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

DEATH ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
APNOEA ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
TRYPTASE INCREASED ( 3 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 3 FDA reports)
SNORING ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
FLUSHING ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)

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