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

FATIGUE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
VOMITING ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)

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