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

ASTHENIA ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DYSPNOEA AT REST ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEPATITIS C ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)

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