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

HYPERTENSION ( 131 FDA reports)
PYREXIA ( 126 FDA reports)
RENAL IMPAIRMENT ( 121 FDA reports)
BLOOD CREATININE INCREASED ( 118 FDA reports)
DIARRHOEA ( 116 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 115 FDA reports)
ANAEMIA ( 106 FDA reports)
DECREASED APPETITE ( 105 FDA reports)
NAUSEA ( 99 FDA reports)
DYSPNOEA ( 95 FDA reports)
PNEUMONIA ( 93 FDA reports)
CARDIAC FAILURE ( 89 FDA reports)
INTERSTITIAL LUNG DISEASE ( 80 FDA reports)
VOMITING ( 80 FDA reports)
PLEURAL EFFUSION ( 78 FDA reports)
RENAL FAILURE ACUTE ( 78 FDA reports)
PLATELET COUNT DECREASED ( 75 FDA reports)
DIZZINESS ( 73 FDA reports)
MALAISE ( 73 FDA reports)
OEDEMA PERIPHERAL ( 71 FDA reports)
RENAL FAILURE ( 66 FDA reports)
DEATH ( 65 FDA reports)
RASH ( 65 FDA reports)
HAEMOGLOBIN DECREASED ( 61 FDA reports)
FALL ( 60 FDA reports)
PAIN ( 59 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 58 FDA reports)
BLOOD UREA INCREASED ( 58 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 57 FDA reports)
CEREBRAL INFARCTION ( 55 FDA reports)
CONDITION AGGRAVATED ( 55 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 54 FDA reports)
MYOCARDIAL INFARCTION ( 54 FDA reports)
BLOOD PRESSURE DECREASED ( 53 FDA reports)
HYPOGLYCAEMIA ( 53 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 53 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 51 FDA reports)
HYPERKALAEMIA ( 51 FDA reports)
INSOMNIA ( 51 FDA reports)
LIVER DISORDER ( 51 FDA reports)
ARTHRALGIA ( 50 FDA reports)
ASCITES ( 48 FDA reports)
BLOOD PRESSURE INCREASED ( 47 FDA reports)
ATRIAL FIBRILLATION ( 45 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 45 FDA reports)
CONSTIPATION ( 45 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 45 FDA reports)
ASTHENIA ( 44 FDA reports)
BACK PAIN ( 43 FDA reports)
DIABETES MELLITUS ( 43 FDA reports)
DEHYDRATION ( 42 FDA reports)
HYPOTENSION ( 41 FDA reports)
FATIGUE ( 40 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 38 FDA reports)
LOSS OF CONSCIOUSNESS ( 38 FDA reports)
ANXIETY ( 37 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 37 FDA reports)
CARDIAC ARREST ( 35 FDA reports)
ABDOMINAL PAIN UPPER ( 34 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 34 FDA reports)
HEADACHE ( 34 FDA reports)
HYPERURICAEMIA ( 34 FDA reports)
PAIN IN EXTREMITY ( 34 FDA reports)
PROTEINURIA ( 34 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 32 FDA reports)
PRURITUS ( 32 FDA reports)
ANGINA PECTORIS ( 31 FDA reports)
DRUG ERUPTION ( 31 FDA reports)
GAIT DISTURBANCE ( 31 FDA reports)
HYPERGLYCAEMIA ( 31 FDA reports)
HYPOKALAEMIA ( 31 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 31 FDA reports)
RENAL FAILURE CHRONIC ( 31 FDA reports)
ANOREXIA ( 30 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 30 FDA reports)
CHEST PAIN ( 30 FDA reports)
DIALYSIS ( 30 FDA reports)
HYPOAESTHESIA ( 30 FDA reports)
URTICARIA ( 30 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 29 FDA reports)
DYSARTHRIA ( 29 FDA reports)
MULTI-ORGAN FAILURE ( 29 FDA reports)
RHABDOMYOLYSIS ( 29 FDA reports)
WEIGHT INCREASED ( 29 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 28 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 28 FDA reports)
BRADYCARDIA ( 28 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 27 FDA reports)
HYPONATRAEMIA ( 27 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 26 FDA reports)
HYPERLIPIDAEMIA ( 26 FDA reports)
PANCYTOPENIA ( 26 FDA reports)
THROMBOCYTOPENIA ( 26 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
BLOOD GLUCOSE INCREASED ( 25 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 25 FDA reports)
DEPRESSION ( 25 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 25 FDA reports)
OSTEOARTHRITIS ( 25 FDA reports)
HAEMATEMESIS ( 24 FDA reports)
HAEMATOCRIT DECREASED ( 24 FDA reports)
INJURY ( 24 FDA reports)
MUSCULAR WEAKNESS ( 24 FDA reports)
RHEUMATOID ARTHRITIS ( 24 FDA reports)
STOMATITIS ( 24 FDA reports)
WEIGHT DECREASED ( 24 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 24 FDA reports)
ERYTHEMA ( 23 FDA reports)
HERPES ZOSTER ( 23 FDA reports)
OEDEMA ( 23 FDA reports)
OSTEONECROSIS ( 23 FDA reports)
CONVULSION ( 22 FDA reports)
DISEASE PROGRESSION ( 22 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 22 FDA reports)
