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

URINARY TRACT INFECTION ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEATH ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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