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

NEOPLASM MALIGNANT ( 1157 FDA reports)
PYREXIA ( 893 FDA reports)
DYSPNOEA ( 878 FDA reports)
DEATH ( 788 FDA reports)
FATIGUE ( 720 FDA reports)
NEOPLASM PROGRESSION ( 719 FDA reports)
ANAEMIA ( 617 FDA reports)
DIARRHOEA ( 612 FDA reports)
COUGH ( 582 FDA reports)
NAUSEA ( 545 FDA reports)
PNEUMONIA ( 479 FDA reports)
MALAISE ( 463 FDA reports)
ASTHENIA ( 451 FDA reports)
HAEMOGLOBIN DECREASED ( 445 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 439 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 439 FDA reports)
VOMITING ( 437 FDA reports)
STOMATITIS ( 417 FDA reports)
DECREASED APPETITE ( 410 FDA reports)
PLEURAL EFFUSION ( 400 FDA reports)
OEDEMA PERIPHERAL ( 383 FDA reports)
INTERSTITIAL LUNG DISEASE ( 378 FDA reports)
PNEUMONITIS ( 310 FDA reports)
DEHYDRATION ( 309 FDA reports)
ABDOMINAL PAIN ( 302 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 290 FDA reports)
PLATELET COUNT DECREASED ( 289 FDA reports)
BLOOD CREATININE INCREASED ( 260 FDA reports)
THROMBOCYTOPENIA ( 250 FDA reports)
WEIGHT DECREASED ( 246 FDA reports)
HYPERGLYCAEMIA ( 234 FDA reports)
PAIN ( 234 FDA reports)
RASH ( 234 FDA reports)
BLOOD GLUCOSE INCREASED ( 225 FDA reports)
LUNG DISORDER ( 217 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 208 FDA reports)
DRUG INEFFECTIVE ( 198 FDA reports)
RENAL IMPAIRMENT ( 198 FDA reports)
MUCOSAL INFLAMMATION ( 193 FDA reports)
RENAL FAILURE ( 191 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 184 FDA reports)
BACK PAIN ( 179 FDA reports)
FEBRILE NEUTROPENIA ( 175 FDA reports)
CONVULSION ( 168 FDA reports)
RENAL FAILURE ACUTE ( 168 FDA reports)
URINARY TRACT INFECTION ( 164 FDA reports)
METASTASES TO LUNG ( 160 FDA reports)
HEADACHE ( 153 FDA reports)
HYPOTENSION ( 152 FDA reports)
ORAL PAIN ( 151 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 146 FDA reports)
LUNG INFILTRATION ( 145 FDA reports)
PAIN IN EXTREMITY ( 145 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 144 FDA reports)
DYSPHAGIA ( 143 FDA reports)
FALL ( 143 FDA reports)
MOUTH ULCERATION ( 142 FDA reports)
SEPSIS ( 140 FDA reports)
EPISTAXIS ( 139 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 138 FDA reports)
ASCITES ( 136 FDA reports)
CHEST PAIN ( 133 FDA reports)
DIZZINESS ( 130 FDA reports)
METASTASES TO BONE ( 130 FDA reports)
HYPOPHAGIA ( 129 FDA reports)
METASTASES TO LIVER ( 126 FDA reports)
PULMONARY EMBOLISM ( 123 FDA reports)
CHILLS ( 119 FDA reports)
OEDEMA ( 117 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 116 FDA reports)
SOMNOLENCE ( 115 FDA reports)
CONFUSIONAL STATE ( 114 FDA reports)
HYPOXIA ( 113 FDA reports)
INFLAMMATION ( 113 FDA reports)
NEUTROPHIL COUNT DECREASED ( 113 FDA reports)
BLOOD UREA INCREASED ( 111 FDA reports)
ABDOMINAL PAIN UPPER ( 110 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 110 FDA reports)
DIABETES MELLITUS ( 106 FDA reports)
NEUTROPENIA ( 104 FDA reports)
ARTHRALGIA ( 103 FDA reports)
OROPHARYNGEAL PAIN ( 103 FDA reports)
DEEP VEIN THROMBOSIS ( 102 FDA reports)
INFECTION ( 102 FDA reports)
RESPIRATORY FAILURE ( 102 FDA reports)
HAEMORRHAGE ( 100 FDA reports)
CONSTIPATION ( 97 FDA reports)
BLOOD PRESSURE INCREASED ( 94 FDA reports)
PERICARDIAL EFFUSION ( 91 FDA reports)
ABDOMINAL DISTENSION ( 90 FDA reports)
RESPIRATORY DISTRESS ( 90 FDA reports)
HYPERTENSION ( 89 FDA reports)
TACHYCARDIA ( 89 FDA reports)
HYPOKALAEMIA ( 88 FDA reports)
ATELECTASIS ( 87 FDA reports)
CEREBRAL HAEMORRHAGE ( 87 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 82 FDA reports)
CARDIAC FAILURE ( 82 FDA reports)
DISEASE PROGRESSION ( 81 FDA reports)
MUSCULAR WEAKNESS ( 81 FDA reports)
BRONCHITIS ( 79 FDA reports)
GAIT DISTURBANCE ( 79 FDA reports)
DYSPEPSIA ( 77 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 77 FDA reports)
MULTI-ORGAN FAILURE ( 76 FDA reports)
PULMONARY OEDEMA ( 76 FDA reports)
ERYTHEMA ( 75 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 73 FDA reports)
HYPONATRAEMIA ( 73 FDA reports)
SEPTIC SHOCK ( 73 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 71 FDA reports)
LETHARGY ( 70 FDA reports)
HAEMATOCRIT DECREASED ( 67 FDA reports)
APHAGIA ( 66 FDA reports)
BONE MARROW FAILURE ( 66 FDA reports)
ABNORMAL BEHAVIOUR ( 65 FDA reports)
ACNE ( 65 FDA reports)
DRUG INTOLERANCE ( 65 FDA reports)
LYMPHADENOPATHY ( 65 FDA reports)
PNEUMONIA BACTERIAL ( 65 FDA reports)
HYPERKALAEMIA ( 63 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 62 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 62 FDA reports)
FEELING ABNORMAL ( 62 FDA reports)
ATRIAL FIBRILLATION ( 61 FDA reports)
DYSGEUSIA ( 61 FDA reports)
PRURITUS ( 61 FDA reports)
ABDOMINAL DISCOMFORT ( 60 FDA reports)
CONTUSION ( 60 FDA reports)
NASOPHARYNGITIS ( 60 FDA reports)
DEPRESSION ( 59 FDA reports)
