lunes, 18 de septiembre de 2017

Press Announcements > FDA approves new treatment for adults with relapsed follicular lymphoma

Press Announcements > FDA approves new treatment for adults with relapsed follicular lymphoma

The Division of Drug Information (DDI) - serving the public by providing information on human drug products and drug product regulation by FDA.


The U.S. Food and Drug Administration granted accelerated approval to Aliqopa (copanlisib) for the treatment of adults with relapsed follicular lymphoma who have received at least two prior treatments known as systemic therapies.

Common side effects of Aliqopa include high blood sugar levels (hyperglycemia), diarrhea, decreased general strength and energy, high blood pressure (hypertension), low levels of certain white blood cells (leukopenia, neutropenia), nausea, lower respiratory tract infections, and low levels of blood platelets (thrombocytopenia).Serious side effects include infections, high blood sugar levels (hyperglycemia), high blood pressure (hypertension), inflammation of the lung tissue (non-infectious pneumonitis), low levels of certain white blood cells (neutropenia), and severe skin reactions. Women who are pregnant or breastfeeding should not take Aliqopa because it may cause harm to a developing fetus or newborn baby.

For more information, please visit: Aliqopa.

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