINENCE ( 67 FDA reports)
MITRAL VALVE INCOMPETENCE ( 66 FDA reports)
OXYGEN SATURATION DECREASED ( 66 FDA reports)
STOMATITIS ( 66 FDA reports)
HYPOTHYROIDISM ( 65 FDA reports)
NERVOUS SYSTEM DISORDER ( 65 FDA reports)
SWELLING FACE ( 65 FDA reports)
EMOTIONAL DISTRESS ( 64 FDA reports)
FLUSHING ( 64 FDA reports)
HEPATITIS ( 64 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 64 FDA reports)
MYOPATHY ( 64 FDA reports)
VISUAL ACUITY REDUCED ( 64 FDA reports)
AGRANULOCYTOSIS ( 62 FDA reports)
INJECTION SITE PAIN ( 62 FDA reports)
MELAENA ( 62 FDA reports)
TOE OPERATION ( 61 FDA reports)
MOBILITY DECREASED ( 60 FDA reports)
MYOSITIS ( 60 FDA reports)
PANCREATITIS ACUTE ( 60 FDA reports)
ACUTE CORONARY SYNDROME ( 59 FDA reports)
CATARACT ( 59 FDA reports)
ENCEPHALOPATHY ( 59 FDA reports)
HEAD INJURY ( 59 FDA reports)
ORTHOSTATIC HYPOTENSION ( 59 FDA reports)
PRURITUS GENERALISED ( 59 FDA reports)
TOXIC SKIN ERUPTION ( 59 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 58 FDA reports)
NEUROPATHY PERIPHERAL ( 58 FDA reports)
PROTEINURIA ( 58 FDA reports)
STEVENS-JOHNSON SYNDROME ( 58 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 58 FDA reports)
WHEEZING ( 58 FDA reports)
AGITATION ( 57 FDA reports)
ECZEMA ( 57 FDA reports)
HAEMATOMA ( 57 FDA reports)
LUNG NEOPLASM ( 57 FDA reports)
OROPHARYNGEAL PAIN ( 57 FDA reports)
POLLAKIURIA ( 57 FDA reports)
PULMONARY HYPERTENSION ( 57 FDA reports)
BALANCE DISORDER ( 56 FDA reports)
CARDIAC MURMUR ( 56 FDA reports)
DIFFICULTY IN WALKING ( 56 FDA reports)
FULL BLOOD COUNT DECREASED ( 56 FDA reports)
HEPATIC FAILURE ( 56 FDA reports)
MUSCULOSKELETAL PAIN ( 56 FDA reports)
PANCREATITIS ( 56 FDA reports)
RESPIRATORY ARREST ( 56 FDA reports)
THROMBOSIS ( 56 FDA reports)
DYSPHONIA ( 55 FDA reports)
FEELING HOT ( 55 FDA reports)
PAIN IN JAW ( 55 FDA reports)
CYTOLYTIC HEPATITIS ( 54 FDA reports)
DYSKINESIA ( 54 FDA reports)
DYSURIA ( 54 FDA reports)
HAEMORRHOIDS ( 54 FDA reports)
LEUKOPENIA ( 54 FDA reports)
THROAT IRRITATION ( 54 FDA reports)
TREATMENT NONCOMPLIANCE ( 54 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 53 FDA reports)
GASTRITIS ( 53 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 53 FDA reports)
HEART RATE IRREGULAR ( 53 FDA reports)
HYPERLIPIDAEMIA ( 53 FDA reports)
SINUS BRADYCARDIA ( 53 FDA reports)
SKIN ULCER ( 53 FDA reports)
ANURIA ( 52 FDA reports)
BLOOD BILIRUBIN INCREASED ( 52 FDA reports)
BLOOD SODIUM DECREASED ( 52 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 52 FDA reports)
PNEUMONIA ASPIRATION ( 52 FDA reports)
PURPURA ( 52 FDA reports)
BLISTER ( 51 FDA reports)
EOSINOPHILIA ( 51 FDA reports)
MYOCARDIAL ISCHAEMIA ( 51 FDA reports)
RASH PRURITIC ( 51 FDA reports)
HEPATIC ENZYME INCREASED ( 50 FDA reports)
HYPOCALCAEMIA ( 50 FDA reports)
LEUKOCYTOSIS ( 50 FDA reports)
OSTEONECROSIS OF JAW ( 50 FDA reports)
SINUSITIS ( 50 FDA reports)
HYPERURICAEMIA ( 49 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 49 FDA reports)
OSTEOPOROSIS ( 49 FDA reports)
RASH GENERALISED ( 49 FDA reports)
RESTLESSNESS ( 49 FDA reports)
FEELING COLD ( 48 FDA reports)
FLUID RETENTION ( 48 FDA reports)
INTENTIONAL OVERDOSE ( 48 FDA reports)
INTESTINAL OBSTRUCTION ( 48 FDA reports)
METASTASES TO LIVER ( 48 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 48 FDA reports)
NEOPLASM MALIGNANT ( 48 FDA reports)
PRODUCT QUALITY ISSUE ( 48 FDA reports)
SKIN TIGHTNESS ( 48 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 47 FDA reports)
CORONARY ARTERY OCCLUSION ( 47 FDA reports)
HAEMATEMESIS ( 47 FDA reports)
HAEMOPTYSIS ( 47 FDA reports)
HEPATIC STEATOSIS ( 47 FDA reports)
NECK PAIN ( 47 FDA reports)
NIGHT SWEATS ( 47 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 47 FDA reports)
RESPIRATORY DISTRESS ( 47 FDA reports)
COGNITIVE DISORDER ( 46 FDA reports)
DELIRIUM ( 46 FDA reports)
HAEMATOCHEZIA ( 46 FDA reports)
HYPOALBUMINAEMIA ( 46 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 45 FDA reports)
ATELECTASIS ( 45 FDA reports)
LACTIC ACIDOSIS ( 45 FDA reports)
PERITONITIS ( 45 FDA reports)
DEMENTIA ( 44 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 44 FDA reports)
DRY SKIN ( 44 FDA reports)
FEMUR FRACTURE ( 44 FDA reports)
GASTRIC CANCER ( 44 FDA reports)
RASH ERYTHEMATOUS ( 44 FDA reports)
RASH MACULO-PAPULAR ( 44 FDA reports)
ROAD TRAFFIC ACCIDENT ( 44 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 44 FDA reports)
VASCULITIS ( 44 FDA reports)
DRUG TOXICITY ( 43 FDA reports)
GALLBLADDER DISORDER ( 43 FDA reports)
HYPERCHOLESTEROLAEMIA ( 43 FDA reports)
INCORRECT DOSE ADMINISTERED ( 43 FDA reports)
INJECTION SITE ERYTHEMA ( 43 FDA reports)
KIDNEY INFECTION ( 43 FDA reports)
ANHEDONIA ( 42 FDA reports)
BLOOD GLUCOSE DECREASED ( 42 FDA reports)
BONE MARROW FAILURE ( 42 FDA reports)
CARDIOGENIC SHOCK ( 42 FDA reports)
DRUG LEVEL INCREASED ( 42 FDA reports)
INFLUENZA ( 42 FDA reports)
PALLOR ( 42 FDA reports)
PETECHIAE ( 42 FDA reports)
SKIN LESION ( 42 FDA reports)
BLOOD ALBUMIN DECREASED ( 41 FDA reports)
BREAST CANCER ( 41 FDA reports)
GASTROENTERITIS ( 41 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 41 FDA reports)
IMPAIRED HEALING ( 41 FDA reports)
NEPHROLITHIASIS ( 41 FDA reports)
OSTEOMYELITIS ( 41 FDA reports)
OSTEONECROSIS ( 41 FDA reports)
PROTHROMBIN TIME PROLONGED ( 41 FDA reports)
CYANOSIS ( 40 FDA reports)
HEART RATE DECREASED ( 40 FDA reports)
ILEUS PARALYTIC ( 40 FDA reports)
INJECTION SITE HAEMORRHAGE ( 40 FDA reports)
MEDICATION ERROR ( 40 FDA reports)
SWOLLEN TONGUE ( 40 FDA reports)
BLOOD URINE PRESENT ( 39 FDA reports)
EMPHYSEMA ( 39 FDA reports)
HALLUCINATION, VISUAL ( 39 FDA reports)
ILEUS ( 39 FDA reports)
OSTEOARTHRITIS ( 39 FDA reports)
PRODUCTIVE COUGH ( 39 FDA reports)
SUBDURAL HAEMATOMA ( 39 FDA reports)
URINE OUTPUT DECREASED ( 39 FDA reports)
BONE DISORDER ( 38 FDA reports)
LYMPHADENOPATHY ( 38 FDA reports)
MENTAL STATUS CHANGES ( 38 FDA reports)
MOUTH ULCERATION ( 38 FDA reports)
MULTIPLE MYELOMA ( 38 FDA reports)
PSORIASIS ( 38 FDA reports)
PULMONARY CONGESTION ( 38 FDA reports)
PULMONARY FIBROSIS ( 38 FDA reports)
RENAL TUBULAR NECROSIS ( 38 FDA reports)
RESPIRATORY RATE INCREASED ( 38 FDA reports)
SKIN EXFOLIATION ( 38 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 37 FDA reports)
ARTERIOSCLEROSIS ( 37 FDA reports)
COAGULOPATHY ( 37 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 37 FDA reports)
MENTAL DISORDER ( 37 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 37 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 37 FDA reports)
SUICIDAL IDEATION ( 37 FDA reports)
UNEVALUABLE EVENT ( 37 FDA reports)
UPPER LIMB FRACTURE ( 36 FDA reports)
CHOLESTASIS ( 36 FDA reports)
COLD SWEAT ( 36 FDA reports)
FLATULENCE ( 36 FDA reports)
INTENTIONAL DRUG MISUSE ( 36 FDA reports)
LIP SWELLING ( 36 FDA reports)
MALNUTRITION ( 36 FDA reports)
PYELONEPHRITIS ( 36 FDA reports)
SCAR ( 36 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 36 FDA reports)
BODY TEMPERATURE INCREASED ( 35 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 35 FDA reports)
DRY EYE ( 35 FDA reports)
EYE PAIN ( 35 FDA reports)
HAEMOLYTIC ANAEMIA ( 35 FDA reports)
NO THERAPEUTIC RESPONSE ( 35 FDA reports)
PANIC ATTACK ( 35 FDA reports)
RHINORRHOEA ( 35 FDA reports)
STRESS ( 35 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 35 FDA reports)
VENTRICULAR TACHYCARDIA ( 35 FDA reports)
UNRESPONSIVE TO STIMULI ( 34 FDA reports)
BRONCHOPNEUMONIA ( 34 FDA reports)
CEREBROVASCULAR DISORDER ( 34 FDA reports)
DRUG ADMINISTRATION ERROR ( 34 FDA reports)
DRUG DOSE OMISSION ( 34 FDA reports)
DYSSTASIA ( 34 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 34 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 34 FDA reports)
POST PROCEDURAL COMPLICATION ( 34 FDA reports)
RESPIRATORY DISORDER ( 34 FDA reports)
SKIN DISCOLOURATION ( 34 FDA reports)
SURGERY ( 34 FDA reports)
TRANSAMINASES INCREASED ( 34 FDA reports)
ABNORMAL BEHAVIOUR ( 33 FDA reports)
ACUTE RESPIRATORY FAILURE ( 33 FDA reports)
GASTROINTESTINAL DISORDER ( 33 FDA reports)
LUNG NEOPLASM MALIGNANT ( 33 FDA reports)
RASH MACULAR ( 33 FDA reports)
RIB FRACTURE ( 33 FDA reports)
