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

HYPOTENSION ( 6 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
SWELLING ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
BLISTER ( 4 FDA reports)
DYSPNOEA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
VOMITING ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
THIRST ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
PAIN ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
KWASHIORKOR ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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