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

HYPERTENSION ( 10 FDA reports)
NAUSEA ( 9 FDA reports)
DIARRHOEA ( 7 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
RENAL FAILURE ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
DEATH ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ASCITES ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
MARCHIAFAVA-BIGNAMI DISEASE ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
BISPECTRAL INDEX DECREASED ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARESIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
COUGH ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
MALAISE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use