SLEEP APNOEA SYNDROME ( 33 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 32 FDA reports)
CARDIOMYOPATHY ( 32 FDA reports)
HOT FLUSH ( 32 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 32 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 32 FDA reports)
NEURALGIA ( 32 FDA reports)
OSTEOPENIA ( 32 FDA reports)
RASH PAPULAR ( 32 FDA reports)
TINNITUS ( 32 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 32 FDA reports)
ATRIOVENTRICULAR BLOCK ( 31 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 31 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 31 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 31 FDA reports)
CARBUNCLE ( 31 FDA reports)
CAROTID ARTERY STENOSIS ( 31 FDA reports)
DIPLOPIA ( 31 FDA reports)
DISCOMFORT ( 31 FDA reports)
HEMIPARESIS ( 31 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 31 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 31 FDA reports)
MUSCLE ATROPHY ( 31 FDA reports)
PNEUMONITIS ( 31 FDA reports)
PRESYNCOPE ( 31 FDA reports)
PROSTATE CANCER ( 31 FDA reports)
ACUTE PULMONARY OEDEMA ( 30 FDA reports)
BONE LESION ( 30 FDA reports)
CHROMATURIA ( 30 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 30 FDA reports)
DERMATITIS ( 30 FDA reports)
EPILEPSY ( 30 FDA reports)
EYE DISORDER ( 30 FDA reports)
HYPERTENSIVE CRISIS ( 30 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 30 FDA reports)
MICTURITION FREQUENCY DECREASED ( 30 FDA reports)
SLEEP DISORDER ( 30 FDA reports)
ANAPHYLACTIC SHOCK ( 29 FDA reports)
APHASIA ( 29 FDA reports)
DERMATITIS EXFOLIATIVE ( 29 FDA reports)
DISTURBANCE IN ATTENTION ( 29 FDA reports)
DIVERTICULUM ( 29 FDA reports)
FUNGAL INFECTION ( 29 FDA reports)
GINGIVAL BLEEDING ( 29 FDA reports)
GUILLAIN-BARRE SYNDROME ( 29 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 29 FDA reports)
OESOPHAGITIS ( 29 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 29 FDA reports)
THIRST ( 29 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 29 FDA reports)
TUBERCULOSIS ( 29 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 28 FDA reports)
VENTRICULAR FIBRILLATION ( 28 FDA reports)
BLOOD CREATINE INCREASED ( 28 FDA reports)
EMOTIONAL DISORDER ( 28 FDA reports)
ERECTILE DYSFUNCTION ( 28 FDA reports)
HIP FRACTURE ( 28 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 28 FDA reports)
METASTASES TO BONE ( 28 FDA reports)
MULTIPLE DRUG OVERDOSE ( 28 FDA reports)
NEOPLASM PROGRESSION ( 28 FDA reports)
NEPHROPATHY ( 28 FDA reports)
OLIGURIA ( 28 FDA reports)
RENAL CYST ( 28 FDA reports)
SPINAL OSTEOARTHRITIS ( 28 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 27 FDA reports)
CIRCULATORY COLLAPSE ( 27 FDA reports)
COORDINATION ABNORMAL ( 27 FDA reports)
CORONARY ARTERY STENOSIS ( 27 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 27 FDA reports)
DEPRESSED MOOD ( 27 FDA reports)
DIVERTICULITIS ( 27 FDA reports)
FLUID OVERLOAD ( 27 FDA reports)
FOOT FRACTURE ( 27 FDA reports)
GLAUCOMA ( 27 FDA reports)
HEPATOMEGALY ( 27 FDA reports)
IRON DEFICIENCY ANAEMIA ( 27 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 27 FDA reports)
PARKINSON'S DISEASE ( 27 FDA reports)
PROTEIN URINE PRESENT ( 27 FDA reports)
PSYCHOTIC DISORDER ( 27 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 27 FDA reports)
URINARY RETENTION ( 27 FDA reports)
AORTIC ANEURYSM ( 26 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 26 FDA reports)
BACTERIAL INFECTION ( 26 FDA reports)
BLOOD CALCIUM INCREASED ( 26 FDA reports)
BLOOD URIC ACID INCREASED ( 26 FDA reports)
COLITIS ( 26 FDA reports)
CONJUNCTIVITIS ( 26 FDA reports)
INFUSION RELATED REACTION ( 26 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 26 FDA reports)
LYMPHOCELE ( 26 FDA reports)
MENTAL IMPAIRMENT ( 26 FDA reports)
OCULAR HYPERAEMIA ( 26 FDA reports)
SHOCK HAEMORRHAGIC ( 26 FDA reports)
SKIN BURNING SENSATION ( 26 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 26 FDA reports)
TACHYPNOEA ( 26 FDA reports)
AGGRESSION ( 25 FDA reports)
BLINDNESS ( 25 FDA reports)
BLOOD CALCIUM DECREASED ( 25 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 25 FDA reports)
DEAFNESS ( 25 FDA reports)
DISEASE RECURRENCE ( 25 FDA reports)
EAR INFECTION ( 25 FDA reports)
HEPATITIS CHOLESTATIC ( 25 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 25 FDA reports)
INFLUENZA LIKE ILLNESS ( 25 FDA reports)
INJECTION SITE HAEMATOMA ( 25 FDA reports)
METASTASES TO LYMPH NODES ( 25 FDA reports)
NASAL CONGESTION ( 25 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 25 FDA reports)
PHOTOSENSITIVITY REACTION ( 25 FDA reports)
PNEUMOTHORAX ( 25 FDA reports)
RALES ( 25 FDA reports)
RENAL ARTERY STENOSIS ( 25 FDA reports)
SENSORY DISTURBANCE ( 25 FDA reports)
SPINAL COLUMN STENOSIS ( 25 FDA reports)
SPINAL COMPRESSION FRACTURE ( 25 FDA reports)
TORSADE DE POINTES ( 25 FDA reports)
ULCER ( 25 FDA reports)
VENTRICULAR HYPERTROPHY ( 25 FDA reports)
CHOKING ( 24 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 24 FDA reports)
EXPOSED BONE IN JAW ( 24 FDA reports)
JOINT INJURY ( 24 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 24 FDA reports)
MIGRAINE ( 24 FDA reports)
MUSCLE TWITCHING ( 24 FDA reports)
NEPHROTIC SYNDROME ( 24 FDA reports)
ORAL PAIN ( 24 FDA reports)
PRIMARY SEQUESTRUM ( 24 FDA reports)
ARTHROPATHY ( 23 FDA reports)
BLADDER CANCER ( 23 FDA reports)
BLOOD CHLORIDE DECREASED ( 23 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 23 FDA reports)
ECCHYMOSIS ( 23 FDA reports)
HIATUS HERNIA ( 23 FDA reports)
HYPERCALCAEMIA ( 23 FDA reports)
HYPOVOLAEMIA ( 23 FDA reports)
LIVER INJURY ( 23 FDA reports)
LUNG INFILTRATION ( 23 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 23 FDA reports)
NEUROPATHY ( 23 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 23 FDA reports)
SINUS TACHYCARDIA ( 23 FDA reports)
SKIN DISORDER ( 23 FDA reports)
SUDDEN DEATH ( 23 FDA reports)
TOOTH FRACTURE ( 23 FDA reports)
VAGINAL HAEMORRHAGE ( 23 FDA reports)
TYPE 2 DIABETES MELLITUS ( 22 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
APLASTIC ANAEMIA ( 22 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 22 FDA reports)
CANDIDIASIS ( 22 FDA reports)
CARDIOVASCULAR DISORDER ( 22 FDA reports)
DRUG DISPENSING ERROR ( 22 FDA reports)
DRUG INTOLERANCE ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
ESCHERICHIA INFECTION ( 22 FDA reports)
FAECES DISCOLOURED ( 22 FDA reports)
FEAR ( 22 FDA reports)
HEPATIC ENCEPHALOPATHY ( 22 FDA reports)
HYPOPHAGIA ( 22 FDA reports)
LABORATORY TEST ABNORMAL ( 22 FDA reports)
LOOSE TOOTH ( 22 FDA reports)
LYMPHOMA ( 22 FDA reports)
MUCOSAL INFLAMMATION ( 22 FDA reports)
NODULE ( 22 FDA reports)
OBESITY ( 22 FDA reports)
ORAL INTAKE REDUCED ( 22 FDA reports)
PARALYSIS ( 22 FDA reports)
SENSATION OF HEAVINESS ( 22 FDA reports)
SKIN INDURATION ( 22 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 22 FDA reports)
ABNORMAL DREAMS ( 21 FDA reports)
ACCIDENTAL OVERDOSE ( 21 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
ADVERSE EVENT ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 21 FDA reports)
BLINDNESS UNILATERAL ( 21 FDA reports)
BRONCHOSPASM ( 21 FDA reports)
COLITIS ISCHAEMIC ( 21 FDA reports)
COLON CANCER ( 21 FDA reports)
ENTERITIS ( 21 FDA reports)
ESCHERICHIA SEPSIS ( 21 FDA reports)
GRANULOCYTOPENIA ( 21 FDA reports)
INJECTION SITE PRURITUS ( 21 FDA reports)
IRRITABILITY ( 21 FDA reports)
ISCHAEMIC STROKE ( 21 FDA reports)
LARGE INTESTINE PERFORATION ( 21 FDA reports)
LIPASE INCREASED ( 21 FDA reports)
PULSE ABSENT ( 21 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 21 FDA reports)
RESTLESS LEGS SYNDROME ( 21 FDA reports)
SPINAL FRACTURE ( 21 FDA reports)
TENDERNESS ( 21 FDA reports)
TOOTH DISORDER ( 21 FDA reports)
VASCULAR PURPURA ( 21 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 20 FDA reports)
APLASIA PURE RED CELL ( 20 FDA reports)
ARTERIAL DISORDER ( 20 FDA reports)
AZOTAEMIA ( 20 FDA reports)
BODY TEMPERATURE DECREASED ( 20 FDA reports)
CARDIAC FAILURE ACUTE ( 20 FDA reports)
CLOSTRIDIAL INFECTION ( 20 FDA reports)
DELUSION ( 20 FDA reports)
DYSLIPIDAEMIA ( 20 FDA reports)
ELECTROLYTE IMBALANCE ( 20 FDA reports)
ENDOCARDITIS ( 20 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 20 FDA reports)
