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

SOMNOLENCE ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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