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Antiretroviral Drug Characteristics, Dosages, Interactions
and
Black-box Warnings
Chinese Version
Updated February, 2009
Hsin-Yun Sun, M.D. Chia-Jui Yang, M.D.
The tables in this chapter are modified from the November 3, 2008
Guidelines for the use of antiretroviral agents in HIV-1-infected adults and
adolescents by Department of Health and Human Services (1).
These tables have been reformatted from the original and revised so that they
are easier to view and printout. Information relevant for the clinician has been
emphasized.
Tables 1 through 4 summarize the formulation, dosing recommendations, food
effect, and specific adverse events of nucleoside reverse trascriptase (NRTIs),
non-nucleoside reverse transcriptase inhibitors (NNRTIs), protease inhibitors
(PIs), fusion inhibitors, CCR5 antagonists, and integrase inhibitors.
Table 5 contains dosing recommendations in
patients with renal and hepatic insufficiency. Tables 6 through 9
describe adverse events and black-box warnings of antiretroviral therapy and
HIV-related drugs with overlapping toxicity. Tables 10
through 12 list the drug interactions among
antiretrovirals and other drugs. The highlighted words in yellow are the changes
made in the current version as compared with the January 29, 2008 version of the
guidelines.
Table 1. Characteristics
of Nucleoside Reverse Transcriptase Inhibitors (NRTIs) (Updated
November 3, 2008)a
(PDF
Version)
Table 2.
Characteristics of Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs)
(Updated
November 3, 2008)a
(PDF
Version)
Table 3. Characteristics
of Protease Inhibitors (PIs) (Updated
November
3, 2008)a
(PDF
Version)
Table 4.
Characteristics of Entry Inhibitors, CCR5 Antagonist and Integrase Inhibitor
(Updated
January
29, 2008)
(PDF
Version)
Table
5. Antiretroviral Dosing Recommendations in
Patients with Renal or Hepatic Insufficiency (Updated
November 3, 2008)a
(PDF
Version)
Table 6a.
Potentially Life-Threatening Adverse Events. (Updated
January 29, 2008)
(PDF
Version)
Table 6b.
Potentially Serious Adverse Events (Updated
January 29, 2008)
(PDF
Version)
Table 6c.
Adverse Events With Potential Long-Term Complications (Updated
January 29, 2008)
(PDF
Version)
Table
6d. Adverse Effects Compromising Quality of Life and/or With Potential Impact on
Medication Adherence (Updated
January 29, 2008)
(PDF
Version)
Table 7.
Antiretroviral Therapy-Associated Adverse Effects and Management Recommendations
(Updated
November 3, 2008)a
(PDF
Version)
Table 8.
HIV-Related Drugs With Overlapping Toxicities (Updated
January 29, 2008) (PDF
Version)
Table 9. Adverse Drug Reactions and Related “Black Box
Warnings” in Product Labeling for Antiretroviral Agents
(Updated January 29, 2008)
(PDF
Version)
Table 10a Drugs
That Should Not Be Used With PI, NNRTI, or CCR5 Antagonist Antiretrovirals
(Updated
November 3, 2008)a
(PDF
Version)
Table
10b. Drugs That Should Not Be Used With PI, NNRTI, or CCR5 Antagonist
Antiretrovirals (continued) (PDF
Version)
Table
11a. Drug Interactions Between Protease Inhibitors (PIs) and Other Drugs
(Updated November 3, 2008)a
(PDF
Version)
Table 11b. Drug Interactions Between NNRTIs and Other Drugs (Updated November 3,
2008)
a (PDF
Version)
Table 11c. Drug Interactions Between NRTIs and Other Drugs (including
antiretroviral agents) (Updated November 3, 2008)
a
(PDF
Version)
Table
11d. Drug
Interactions Between CCR5 Antagonists and Other Drugs (Updated November 3, 2008)a (PDF
Version)
Table 11e. Drug Interactions Between Antiretrovirals
and Other Drugs: Integrase Inhibitors (Updated November 3, 2008) (PDF
Version)
Table
12a. Drug Effects
on Concentration of PIs
(Updated
November 3, 2008)
a (PDF
Version)
Table
12b. Drug Effects on Concentration of NNRTIs and Maraviroc
(Updated
November 3, 2008)
a (PDF
Version)
REFERENCES
1. Panel on Antiretroviral Guidelines for Adult and
Adolescents. Guidelines for the use of antiretroviral agents in HIV-1-infected
adults and adolescents. Department of Health and Human Services. November 3,
2008,
1-146. Available at
http://www.aidsinfo.nih.gov/ContentFiles/AdultandAdolescentGL.pdf.
Accessed on December 1, 2008
[Table 13-16; Appendix Table 2-8].
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