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

SEPSIS ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
SHOCK ( 4 FDA reports)
ASCITES ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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