HERPES ZOSTER ( 59 FDA reports)
LUNG CONSOLIDATION ( 59 FDA reports)
BLOOD PRESSURE DECREASED ( 58 FDA reports)
WHEEZING ( 58 FDA reports)
CONDITION AGGRAVATED ( 57 FDA reports)
SWELLING ( 57 FDA reports)
LIVER DISORDER ( 56 FDA reports)
PRODUCTIVE COUGH ( 56 FDA reports)
DISORIENTATION ( 55 FDA reports)
NASAL CONGESTION ( 55 FDA reports)
PARAESTHESIA ( 55 FDA reports)
CARDIAC ARREST ( 54 FDA reports)
MUSCULOSKELETAL PAIN ( 54 FDA reports)
JAUNDICE ( 53 FDA reports)
MYOCARDIAL INFARCTION ( 53 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 52 FDA reports)
INTESTINAL OBSTRUCTION ( 52 FDA reports)
LOCALISED INFECTION ( 52 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 52 FDA reports)
ANXIETY ( 51 FDA reports)
INGROWING NAIL ( 51 FDA reports)
WEIGHT INCREASED ( 51 FDA reports)
ANAL ABSCESS ( 50 FDA reports)
GENERALISED OEDEMA ( 50 FDA reports)
JOINT SWELLING ( 50 FDA reports)
ECZEMA ( 49 FDA reports)
INSOMNIA ( 49 FDA reports)
URINE OUTPUT DECREASED ( 49 FDA reports)
HAEMATEMESIS ( 48 FDA reports)
LUNG INFECTION ( 48 FDA reports)
SYNCOPE ( 48 FDA reports)
TOOTHACHE ( 48 FDA reports)
CHEST DISCOMFORT ( 47 FDA reports)
DYSPNOEA EXERTIONAL ( 47 FDA reports)
TONGUE ULCERATION ( 47 FDA reports)
HAEMOPTYSIS ( 46 FDA reports)
PNEUMONIA ASPIRATION ( 46 FDA reports)
RESPIRATORY DISORDER ( 46 FDA reports)
FAECES DISCOLOURED ( 45 FDA reports)
OSTEONECROSIS OF JAW ( 45 FDA reports)
PANCYTOPENIA ( 45 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 45 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 44 FDA reports)
DRUG INTERACTION ( 44 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 44 FDA reports)
EJECTION FRACTION DECREASED ( 44 FDA reports)
SWOLLEN TONGUE ( 44 FDA reports)
BLOOD POTASSIUM DECREASED ( 43 FDA reports)
CYANOSIS ( 43 FDA reports)
RASH PRURITIC ( 43 FDA reports)
ELECTROLYTE IMBALANCE ( 42 FDA reports)
HAEMORRHOIDS ( 42 FDA reports)
HYPERCALCAEMIA ( 42 FDA reports)
INFLUENZA LIKE ILLNESS ( 42 FDA reports)
ESCHERICHIA INFECTION ( 41 FDA reports)
ILEUS ( 41 FDA reports)
OXYGEN SATURATION DECREASED ( 41 FDA reports)
SWELLING FACE ( 41 FDA reports)
CEREBROVASCULAR ACCIDENT ( 40 FDA reports)
FEMUR FRACTURE ( 40 FDA reports)
MYALGIA ( 40 FDA reports)
PROTEINURIA ( 40 FDA reports)
HAEMATURIA ( 39 FDA reports)
PALLOR ( 39 FDA reports)
SINUSITIS ( 39 FDA reports)
SLEEP DISORDER ( 39 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 39 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 38 FDA reports)
DRY SKIN ( 38 FDA reports)
HEPATIC ENZYME INCREASED ( 38 FDA reports)
LUNG NEOPLASM ( 38 FDA reports)
MELAENA ( 38 FDA reports)
PNEUMOTHORAX ( 38 FDA reports)
PERFORMANCE STATUS DECREASED ( 37 FDA reports)
SHOCK ( 37 FDA reports)
TESTICULAR PAIN ( 37 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 36 FDA reports)
CELL MARKER INCREASED ( 36 FDA reports)
EAR INFECTION ( 36 FDA reports)
GASTRITIS ( 36 FDA reports)
RHINORRHOEA ( 36 FDA reports)
BLOOD ALBUMIN DECREASED ( 35 FDA reports)
CARDIOMEGALY ( 35 FDA reports)
MENTAL STATUS CHANGES ( 35 FDA reports)
ORAL HERPES ( 35 FDA reports)
RASH GENERALISED ( 35 FDA reports)
ANGIOEDEMA ( 34 FDA reports)
GRAND MAL CONVULSION ( 34 FDA reports)
HEPATIC FAILURE ( 34 FDA reports)
LEUKOPENIA ( 34 FDA reports)
PALPITATIONS ( 34 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 34 FDA reports)
CHOLELITHIASIS ( 33 FDA reports)
HYPOVOLAEMIA ( 33 FDA reports)
LOSS OF CONSCIOUSNESS ( 33 FDA reports)
THORACIC CAVITY DRAINAGE ( 33 FDA reports)
ASTHMA ( 32 FDA reports)
FLUSHING ( 32 FDA reports)
GASTRIC HAEMORRHAGE ( 32 FDA reports)
HYPOPHOSPHATAEMIA ( 32 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 32 FDA reports)
METASTASIS ( 32 FDA reports)
PANCREATITIS ( 32 FDA reports)
PULMONARY FIBROSIS ( 32 FDA reports)
SKIN DISORDER ( 32 FDA reports)
SKIN EXFOLIATION ( 32 FDA reports)
URTICARIA ( 32 FDA reports)
BLOOD COUNT ABNORMAL ( 31 FDA reports)
CARDIOMYOPATHY ( 31 FDA reports)
CELLULITIS ( 31 FDA reports)
CHOLANGITIS ( 31 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 31 FDA reports)
FLUID RETENTION ( 31 FDA reports)
INTESTINAL PERFORATION ( 31 FDA reports)
LYMPHOEDEMA ( 31 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 31 FDA reports)
AMYLASE INCREASED ( 30 FDA reports)
ANGER ( 30 FDA reports)
COGNITIVE DISORDER ( 30 FDA reports)
NEPHROLITHIASIS ( 30 FDA reports)
SURGERY ( 30 FDA reports)
ANAL FISSURE ( 29 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 29 FDA reports)
CACHEXIA ( 29 FDA reports)
FAILURE TO THRIVE ( 29 FDA reports)
IRRITABILITY ( 29 FDA reports)
LIP SWELLING ( 29 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 29 FDA reports)
RENAL FAILURE CHRONIC ( 29 FDA reports)
EOSINOPHIL COUNT INCREASED ( 28 FDA reports)
MUSCLE SPASMS ( 28 FDA reports)
RENAL DISORDER ( 28 FDA reports)
UROSEPSIS ( 28 FDA reports)
BLADDER DISORDER ( 27 FDA reports)
