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FEMUR FRACTURE ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
BONE METABOLISM DISORDER ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
MALAISE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PERIPHERAL NERVE PALSY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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