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

DIZZINESS ( 4 FDA reports)
PNEUMONIA ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)

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