CRYING ( 27 FDA reports)
RESPIRATORY ARREST ( 27 FDA reports)
AGITATION ( 26 FDA reports)
BODY TEMPERATURE INCREASED ( 26 FDA reports)
CHEST X-RAY ABNORMAL ( 26 FDA reports)
COMPLEX PARTIAL SEIZURES ( 26 FDA reports)
FUNGAL INFECTION ( 26 FDA reports)
HAEMATOCHEZIA ( 26 FDA reports)
HYPOGLYCAEMIA ( 26 FDA reports)
INJURY ( 26 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 26 FDA reports)
METASTASES TO ADRENALS ( 26 FDA reports)
OSTEOMYELITIS ( 26 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 26 FDA reports)
RECTAL HAEMORRHAGE ( 26 FDA reports)
TUMOUR HAEMORRHAGE ( 26 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 25 FDA reports)
APHTHOUS STOMATITIS ( 25 FDA reports)
ARRHYTHMIA ( 25 FDA reports)
BLOOD BILIRUBIN INCREASED ( 25 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 25 FDA reports)
LACRIMATION INCREASED ( 25 FDA reports)
LEUKOCYTOSIS ( 25 FDA reports)
LOCAL SWELLING ( 25 FDA reports)
OSTEONECROSIS ( 25 FDA reports)
SPEECH DISORDER ( 25 FDA reports)
TERMINAL STATE ( 25 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 25 FDA reports)
BLISTER ( 24 FDA reports)
DELIRIUM ( 24 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 24 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 24 FDA reports)
INFLUENZA ( 24 FDA reports)
OCULAR HYPERAEMIA ( 24 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 24 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 24 FDA reports)
SECRETION DISCHARGE ( 24 FDA reports)
ASPIRATION PLEURAL CAVITY ( 23 FDA reports)
BLOOD AMYLASE INCREASED ( 23 FDA reports)
CIRCULATORY COLLAPSE ( 23 FDA reports)
COMA ( 23 FDA reports)
DEPRESSED MOOD ( 23 FDA reports)
GASTRIC ULCER ( 23 FDA reports)
GASTROENTERITIS ( 23 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 23 FDA reports)
GOUT ( 23 FDA reports)
HEART RATE INCREASED ( 23 FDA reports)
HYPOCALCAEMIA ( 23 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 23 FDA reports)
RALES ( 23 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 23 FDA reports)
ABSCESS ORAL ( 22 FDA reports)
ARTHRITIS ( 22 FDA reports)
BONE PAIN ( 22 FDA reports)
EYELID OEDEMA ( 22 FDA reports)
FLATULENCE ( 22 FDA reports)
GASTROINTESTINAL PERFORATION ( 22 FDA reports)
HYPERCHOLESTEROLAEMIA ( 22 FDA reports)
HYPERLIPIDAEMIA ( 22 FDA reports)
HYPERSENSITIVITY ( 22 FDA reports)
HYPOAESTHESIA ORAL ( 22 FDA reports)
HYPOTHYROIDISM ( 22 FDA reports)
PATHOLOGICAL FRACTURE ( 22 FDA reports)
THROMBOSIS ( 22 FDA reports)
ACUTE RESPIRATORY FAILURE ( 21 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 21 FDA reports)
BLOOD GLUCOSE DECREASED ( 21 FDA reports)
CARDIAC DISORDER ( 21 FDA reports)
ENDOTRACHEAL INTUBATION ( 21 FDA reports)
INFANTILE SPASMS ( 21 FDA reports)
PULMONARY CONGESTION ( 21 FDA reports)
SINUS TACHYCARDIA ( 21 FDA reports)
SKIN LESION ( 21 FDA reports)
AGGRESSION ( 20 FDA reports)
ANURIA ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 20 FDA reports)
DISCOMFORT ( 20 FDA reports)
DYSURIA ( 20 FDA reports)
FEELING HOT ( 20 FDA reports)
GLOSSODYNIA ( 20 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 20 FDA reports)
METASTASES TO SPINE ( 20 FDA reports)
NEUROPATHY PERIPHERAL ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
ORAL DISCOMFORT ( 20 FDA reports)
PERIODONTITIS ( 20 FDA reports)
PLEURODESIS ( 20 FDA reports)
PULMONARY TOXICITY ( 20 FDA reports)
RESPIRATORY TRACT INFECTION ( 20 FDA reports)
AZOTAEMIA ( 19 FDA reports)
BACTERIAL INFECTION ( 19 FDA reports)
BLOOD POTASSIUM INCREASED ( 19 FDA reports)
CANCER PAIN ( 19 FDA reports)
CHEILITIS ( 19 FDA reports)
CHOLECYSTITIS ( 19 FDA reports)
COLITIS ISCHAEMIC ( 19 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 19 FDA reports)
HEAD BANGING ( 19 FDA reports)
HEPATITIS B ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
HYPOAESTHESIA ( 19 FDA reports)
HYPOALBUMINAEMIA ( 19 FDA reports)
MOUTH HAEMORRHAGE ( 19 FDA reports)
NIGHT SWEATS ( 19 FDA reports)
OESOPHAGITIS ( 19 FDA reports)
POOR QUALITY SLEEP ( 19 FDA reports)
RASH ERYTHEMATOUS ( 19 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
CLOSTRIDIAL INFECTION ( 18 FDA reports)
EPILEPSY ( 18 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 18 FDA reports)
HEMIPLEGIA ( 18 FDA reports)
NAIL DISORDER ( 18 FDA reports)
ORTHOPNOEA ( 18 FDA reports)
OSTEOARTHRITIS ( 18 FDA reports)
PETECHIAE ( 18 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 18 FDA reports)
RASH MACULAR ( 18 FDA reports)
RENAL CELL CARCINOMA ( 18 FDA reports)
SCRATCH ( 18 FDA reports)
TONGUE OEDEMA ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 18 FDA reports)
BURNING SENSATION ( 17 FDA reports)
CHOLESTASIS ( 17 FDA reports)
DROOLING ( 17 FDA reports)
DRY MOUTH ( 17 FDA reports)
FRACTURE ( 17 FDA reports)
GASTROINTESTINAL ULCER ( 17 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 17 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 17 FDA reports)
