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

ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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