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

SINUS BRADYCARDIA ( 5 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
TREMOR ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
COUGH ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COMA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)

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