HEPATOMEGALY ( 17 FDA reports)
LIGAMENT SPRAIN ( 17 FDA reports)
LYMPHOPENIA ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
METABOLIC ACIDOSIS ( 17 FDA reports)
MYOCARDIAL ISCHAEMIA ( 17 FDA reports)
ODYNOPHAGIA ( 17 FDA reports)
OROPHARYNGEAL BLISTERING ( 17 FDA reports)
PNEUMONIA FUNGAL ( 17 FDA reports)
POLLAKIURIA ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
TENDERNESS ( 17 FDA reports)
TONGUE DISORDER ( 17 FDA reports)
UNRESPONSIVE TO STIMULI ( 17 FDA reports)
VENTRICULAR TACHYCARDIA ( 17 FDA reports)
VISION BLURRED ( 17 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 16 FDA reports)
CANDIDIASIS ( 16 FDA reports)
CARDIAC TAMPONADE ( 16 FDA reports)
COLITIS ( 16 FDA reports)
DRUG TOXICITY ( 16 FDA reports)
INJECTION SITE ERYTHEMA ( 16 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
LIPASE INCREASED ( 16 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
MITRAL VALVE INCOMPETENCE ( 16 FDA reports)
NECK PAIN ( 16 FDA reports)
NEUTROPENIC SEPSIS ( 16 FDA reports)
PAIN IN JAW ( 16 FDA reports)
PARACENTESIS ( 16 FDA reports)
PERICARDIAL DRAINAGE ( 16 FDA reports)
PYELONEPHRITIS ACUTE ( 16 FDA reports)
SALIVARY GLAND CALCULUS ( 16 FDA reports)
SKIN NECROSIS ( 16 FDA reports)
TREMOR ( 16 FDA reports)
VENA CAVA FILTER INSERTION ( 16 FDA reports)
ABDOMINAL PAIN LOWER ( 15 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
BLOOD CALCIUM DECREASED ( 15 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 15 FDA reports)
COLD SWEAT ( 15 FDA reports)
CREPITATIONS ( 15 FDA reports)
CYSTITIS ( 15 FDA reports)
DRUG LEVEL DECREASED ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
GASTROENTERITIS RADIATION ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
GASTROINTESTINAL INFECTION ( 15 FDA reports)
GLOSSITIS ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
KLEBSIELLA SEPSIS ( 15 FDA reports)
MALNUTRITION ( 15 FDA reports)
NEUTROPHIL COUNT INCREASED ( 15 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 15 FDA reports)
SKIN ULCER ( 15 FDA reports)
SPUTUM DISCOLOURED ( 15 FDA reports)
SUBILEUS ( 15 FDA reports)
SURFACTANT PROTEIN INCREASED ( 15 FDA reports)
TUMOUR NECROSIS ( 15 FDA reports)
VENTRICULAR HYPOKINESIA ( 15 FDA reports)
ABDOMINAL ABSCESS ( 14 FDA reports)
ABDOMINAL HERNIA ( 14 FDA reports)
ALOPECIA ( 14 FDA reports)
DYSSTASIA ( 14 FDA reports)
ENTERITIS ( 14 FDA reports)
ERYTHEMA MULTIFORME ( 14 FDA reports)
FISTULA ( 14 FDA reports)
GASTROENTERITIS VIRAL ( 14 FDA reports)
HAEMATOTOXICITY ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 14 FDA reports)
INJECTION SITE PAIN ( 14 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 14 FDA reports)
METASTATIC PAIN ( 14 FDA reports)
MOBILITY DECREASED ( 14 FDA reports)
PERITONITIS ( 14 FDA reports)
PRURITUS GENERALISED ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RADIATION PNEUMONITIS ( 14 FDA reports)
RENAL CANCER ( 14 FDA reports)
RENAL CYST ( 14 FDA reports)
SMALL INTESTINAL PERFORATION ( 14 FDA reports)
STRIDOR ( 14 FDA reports)
SUDDEN DEATH ( 14 FDA reports)
URINARY RETENTION ( 14 FDA reports)
VERTIGO ( 14 FDA reports)
VIRAL INFECTION ( 14 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 13 FDA reports)
ABDOMINAL TENDERNESS ( 13 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 13 FDA reports)
ANGIOMYOLIPOMA ( 13 FDA reports)
ATONIC SEIZURES ( 13 FDA reports)
BLADDER TAMPONADE ( 13 FDA reports)
BLOOD CALCIUM INCREASED ( 13 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 13 FDA reports)
CATHETERISATION CARDIAC ( 13 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
DERMATITIS ( 13 FDA reports)
DIABETIC KETOACIDOSIS ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
FLANK PAIN ( 13 FDA reports)
FOAMING AT MOUTH ( 13 FDA reports)
FOLLICULITIS ( 13 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 13 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 13 FDA reports)
HEPATITIS FULMINANT ( 13 FDA reports)
HERPANGINA ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 13 FDA reports)
LUNG INFILTRATION MALIGNANT ( 13 FDA reports)
METASTASES TO LYMPH NODES ( 13 FDA reports)
NO ADVERSE EVENT ( 13 FDA reports)
OSTEOLYSIS ( 13 FDA reports)
POLYDIPSIA ( 13 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 13 FDA reports)
RENAL MASS ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 13 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
APHASIA ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD CREATININE DECREASED ( 12 FDA reports)
BLOOD SODIUM DECREASED ( 12 FDA reports)
CARDIAC ENZYMES INCREASED ( 12 FDA reports)
COAGULOPATHY ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
DYSPLASIA ( 12 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 12 FDA reports)
HAEMODYNAMIC INSTABILITY ( 12 FDA reports)
