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

ATRIAL FIBRILLATION ( 524 FDA reports)
DYSPNOEA ( 407 FDA reports)
PAIN ( 395 FDA reports)
ASTHENIA ( 342 FDA reports)
RENAL FAILURE ( 341 FDA reports)
ANXIETY ( 315 FDA reports)
DRUG INTERACTION ( 302 FDA reports)
HYPOTENSION ( 300 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 299 FDA reports)
INJURY ( 288 FDA reports)
DIZZINESS ( 284 FDA reports)
NAUSEA ( 256 FDA reports)
RENAL FAILURE ACUTE ( 255 FDA reports)
OEDEMA PERIPHERAL ( 238 FDA reports)
FATIGUE ( 237 FDA reports)
PNEUMONIA ( 232 FDA reports)
ANAEMIA ( 216 FDA reports)
VENTRICULAR TACHYCARDIA ( 216 FDA reports)
FALL ( 207 FDA reports)
PLEURAL EFFUSION ( 199 FDA reports)
MULTI-ORGAN FAILURE ( 197 FDA reports)
UNEVALUABLE EVENT ( 192 FDA reports)
EMOTIONAL DISTRESS ( 181 FDA reports)
VOMITING ( 174 FDA reports)
DEATH ( 173 FDA reports)
CHEST PAIN ( 172 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 172 FDA reports)
BRADYCARDIA ( 171 FDA reports)
DEPRESSION ( 165 FDA reports)
ANHEDONIA ( 162 FDA reports)
CARDIAC ARREST ( 161 FDA reports)
FEAR ( 159 FDA reports)
RENAL IMPAIRMENT ( 158 FDA reports)
MYOCARDIAL INFARCTION ( 155 FDA reports)
DIARRHOEA ( 146 FDA reports)
SEPSIS ( 143 FDA reports)
DRUG INEFFECTIVE ( 142 FDA reports)
HYPERTENSION ( 141 FDA reports)
PAIN IN EXTREMITY ( 140 FDA reports)
CARDIAC FAILURE ( 137 FDA reports)
CONFUSIONAL STATE ( 137 FDA reports)
RESPIRATORY FAILURE ( 136 FDA reports)
SYNCOPE ( 135 FDA reports)
PYREXIA ( 132 FDA reports)
DEHYDRATION ( 130 FDA reports)
WEIGHT DECREASED ( 129 FDA reports)
ARRHYTHMIA ( 127 FDA reports)
RENAL INJURY ( 124 FDA reports)
ECONOMIC PROBLEM ( 119 FDA reports)
CORONARY ARTERY DISEASE ( 117 FDA reports)
STRESS ( 113 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 112 FDA reports)
PARAESTHESIA ( 112 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 111 FDA reports)
PALPITATIONS ( 111 FDA reports)
URINARY TRACT INFECTION ( 111 FDA reports)
BACK PAIN ( 110 FDA reports)
THROMBOCYTOPENIA ( 109 FDA reports)
FEELING ABNORMAL ( 108 FDA reports)
HYPOKALAEMIA ( 108 FDA reports)
CONDITION AGGRAVATED ( 107 FDA reports)
ARTHRALGIA ( 106 FDA reports)
BLOOD CREATININE INCREASED ( 106 FDA reports)
VENTRICULAR FIBRILLATION ( 104 FDA reports)
MYOSITIS ( 103 FDA reports)
MITRAL VALVE INCOMPETENCE ( 102 FDA reports)
CARDIOMEGALY ( 100 FDA reports)
COUGH ( 99 FDA reports)
PULMONARY EMBOLISM ( 99 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 97 FDA reports)
OEDEMA ( 95 FDA reports)
PERICARDIAL EFFUSION ( 95 FDA reports)
MALAISE ( 94 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 94 FDA reports)
HAEMOGLOBIN DECREASED ( 93 FDA reports)
CEREBROVASCULAR ACCIDENT ( 92 FDA reports)
DECREASED APPETITE ( 92 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 92 FDA reports)
RHABDOMYOLYSIS ( 92 FDA reports)
HEADACHE ( 91 FDA reports)
LOSS OF CONSCIOUSNESS ( 91 FDA reports)
CARDIOMYOPATHY ( 88 FDA reports)
TORSADE DE POINTES ( 88 FDA reports)
HYPERKALAEMIA ( 87 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 87 FDA reports)
ABDOMINAL PAIN ( 86 FDA reports)
PULMONARY OEDEMA ( 85 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 84 FDA reports)
MUSCULAR WEAKNESS ( 84 FDA reports)
RENAL FAILURE CHRONIC ( 84 FDA reports)
DYSPNOEA EXERTIONAL ( 81 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 79 FDA reports)
MULTIPLE INJURIES ( 78 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 77 FDA reports)
ERYTHEMA ( 75 FDA reports)
INSOMNIA ( 75 FDA reports)
MYALGIA ( 75 FDA reports)
HEART RATE INCREASED ( 73 FDA reports)
HYPONATRAEMIA ( 73 FDA reports)
PRURITUS ( 73 FDA reports)
INFECTION ( 69 FDA reports)
RECTAL HAEMORRHAGE ( 69 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 69 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 67 FDA reports)
CARDIAC DISORDER ( 66 FDA reports)
CARDIAC MURMUR ( 66 FDA reports)
CARDIOGENIC SHOCK ( 66 FDA reports)
EPISTAXIS ( 66 FDA reports)
HYPOTHYROIDISM ( 66 FDA reports)
PLATELET COUNT DECREASED ( 66 FDA reports)
BLOOD UREA INCREASED ( 65 FDA reports)
WEIGHT INCREASED ( 65 FDA reports)
MOBILITY DECREASED ( 64 FDA reports)
GAIT DISTURBANCE ( 62 FDA reports)
HYPERHIDROSIS ( 62 FDA reports)
HYPERTHYROIDISM ( 60 FDA reports)
TACHYCARDIA ( 60 FDA reports)
