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

CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)

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