UNEVALUABLE EVENT ( 22 FDA reports)
CARDIO-RESPIRATORY ARREST ( 21 FDA reports)
CHEST DISCOMFORT ( 21 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
DYSURIA ( 21 FDA reports)
OSTEOMYELITIS ( 21 FDA reports)
PROSTATITIS ( 21 FDA reports)
PULMONARY OEDEMA ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 21 FDA reports)
ABDOMINAL DISTENSION ( 20 FDA reports)
HEPATIC ENCEPHALOPATHY ( 20 FDA reports)
SOMNOLENCE ( 20 FDA reports)
TINNITUS ( 20 FDA reports)
TREMOR ( 20 FDA reports)
VISION BLURRED ( 20 FDA reports)
BLOOD SODIUM DECREASED ( 19 FDA reports)
CEREBROVASCULAR ACCIDENT ( 19 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
DYSGEUSIA ( 19 FDA reports)
INFECTION ( 19 FDA reports)
NOCTURIA ( 19 FDA reports)
PNEUMONIA BACTERIAL ( 19 FDA reports)
BLOOD POTASSIUM INCREASED ( 18 FDA reports)
BLOOD URIC ACID INCREASED ( 18 FDA reports)
CELLULITIS ( 18 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 18 FDA reports)
COUGH ( 18 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 18 FDA reports)
EMOTIONAL DISTRESS ( 18 FDA reports)
GENERALISED OEDEMA ( 18 FDA reports)
HAEMODIALYSIS ( 18 FDA reports)
HALLUCINATION ( 18 FDA reports)
MELAENA ( 18 FDA reports)
NEOPLASM MALIGNANT ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
MYALGIA ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
OVERDOSE ( 17 FDA reports)
RENAL DISORDER ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
AORTIC DISSECTION ( 16 FDA reports)
ARRHYTHMIA ( 16 FDA reports)
ENCEPHALOPATHY ( 16 FDA reports)
FEBRILE NEUTROPENIA ( 16 FDA reports)
FEELING ABNORMAL ( 16 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 16 FDA reports)
GASTRITIS ( 16 FDA reports)
HYPOXIA ( 16 FDA reports)
IMPAIRED HEALING ( 16 FDA reports)
MUSCULOSKELETAL PAIN ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
OXYGEN SATURATION DECREASED ( 16 FDA reports)
PROTEIN URINE PRESENT ( 16 FDA reports)
RENAL CELL CARCINOMA ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
SWELLING ( 16 FDA reports)
THROMBOSIS ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
CARDIAC FAILURE CHRONIC ( 15 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
DECREASED ACTIVITY ( 15 FDA reports)
EATING DISORDER ( 15 FDA reports)
FEMUR FRACTURE ( 15 FDA reports)
GASTROINTESTINAL NECROSIS ( 15 FDA reports)
JAUNDICE ( 15 FDA reports)
LEUKOPENIA ( 15 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
PANCREATITIS ACUTE ( 15 FDA reports)
RECTAL HAEMORRHAGE ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
TOXIC SKIN ERUPTION ( 15 FDA reports)
VENTRICULAR FIBRILLATION ( 15 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
ANGIOEDEMA ( 14 FDA reports)
ASTHMA ( 14 FDA reports)
CATARACT ( 14 FDA reports)
CEREBRAL HAEMORRHAGE ( 14 FDA reports)
FACE OEDEMA ( 14 FDA reports)
HAEMATOMA ( 14 FDA reports)
HEPATIC FAILURE ( 14 FDA reports)
JOINT SWELLING ( 14 FDA reports)
OROPHARYNGEAL PAIN ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
REFLUX OESOPHAGITIS ( 14 FDA reports)
SHOCK ( 14 FDA reports)
SWELLING FACE ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 13 FDA reports)
EXOSTOSIS ( 13 FDA reports)
FEAR ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
INTESTINAL OBSTRUCTION ( 13 FDA reports)
MITRAL VALVE INCOMPETENCE ( 13 FDA reports)
NEPHROTIC SYNDROME ( 13 FDA reports)
PNEUMONIA ASPIRATION ( 13 FDA reports)
PULMONARY CONGESTION ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
URINE OUTPUT DECREASED ( 13 FDA reports)
DIABETIC NEPHROPATHY ( 12 FDA reports)
DYSLIPIDAEMIA ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
ENTEROCOLITIS ( 12 FDA reports)
GASTRIC ULCER ( 12 FDA reports)
GASTROINTESTINAL PERFORATION ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
PRINZMETAL ANGINA ( 12 FDA reports)
RESTLESSNESS ( 12 FDA reports)
SEPTIC SHOCK ( 12 FDA reports)
SHUNT MALFUNCTION ( 12 FDA reports)
STRESS ( 12 FDA reports)
SUDDEN DEATH ( 12 FDA reports)
THROMBOPHLEBITIS ( 12 FDA reports)
ALOPECIA ( 11 FDA reports)
CARDIAC DISORDER ( 11 FDA reports)
COMA ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
FUNGAL INFECTION ( 11 FDA reports)
IRON DEFICIENCY ANAEMIA ( 11 FDA reports)
LYMPHOMA ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
NECK PAIN ( 11 FDA reports)
NEPHROGENIC ANAEMIA ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
PARALYSIS ( 11 FDA reports)