CARDIO-RESPIRATORY ARREST ( 59 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 59 FDA reports)
RASH ( 58 FDA reports)
CONSTIPATION ( 57 FDA reports)
ABDOMINAL DISTENSION ( 56 FDA reports)
BONE DISORDER ( 56 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 56 FDA reports)
CONTUSION ( 56 FDA reports)
CONVULSION ( 56 FDA reports)
SHOCK ( 56 FDA reports)
DIABETES MELLITUS ( 55 FDA reports)
BLOOD PRESSURE INCREASED ( 53 FDA reports)
CELLULITIS ( 53 FDA reports)
HEPATIC FAILURE ( 53 FDA reports)
HYPOXIA ( 53 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 53 FDA reports)
ATELECTASIS ( 52 FDA reports)
BLOOD GLUCOSE INCREASED ( 52 FDA reports)
DYSPEPSIA ( 52 FDA reports)
HEART RATE IRREGULAR ( 52 FDA reports)
UNRESPONSIVE TO STIMULI ( 52 FDA reports)
ATRIAL FLUTTER ( 51 FDA reports)
ABDOMINAL DISCOMFORT ( 50 FDA reports)
CHEST DISCOMFORT ( 50 FDA reports)
MENTAL STATUS CHANGES ( 50 FDA reports)
SEPTIC SHOCK ( 50 FDA reports)
SLEEP APNOEA SYNDROME ( 50 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 49 FDA reports)
TREMOR ( 49 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 49 FDA reports)
FLUSHING ( 48 FDA reports)
HAEMORRHAGE ( 48 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 47 FDA reports)
DEEP VEIN THROMBOSIS ( 47 FDA reports)
DYSPHAGIA ( 47 FDA reports)
EJECTION FRACTION DECREASED ( 47 FDA reports)
HAEMATOCRIT DECREASED ( 47 FDA reports)
BRONCHITIS ( 46 FDA reports)
HYPOKINESIA ( 46 FDA reports)
PULMONARY HYPERTENSION ( 46 FDA reports)
RESPIRATORY DISTRESS ( 46 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 46 FDA reports)
LETHARGY ( 45 FDA reports)
HYPOAESTHESIA ( 44 FDA reports)
LEUKOCYTOSIS ( 44 FDA reports)
SURGERY ( 44 FDA reports)
NEUROPATHY PERIPHERAL ( 43 FDA reports)
SOMNOLENCE ( 43 FDA reports)
VERTIGO ( 43 FDA reports)
DIPLOPIA ( 42 FDA reports)
FLUID OVERLOAD ( 42 FDA reports)
OSTEOARTHRITIS ( 42 FDA reports)
BLOOD PRESSURE DECREASED ( 41 FDA reports)
MYOCARDIAL ISCHAEMIA ( 41 FDA reports)
PULMONARY FIBROSIS ( 41 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 40 FDA reports)
ACUTE RESPIRATORY FAILURE ( 40 FDA reports)
OSTEONECROSIS OF JAW ( 40 FDA reports)
TREATMENT NONCOMPLIANCE ( 40 FDA reports)
ASTHMA ( 39 FDA reports)
HYPOGLYCAEMIA ( 39 FDA reports)
LEFT VENTRICULAR FAILURE ( 39 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 38 FDA reports)
COLITIS ( 38 FDA reports)
DRUG TOXICITY ( 38 FDA reports)
HYPERLIPIDAEMIA ( 38 FDA reports)
INCORRECT DOSE ADMINISTERED ( 38 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 38 FDA reports)
NEUTROPENIA ( 38 FDA reports)
POST PROCEDURAL COMPLICATION ( 38 FDA reports)
SKIN DISCOLOURATION ( 38 FDA reports)
COAGULOPATHY ( 37 FDA reports)
HAEMATEMESIS ( 37 FDA reports)
HYPERGLYCAEMIA ( 37 FDA reports)
SKIN INDURATION ( 37 FDA reports)
THROMBOSIS ( 37 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 37 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 36 FDA reports)
DISSOCIATION ( 36 FDA reports)
HAEMATOMA ( 36 FDA reports)
HAEMODIALYSIS ( 36 FDA reports)
MYOPATHY ( 36 FDA reports)
OVERDOSE ( 36 FDA reports)
SWELLING ( 36 FDA reports)
ASCITES ( 35 FDA reports)
CHOLELITHIASIS ( 35 FDA reports)
INTERSTITIAL LUNG DISEASE ( 35 FDA reports)
MELAENA ( 35 FDA reports)
OSTEOMYELITIS ( 35 FDA reports)
OSTEONECROSIS ( 35 FDA reports)
HEART RATE DECREASED ( 34 FDA reports)
JAUNDICE ( 34 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 34 FDA reports)
MULTIPLE MYELOMA ( 34 FDA reports)
PANCYTOPENIA ( 34 FDA reports)
TOOTH EXTRACTION ( 34 FDA reports)
ABDOMINAL PAIN UPPER ( 33 FDA reports)
ANGINA UNSTABLE ( 33 FDA reports)
DISORIENTATION ( 33 FDA reports)
PERITONITIS ( 33 FDA reports)
SKIN HYPERTROPHY ( 33 FDA reports)
STAPHYLOCOCCAL INFECTION ( 33 FDA reports)
VISION BLURRED ( 33 FDA reports)
BLOOD POTASSIUM DECREASED ( 32 FDA reports)
FLUID RETENTION ( 32 FDA reports)
HEPATIC ENZYME INCREASED ( 32 FDA reports)
ATAXIA ( 31 FDA reports)
BALANCE DISORDER ( 31 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 31 FDA reports)
BLOOD POTASSIUM INCREASED ( 31 FDA reports)
COMA ( 31 FDA reports)
HAEMATURIA ( 31 FDA reports)
RESPIRATORY ARREST ( 31 FDA reports)
BLOOD BILIRUBIN INCREASED ( 30 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 30 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 30 FDA reports)
DEFORMITY ( 30 FDA reports)
