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

DRUG INTERACTION ( 199 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 116 FDA reports)
CARDIAC FAILURE ( 91 FDA reports)
ANAEMIA ( 78 FDA reports)
FALL ( 68 FDA reports)
RENAL FAILURE ( 61 FDA reports)
ATRIAL FIBRILLATION ( 53 FDA reports)
FATIGUE ( 53 FDA reports)
VOMITING ( 53 FDA reports)
DIZZINESS ( 51 FDA reports)
DYSPNOEA ( 49 FDA reports)
RENAL FAILURE ACUTE ( 49 FDA reports)
PYREXIA ( 48 FDA reports)
HAEMATOMA ( 46 FDA reports)
NAUSEA ( 44 FDA reports)
DEATH ( 43 FDA reports)
HYPOTENSION ( 43 FDA reports)
MALAISE ( 41 FDA reports)
HAEMOGLOBIN DECREASED ( 40 FDA reports)
PULMONARY EMBOLISM ( 39 FDA reports)
CARDIOGENIC SHOCK ( 38 FDA reports)
DIARRHOEA ( 38 FDA reports)
OVERDOSE ( 38 FDA reports)
ARRHYTHMIA ( 36 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 35 FDA reports)
PNEUMONIA ( 35 FDA reports)
DRUG INEFFECTIVE ( 34 FDA reports)
ASTHENIA ( 32 FDA reports)
HYPERKALAEMIA ( 32 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 30 FDA reports)
SYNCOPE ( 28 FDA reports)
LOSS OF CONSCIOUSNESS ( 27 FDA reports)
OEDEMA PERIPHERAL ( 27 FDA reports)
BLOOD CREATININE INCREASED ( 26 FDA reports)
BRADYCARDIA ( 23 FDA reports)
PROTHROMBIN TIME PROLONGED ( 23 FDA reports)
THROMBOSIS ( 23 FDA reports)
WEIGHT DECREASED ( 23 FDA reports)
CONSTIPATION ( 22 FDA reports)
DISORIENTATION ( 22 FDA reports)
HAEMATURIA ( 22 FDA reports)
CONFUSIONAL STATE ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
RHABDOMYOLYSIS ( 21 FDA reports)
HYPONATRAEMIA ( 20 FDA reports)
MELAENA ( 20 FDA reports)
ABDOMINAL PAIN ( 19 FDA reports)
DEHYDRATION ( 19 FDA reports)
HEPATIC FAILURE ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
PALLOR ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
PAIN ( 18 FDA reports)
THROMBOCYTOPENIA ( 18 FDA reports)
VENTRICULAR FIBRILLATION ( 18 FDA reports)
EPISTAXIS ( 17 FDA reports)
HEADACHE ( 17 FDA reports)
ISCHAEMIC STROKE ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
CHEST PAIN ( 16 FDA reports)
DIPLOPIA ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
HAEMORRHAGE ( 16 FDA reports)
HEPATOTOXICITY ( 16 FDA reports)
HYPOGLYCAEMIA ( 16 FDA reports)
MYOCARDIAL ISCHAEMIA ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
STAPHYLOCOCCAL INFECTION ( 16 FDA reports)
VENTRICULAR ARRHYTHMIA ( 16 FDA reports)
VENTRICULAR TACHYCARDIA ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 15 FDA reports)
CONVULSION ( 15 FDA reports)
COUGH ( 15 FDA reports)
HAEMATEMESIS ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
CARDIO-RESPIRATORY ARREST ( 14 FDA reports)
COAGULOPATHY ( 14 FDA reports)
DELIRIUM ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
MUSCULAR WEAKNESS ( 14 FDA reports)
PARAESTHESIA ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
SUBDURAL HAEMATOMA ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
HALLUCINATION ( 12 FDA reports)
HEPATIC ENZYME INCREASED ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 12 FDA reports)
PULMONARY OEDEMA ( 12 FDA reports)
RESPIRATORY TRACT INFECTION ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 11 FDA reports)
BLOOD UREA INCREASED ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CONTUSION ( 11 FDA reports)
DEMENTIA ( 11 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
DYSURIA ( 11 FDA reports)
HYPERGLYCAEMIA ( 11 FDA reports)
MYALGIA ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
SUDDEN DEATH ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
TREMOR ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
LEUKOCYTOSIS ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 10 FDA reports)
RASH ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
TOXIC SKIN ERUPTION ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
FEMUR FRACTURE ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HALLUCINATION, VISUAL ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
ILEUS ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
STATUS EPILEPTICUS ( 9 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
ANXIETY ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
HAEMODYNAMIC INSTABILITY ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
INFANTILE SPITTING UP ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 7 FDA reports)
ALOPECIA ( 7 FDA reports)
APHASIA ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
FRACTURE ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PLATELET COUNT INCREASED ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
BLADDER CANCER ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 6 FDA reports)
CAST APPLICATION ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
EMBOLISM ARTERIAL ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
METASTASES TO LIVER ( 6 FDA reports)
MUSCLE HAEMORRHAGE ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
WOUND INFECTION ( 6 FDA reports)
ACNE ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ASCITES ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
COMA ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 5 FDA reports)
GOITRE ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYDROTHORAX ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
LEG AMPUTATION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
POOR PERSONAL HYGIENE ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
TERMINAL STATE ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
COAGULATION TEST ABNORMAL ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ENDOPHTHALMITIS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
ORAL FUNGAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PENILE NECROSIS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SPONTANEOUS HAEMATOMA ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
ULCER ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VESTIBULAR DISORDER ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMNIOTIC FLUID VOLUME ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BILIARY CIRRHOSIS ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COAGULATION TIME SHORTENED ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORNEAL ABSCESS ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRESSLER'S SYNDROME ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
HYPERALDOSTERONISM ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NASAL NECROSIS ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PENILE VEIN THROMBOSIS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL CANCER STAGE 0 ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APNOEA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CERVIX HAEMATOMA UTERINE ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE TYPE STAGE UNSPECIFIED ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROGENIC SHOCK ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
OSTEOARTHROPATHY ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHAEHYPHOMYCOSIS ( 2 FDA reports)
PHARYNGEAL HAEMATOMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROMINENT EPICANTHAL FOLDS ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE AMYLASE INCREASED ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR SKIN DISORDER ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACANTHOMA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
AMPUTATION OF PENIS ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL CANCER RECURRENT ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FISTULA INFECTION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL HAEMORRHAGE ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHANGIOPATHY ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS NONINFECTIVE ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STOMA CARE ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
ULTRASOUND ABDOMEN NORMAL ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERAL NECROSIS ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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