HERNIAL EVENTRATION ( 12 FDA reports)
HERPES SIMPLEX ( 12 FDA reports)
HILAR LYMPHADENOPATHY ( 12 FDA reports)
HYPERTENSIVE CRISIS ( 12 FDA reports)
HYPOVOLAEMIC SHOCK ( 12 FDA reports)
IMPAIRED HEALING ( 12 FDA reports)
INTESTINAL DILATATION ( 12 FDA reports)
LEUKOENCEPHALOPATHY ( 12 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 12 FDA reports)
METABOLIC SYNDROME ( 12 FDA reports)
MOOD ALTERED ( 12 FDA reports)
MOVEMENT DISORDER ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
RENAL TUBULAR NECROSIS ( 12 FDA reports)
RESTLESSNESS ( 12 FDA reports)
SKIN DISCOLOURATION ( 12 FDA reports)
SKIN SWELLING ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
TONGUE BLISTERING ( 12 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ACUTE PULMONARY OEDEMA ( 11 FDA reports)
ADNEXA UTERI CYST ( 11 FDA reports)
BACTERIAL TEST POSITIVE ( 11 FDA reports)
BILIARY ANASTOMOSIS ( 11 FDA reports)
CARDIAC MURMUR ( 11 FDA reports)
CATHETER PLACEMENT ( 11 FDA reports)
CATHETER SITE INFECTION ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DUODENAL ULCER ( 11 FDA reports)
ECCHYMOSIS ( 11 FDA reports)
EMPHYSEMA ( 11 FDA reports)
GASTROINTESTINAL OEDEMA ( 11 FDA reports)
HEART RATE ABNORMAL ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HEPATORENAL SYNDROME ( 11 FDA reports)
HYPERURICAEMIA ( 11 FDA reports)
HYPOACUSIS ( 11 FDA reports)
IRON DEFICIENCY ANAEMIA ( 11 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
NERVOUSNESS ( 11 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
PROCTALGIA ( 11 FDA reports)
PROTEIN TOTAL INCREASED ( 11 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 11 FDA reports)
PULSE ABSENT ( 11 FDA reports)
RECALL PHENOMENON ( 11 FDA reports)
RESPIRATORY RATE INCREASED ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
RIB FRACTURE ( 11 FDA reports)
SLEEP APNOEA SYNDROME ( 11 FDA reports)
STAPHYLOCOCCAL INFECTION ( 11 FDA reports)
ABASIA ( 10 FDA reports)
BILE DUCT STENOSIS ( 10 FDA reports)
BILE DUCT STENT INSERTION ( 10 FDA reports)
BONE DISORDER ( 10 FDA reports)
BRAIN MASS ( 10 FDA reports)
BRAIN OEDEMA ( 10 FDA reports)
BRONCHOPNEUMONIA ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CARDIAC FAILURE ACUTE ( 10 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 10 FDA reports)
CYST ( 10 FDA reports)
DIPLEGIA ( 10 FDA reports)
DIVERTICULITIS ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
FOOD INTOLERANCE ( 10 FDA reports)
GALLBLADDER OBSTRUCTION ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
HERNIA ( 10 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
HYPERSOMNIA ( 10 FDA reports)
INTERNAL HERNIA ( 10 FDA reports)
JAUNDICE CHOLESTATIC ( 10 FDA reports)
JOINT EFFUSION ( 10 FDA reports)
JOINT INJURY ( 10 FDA reports)
MASS ( 10 FDA reports)
NODULE ( 10 FDA reports)
OESOPHAGEAL STENOSIS ( 10 FDA reports)
PLATELET COUNT INCREASED ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
PROTEIN TOTAL DECREASED ( 10 FDA reports)
PULMONARY HYPERTENSION ( 10 FDA reports)
RADIATION OESOPHAGITIS ( 10 FDA reports)
RASH MACULO-PAPULAR ( 10 FDA reports)
RENAL CANCER METASTATIC ( 10 FDA reports)
RESPIRATORY TRACT CONGESTION ( 10 FDA reports)
SCREAMING ( 10 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 10 FDA reports)
SINUS HEADACHE ( 10 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
ABSCESS ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ANAPHYLACTIC REACTION ( 9 FDA reports)
ANGIOFIBROMA ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
BILE DUCT OBSTRUCTION ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 9 FDA reports)
BLOOD CREATINE INCREASED ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
CATARACT ( 9 FDA reports)
CEREBRAL ATROPHY ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 9 FDA reports)
COLECTOMY ( 9 FDA reports)
DENTAL CARIES ( 9 FDA reports)
DERMATITIS CONTACT ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
DRUG ADMINISTRATION ERROR ( 9 FDA reports)
DYSLIPIDAEMIA ( 9 FDA reports)
EATING DISORDER ( 9 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
ERYSIPELAS ( 9 FDA reports)
GALLBLADDER DISORDER ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
INFECTIOUS PERITONITIS ( 9 FDA reports)
INJECTION SITE MASS ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 9 FDA reports)
LEFT VENTRICULAR FAILURE ( 9 FDA reports)
LIPID METABOLISM DISORDER ( 9 FDA reports)
LIVER ABSCESS ( 9 FDA reports)
LOCALISED OEDEMA ( 9 FDA reports)
LUNG ABSCESS ( 9 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 9 FDA reports)
MECHANICAL ILEUS ( 9 FDA reports)
MENORRHAGIA ( 9 FDA reports)
NEOPLASM ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NON-CARDIAC CHEST PAIN ( 9 FDA reports)
OBESITY ( 9 FDA reports)
ONYCHOCLASIS ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
OSTEOSCLEROSIS ( 9 FDA reports)
POLYMYOSITIS ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