GOUT ( 30 FDA reports)
HAEMODYNAMIC INSTABILITY ( 30 FDA reports)
JOINT SWELLING ( 30 FDA reports)
PNEUMONITIS ( 30 FDA reports)
SKIN TIGHTNESS ( 30 FDA reports)
ABASIA ( 29 FDA reports)
CHILLS ( 29 FDA reports)
DIALYSIS ( 29 FDA reports)
GASTRITIS EROSIVE ( 29 FDA reports)
METABOLIC ACIDOSIS ( 29 FDA reports)
VISUAL IMPAIRMENT ( 29 FDA reports)
WHEEZING ( 29 FDA reports)
DECUBITUS ULCER ( 28 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 28 FDA reports)
DRY SKIN ( 28 FDA reports)
HYPOPHAGIA ( 28 FDA reports)
HYPOTONIA ( 28 FDA reports)
NECK PAIN ( 28 FDA reports)
SINUS BRADYCARDIA ( 28 FDA reports)
SKIN ULCER ( 28 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 28 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 27 FDA reports)
CEREBRAL HAEMORRHAGE ( 27 FDA reports)
DRUG HYPERSENSITIVITY ( 27 FDA reports)
HALLUCINATION ( 27 FDA reports)
HYPERSENSITIVITY ( 27 FDA reports)
NERVOUSNESS ( 27 FDA reports)
SKIN HYPERPIGMENTATION ( 27 FDA reports)
VENTRICULAR HYPOKINESIA ( 27 FDA reports)
ANGINA PECTORIS ( 26 FDA reports)
BURNING SENSATION ( 26 FDA reports)
DELIRIUM ( 26 FDA reports)
JOINT STIFFNESS ( 26 FDA reports)
LUNG DISORDER ( 26 FDA reports)
LUNG INFILTRATION ( 26 FDA reports)
MALNUTRITION ( 26 FDA reports)
MEDICATION ERROR ( 26 FDA reports)
MENTAL DISORDER ( 26 FDA reports)
OXYGEN SATURATION DECREASED ( 26 FDA reports)
AGITATION ( 25 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 25 FDA reports)
CORONARY ARTERY OCCLUSION ( 25 FDA reports)
DYSURIA ( 25 FDA reports)
HAEMOPTYSIS ( 25 FDA reports)
MOUTH HAEMORRHAGE ( 25 FDA reports)
MUSCULOSKELETAL PAIN ( 25 FDA reports)
ORTHOPNOEA ( 25 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 25 FDA reports)
RENAL DISORDER ( 25 FDA reports)
DEVELOPMENTAL DELAY ( 24 FDA reports)
IMPAIRED HEALING ( 24 FDA reports)
NASOPHARYNGITIS ( 24 FDA reports)
PROTHROMBIN TIME PROLONGED ( 24 FDA reports)
TALIPES ( 24 FDA reports)
AMNESIA ( 23 FDA reports)
AORTIC VALVE INCOMPETENCE ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 23 FDA reports)
BLOOD SODIUM DECREASED ( 23 FDA reports)
CARDIAC PACEMAKER INSERTION ( 23 FDA reports)
CARDIOVASCULAR DISORDER ( 23 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 23 FDA reports)
DILATATION VENTRICULAR ( 23 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 23 FDA reports)
DYSPHONIA ( 23 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 23 FDA reports)
PAIN IN JAW ( 23 FDA reports)
SKIN EXFOLIATION ( 23 FDA reports)
DEAFNESS ( 22 FDA reports)
DIVERTICULUM ( 22 FDA reports)
GASTRIC ULCER ( 22 FDA reports)
MEMORY IMPAIRMENT ( 22 FDA reports)
MUSCLE SPASMS ( 22 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 22 FDA reports)
NIGHT SWEATS ( 22 FDA reports)
SCAR ( 22 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
BLISTER ( 21 FDA reports)
DISEASE PROGRESSION ( 21 FDA reports)
HEPATIC STEATOSIS ( 21 FDA reports)
IRRITABILITY ( 21 FDA reports)
LEFT ATRIAL DILATATION ( 21 FDA reports)
OLIGURIA ( 21 FDA reports)
ORTHOSTATIC HYPOTENSION ( 21 FDA reports)
PNEUMOTHORAX ( 21 FDA reports)
PULMONARY CONGESTION ( 21 FDA reports)
SINUSITIS ( 21 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 21 FDA reports)
SUBDURAL HAEMATOMA ( 21 FDA reports)
ADVERSE EVENT ( 20 FDA reports)
ANOREXIA ( 20 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 20 FDA reports)
EAR PAIN ( 20 FDA reports)
ENCEPHALOPATHY ( 20 FDA reports)
HEAD INJURY ( 20 FDA reports)
INFLUENZA ( 20 FDA reports)
JOINT CONTRACTURE ( 20 FDA reports)
OBESITY ( 20 FDA reports)
PNEUMATOSIS INTESTINALIS ( 20 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 20 FDA reports)
VISUAL ACUITY REDUCED ( 20 FDA reports)
AORTIC STENOSIS ( 19 FDA reports)
CARDIAC VALVE DISEASE ( 19 FDA reports)
EXTREMITY CONTRACTURE ( 19 FDA reports)
HAEMATOCHEZIA ( 19 FDA reports)
HEPATIC CIRRHOSIS ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
IRRITABLE BOWEL SYNDROME ( 19 FDA reports)
OROPHARYNGEAL PAIN ( 19 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 19 FDA reports)
SICK SINUS SYNDROME ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK ( 18 FDA reports)
AZOTAEMIA ( 18 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 18 FDA reports)
CEREBRAL ATROPHY ( 18 FDA reports)
CHOLESTASIS ( 18 FDA reports)
DEVICE MALFUNCTION ( 18 FDA reports)
