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

COUGH ( 9 FDA reports)
VOMITING ( 9 FDA reports)
PYREXIA ( 8 FDA reports)
NAUSEA ( 7 FDA reports)
DIARRHOEA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CROUP INFECTIOUS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FISTULA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
INFANTILE SPITTING UP ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 2 FDA reports)
APNOEA ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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