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ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
TREMOR ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DEATH ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)

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