EYELID OEDEMA ( 20 FDA reports)
GENERALISED ERYTHEMA ( 20 FDA reports)
GINGIVAL DISORDER ( 20 FDA reports)
GINGIVAL HYPERPLASIA ( 20 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 20 FDA reports)
HYPOTONIA ( 20 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 20 FDA reports)
LACERATION ( 20 FDA reports)
LACRIMATION INCREASED ( 20 FDA reports)
LARGE INTESTINE CARCINOMA ( 20 FDA reports)
METABOLIC ENCEPHALOPATHY ( 20 FDA reports)
MUSCLE TIGHTNESS ( 20 FDA reports)
MYELODYSPLASTIC SYNDROME ( 20 FDA reports)
NEPHROGENIC ANAEMIA ( 20 FDA reports)
NOCTURIA ( 20 FDA reports)
PEMPHIGOID ( 20 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 20 FDA reports)
SINUS DISORDER ( 20 FDA reports)
SKIN HYPERTROPHY ( 20 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 20 FDA reports)
TENDON RUPTURE ( 20 FDA reports)
ANGER ( 19 FDA reports)
APNOEA ( 19 FDA reports)
ASPIRATION ( 19 FDA reports)
BILE DUCT STONE ( 19 FDA reports)
CHEST X-RAY ABNORMAL ( 19 FDA reports)
COMPRESSION FRACTURE ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
ECONOMIC PROBLEM ( 19 FDA reports)
EOSINOPHIL COUNT INCREASED ( 19 FDA reports)
ERYTHEMA MULTIFORME ( 19 FDA reports)
EXCORIATION ( 19 FDA reports)
GANGRENE ( 19 FDA reports)
GINGIVITIS ( 19 FDA reports)
GOUT ( 19 FDA reports)
HEPATIC CIRRHOSIS ( 19 FDA reports)
HICCUPS ( 19 FDA reports)
HYPERTHERMIA ( 19 FDA reports)
ILL-DEFINED DISORDER ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
INGUINAL HERNIA ( 19 FDA reports)
MACULAR DEGENERATION ( 19 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 19 FDA reports)
NIGHTMARE ( 19 FDA reports)
ORGANISING PNEUMONIA ( 19 FDA reports)
PERIORBITAL OEDEMA ( 19 FDA reports)
POST HERPETIC NEURALGIA ( 19 FDA reports)
RESPIRATORY TRACT INFECTION ( 19 FDA reports)
RHINITIS ALLERGIC ( 19 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 19 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 19 FDA reports)
TRANSPLANT REJECTION ( 19 FDA reports)
TUMOUR LYSIS SYNDROME ( 19 FDA reports)
VIITH NERVE PARALYSIS ( 19 FDA reports)
VISUAL DISTURBANCE ( 19 FDA reports)
WOUND ( 18 FDA reports)
WOUND SECRETION ( 18 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 18 FDA reports)
BLOOD MAGNESIUM DECREASED ( 18 FDA reports)
BLOOD PRESSURE ABNORMAL ( 18 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 18 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 18 FDA reports)
CEREBRAL ATROPHY ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
CHOLECYSTITIS ( 18 FDA reports)
COELIAC DISEASE ( 18 FDA reports)
DECUBITUS ULCER ( 18 FDA reports)
EXOSTOSIS ( 18 FDA reports)
EYE IRRITATION ( 18 FDA reports)
FAILURE TO THRIVE ( 18 FDA reports)
FOOT DEFORMITY ( 18 FDA reports)
GASTRITIS EROSIVE ( 18 FDA reports)
GLOSSODYNIA ( 18 FDA reports)
HEPATIC LESION ( 18 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 18 FDA reports)
HYDRONEPHROSIS ( 18 FDA reports)
HYPERNATRAEMIA ( 18 FDA reports)
HYPOMAGNESAEMIA ( 18 FDA reports)
INTESTINAL PERFORATION ( 18 FDA reports)
LARYNGEAL OEDEMA ( 18 FDA reports)
MOUTH HAEMORRHAGE ( 18 FDA reports)
MYOCLONUS ( 18 FDA reports)
NECK INJURY ( 18 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 18 FDA reports)
ORTHOPNOEA ( 18 FDA reports)
PANCREATIC CARCINOMA ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
PYELONEPHRITIS ACUTE ( 18 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 18 FDA reports)
ANGIOPATHY ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 17 FDA reports)
CAESAREAN SECTION ( 17 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 17 FDA reports)
DECREASED ACTIVITY ( 17 FDA reports)
DERMAL CYST ( 17 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 17 FDA reports)
ENTEROCOLITIS ( 17 FDA reports)
EXTRASYSTOLES ( 17 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 17 FDA reports)
HEPATIC CYST ( 17 FDA reports)
MASS ( 17 FDA reports)
METABOLIC DISORDER ( 17 FDA reports)
PERIPHERAL ISCHAEMIA ( 17 FDA reports)
POLYMYOSITIS ( 17 FDA reports)
PSEUDOMONAS INFECTION ( 17 FDA reports)
ROTATOR CUFF SYNDROME ( 17 FDA reports)
SPLENOMEGALY ( 17 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 17 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 17 FDA reports)
THERAPY NON-RESPONDER ( 17 FDA reports)
VITREOUS FLOATERS ( 17 FDA reports)
WRIST FRACTURE ( 17 FDA reports)
VITREOUS HAEMORRHAGE ( 16 FDA reports)
WRONG DRUG ADMINISTERED ( 16 FDA reports)
ADVERSE DRUG REACTION ( 16 FDA reports)
AORTIC DISSECTION ( 16 FDA reports)
AORTIC VALVE INCOMPETENCE ( 16 FDA reports)
BEDRIDDEN ( 16 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 16 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 16 FDA reports)
CHOLECYSTITIS CHRONIC ( 16 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 16 FDA reports)
CREPITATIONS ( 16 FDA reports)
CYST ( 16 FDA reports)
CYSTITIS HAEMORRHAGIC ( 16 FDA reports)
DERMATITIS ALLERGIC ( 16 FDA reports)
DEVICE RELATED INFECTION ( 16 FDA reports)
DIASTOLIC DYSFUNCTION ( 16 FDA reports)
DRUG PRESCRIBING ERROR ( 16 FDA reports)
EJECTION FRACTION DECREASED ( 16 FDA reports)
ENTEROCOCCAL INFECTION ( 16 FDA reports)
ERYSIPELAS ( 16 FDA reports)
FAECALOMA ( 16 FDA reports)
HAEMOLYSIS ( 16 FDA reports)
HEPATIC CANCER METASTATIC ( 16 FDA reports)
IMMUNOSUPPRESSION ( 16 FDA reports)
INTESTINAL ISCHAEMIA ( 16 FDA reports)
KYPHOSIS ( 16 FDA reports)
LEG AMPUTATION ( 16 FDA reports)
LOBAR PNEUMONIA ( 16 FDA reports)
MIDDLE INSOMNIA ( 16 FDA reports)
MIOSIS ( 16 FDA reports)
MONOCLONAL GAMMOPATHY ( 16 FDA reports)
MUSCLE DISORDER ( 16 FDA reports)
MUSCLE HAEMORRHAGE ( 16 FDA reports)
PLEURAL FIBROSIS ( 16 FDA reports)
ALVEOLITIS ( 15 FDA reports)
ANGINA UNSTABLE ( 15 FDA reports)
AORTIC STENOSIS ( 15 FDA reports)
BASAL CELL CARCINOMA ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 15 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 15 FDA reports)
BLOOD IRON DECREASED ( 15 FDA reports)
BODY HEIGHT DECREASED ( 15 FDA reports)
BRADYARRHYTHMIA ( 15 FDA reports)
DERMATITIS BULLOUS ( 15 FDA reports)
DERMATOMYOSITIS ( 15 FDA reports)
EATING DISORDER ( 15 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 15 FDA reports)
FEELING JITTERY ( 15 FDA reports)
FRACTURE ( 15 FDA reports)
GLUCOSE URINE PRESENT ( 15 FDA reports)
HEPATOCELLULAR DAMAGE ( 15 FDA reports)
HEPATOCELLULAR INJURY ( 15 FDA reports)
HIP ARTHROPLASTY ( 15 FDA reports)
HYPOAESTHESIA ORAL ( 15 FDA reports)
HYPOKINESIA ( 15 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 15 FDA reports)
KNEE ARTHROPLASTY ( 15 FDA reports)
LUNG INFECTION ( 15 FDA reports)
MUSCLE CRAMP ( 15 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 15 FDA reports)
OPEN WOUND ( 15 FDA reports)
ORAL CANDIDIASIS ( 15 FDA reports)
ORAL DISORDER ( 15 FDA reports)
PLATELET COUNT INCREASED ( 15 FDA reports)
PNEUMONIA BACTERIAL ( 15 FDA reports)
PROTHROMBIN TIME SHORTENED ( 15 FDA reports)
RADIUS FRACTURE ( 15 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 15 FDA reports)
RETINAL DETACHMENT ( 15 FDA reports)
RETINAL HAEMORRHAGE ( 15 FDA reports)
STOMACH DISCOMFORT ( 15 FDA reports)
TROPONIN INCREASED ( 15 FDA reports)
ABDOMINAL TENDERNESS ( 14 FDA reports)
BILE DUCT CANCER ( 14 FDA reports)
BLOOD SODIUM INCREASED ( 14 FDA reports)
BREAST CANCER FEMALE ( 14 FDA reports)
CEREBRAL HAEMATOMA ( 14 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 14 FDA reports)
DIABETIC NEPHROPATHY ( 14 FDA reports)
DIVERTICULUM INTESTINAL ( 14 FDA reports)
EAR PAIN ( 14 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 14 FDA reports)
EYE SWELLING ( 14 FDA reports)
GASTROENTERITIS RADIATION ( 14 FDA reports)
HAEMODYNAMIC INSTABILITY ( 14 FDA reports)
HALLUCINATION, AUDITORY ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HERPES VIRUS INFECTION ( 14 FDA reports)
HYPERSOMNIA ( 14 FDA reports)
INCOHERENT ( 14 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 14 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 14 FDA reports)
LEFT VENTRICULAR FAILURE ( 14 FDA reports)
LIMB INJURY ( 14 FDA reports)
LOCAL SWELLING ( 14 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 14 FDA reports)
MENISCUS LESION ( 14 FDA reports)
MUSCLE STRAIN ( 14 FDA reports)
NEPHROPATHY TOXIC ( 14 FDA reports)
NEUROGENIC BLADDER ( 14 FDA reports)