DYSGEUSIA ( 18 FDA reports)
ECCHYMOSIS ( 18 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 18 FDA reports)
EMOTIONAL DISORDER ( 18 FDA reports)
FIBROSIS ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
GASTROINTESTINAL DISORDER ( 18 FDA reports)
IRON DEFICIENCY ANAEMIA ( 18 FDA reports)
JAW FRACTURE ( 18 FDA reports)
RENAL TUBULAR NECROSIS ( 18 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 18 FDA reports)
VENTRICULAR DYSFUNCTION ( 18 FDA reports)
ARTHRITIS ( 17 FDA reports)
CORONARY ARTERY STENOSIS ( 17 FDA reports)
CYANOSIS ( 17 FDA reports)
DYSARTHRIA ( 17 FDA reports)
ENDODONTIC PROCEDURE ( 17 FDA reports)
FLATULENCE ( 17 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 17 FDA reports)
HIP FRACTURE ( 17 FDA reports)
HYPOVOLAEMIA ( 17 FDA reports)
LYMPHADENOPATHY ( 17 FDA reports)
PNEUMONIA ASPIRATION ( 17 FDA reports)
POLLAKIURIA ( 17 FDA reports)
RASH ERYTHEMATOUS ( 17 FDA reports)
RENAL CYST ( 17 FDA reports)
SKIN FIBROSIS ( 17 FDA reports)
SKIN LESION ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 17 FDA reports)
TINNITUS ( 17 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 17 FDA reports)
ALOPECIA ( 16 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 16 FDA reports)
BACTERAEMIA ( 16 FDA reports)
DYSSTASIA ( 16 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 16 FDA reports)
GANGRENE ( 16 FDA reports)
HEMIPARESIS ( 16 FDA reports)
HYPOAESTHESIA ORAL ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 16 FDA reports)
KLEBSIELLA INFECTION ( 16 FDA reports)
LEUKOPENIA ( 16 FDA reports)
LOBAR PNEUMONIA ( 16 FDA reports)
PERIPHERAL ISCHAEMIA ( 16 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 16 FDA reports)
PRESYNCOPE ( 16 FDA reports)
PULMONARY TOXICITY ( 16 FDA reports)
PURPURA ( 16 FDA reports)
SPINAL OSTEOARTHRITIS ( 16 FDA reports)
TYPE 2 DIABETES MELLITUS ( 16 FDA reports)
URINARY RETENTION ( 16 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 15 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 15 FDA reports)
ANURIA ( 15 FDA reports)
ARTERIOSCLEROSIS ( 15 FDA reports)
BLOOD CHLORIDE DECREASED ( 15 FDA reports)
COMPLETED SUICIDE ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
HEPATITIS ( 15 FDA reports)
INFLUENZA LIKE ILLNESS ( 15 FDA reports)
ISCHAEMIA ( 15 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
PHARYNGEAL OEDEMA ( 15 FDA reports)
PHOTOSENSITIVITY REACTION ( 15 FDA reports)
POLYNEUROPATHY ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
PULSE ABSENT ( 15 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 15 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
ABSCESS DRAINAGE ( 14 FDA reports)
ACCIDENTAL OVERDOSE ( 14 FDA reports)
ANKLE FRACTURE ( 14 FDA reports)
BRONCHOPNEUMONIA ( 14 FDA reports)
CATARACT ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
COGNITIVE DISORDER ( 14 FDA reports)
DECREASED INTEREST ( 14 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 14 FDA reports)
EXERCISE TOLERANCE DECREASED ( 14 FDA reports)
FEELING HOT ( 14 FDA reports)
GINGIVAL SWELLING ( 14 FDA reports)
HAEMORRHOIDS ( 14 FDA reports)
ILL-DEFINED DISORDER ( 14 FDA reports)
OSTEOPENIA ( 14 FDA reports)
PANCREATITIS ( 14 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 14 FDA reports)
RIGHT VENTRICULAR FAILURE ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
SUDDEN DEATH ( 14 FDA reports)
ACUTE PULMONARY OEDEMA ( 13 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 13 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 13 FDA reports)
DEMENTIA ( 13 FDA reports)
DRUG INTOLERANCE ( 13 FDA reports)
GENERALISED OEDEMA ( 13 FDA reports)
HERPES ZOSTER ( 13 FDA reports)
INFLAMMATION ( 13 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 13 FDA reports)
JAW DISORDER ( 13 FDA reports)
LACERATION ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
MITRAL VALVE CALCIFICATION ( 13 FDA reports)
NASAL CONGESTION ( 13 FDA reports)
ODYNOPHAGIA ( 13 FDA reports)
PALLOR ( 13 FDA reports)
RALES ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
RHEUMATOID ARTHRITIS ( 13 FDA reports)
STEVENS-JOHNSON SYNDROME ( 13 FDA reports)
TOOTH FRACTURE ( 13 FDA reports)
TOOTHACHE ( 13 FDA reports)
TRANSAMINASES INCREASED ( 13 FDA reports)
URINE OUTPUT DECREASED ( 13 FDA reports)
ANAPHYLACTIC REACTION ( 12 FDA reports)
