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HIV/AIDS Treatment and Care : Clinical protocols for the European ...

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190<br />

<strong>HIV</strong>/<strong>AIDS</strong> TREATMENT AND CARE CLINICAL PROTOCOLS FOR THE WHO EUROPEAN REGION<br />

O<strong>the</strong>r medications Use<br />

Interaction with<br />

methadone<br />

Fluconazole Antifungal Increased methadone levels<br />

(35%).<br />

<strong>Clinical</strong> significance<br />

unknown, although cases<br />

requiring dose reduction<br />

reported.<br />

No signs of methadone<br />

toxicity reported.<br />

O<strong>the</strong>r azole antifungal<br />

antibiotics may potentially<br />

influence opioid toxicity.<br />

e.g. itraconzale, ketoconazole,<br />

voriconazole.<br />

Interferon-α + ribavirin Anti hepatitis C treatment Side-effects can mimic opioid<br />

withdrawal symptoms<br />

<strong>and</strong> methadone dose is<br />

often increased.<br />

In a study of HCV patients<br />

concomitantly receiving<br />

methadone <strong>and</strong> peginterferon-alfa<br />

2a methadone<br />

levels increased 10-15%.<br />

<strong>Clinical</strong> significance unknown.<br />

Patients should be<br />

monitored <strong>for</strong> signs <strong>and</strong><br />

symptoms <strong>for</strong> methadone<br />

toxicity.<br />

Phenobarbital<br />

(barbiturate)<br />

Anticonvulsant, sedative Decreases methadone<br />

levels, often sharply.<br />

May cause withdrawal.<br />

A methadone dosage increase<br />

may be required.<br />

Phenytoin Anticonvulsant Decreases methadone<br />

levels, often sharply.<br />

May cause withdrawal.<br />

A methadone dosage increase<br />

may be required.<br />

Rifabutin Anti-mycobacterial treatment<br />

of pulmonary TB<br />

No change in methadone<br />

levels.<br />

Mild narcotic withdrawal<br />

symptoms.<br />

Interaction with ARV<br />

medications<br />

Potential <strong>for</strong> bi-directional<br />

inhibition between some<br />

azole antifungal antibiotics<br />

<strong>and</strong> PIs. Monitor <strong>for</strong> toxicities<br />

<strong>and</strong> dose adjustments.<br />

Toxicity <strong>and</strong> anti-fugal<br />

outcomes observed with<br />

NNRTIs.<br />

Refer to Protocol 1, Patient<br />

evaluation <strong>and</strong> antiretroviral<br />

treatment in adults <strong>and</strong><br />

adolescents.<br />

Hepatitis C infection can<br />

aggravate <strong>the</strong> hepatotoxicity<br />

of several ARV regimens.<br />

(Refer to Protocol 6,<br />

Management of hepatitis C<br />

<strong>and</strong> <strong>HIV</strong> coinfection.)<br />

Barbiturates such as phenobarbital<br />

are potent inducers<br />

of CYP3A4. Clinicians<br />

should consider avoiding<br />

concurrent administration<br />

of o<strong>the</strong>r potent inducers<br />

(e.g. EFV <strong>and</strong> NVP) in<br />

patients misusing barbiturates.<br />

May decrease NFV concentrations.<br />

Some interactions (refer to<br />

Protocol 1, Patient evaluation<br />

<strong>and</strong> antiretroviral<br />

treatment in adults <strong>and</strong><br />

adolescents.) Monitor <strong>for</strong><br />

toxicities <strong>and</strong> dose adjustments.<br />

Some interactions (refer to<br />

Protocol 1, Patient evaluation<br />

<strong>and</strong> antiretroviral<br />

treatment in adults <strong>and</strong><br />

adolescents) but rifabutin<br />

may be a preferred option<br />

<strong>for</strong> <strong>the</strong> treatment of pulmonary<br />

TB as an alternative<br />

to rifampicin. Monitor <strong>for</strong><br />

toxicities <strong>and</strong> dose adjustments.

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