PARALYSIS FLACCID ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
SHUNT OCCLUSION ( 11 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
ANHEDONIA ( 10 FDA reports)
CARDIOGENIC SHOCK ( 10 FDA reports)
DEPRESSED MOOD ( 10 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
EMPHYSEMA ( 10 FDA reports)
EOSINOPHIL COUNT INCREASED ( 10 FDA reports)
GASTROENTERITIS ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HEPATIC STEATOSIS ( 10 FDA reports)
HEPATITIS B ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
INFLAMMATION ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
METASTATIC NEOPLASM ( 10 FDA reports)
NEPHROPATHY ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
RENAL INJURY ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
TOOTH EXTRACTION ( 10 FDA reports)
TOOTHACHE ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
ABDOMINAL PAIN LOWER ( 9 FDA reports)
ACTINOMYCOSIS ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
AMNESIA ( 9 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 9 FDA reports)
ASPIRATION PLEURAL CAVITY ( 9 FDA reports)
BONE DEBRIDEMENT ( 9 FDA reports)
BONE DISORDER ( 9 FDA reports)
BREATH ODOUR ( 9 FDA reports)
CAROTID ARTERY OCCLUSION ( 9 FDA reports)
CEREBRAL ATROPHY ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
DENTAL OPERATION ( 9 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
DYSSTASIA ( 9 FDA reports)
ENDODONTIC PROCEDURE ( 9 FDA reports)
EPIDURAL LIPOMATOSIS ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 9 FDA reports)
HAEMORRHOIDS ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HEPATITIS FULMINANT ( 9 FDA reports)
HERNIA REPAIR ( 9 FDA reports)
HYPERAMYLASAEMIA ( 9 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
LARGE INTESTINE CARCINOMA ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
MYOCARDIAL ISCHAEMIA ( 9 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
ORAL DISORDER ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PERICARDIAL EFFUSION ( 9 FDA reports)
PERIODONTAL OPERATION ( 9 FDA reports)
POOR PERSONAL HYGIENE ( 9 FDA reports)
PURULENCE ( 9 FDA reports)
SUBCUTANEOUS ABSCESS ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 9 FDA reports)
TOOTH IMPACTED ( 9 FDA reports)
VASCULAR OPERATION ( 9 FDA reports)
VENA CAVA FILTER INSERTION ( 9 FDA reports)
ABASIA ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BLOOD GLUCOSE DECREASED ( 8 FDA reports)
BONE MARROW TOXICITY ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DYSLALIA ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
GOUT ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HYPOPHAGIA ( 8 FDA reports)
ILEUS ( 8 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
LACUNAR INFARCTION ( 8 FDA reports)
LARGE INTESTINAL ULCER ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LUNG OPERATION ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
NEPHRITIS ( 8 FDA reports)
ORAL HERPES ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
SINUS DISORDER ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
SPINAL CORD DISORDER ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
WHEELCHAIR USER ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
ANGIOPATHY ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BASEDOW'S DISEASE ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 7 FDA reports)
CAROTID ARTERY STENOSIS ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
CUTANEOUS VASCULITIS ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
DRY EYE ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPERTHYROIDISM ( 7 FDA reports)
ISCHAEMIC HEPATITIS ( 7 FDA reports)
LOBAR PNEUMONIA ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PARESIS ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
PLEURISY ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
PSORIASIS ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ACUTE SINUSITIS ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CATHETER SITE PAIN ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CHONDROCALCINOSIS ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
HEPATIC ISCHAEMIA ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
INCOHERENT ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MENISCUS LESION ( 6 FDA reports)
MENOPAUSAL SYMPTOMS ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
