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262 PART 6 Antiparasitic Drugs<br />

ability of the malaria parasite to detoxify hemoglobin<br />

metabolites. Primaquine appears to affect<br />

parasitic mitochondrial function.<br />

Spectrum<br />

Protozoa (activity variable by region): Plasmodium<br />

falciparum, P. malariae, P. ovale, P. vivax<br />

Like-a-parasite-but-technically-a-fungus: Pneumocystis<br />

jirovecii (primaquine)<br />

Adverse Effects<br />

Cardiovascular: The quinolines can cause doserelated<br />

cardiovascular toxicity, including QT<br />

interval prolongation, hypotension, and potentially<br />

fatal ventricular arrhythmias. Quinidine<br />

is a class IA antiarrhythmic, and it is also used<br />

therapeutically in the treatment of some arrhythmias<br />

(however, like many antiarrhythmics, it<br />

can be proarrhythmic). Cardiovascular effects<br />

are most likely with IV quinidine; less common<br />

with quinine, mefloquine, and chloroquine; and<br />

rare with primaquine.<br />

Hematologic: Primaquine can cause hemolysis in<br />

patients deficient in glucose-6-phosphate dehydrogenase<br />

(G6PD); testing for G6PD deficiency<br />

is required before use.<br />

Metabolic: Quinidine and quinine can cause profound<br />

hypoglycemia resulting from the stimulated<br />

release of insulin.<br />

Psychiatric: Mefloquine is associated with a range<br />

of psychiatric disturbances ranging from<br />

insomnia, vivid dreams, and mood swings to<br />

depression, psychosis, and suicide. Although<br />

mefloquine is well tolerated by the vast

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