Παρασκευή 12 Σεπτεμβρίου 2008

FDA: Οι αναστολείς TNF αυξάνουν τον κίνδυνο ανάπτυξης επιθετικών μυκυσιακών λοιμώξεων που μπορούν να οδηγήσουν στο θάνατο

ROCKVILLE, Md -- September 4, 2008 –


The US Food and Drug Administration (FDA) 

is notifying healthcare professionals that histoplasmosis and other invasive 

fungal infections are not consistently recognised in 

patients taking tumor necrosis factor-alpha blockers (TNF blockers)

certolizumab pegol (Cimzia), etanercept (Enbrel), adalimumab (Humira), and infliximab (Remicade)

This has resulted in delays in appropriate treatment, sometimes resulting in death.

The FDA has received reports of patients developing pulmonary and disseminated

histoplasmosis, coccidioidomycosis, blastomycosis and other opportunistic infections while taking TNF blockers.


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