NIGHT SWEATS ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PARACENTESIS ( 6 FDA reports)
PARONYCHIA ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PERITONEAL PERMEABILITY INCREASED ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
POLYNEUROPATHY ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SYNOVIAL CYST ( 6 FDA reports)
THORACIC CAVITY DRAINAGE ( 6 FDA reports)
UMBILICAL CORD AROUND NECK ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VERTIGO POSITIONAL ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BILE DUCT CANCER ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
COLITIS COLLAGENOUS ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CYST ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DERMATOMYOSITIS ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DROWNING ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ELECTROLYTE DEPLETION ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
FANCONI SYNDROME ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
JAW FRACTURE ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PLEURODESIS ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
PURPURA ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
VIITH NERVE PARALYSIS ( 5 FDA reports)
ACCIDENT ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AGITATION ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANURIA ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 4 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BENIGN NEOPLASM OF SKIN ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CATARACT CORTICAL ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERCREATININAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
IMPAIRED FASTING GLUCOSE ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
KNEE DEFORMITY ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
RETINAL DEGENERATION ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
VENTRICULAR ARRHYTHMIA ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE EROSION ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CLEFT PALATE ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL HAEMATOMA ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NASAL SEPTUM PERFORATION ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY HILUM MASS ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STILL'S DISEASE ADULT ONSET ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VERTIGO LABYRINTHINE ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLIGHTED OVUM ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRANIAL NEUROPATHY ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVAL HYPOPLASIA ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERPES DERMATITIS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPNAGOGIC HALLUCINATION ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODULE ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
ORAL FIBROMA ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 2 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RADIATION NECROSIS ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCEDOSPORIUM INFECTION ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYROIDITIS CHRONIC ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AIRWAY BURNS ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPHARYNGEAL NEOPLASM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASOPHARYNGEAL CANCER RECURRENT ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
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NEPHROPATHY TOXIC ( 1 FDA reports)
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NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
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NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OPTIC PATHWAY INJURY ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAESTHESIA CIRCUMORAL ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENETRATING ABDOMINAL TRAUMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CANCER STAGE I ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENSION ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEAL FISTULA ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN WALL HYPERTROPHY ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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