APHASIA ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
DRUG LEVEL INCREASED ( 12 FDA reports)
DRY MOUTH ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 12 FDA reports)
EMPHYSEMA ( 12 FDA reports)
ENTEROBACTER PNEUMONIA ( 12 FDA reports)
ENTEROCOCCAL INFECTION ( 12 FDA reports)
EOSINOPHILIA ( 12 FDA reports)
FAILURE TO THRIVE ( 12 FDA reports)
GINGIVAL DISORDER ( 12 FDA reports)
HELICOBACTER INFECTION ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HEPATOCELLULAR INJURY ( 12 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
MOUTH ULCERATION ( 12 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 12 FDA reports)
NODAL RHYTHM ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
PERIPHERAL COLDNESS ( 12 FDA reports)
PETECHIAE ( 12 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 12 FDA reports)
RIB FRACTURE ( 12 FDA reports)
SKIN NECROSIS ( 12 FDA reports)
SPLENOMEGALY ( 12 FDA reports)
THERAPY NON-RESPONDER ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
ABSCESS ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ANOXIC ENCEPHALOPATHY ( 11 FDA reports)
AORTIC VALVE CALCIFICATION ( 11 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 11 FDA reports)
BRONCHOSPASM ( 11 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 11 FDA reports)
CANDIDIASIS ( 11 FDA reports)
CARDIAC ANEURYSM ( 11 FDA reports)
CARDIAC FLUTTER ( 11 FDA reports)
CARDIORENAL SYNDROME ( 11 FDA reports)
CLOSTRIDIAL INFECTION ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
DERMATITIS EXFOLIATIVE ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
DYSLIPIDAEMIA ( 11 FDA reports)
EAR DISORDER ( 11 FDA reports)
FEAR OF DEATH ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
ILEUS PARALYTIC ( 11 FDA reports)
INTENTIONAL OVERDOSE ( 11 FDA reports)
INTERMITTENT CLAUDICATION ( 11 FDA reports)
LONG QT SYNDROME ( 11 FDA reports)
MITRAL VALVE PROLAPSE ( 11 FDA reports)
NODAL ARRHYTHMIA ( 11 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 11 FDA reports)
ORGAN FAILURE ( 11 FDA reports)
RASH PAPULAR ( 11 FDA reports)
SOCIAL PROBLEM ( 11 FDA reports)
SYSTEMIC CANDIDA ( 11 FDA reports)
THYROID DISORDER ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ACIDOSIS ( 10 FDA reports)
ADRENAL NEOPLASM ( 10 FDA reports)
AGEUSIA ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 10 FDA reports)
BREAST CANCER ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 10 FDA reports)
COLONIC POLYP ( 10 FDA reports)
DERMATITIS ( 10 FDA reports)
DIVERTICULITIS ( 10 FDA reports)
DRUG EFFECT DECREASED ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
FEMUR FRACTURE ( 10 FDA reports)
FISTULA ( 10 FDA reports)
GLAUCOMA ( 10 FDA reports)
HAEMATOMA INFECTION ( 10 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 10 FDA reports)
HEART TRANSPLANT ( 10 FDA reports)
HEPATOMEGALY ( 10 FDA reports)
JAUNDICE CHOLESTATIC ( 10 FDA reports)
JUGULAR VEIN DISTENSION ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MOTOR DYSFUNCTION ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
NERVOUS SYSTEM DISORDER ( 10 FDA reports)
ORAL PAIN ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
RASH MACULO-PAPULAR ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
ROAD TRAFFIC ACCIDENT ( 10 FDA reports)
SHOCK HAEMORRHAGIC ( 10 FDA reports)
SINUS HEADACHE ( 10 FDA reports)
SMALL INTESTINE OPERATION ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
SPINAL LAMINECTOMY ( 10 FDA reports)
SPINAL OPERATION ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 10 FDA reports)
TOOTH ABSCESS ( 10 FDA reports)
TOOTH INFECTION ( 10 FDA reports)
VENOUS INSUFFICIENCY ( 10 FDA reports)
VIRAL INFECTION ( 10 FDA reports)
WOUND ( 10 FDA reports)
AORTIC VALVE STENOSIS ( 9 FDA reports)
AREFLEXIA ( 9 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 9 FDA reports)
ASPIRATION JOINT ( 9 FDA reports)
ATRIAL TACHYCARDIA ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CACHEXIA ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
DEBRIDEMENT ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
DISEASE RECURRENCE ( 9 FDA reports)
DIVERTICULUM INTESTINAL ( 9 FDA reports)
EYE HAEMORRHAGE ( 9 FDA reports)
GLOSSODYNIA ( 9 FDA reports)
HEPATOJUGULAR REFLUX ( 9 FDA reports)
HIATUS HERNIA ( 9 FDA reports)
HYDRONEPHROSIS ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
