Abacavir (Ziagen)
Pharmacology
- Nucleoside Reverse Transcriptase Inhibitor
Adverse Effects
General Adverse Effects
Abacavir Hypersensitivity Reaction
- Epidemiology
- Relationship to Abacavir Dosing Frequency
- Hypersensitivity reaction may be more severe with once daily dosing
- Risk Factors
- HLA B*5701 -> can screen for this prior to abacavir administration
- Temporal Relationship to Abacavir Administration
- During Abacavir Therapy
- Occurs within few days-6 weeks (median = 11 days) after start of therapy
- Symptoms usually worsen with continuation of therapy
- After Re-Introduction of Abacavir
- Occurs within hours of re-introduction after an interruption in therapy
- Particularly severe reactions can occur with re-challenge in patients with a previous hypersensitivity reaction
- Physiology
- Hypersensitivity (immune)-mediated reaction
- Clinical
- General: 98% of cases have fever or rash or both
- Fever (80%) (see Fever)
- Rash (70%)
- Malaise (40%)
- Myalgias
- Arthralgias
- Lymphadenopathy
- GI (50%)
- Pulmonary (18%)
- Renal
- Cardiac
- Neurologic
- Treatment
- Immediate Withdrawal of Drug: avoid re-challenge with drug in the future if hypersensitivity reaction occurs
- Supportive Care
- Prognosis
- Death: may occur in severe cases
References
- HLA-B*5701 Screening for Hypersensitivity to Abacavir. N Engl J Med 2008; 358:568-579