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

PULMONARY OEDEMA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
TACHYCARDIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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