OSTEOSCLEROSIS ( 14 FDA reports)
PARESIS ( 14 FDA reports)
PELVIC FRACTURE ( 14 FDA reports)
PERIPHERAL COLDNESS ( 14 FDA reports)
PHARYNGEAL OEDEMA ( 14 FDA reports)
PROCEDURAL COMPLICATION ( 14 FDA reports)
PROSTATITIS ( 14 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 14 FDA reports)
THROAT TIGHTNESS ( 14 FDA reports)
TONSILLITIS ( 14 FDA reports)
TOOTH EXTRACTION ( 14 FDA reports)
ABDOMINAL PAIN LOWER ( 13 FDA reports)
ACUTE PRERENAL FAILURE ( 13 FDA reports)
ALDOLASE INCREASED ( 13 FDA reports)
ATRIAL FLUTTER ( 13 FDA reports)
ATROPHY ( 13 FDA reports)
BACTERAEMIA ( 13 FDA reports)
BLOOD AMYLASE INCREASED ( 13 FDA reports)
CARDIAC PACEMAKER INSERTION ( 13 FDA reports)
CHOLANGITIS ( 13 FDA reports)
COLONIC POLYP ( 13 FDA reports)
DENTURE WEARER ( 13 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 13 FDA reports)
EYE HAEMORRHAGE ( 13 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 13 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
HEPATITIS ACUTE ( 13 FDA reports)
HERNIA ( 13 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 13 FDA reports)
HYDROCEPHALUS ( 13 FDA reports)
INJECTION SITE IRRITATION ( 13 FDA reports)
INJECTION SITE SWELLING ( 13 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 13 FDA reports)
JAUNDICE CHOLESTATIC ( 13 FDA reports)
LIMB DISCOMFORT ( 13 FDA reports)
LISTLESS ( 13 FDA reports)
MANIA ( 13 FDA reports)
MULTIPLE SCLEROSIS ( 13 FDA reports)
NECROSIS ( 13 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 13 FDA reports)
PO2 DECREASED ( 13 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 13 FDA reports)
RESPIRATORY DEPRESSION ( 13 FDA reports)
RHINITIS ( 13 FDA reports)
SCIATICA ( 13 FDA reports)
SEXUAL DYSFUNCTION ( 13 FDA reports)
SNEEZING ( 13 FDA reports)
TOOTH LOSS ( 13 FDA reports)
TUBERCULOUS PLEURISY ( 13 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 13 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 13 FDA reports)
WALKING AID USER ( 13 FDA reports)
VISUAL FIELD DEFECT ( 12 FDA reports)
WOUND DEHISCENCE ( 12 FDA reports)
ARTHRITIS BACTERIAL ( 12 FDA reports)
ASPHYXIA ( 12 FDA reports)
BONE MARROW DEPRESSION ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 12 FDA reports)
CRYING ( 12 FDA reports)
DECREASED INTEREST ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
FIBROMYALGIA ( 12 FDA reports)
HAEMORRHAGIC DIATHESIS ( 12 FDA reports)
HAEMORRHAGIC STROKE ( 12 FDA reports)
HEPATOTOXICITY ( 12 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 12 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 12 FDA reports)
INFARCTION ( 12 FDA reports)
INJECTION SITE NODULE ( 12 FDA reports)
IRITIS ( 12 FDA reports)
JOINT CONTRACTURE ( 12 FDA reports)
JOINT STIFFNESS ( 12 FDA reports)
KLEBSIELLA INFECTION ( 12 FDA reports)
LUNG ADENOCARCINOMA ( 12 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 12 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 12 FDA reports)
MELANOCYTIC NAEVUS ( 12 FDA reports)
METASTASES TO LUNG ( 12 FDA reports)
MUSCLE RIGIDITY ( 12 FDA reports)
NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
NODAL RHYTHM ( 12 FDA reports)
OEDEMA MOUTH ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 12 FDA reports)
PHLEBITIS ( 12 FDA reports)
PHOTOPSIA ( 12 FDA reports)
PLEURISY ( 12 FDA reports)
POOR PERIPHERAL CIRCULATION ( 12 FDA reports)
POSTRENAL FAILURE ( 12 FDA reports)
PYURIA ( 12 FDA reports)
RENAL TUBULAR DISORDER ( 12 FDA reports)
RHONCHI ( 12 FDA reports)
SEBORRHOEIC DERMATITIS ( 12 FDA reports)
SELF-MEDICATION ( 12 FDA reports)
SICK SINUS SYNDROME ( 12 FDA reports)
STENT PLACEMENT ( 12 FDA reports)
STILLBIRTH ( 12 FDA reports)
TARDIVE DYSKINESIA ( 12 FDA reports)
THINKING ABNORMAL ( 12 FDA reports)
THYROID NEOPLASM ( 12 FDA reports)
TONGUE DISORDER ( 12 FDA reports)
TONGUE OEDEMA ( 12 FDA reports)
TOOTH ABSCESS ( 12 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
ARTERIOSPASM CORONARY ( 11 FDA reports)
ASTHENOPIA ( 11 FDA reports)
BLOOD BICARBONATE DECREASED ( 11 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 11 FDA reports)
BRAIN OEDEMA ( 11 FDA reports)
BRAIN STEM HAEMORRHAGE ( 11 FDA reports)
BRONCHIECTASIS ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
CATARACT OPERATION ( 11 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 11 FDA reports)
COLITIS ULCERATIVE ( 11 FDA reports)
CROHN'S DISEASE ( 11 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 11 FDA reports)
DROOLING ( 11 FDA reports)
FEMORAL NECK FRACTURE ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
FOREIGN BODY ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 11 FDA reports)
GRAND MAL CONVULSION ( 11 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 11 FDA reports)
HAND FRACTURE ( 11 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 11 FDA reports)
HOSPITALISATION ( 11 FDA reports)
HYPERCAPNIA ( 11 FDA reports)
HYPERPHOSPHATAEMIA ( 11 FDA reports)
HYPERTHYROIDISM ( 11 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 11 FDA reports)
HYPOPERFUSION ( 11 FDA reports)
HYPOTHERMIA ( 11 FDA reports)
INITIAL INSOMNIA ( 11 FDA reports)
IRRITABLE BOWEL SYNDROME ( 11 FDA reports)
LOCALISED INFECTION ( 11 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 11 FDA reports)
MEAN CELL VOLUME INCREASED ( 11 FDA reports)
MYOCARDITIS ( 11 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 11 FDA reports)
NO ADVERSE EVENT ( 11 FDA reports)
NON-CARDIAC CHEST PAIN ( 11 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 11 FDA reports)
OTITIS MEDIA CHRONIC ( 11 FDA reports)
PAROSMIA ( 11 FDA reports)
PIGMENTATION DISORDER ( 11 FDA reports)
PRESBYOPIA ( 11 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 11 FDA reports)
PSEUDOLYMPHOMA ( 11 FDA reports)
PSYCHIATRIC SYMPTOM ( 11 FDA reports)
RENAL INJURY ( 11 FDA reports)
RIGHT VENTRICULAR FAILURE ( 11 FDA reports)
SINUS ARREST ( 11 FDA reports)
SKIN HAEMORRHAGE ( 11 FDA reports)
SUBILEUS ( 11 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 11 FDA reports)
URETERIC STENOSIS ( 11 FDA reports)
WOUND INFECTION ( 11 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 10 FDA reports)
VENOUS OCCLUSION ( 10 FDA reports)
VENTRICULAR DYSFUNCTION ( 10 FDA reports)
VITAMIN B12 DEFICIENCY ( 10 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 10 FDA reports)
ALCOHOL USE ( 10 FDA reports)
ANAEMIA MACROCYTIC ( 10 FDA reports)
ANKLE FRACTURE ( 10 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 10 FDA reports)
BACTERIAL SEPSIS ( 10 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 10 FDA reports)
BLOOD LACTIC ACID INCREASED ( 10 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 10 FDA reports)
COLLAPSE OF LUNG ( 10 FDA reports)
COMA SCALE ABNORMAL ( 10 FDA reports)
CORONARY ARTERY BYPASS ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DEPRESSIVE SYMPTOM ( 10 FDA reports)
DIABETIC RETINOPATHY ( 10 FDA reports)
DIZZINESS POSTURAL ( 10 FDA reports)
EMBOLISM ( 10 FDA reports)
GINGIVAL HYPERTROPHY ( 10 FDA reports)
GINGIVAL PAIN ( 10 FDA reports)
GINGIVAL SWELLING ( 10 FDA reports)
HEAD DISCOMFORT ( 10 FDA reports)
HEPATIC FIBROSIS ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HUMERUS FRACTURE ( 10 FDA reports)
HYPERVENTILATION ( 10 FDA reports)
IMMUNE SYSTEM DISORDER ( 10 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 10 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 10 FDA reports)
KELOID SCAR ( 10 FDA reports)
LACUNAR INFARCTION ( 10 FDA reports)
LIP DRY ( 10 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 10 FDA reports)
MICROCYTIC ANAEMIA ( 10 FDA reports)
MONOPLEGIA ( 10 FDA reports)
MYOPIA ( 10 FDA reports)
NEPHRITIS INTERSTITIAL ( 10 FDA reports)
NERVE INJURY ( 10 FDA reports)
NODULE ON EXTREMITY ( 10 FDA reports)
NOSOCOMIAL INFECTION ( 10 FDA reports)
ORAL DISCOMFORT ( 10 FDA reports)
OSTEITIS ( 10 FDA reports)
PERITONEAL ADHESIONS ( 10 FDA reports)
PHYSICAL DISABILITY ( 10 FDA reports)
POLYURIA ( 10 FDA reports)
POOR QUALITY SLEEP ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
PURULENT DISCHARGE ( 10 FDA reports)
RETCHING ( 10 FDA reports)
RETINAL VEIN OCCLUSION ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
SKIN REACTION ( 10 FDA reports)
