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

HYPOGLYCAEMIA ( 7 FDA reports)
HYPERTENSION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
PAIN ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
DIABETIC FOETOPATHY ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ACETONAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
ABASIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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