ILEUS ( 9 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
ISCHAEMIC STROKE ( 9 FDA reports)
LEG AMPUTATION ( 9 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 9 FDA reports)
MORTON'S NEUROMA ( 9 FDA reports)
NEURALGIA ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
PAIN OF SKIN ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
RESTLESS LEGS SYNDROME ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
SKIN DISORDER ( 9 FDA reports)
SKIN PLAQUE ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
THROAT IRRITATION ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
TROPONIN INCREASED ( 9 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 9 FDA reports)
WOUND SECRETION ( 9 FDA reports)
WRIST FRACTURE ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 8 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
AGGRESSION ( 8 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 8 FDA reports)
APNOEA ( 8 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
BLOOD CULTURE POSITIVE ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CEREBRAL ISCHAEMIA ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
CHOLECYSTECTOMY ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
COLITIS ISCHAEMIC ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
CORONARY ARTERY BYPASS ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
HEART INJURY ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPERCHOLESTEROLAEMIA ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 8 FDA reports)
INFUSION RELATED REACTION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
INTRACARDIAC THROMBUS ( 8 FDA reports)
ISCHAEMIC HEPATITIS ( 8 FDA reports)
LABORATORY TEST ABNORMAL ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
PEMPHIGOID ( 8 FDA reports)
PITTING OEDEMA ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
RASH MACULAR ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 8 FDA reports)
RETROPERITONEAL HAEMATOMA ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
RIGHT ATRIAL DILATATION ( 8 FDA reports)
TREATMENT FAILURE ( 8 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 8 FDA reports)
VASCULAR GRAFT ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VISUAL DISTURBANCE ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
BRAIN OEDEMA ( 7 FDA reports)
BREAST OEDEMA ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CORONARY ARTERY THROMBOSIS ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
DIASTOLIC DYSFUNCTION ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
FAECES DISCOLOURED ( 7 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 7 FDA reports)
GYNAECOMASTIA ( 7 FDA reports)
HALLUCINATION, VISUAL ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HEPATORENAL SYNDROME ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 7 FDA reports)
JOINT INJURY ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
LIFE EXPECTANCY SHORTENED ( 7 FDA reports)
LUNG CONSOLIDATION ( 7 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
NASAL ULCER ( 7 FDA reports)
NOCTURIA ( 7 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
ORAL INFECTION ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PEAU D'ORANGE ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
PERITONEAL HAEMORRHAGE ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
POLYP ( 7 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 7 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 7 FDA reports)
PULMONARY MASS ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
QUALITY OF LIFE DECREASED ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 7 FDA reports)
ROSACEA ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
SWOLLEN TONGUE ( 7 FDA reports)
TENDERNESS ( 7 FDA reports)
TENDON INJURY ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
TRANSFUSION ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
TUMOUR HAEMORRHAGE ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
URINE ABNORMALITY ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ANGER ( 6 FDA reports)
ANGIONEUROTIC OEDEMA ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
ARTHRITIS BACTERIAL ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
CALCIPHYLAXIS ( 6 FDA reports)
