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

WRONG DRUG ADMINISTERED ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
DEATH ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
FALL ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
CONSTIPATION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)

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