SNORING ( 10 FDA reports)
SPINAL DISORDER ( 10 FDA reports)
SPLENIC GRANULOMA ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SYNCOPE VASOVAGAL ( 10 FDA reports)
THYROID CANCER ( 10 FDA reports)
ABDOMINAL INFECTION ( 9 FDA reports)
ABSCESS ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
AFFECTIVE DISORDER ( 9 FDA reports)
ANAPHYLACTOID REACTION ( 9 FDA reports)
AORTIC VALVE DISEASE ( 9 FDA reports)
BLADDER DISORDER ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
CARDIOPULMONARY FAILURE ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
CHRONIC SINUSITIS ( 9 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 9 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 9 FDA reports)
CONTRAST MEDIA REACTION ( 9 FDA reports)
CRYSTALLURIA ( 9 FDA reports)
DEAFNESS NEUROSENSORY ( 9 FDA reports)
DERMATITIS CONTACT ( 9 FDA reports)
DERMATOSIS ( 9 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 9 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 9 FDA reports)
ESSENTIAL HYPERTENSION ( 9 FDA reports)
FAECAL INCONTINENCE ( 9 FDA reports)
FIBROSIS ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GASTROINTESTINAL PERFORATION ( 9 FDA reports)
GYNAECOMASTIA ( 9 FDA reports)
HODGKIN'S DISEASE ( 9 FDA reports)
HYPOAESTHESIA FACIAL ( 9 FDA reports)
HYPOCHLORAEMIA ( 9 FDA reports)
HYPOGLYCAEMIC COMA ( 9 FDA reports)
HYPOPROTEINAEMIA ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INJECTION SITE REACTION ( 9 FDA reports)
INTRACRANIAL ANEURYSM ( 9 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
JOINT EFFUSION ( 9 FDA reports)
KERATITIS ( 9 FDA reports)
LIP BLISTER ( 9 FDA reports)
LYMPHOPENIA ( 9 FDA reports)
MENINGITIS NONINFECTIVE ( 9 FDA reports)
MERALGIA PARAESTHETICA ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
NEPHRITIS ( 9 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
OCULAR ICTERUS ( 9 FDA reports)
ODYNOPHAGIA ( 9 FDA reports)
PARTIAL SEIZURES ( 9 FDA reports)
PERICARDITIS ( 9 FDA reports)
PERITONEAL TUBERCULOSIS ( 9 FDA reports)
PETIT MAL EPILEPSY ( 9 FDA reports)
PHARYNGEAL DISORDER ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
PLEURITIC PAIN ( 9 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 9 FDA reports)
PNEUMOPERITONEUM ( 9 FDA reports)
PROCTALGIA ( 9 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 9 FDA reports)
PULMONARY MASS ( 9 FDA reports)
PYOTHORAX ( 9 FDA reports)
REFLUX LARYNGITIS ( 9 FDA reports)
REITER'S SYNDROME ( 9 FDA reports)
RENAL ARTERY OCCLUSION ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RENAL TRANSPLANT ( 9 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 9 FDA reports)
SALIVARY HYPERSECRETION ( 9 FDA reports)
SEROTONIN SYNDROME ( 9 FDA reports)
SINUS PAIN ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
SKIN PLAQUE ( 9 FDA reports)
SPUTUM DISCOLOURED ( 9 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 9 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 9 FDA reports)
TOOTH INFECTION ( 9 FDA reports)
TOOTHACHE ( 9 FDA reports)
TRANSPLANT FAILURE ( 9 FDA reports)
VENTRICULAR ARRHYTHMIA ( 9 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
AGEUSIA ( 8 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 8 FDA reports)
APHAGIA ( 8 FDA reports)
APTYALISM ( 8 FDA reports)
BLADDER NEOPLASM ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
BLOOD PH DECREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
BUNDLE BRANCH BLOCK ( 8 FDA reports)
CANDIDA TEST POSITIVE ( 8 FDA reports)
CARDIOTOXICITY ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 8 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 8 FDA reports)
CULTURE URINE POSITIVE ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DRUG LEVEL DECREASED ( 8 FDA reports)
DRY THROAT ( 8 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
ENCEPHALITIS ( 8 FDA reports)
ENDOTRACHEAL INTUBATION ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 8 FDA reports)
FLANK PAIN ( 8 FDA reports)
GASTRIC PERFORATION ( 8 FDA reports)
GASTRIC POLYPS ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GINGIVAL RECESSION ( 8 FDA reports)
GRAFT DYSFUNCTION ( 8 FDA reports)
HELICOBACTER INFECTION ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
HYPERKERATOSIS ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 8 FDA reports)
INJECTION SITE BURNING ( 8 FDA reports)
INTESTINAL STENOSIS ( 8 FDA reports)
JAW DISORDER ( 8 FDA reports)
JOINT CREPITATION ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LARYNGOCELE ( 8 FDA reports)
LIP PAIN ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
MACROGLOSSIA ( 8 FDA reports)
MENORRHAGIA ( 8 FDA reports)
MOOD ALTERED ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PERFORMANCE STATUS DECREASED ( 8 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 8 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 8 FDA reports)
PERSONALITY CHANGE ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 8 FDA reports)
POLYARTHRITIS ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
POLYP ( 8 FDA reports)
PORTAL VEIN THROMBOSIS ( 8 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 8 FDA reports)
PYELOCALIECTASIS ( 8 FDA reports)
RADIATION PNEUMONITIS ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
RAYNAUD'S PHENOMENON ( 8 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 8 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 8 FDA reports)
SARCOIDOSIS ( 8 FDA reports)
SCAB ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SKIN FIBROSIS ( 8 FDA reports)
SKIN FISSURES ( 8 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 8 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 8 FDA reports)
THROMBOCYTOSIS ( 8 FDA reports)
TOOTH INJURY ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ACIDOSIS ( 7 FDA reports)
ACNE ( 7 FDA reports)
ADENOCARCINOMA ( 7 FDA reports)
ALCOHOLISM ( 7 FDA reports)
ALLERGY TO ANIMAL ( 7 FDA reports)
APHTHOUS STOMATITIS ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 7 FDA reports)
BLOOD PH INCREASED ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
CACHEXIA ( 7 FDA reports)
CALCINOSIS ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CARDIAC FIBRILLATION ( 7 FDA reports)
CATHETER RELATED INFECTION ( 7 FDA reports)
CATHETER SITE HAEMORRHAGE ( 7 FDA reports)
CEREBRAL THROMBOSIS ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DEMYELINATION ( 7 FDA reports)
DRUG DEPENDENCE ( 7 FDA reports)
DYSLALIA ( 7 FDA reports)
DYSPAREUNIA ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
FAECES HARD ( 7 FDA reports)
FAT EMBOLISM ( 7 FDA reports)
FOETAL GROWTH RESTRICTION ( 7 FDA reports)
FOOD ALLERGY ( 7 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 7 FDA reports)
GROIN PAIN ( 7 FDA reports)
HAEMATOSPERMIA ( 7 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HEPATOJUGULAR REFLUX ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
INADEQUATE ANALGESIA ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
INHIBITORY DRUG INTERACTION ( 7 FDA reports)
LABYRINTHITIS ( 7 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MECHANICAL VENTILATION ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MOTOR DYSFUNCTION ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
NONSPECIFIC REACTION ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
OPPORTUNISTIC INFECTION ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PERIODONTAL DISEASE ( 7 FDA reports)
PERIPHERAL EMBOLISM ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PNEUMONIA FUNGAL ( 7 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PROTEIN TOTAL INCREASED ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
QUADRIPARESIS ( 7 FDA reports)
QUADRIPLEGIA ( 7 FDA reports)
RECTAL POLYP ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
REGRESSIVE BEHAVIOUR ( 7 FDA reports)
RESPIRATORY ACIDOSIS ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SENSORY LOSS ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SKIN OEDEMA ( 7 FDA reports)
SLUGGISHNESS ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
SOFT TISSUE INFECTION ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 7 FDA reports)
TENDON PAIN ( 7 FDA reports)
TRANSFUSION ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