CARDIAC FIBRILLATION ( 6 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 6 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
CLOSED HEAD INJURY ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 6 FDA reports)
CREPITATIONS ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
CYST ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
DENTAL FISTULA ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
EJECTION FRACTION ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
EMPTY SELLA SYNDROME ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FUSOBACTERIUM INFECTION ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GOUTY ARTHRITIS ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
MASS ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
NECK MASS ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
OSTEOLYSIS ( 6 FDA reports)
OSTEORADIONECROSIS ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PARKINSONISM ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PHLEBITIS ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 6 FDA reports)
RADICULOPATHY ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
THIRST ( 6 FDA reports)
THROMBOPHLEBITIS ( 6 FDA reports)
TOOTH LOSS ( 6 FDA reports)
ULCER ( 6 FDA reports)
URINARY INCONTINENCE ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
VERTEBROPLASTY ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
WALKING AID USER ( 6 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
ALCOHOLIC LIVER DISEASE ( 5 FDA reports)
AORTIC DISSECTION ( 5 FDA reports)
ARTERIAL INSUFFICIENCY ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BENIGN BONE NEOPLASM ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BONE NEOPLASM ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
ESSENTIAL HYPERTENSION ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE SWELLING ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
GINGIVAL ULCERATION ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMPATIENCE ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFECTION PROTOZOAL ( 5 FDA reports)
INGROWING NAIL ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
JOINT INSTABILITY ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 5 FDA reports)
MULTIPLE ALLERGIES ( 5 FDA reports)
MUSCLE CONTRACTURE ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
MUSCULAR DYSTROPHY ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL CANCER ( 5 FDA reports)
RENAL PAIN ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
SELF ESTEEM DECREASED ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SEQUESTRECTOMY ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SPINAL FRACTURE ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 5 FDA reports)
WEANING FAILURE ( 5 FDA reports)
ABDOMINAL HAEMATOMA ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAL FISTULA ( 4 FDA reports)
ANEURYSM REPAIR ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
BLADDER MASS ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CRYING ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DENTAL CARE ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DEVICE ISSUE ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 4 FDA reports)
EARLY SATIETY ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
FISTULA REPAIR ( 4 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GASTROENTERITIS RADIATION ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GLARE ( 4 FDA reports)
GOITRE ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
ILIAC ARTERY STENOSIS ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INFUSION SITE NECROSIS ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
IRITIS ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KERATOPATHY ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LISTLESS ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NON-CARDIAC CHEST PAIN ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PRODUCT TASTE ABNORMAL ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SEPTIC EMBOLUS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TOOTH REPAIR ( 4 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 4 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
URGE INCONTINENCE ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
ALOPECIA EFFLUVIUM ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
