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

SURGERY ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
OMENTUM NEOPLASM ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 3 FDA reports)
INCISIONAL HERNIA REPAIR ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
METASTATIC CARCINOID TUMOUR ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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