UNDERDOSE ( 7 FDA reports)
URINOMA ( 7 FDA reports)
UROSEPSIS ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 7 FDA reports)
VITAMIN D DEFICIENCY ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
URINARY TRACT OBSTRUCTION ( 6 FDA reports)
UTERINE LEIOMYOMA ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VITAMIN B12 INCREASED ( 6 FDA reports)
VITAMIN D DECREASED ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
ALBUMIN URINE PRESENT ( 6 FDA reports)
ALCOHOLIC LIVER DISEASE ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
ATHEROSCLEROSIS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 6 FDA reports)
BACK DISORDER ( 6 FDA reports)
BACK INJURY ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLADDER DILATATION ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 6 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BRAIN ABSCESS ( 6 FDA reports)
BRAIN HERNIATION ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
BRONCHIAL OBSTRUCTION ( 6 FDA reports)
BULIMIA NERVOSA ( 6 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CARDIAC FLUTTER ( 6 FDA reports)
CARDIAC INFECTION ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CEREBRAL ASPERGILLOSIS ( 6 FDA reports)
CHOLANGITIS ACUTE ( 6 FDA reports)
COLLAGEN DISORDER ( 6 FDA reports)
COLON CANCER RECURRENT ( 6 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
DRUG-INDUCED LIVER INJURY ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 6 FDA reports)
ENURESIS ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 6 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 6 FDA reports)
HAEMATOCRIT INCREASED ( 6 FDA reports)
HAPTOGLOBIN DECREASED ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
IDIOPATHIC URTICARIA ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
IMPLANT SITE INFECTION ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INJECTION SITE RASH ( 6 FDA reports)
INJECTION SITE STINGING ( 6 FDA reports)
INJECTION SITE WARMTH ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
LARGE INTESTINAL ULCER ( 6 FDA reports)
LARYNGEAL MASS ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
LOWER LIMB FRACTURE ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MELANOSIS ( 6 FDA reports)
MENIERE'S DISEASE ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
METAMORPHOPSIA ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MITRAL VALVE CALCIFICATION ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MUCOSAL EROSION ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
NAIL DISORDER ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NODAL ARRHYTHMIA ( 6 FDA reports)
OSTEOLYSIS ( 6 FDA reports)
PATHOLOGICAL GAMBLING ( 6 FDA reports)
PEMPHIGUS ( 6 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 6 FDA reports)
PERITONEAL DISORDER ( 6 FDA reports)
PERITONITIS SCLEROSING ( 6 FDA reports)
POLYMYALGIA RHEUMATICA ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
POST PROCEDURAL PAIN ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 6 FDA reports)
PUPIL FIXED ( 6 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RADIATION OESOPHAGITIS ( 6 FDA reports)
RADIOTHERAPY ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 6 FDA reports)
SEQUESTRECTOMY ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
SMALL INTESTINE ULCER ( 6 FDA reports)
SOMNAMBULISM ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUFFOCATION FEELING ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
TETANY ( 6 FDA reports)
THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 6 FDA reports)
ABDOMINAL HERNIA ( 5 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
ANASTOMOTIC STENOSIS ( 5 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 5 FDA reports)
ANOSMIA ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
APHONIA ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
BILE DUCT CANCER STAGE III ( 5 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
BLADDER CATHETERISATION ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 5 FDA reports)
BONE METABOLISM DISORDER ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 5 FDA reports)
CANDIDA SEPSIS ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CELL MARKER INCREASED ( 5 FDA reports)
CEREBELLAR SYNDROME ( 5 FDA reports)
CHOLESTEATOMA ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 5 FDA reports)
CIRCUMORAL OEDEMA ( 5 FDA reports)
COLITIS MICROSCOPIC ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CYSTITIS KLEBSIELLA ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
DARK CIRCLES UNDER EYES ( 5 FDA reports)
DENGUE FEVER ( 5 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DRUG EFFECT INCREASED ( 5 FDA reports)
DUODENAL POLYP ( 5 FDA reports)
DYSPNOEA AT REST ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
EMPYEMA ( 5 FDA reports)
ENDOCARDITIS BACTERIAL ( 5 FDA reports)
ENDOTOXIC SHOCK ( 5 FDA reports)
ENTEROCOLITIS BACTERIAL ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 5 FDA reports)
FOETAL DEATH ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GALLBLADDER PERFORATION ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 5 FDA reports)
GRIP STRENGTH DECREASED ( 5 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HEMIANOPIA HOMONYMOUS ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HYDROCELE ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
HYPOMANIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
JOINT LOCK ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
KLEBSIELLA SEPSIS ( 5 FDA reports)
LEUKOCYTURIA ( 5 FDA reports)
LEUKOPLAKIA ORAL ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
LIP INJURY ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
LYSOZYME INCREASED ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
MITRAL VALVE PROLAPSE ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
NEURITIS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 5 FDA reports)
OPTIC DISC DISORDER ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
PANCREATIC NEOPLASM ( 5 FDA reports)
PANCREATITIS NECROTISING ( 5 FDA reports)
PANCREATITIS RELAPSING ( 5 FDA reports)
PCO2 DECREASED ( 5 FDA reports)
PNEUMOBILIA ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POISONING ( 5 FDA reports)
POLYMYALGIA ( 5 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROTEIN URINE ( 5 FDA reports)
PRURIGO ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RED BLOOD CELL ROULEAUX FORMATION PRESENT ( 5 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
RENAL OSTEODYSTROPHY ( 5 FDA reports)
RENAL VESSEL DISORDER ( 5 FDA reports)
RENIN INCREASED ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 5 FDA reports)
RETINAL ARTERY EMBOLISM ( 5 FDA reports)
RETINOPATHY HYPERTENSIVE ( 5 FDA reports)
RETINOPATHY PROLIFERATIVE ( 5 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 5 FDA reports)
SCHAMBERG'S DISEASE ( 5 FDA reports)
SCROTAL ABSCESS ( 5 FDA reports)
SCROTAL PAIN ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 5 FDA reports)
SKIN CANCER ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
STARING ( 5 FDA reports)
STEM CELL TRANSPLANT ( 5 FDA reports)
STERNAL FRACTURE ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
SYNOVITIS ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
THROMBOPHLEBITIS ( 5 FDA reports)
THROMBOSIS IN DEVICE ( 5 FDA reports)
TINEA INFECTION ( 5 FDA reports)
TRAUMATIC FRACTURE ( 5 FDA reports)
TRICUSPID VALVE DISEASE ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VASCULAR BYPASS GRAFT ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
VASCULAR DEMENTIA ( 5 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VITREOUS DISORDER ( 5 FDA reports)
VULVAL CANCER ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
WOUND DRAINAGE ( 5 FDA reports)
TRIFASCICULAR BLOCK ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE CYST ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 4 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
ZINC DEFICIENCY ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 4 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACNE CYSTIC ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANION GAP INCREASED ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