AMAUROSIS ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
APATHY ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 3 FDA reports)
CARDIAC ABLATION ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CARDIOTOXICITY ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 3 FDA reports)
COCCYDYNIA ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
COLON POLYPECTOMY ( 3 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIABETIC GASTROPARESIS ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ERYTHEMA INDURATUM ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GASTRIC INFECTION ( 3 FDA reports)
GASTRIC VARICES ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MIXED LIVER INJURY ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYXOEDEMA COMA ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PLASMAPHERESIS ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PLEURAL CALCIFICATION ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
RECTAL POLYP ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETINAL ARTERY EMBOLISM ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
SCAB ( 3 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 3 FDA reports)
SERRATIA BACTERAEMIA ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TESTICULAR ATROPHY ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TONGUE HAEMATOMA ( 3 FDA reports)
TOOTH INJURY ( 3 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WEIGHT ABNORMAL ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ALVEOLOPLASTY ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC REHABILITATION THERAPY ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CAST APPLICATION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECALITH ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLAT FEET ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GAMMA RADIATION THERAPY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRANSAMINASAEMIA ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACULAR PSEUDOHOLE ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUROPATHIC PAIN ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PNEUMONITIS CHEMICAL ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTAL FISTULA REPAIR ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINITIS SEASONAL ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR RETRACTION ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROIDITIS ACUTE ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE CYTOLOGY ABNORMAL ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICOCELE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VASCULITIS GASTROINTESTINAL ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WANDERING PACEMAKER ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BILIRUBIN CONJUGATED ( 1 FDA reports)
BIOPSY ARTERY ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE NORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL PIGMENTATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTATIN C INCREASED ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMOID CYST ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIA MYALGIA SYNDROME ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC DYSPLASIA ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFECTION BACTERIAL ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS EXFOLIATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATITIS INTERSTITIAL ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROBIOLOGY TEST ABNORMAL ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIOTOMY ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL EXAMINATION ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTPARTUM DISORDER ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CANCER RECURRENT ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTIC PHLEBITIS ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STARING ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR GERM CELL CANCER METASTATIC ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID ATROPHY ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROTOXIC PERIODIC PARALYSIS ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
UREA RENAL CLEARANCE DECREASED ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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