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

EPISTAXIS ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MURDER ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RALES ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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