AORTIC CALCIFICATION ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
APATHY ( 4 FDA reports)
APPARENT LIFE THREATENING EVENT ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ASPERGILLUS TEST POSITIVE ( 4 FDA reports)
ATONIC SEIZURES ( 4 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BACTERIAL PYELONEPHRITIS ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 4 FDA reports)
BICYTOPENIA ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BONE NEOPLASM ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BRONCHIAL INFECTION ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BRONCHOSTENOSIS ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CALCULUS PROSTATIC ( 4 FDA reports)
CAPILLARY FRAGILITY ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CATHETER SITE PHLEBITIS ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CEREBELLAR ATROPHY ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHOREA ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
CONTRACTED BLADDER ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DEVICE INTERACTION ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DIABETIC FOOT INFECTION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DISLOCATION OF VERTEBRA ( 4 FDA reports)
DISTRACTIBILITY ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
DYSPHORIA ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
EMBOLISM ARTERIAL ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FLUID IMBALANCE ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
GALLBLADDER CANCER ( 4 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 4 FDA reports)
GLOSSOPTOSIS ( 4 FDA reports)
GOITRE ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEAT ILLNESS ( 4 FDA reports)
HELLP SYNDROME ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOCAPNIA ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IMMUNOGLOBULINS INCREASED ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INCISIONAL HERNIA ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INTENTIONAL SELF-INJURY ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
JOINT INSTABILITY ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LIBIDO INCREASED ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METAPLASIA ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MOUTH BREATHING ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEUROMUSCULAR BLOCKADE ( 4 FDA reports)
NEUROSURGERY ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PANCREAS TRANSPLANT ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PH URINE DECREASED ( 4 FDA reports)
PNEUMONIA ESCHERICHIA ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRINZMETAL ANGINA ( 4 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 4 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULMONARY AIR LEAKAGE ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 4 FDA reports)
RENAL CYST RUPTURED ( 4 FDA reports)
RENAL EMBOLISM ( 4 FDA reports)
RENAL GRAFT LOSS ( 4 FDA reports)
RENAL HAEMATOMA ( 4 FDA reports)
RENAL LYMPHOCELE ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
SALMONELLA SEPSIS ( 4 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SLEEP-RELATED EATING DISORDER ( 4 FDA reports)
SOFT TISSUE INJURY ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SPLINTER HAEMORRHAGES ( 4 FDA reports)
SPONDYLOLISTHESIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
TABLET PHYSICAL ISSUE ( 4 FDA reports)
TEMPORAL ARTERITIS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
ADRENALECTOMY ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 3 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ASPIRATION BIOPSY ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
BASOPHIL COUNT DECREASED ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BILIARY NEOPLASM ( 3 FDA reports)
BLADDER DISTENSION ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD URIC ACID ABNORMAL ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE FRAGMENTATION ( 3 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BOWEN'S DISEASE ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CAMPYLOBACTER INFECTION ( 3 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST CRUSHING ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 3 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CORNEAL ABSCESS ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CRANIOPHARYNGIOMA ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CUTANEOUS CONTOUR DEFORMITY ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG INTERACTION POTENTIATION ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
ECZEMA ASTEATOTIC ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
EPIGLOTTIC OEDEMA ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXTREMITY CONTRACTURE ( 3 FDA reports)
EYE BURNS ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FEMORAL ARTERY EMBOLISM ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 3 FDA reports)
GASTRIC CANCER STAGE II ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
GRIMACING ( 3 FDA reports)
HAEMANGIOMA ( 3 FDA reports)
HAEMANGIOMA OF SKIN ( 3 FDA reports)
HAEMOBILIA ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HEPATITIS INFECTIOUS ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYDROPNEUMOTHORAX ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPHAEMA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOCOMPLEMENTAEMIA ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INGUINAL HERNIA REPAIR ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
JAPAN COMA SCALE ABNORMAL ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KERATOACANTHOMA ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LEISHMANIASIS ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LIBIDO DISORDER ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LUNG LOBECTOMY ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEDIASTINAL CYST ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYELOID MATURATION ARREST ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
MYOGLOBINAEMIA ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 3 FDA reports)
NEURILEMMOMA ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
ORAL CAVITY FISTULA ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
OSMOLAR GAP ABNORMAL ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PANOPHTHALMITIS ( 3 FDA reports)
PARKINSONIAN REST TREMOR ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PENILE OEDEMA ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERICORONITIS ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHOTODERMATOSIS ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST PROCEDURAL PNEUMONIA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROSTATIC ABSCESS ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PSORIATIC ARTHROPATHY ( 3 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL HYPERTROPHY ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESPIRATORY FATIGUE ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETICULOCYTE COUNT INCREASED ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETROGRADE AMNESIA ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SCIATIC NERVE INJURY ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SENSATION OF BLOOD FLOW ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STASIS DERMATITIS ( 3 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SUPERFICIAL INJURY OF EYE ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
TABLET ISSUE ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TENSION ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 3 FDA reports)
YAWNING ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URATE NEPHROPATHY ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VIRAL TEST NEGATIVE ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
AIDS RETINOPATHY ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-B ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE ECZEMA ( 2 FDA reports)
