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

NAUSEA ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SHOCK ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
VOMITING ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
SCAR ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FATIGUE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)

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