RIGHT VENTRICULAR FAILURE ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
TINNITUS ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
URINE COLOUR ABNORMAL ( 9 FDA reports)
VASCULAR INSUFFICIENCY ( 9 FDA reports)
WOUND ( 9 FDA reports)
WOUND DEHISCENCE ( 9 FDA reports)
ABDOMINAL SYMPTOM ( 8 FDA reports)
AGEUSIA ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
BLADDER CATHETERISATION ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BRAIN NEOPLASM ( 8 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 8 FDA reports)
CEREBRAL DISORDER ( 8 FDA reports)
CORONARY ARTERY OCCLUSION ( 8 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 8 FDA reports)
CYSTITIS HAEMORRHAGIC ( 8 FDA reports)
DIASTOLIC DYSFUNCTION ( 8 FDA reports)
DILATATION VENTRICULAR ( 8 FDA reports)
DIPLOPIA ( 8 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 8 FDA reports)
DYSPNOEA AT REST ( 8 FDA reports)
EAR PAIN ( 8 FDA reports)
ENTEROCOLITIS BACTERIAL ( 8 FDA reports)
FEBRILE BONE MARROW APLASIA ( 8 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 8 FDA reports)
GINGIVAL BLEEDING ( 8 FDA reports)
GINGIVAL INFECTION ( 8 FDA reports)
GINGIVAL SWELLING ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HELICOBACTER INFECTION ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERCREATININAEMIA ( 8 FDA reports)
KARNOFSKY SCALE WORSENED ( 8 FDA reports)
LYMPHANGITIS ( 8 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
METASTASES TO ABDOMINAL WALL ( 8 FDA reports)
METASTASES TO RETROPERITONEUM ( 8 FDA reports)
MICROCYTIC ANAEMIA ( 8 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
NOCARDIOSIS ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
PHARYNGEAL ULCERATION ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
PNEUMONIA LEGIONELLA ( 8 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 8 FDA reports)
RENAL HAEMORRHAGE ( 8 FDA reports)
SCAB ( 8 FDA reports)
SOFT TISSUE INJURY ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
THROMBOPHLEBITIS ( 8 FDA reports)
TONIC CONVULSION ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
VENOUS INSUFFICIENCY ( 8 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
ACIDOSIS ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 7 FDA reports)
ADENOCARCINOMA PANCREAS ( 7 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
ARTERIAL STENT INSERTION ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BILIARY TRACT INFECTION ( 7 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
CARBON DIOXIDE INCREASED ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
CHAPPED LIPS ( 7 FDA reports)
COLOSTOMY ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DIZZINESS POSTURAL ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
EMPYEMA ( 7 FDA reports)
ENTEROSTOMY ( 7 FDA reports)
FLUID INTAKE REDUCED ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
GLOBULINS INCREASED ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HEPATIC ATROPHY ( 7 FDA reports)
HYPERPLASIA ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
INCISION SITE HAEMORRHAGE ( 7 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LIP DISORDER ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
MALIGNANT ASCITES ( 7 FDA reports)
MECHANICAL VENTILATION ( 7 FDA reports)
METASTATIC NEOPLASM ( 7 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 7 FDA reports)
OCULAR DISCOMFORT ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
OESOPHAGOSTOMY ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PERSONALITY CHANGE ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PLATELET DISORDER ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
STENT REMOVAL ( 7 FDA reports)
STRESS ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
TOXIC ENCEPHALOPATHY ( 7 FDA reports)
TROPONIN T INCREASED ( 7 FDA reports)
VENTRICULAR DYSFUNCTION ( 7 FDA reports)
ACNE PUSTULAR ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
APNOEA ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CRANIAL NERVE PARALYSIS ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DEVICE OCCLUSION ( 6 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 6 FDA reports)
DIABETIC ULCER ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 6 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
HAIR TEXTURE ABNORMAL ( 6 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
METASTASES TO PERITONEUM ( 6 FDA reports)
METASTASES TO STOMACH ( 6 FDA reports)
MICTURITION DISORDER ( 6 FDA reports)
NEUROENDOCRINE TUMOUR ( 6 FDA reports)
OESOPHAGEAL PERFORATION ( 6 FDA reports)
ONCOLOGIC COMPLICATION ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
ORAL CANDIDIASIS ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
SEPSIS SYNDROME ( 6 FDA reports)
SIALOADENITIS ( 6 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
