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

HYPONATRAEMIA ( 5 FDA reports)
FALL ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
RETROGRADE P-WAVES ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
INFLAMMATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUPERFICIAL SIDEROSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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