Trade Names:Malarone- Tablets 250 mg atovaquone and 100 mg proguanil hydrochloride
Trade Names:Malarone Pediatric- Tablets 62.5 mg atovaquone and 25 mg proguanil hydrochloride
Atovaquone inhibits mitochondrial electron transport in parasites, causing inhibition of nucleic acid synthesis.
Proguanil exerts its effect by means of the metabolite cycloguanil, which inhibits dihydrofolate reductase in the malarial parasite, disrupting deoxythymidylate synthesis.
Prophylaxis of Plasmodium falciparum malaria; treatment of acute, uncomplicated P. falciparum malaria.
Prophylaxis of P. falciparum in patients with severe renal function impairment (Ccr less than 30 mL/min); hypersensitivity to any component of the product.
Start prophylaxis 1 or 2 days before entering a malaria-endemic area and continue during the stay and for 7 days after return.Adults
PO 250 mg atovaquone/100 mg proguanil daily.Children
PO Based on body weight. 11 to 20 kg: 62.5 mg atovaquone/25 mg proguanil daily; 21 to 30 kg: 125 mg atovaquone/50 mg proguanil daily; 31 to 40 kg: 187.5 mg atovaquone/75 mg proguanil; more than 40 kg: 250 mg atovaquone/100 mg proguanil.Treatment of Acute MalariaAdults
PO 1 g atovaquone/400 mg proguanil as a single daily dose for 3 consecutive days.Children
PO Based on body weight. 5 to 8 kg: 125 mg atovaquone/50 mg proguanil daily for 3 consecutive days; 9 to 10 kg: 187.5 mg atovaquone/75 mg proguanil daily for 3 consecutive days; 11 to 20 kg: 250 mg atovaquone/100 mg proguanil daily for 3 consecutive days; 21 to 30 kg: 500 mg atovaquone/200 mg proguanil daily for 3 consecutive days; 31 to 40 kg: 750 mg atovaquone/300 mg proguanil daily for 3 consecutive days; more than 40 kg: 1 g atovaquone/400 mg proguanil daily for 3 consecutive days.
Store tablets at controlled room temperature (59° to 86°F).
May reduce the bioavailability of atovaquone, decreasing the therapeutic effect.Rifamycins (eg, rifampin, rifabutin)
Because atovaquone concentrations may be reduced, coadministration is not recommended.Tetracycline
May reduce plasma concentrations of atovaquone, decreasing the therapeutic effect.
None well documented.
Headache, anorexia, dizziness, abnormal dreams, insomnia (5% or more); psychotic events (eg, hallucinations), seizures (postmarketing).
Pruritus (1% or more); angioedema, photosensitivity, urticaria, erythema multiforme, Stevens-Johnson syndrome (postmarketing).
Visual difficulties (2%).
Abdominal pain, nausea, vomiting, diarrhea, oral ulcers (5% or more); gastritis (3%); dyspepsia (2%).
Cough (5% or more).
Asthenia (5% or more); anaphylaxis (postmarketing).
Category C .
Safety and efficacy not established for the treatment of malaria in children weighing less than 5 kg or for the prophylaxis of malaria in children weighing less than 11 kg.
Use with caution because of the greater frequency of decreased hepatic, renal, or cardiac function, and concomitant diseases or other drug therapy.
Atovaquone/proguanil is contraindicated for malaria prophylaxis in patients with severe renal function impairment (Ccr less than 30 mL/min). May be used with caution for treatment of malaria in patients with severe renal function impairment if benefits of 3-day treatment regimen outweigh potential risks associated with increased drug exposure.
Absorption of atovaquone/proguanil may be reduced. Consider use of antiemetic in patient who has frequent or persistent vomiting. Consider alternative antimalarial therapy in patients with severe or persistent diarrhea or vomiting.
In the event of recrudescent P. falciparum infections after treatment or failure of chemoprophylaxis with atovaquone/proguanil, treat patients with a different blood schizonticide.
Because atovaquone/proguanil has not been evaluated for treatment of cerebral malaria or other severe manifestations of complicated malaria, patients with these conditions are not candidates for oral therapy.
Epigastric discomfort, rash, vomiting.
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