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

GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
CHEST PAIN ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
ASTHMA ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NAUSEA ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
FALL ( 2 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
COUGH ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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