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

DRUG INTERACTION ( 6 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERFORMANCE FEAR ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)

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