The Food and Drug Administration is announcing that the following HIV drug labels have been updated to include Latuda (lurasidone), an antipsychotic used to treat adult patients with depressive episodes in bipolar I disorder (bipolar depression), and schizophrenia, in adults. Lurasidone was added to Section 4 of the label, Contraindications, due to the potential for serious and/or life-threatening reactions to the following product labels:
Aptivus (tipranavir)
Crixivan (indinavir)
Genvoya (elvitegravir, cobicistat, emtricitabine, and tenofovir alafenamide)
Invirase (saquinavir)
Kaletra (lopinavir/ritonavir)
Lexiva (fosamprenavir) note: lurasidone is contraindicated due to the potential for serious and/or life-threatening reactions if Lexiva is coadministered with ritonavir.
Norvir (ritonavir)
Prezista (darunavir)
Reyataz (atazanavir) – note: lurasidone is contraindicated due to the potential for serious and/or life-threatening reactions if Reyataz is coadministered with ritonavir.
Stribild (elvitegravir, cobicistat, emtricitabine, tenofovir disoproxil fumarate)
Viracept (nelfinavir)
Of note, Evotaz (atazanavir/cobicistat) and Prezcobix (darunavir/cobicistat) labels already include lurasidone as a contraindicated medication in section 4.
Richard Klein
Office of Health and Constituent Affairs
Food and Drug Administration
Office of Health and Constituent Affairs
Food and Drug Administration
Kimberly Struble
Division of Antiviral Products
Food and Drug Administration
Division of Antiviral Products
Food and Drug Administration
Steve Morin
Office of Health and Constituent Affairs
Food and Drug Administration
Office of Health and Constituent Affairs
Food and Drug Administration
For more information about the HIV Liaison Program visit the FDA Patient Network
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