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

ATRIAL FIBRILLATION ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
OSTEOMYELITIS CHRONIC ( 5 FDA reports)
PERICARDITIS ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
PERICARDITIS INFECTIVE ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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