APPLICATION SITE PUSTULES ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURA ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER CATHETER TEMPORARY ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLEEDING TIME SHORTENED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE SCAN ABNORMAL ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BREAST INJURY ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BUNION ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CAPILLARITIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOROIDAL DETACHMENT ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COLD AGGLUTININS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C1 DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRYOGLOBULINS PRESENT ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CSF GLUCOSE DECREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION IN NEWBORN ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DISSOCIATIVE AMNESIA ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECTHYMA ( 2 FDA reports)
ECZEMA EYELIDS ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GALLSTONE ILEUS ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HELICOBACTER SEPSIS ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HERPES SIMPLEX HEPATITIS ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HTLV-1 ANTIBODY POSITIVE ( 2 FDA reports)
HTLV-1 TEST POSITIVE ( 2 FDA reports)
HTLV-2 TEST POSITIVE ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
ICHTHYOSIS ACQUIRED ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNISATION ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE LACERATION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL POLYP ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP HAEMATOMA ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPASE DECREASED ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
LYMPHOSTASIS ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEDIASTINAL FIBROSIS ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MESENTERIC PANNICULITIS ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METASTASES TO PROSTATE ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MUCORMYCOSIS ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NON-DIPPING ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OPTIC DISC HAEMORRHAGE ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEDAL PULSE ABSENT ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL EFFLUENT LEUKOCYTE COUNT INCREASED ( 2 FDA reports)
PERITONEAL FIBROSIS ( 2 FDA reports)
PH BODY FLUID DECREASED ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATIC HAEMORRHAGE ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTEUS TEST POSITIVE ( 2 FDA reports)
PSYCHOMOTOR AGITATION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY FISTULA ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL NEOPLASM ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RECTAL SPASM ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CYST INFECTION ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENIN DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SARCOMA OF SKIN ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SOLITARY KIDNEY ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STOMATITIS HAEMORRHAGIC ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TORULOPSIS INFECTION ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
ALVEOLAR SOFT PART SARCOMA ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMPUTATION REVISION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANKLE ARTHROPLASTY ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATLANTOAXIAL INSTABILITY ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATROPHIC GLOSSITIS ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 1 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASOPHIL COUNT ABNORMAL ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY THYROID GLAND ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS PNEUMOCOCCAL ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOMA EXCISION ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER SITE RASH ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHLAMYDIA TEST POSITIVE ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONJUNCTIVAL BLEB ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONTACT LENS COMPLICATION ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL DECOMPENSATION ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE NEGATIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUBIN-JOHNSON SYNDROME ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR NEOPLASM ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHO VIRUS INFECTION ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLECTOMY ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCLYSIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS FUNGAL ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF ANIMALS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRIN D DIMER NORMAL ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC CANCER STAGE IV WITH METASTASES ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATOSALPINX ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIGH GRADE B-CELL LYMPHOMA BURKITT-LIKE LYMPHOMA STAGE II ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOFFMANN'S SIGN ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYGROMA COLLI ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFLUENZA B VIRUS TEST POSITIVE ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE EROSION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOPLAKIA OESOPHAGEAL ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE 0 ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
MACROAMYLASAEMIA ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROGENIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENISCUS OPERATION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MOYAMOYA DISEASE ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL HYPERAEMIA ( 1 FDA reports)
MUCOSAL INFECTION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIA URINE TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOTIC ANEURYSM ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NATURAL KILLER CELL COUNT DECREASED ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECK SURGERY ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSSICLE DISORDER ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARASITIC GASTROENTERITIS ( 1 FDA reports)
PARASITIC TEST POSITIVE ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN INCREASED ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERICARDITIS URAEMIC ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERITONEAL NECROSIS ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PINEAL NEOPLASM ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA SALMONELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE DIZZINESS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT FRIABLE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADICULOTOMY ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL MICROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SALPINGITIS TUBERCULOUS ( 1 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELECTIVE MUTISM ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN DYSTROPHY ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN SQUAMOUS CELL CARCINOMA SURGERY ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPERMATIC CORD DISORDER ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCHORIONIC HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBIN TIME SHORTENED ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE CANCER METASTATIC ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSPLANT EVALUATION ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TYMPANOSCLEROSIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER NORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URETERAL NECROSIS ( 1 FDA reports)
URETERIC REPAIR ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
URINE ARSENIC INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VESSEL PUNCTURE SITE BRUISE ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL SWELLING ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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