| The Food and Drug Administration (FDA) is
reviewing clinical trial data about a potentially serious effect on the
heart from the use of Invirase (saquinavir) in combination with Norvir (ritonavir).
The data suggest that together the two drugs may affect the electrical
activity of the heart.
The changes to the electrical activity of the heart
possibly associated with these drugs, known as prolonged QT or PR intervals,
can be seen on an electrocardiogram (EKG). A prolonged QT interval can
increase the risk for abnormal heart rhythms, including a serious abnormal
rhythm called torsades de pointes. A prolonged PR interval can cause the
electrical signal responsible for generating a heart beat to slow or even
stop; this is known as heart block and can affect how fast the heart is able
to beat.
Invirase and Norvir are antiviral medications given
together to treat HIV infection. Norvir is given at a low dose with Invirase
in order to increase the level of Invirase in the body. This is a process
known as "boosting."
FDA's analysis of these data is ongoing. However,
healthcare professionals should be aware of this potential risk for changes
to the electrical activity of the heart. Invirase and Norvir should not be
used in patients already taking medications known to cause QT interval
prolongation such as Class IA (such as quinidine,) or Class III (such as
amiodarone) antiarrhythmic drugs; or in patients with a history of QT
interval prolongation.
Patients should not stop taking their prescribed antiviral
medications. Patients who are concerned about possible risks associated with
using Invirase and Norvir should talk to their healthcare professional.
This communication is in keeping with FDA's commitment to
inform the public about its ongoing safety review of drugs. The agency will
update the public as soon as this review is complete.
Additional Information for Patients
Patients currently using Invirase should:
- Not stop taking Invirase without talking with their
healthcare professional.
- Discuss any questions or concerns they have about
Invirase with their healthcare professional.
- Review their cardiovascular medical history and current
medications with their healthcare professional to determine if they should
continue using Invirase.
- Report any side effects with Invirase to FDA's MedWatch
program using the information at the bottom of the page.
Additional Information for Healthcare Professionals
FDA recommends that healthcare professionals:
- Not use Invirase in patients with a history of QT
interval prolongation, preexisting conduction system disease, ischemic
heart disease, cardiomyopathy, or underlying structural heart disease.
- Not use Invirase in patients who are currently using
Class IA (such as quinidine) or Class III (such as amiodarone)
antiarrhythmic drugs or other drugs that may prolong the QT or PR
interval.
- Report any adverse events associated with the use of
Invirase to FDA's MedWatch program at 1-800-332-1088, or MedWatch Online.
Data Summary
The study data were submitted by Roche, the manufacturer
of Invirase, based on FDA's request that all manufacturers of protease
inhibitors, including Invirase, conduct a thorough QT study to evaluate the
effect these drugs have on the QT and PR intervals.
The preliminary data show that when Invirase boosted with
Norvir (1000mg/100mg) was given to healthy patients, ages 18 to 55 years,
there was a dose-dependent prolongation of the QT and PR intervals. The
magnitude of the effect and clinical implications of QT and PR interval
prolongation are still being reviewed by FDA.
These findings suggest that some patients using Invirase
boosted with Norvir may be at an increased risk for developing abnormal
heart rhythms. In particular, this risk may be increased in patients using
other medications known to cause QT interval prolongation such as Class IA
and Class III antiarrhythmic drugs or in patients with a history of QT
interval prolongation.
Richard Klein
Office of Special Health Issues
Food and Drug Administration
Kimberly Struble
Division of Antiviral Drug Products
Food and Drug Administration |