THYROIDITIS SUBACUTE ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
ULCER ( 6 FDA reports)
URINARY INCONTINENCE ( 6 FDA reports)
VARICELLA ( 6 FDA reports)
VASCULAR CAUTERISATION ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
AKINESIA ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
DRAIN REMOVAL ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
DUODENAL SPHINCTEROTOMY ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HERPES DERMATITIS ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
JOINT STABILISATION ( 5 FDA reports)
KETOACIDOSIS ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
METASTASES TO HEART ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MITRAL VALVE CALCIFICATION ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NON-HIGH-DENSITY LIPOPROTEIN CHOLESTEROL INCREASED ( 5 FDA reports)
OVARIAN CYST RUPTURED ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PRIMARY SEQUESTRUM ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SKIN INFECTION ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
SPUTUM INCREASED ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
STARING ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TOOTH DISORDER ( 5 FDA reports)
TOOTH EROSION ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
VOCAL CORD PARALYSIS ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ACQUIRED PHIMOSIS ( 4 FDA reports)
ADENOMYOSIS ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
ANORECTAL DISCOMFORT ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
AXILLARY PAIN ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BONE OEDEMA ( 4 FDA reports)
BRADYPHRENIA ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BREAST HYPOPLASIA ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHOLANGITIS ACUTE ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 4 FDA reports)
DROWNING ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENTERITIS NECROTICANS ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EXPOSED BONE IN JAW ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GASTROINTESTINAL NEOPLASM ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAEMOSTASIS ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEAT ILLNESS ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPOSIDERAEMIA ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INFECTED EPIDERMAL CYST ( 4 FDA reports)
INFERIOR VENA CAVA DILATATION ( 4 FDA reports)
INSULINOMA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KUSSMAUL RESPIRATION ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LIP HAEMORRHAGE ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LISTERIA SEPSIS ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METASTASES TO SKIN ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
PALLIATIVE CARE ( 4 FDA reports)
PANCREATIC DUCT DILATATION ( 4 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PERICARDIAL EXCISION ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PINEAL GLAND CYST ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PURPURA ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RENAL STONE REMOVAL ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
RIGHT ATRIAL DILATATION ( 4 FDA reports)
SALMONELLA SEPSIS ( 4 FDA reports)
SCAPULA FRACTURE ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SPINAL CORD INJURY ( 4 FDA reports)
SPINAL CORD PARALYSIS ( 4 FDA reports)
SPINAL FUSION ACQUIRED ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
URETERIC OBSTRUCTION ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANGIODYSPLASIA ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
AORTIC INJURY ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BILIARY ISCHAEMIA ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD INSULIN INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
BONE MARROW OEDEMA ( 3 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
CARCINOID SYNDROME ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CELLS IN URINE ( 3 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLONIC OBSTRUCTION ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CYANOSIS CENTRAL ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
EARLY SATIETY ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
EMPYEMA DRAINAGE ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 3 FDA reports)
EXTUBATION ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTROOESOPHAGEAL CANCER ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMANGIOMA ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERPES OESOPHAGITIS ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILEOSTOMY ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MAXILLOFACIAL SINUS NEOPLASM ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 3 FDA reports)
MENINGIOMA MALIGNANT ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTASES TO BONE MARROW ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTASES TO PANCREAS ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MULTIFOCAL MICRONODULAR PNEUMOCYTE HYPERPLASIA ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PERIOSTITIS ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA HERPES VIRAL ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PROCALCITONIN INCREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PSEUDOCYST ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RADIATION SKIN INJURY ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY FATIGUE ( 3 FDA reports)
RESPIRATORY TRACT OEDEMA ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SEBACEOUS CARCINOMA ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPINAL CORD NEOPLASM ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
THIRST ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUMOUR ASSOCIATED FEVER ( 3 FDA reports)
TUMOUR RUPTURE ( 3 FDA reports)
URETERIC OPERATION ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VITRECTOMY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANTIANGIOGENIC THERAPY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD BICARBONATE ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETERISATION VENOUS ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CHOLANGIOGRAM ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHYLOTHORAX ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CRYSTAL ARTHROPATHY ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DEBRIDEMENT ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
ECZEMA INFECTED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROLYTE DEPLETION ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOMETABOLISM ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMMOBILISATION PROLONGED ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPLANTABLE PLEURAL CATHETER INSERTION ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INSTILLATION SITE PAIN ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL STENT INSERTION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT FLUID DRAINAGE ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKAEMIC INFILTRATION GINGIVA ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO EYE ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTATIC CARCINOID TUMOUR ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NAIL BED INFLAMMATION ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OCULAR SURFACE DISEASE ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OSTEOTOMY ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONITIS CHEMICAL ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RASH FOLLICULAR ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 2 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID ATROPHY ( 2 FDA reports)
TICK-BORNE FEVER ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE PIGMENTATION ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
UROGENITAL ATROPHY ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL FISTULA EXCISION ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTRINGENT THERAPY ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRANIECTOMY ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUODENOSTOMY ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROCAUTERISATION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIDURITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRINOMA ( 1 FDA reports)
GASTRITIS HERPES ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GROWTH HORMONE-PRODUCING PITUITARY TUMOUR ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ITCHING SCAR ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO PITUITARY GLAND ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE FLAP OPERATION ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA METASTATIC ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOCALCIN INCREASED ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERITONEAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMONIA SALMONELLA ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PODAGRA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUS IN STOOL ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL TUBE INSERTION ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBACUTE HEPATIC FAILURE ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VALVULOPLASTY CARDIAC ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR COMPRESSION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL TEST POSITIVE ( 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)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOCAL CORD LIPOINJECTION ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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