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1 integrated treatment (both praziquantel and albendazole).
2 es for praziquantel and two times higher for albendazole.
3 All patients received albendazole.
4 errupted, rather than continuous, courses of albendazole.
5 Surviving recipients received albendazole.
6 solubilize the insoluble benzimidazole drug albendazole.
7 in all six rounds of mass administration of albendazole.
9 g per treatment) against schistosomiasis and albendazole (400 mg per treatment) against soil-transmit
11 azole (2.6%) and the egg-reduction rate with albendazole (45.0%; 95% CI, 32.0 to 56.4) were significa
12 plied to different milk samples, residues of albendazole (49mugkg(-1)), sulfamethazine (<LOQ) and meb
13 r intestinal parasites with a single dose of albendazole (600 mg), administered overseas before depar
14 dentified a synergy between the anthelmintic albendazole (ABZ) and drugs depleting the filarial endos
15 bral Taenia solium cysticercosis with either albendazole (ABZ) or praziquantel (PZQ) is suboptimal.
16 per kilogram of body weight, plus 400 mg of albendazole, administered on consecutive days; oxantel p
17 of coinfected children with praziquantel and albendazole affected schistosome- and hookworm-specific
19 rected treatment with praziquantel (PZQ) and albendazole (ALB) was analyzed in 17 villages of Mayuge
20 1.4%), and whipworm (86.8% to 59.5%), while albendazole alone significantly reduced prevalence of ho
21 her three groups (20 [69%] placebo, 22 [76%] albendazole alone, 17 [61%] ivermectin alone remained po
22 per 20 microL blood among those who received albendazole alone; and from 13.7 to 0.3 per 20 microL bl
24 locks of 100, we assigned patients to 440 mg albendazole and 40 mg/kg praziquantel (n=628), 440 mg al
25 le and 40 mg/kg praziquantel (n=628), 440 mg albendazole and a praziquantel-matching placebo (n=625),
27 ed study of the concurrent administration of albendazole and praziquantel was conducted in>1500 child
28 ed for helminths, treated presumptively with albendazole and selectively with praziquantel, and monit
30 either 4 repeated doses or a single dose of albendazole and were followed up during 13 months to ass
31 benzimidazole anthelmintics, mebendazole and albendazole, are commonly used to remove these infection
32 5 days of azithromycin, and a single dose of albendazole, as compared with standard prophylaxis (trim
33 oate at a single dose of 20 mg per kilogram; albendazole at a single dose of 400 mg; or mebendazole a
37 1:1) eligible participants to either empiric albendazole every 3 months plus praziquantel annually (t
39 ass drug administration with ivermectin plus albendazole for lymphatic filariasis cannot be applied i
41 ted with integrated MDA (of praziquantel and albendazole) for schistosomiasis and soil-transmitted he
42 s significantly lower in the ivermectin plus albendazole group (four [17%]), but there were no signif
43 nd geometric mean titer were observed in the albendazole group in subjects with non-O ABO blood group
45 regimen (ivermectin, diethylcarbamazine, and albendazole) has been shown to clear the transmissible s
52 hese nematode species, e.g., the efficacy of albendazole is strong on A. ceylanicum but weak on H. ba
54 lacebo (n=625), 40 mg/kg praziquantel and an albendazole-matching placebo (n=626), or an albendazole-
55 albendazole-matching placebo (n=626), or an albendazole-matching placebo and praziquantel-matching p
57 in (mean, 273 micrograms/kg, n = 28), 400 mg albendazole (n = 29), or a combination of 200-400 microg
59 ertical transmission was not associated with albendazole (odds ratio 0.70, 95% CI 0.35-1.42) or prazi
62 Current MDA approaches using single-dose albendazole or mebendazole are effective for ascariasis,
63 c-worm infections are typically treated with albendazole or mebendazole, but both drugs show low effi
65 e-blind study to receive two doses of either albendazole or placebo prior to vaccination and in a gro
73 lumbricoides and investigated the effect of albendazole pretreatment on the postvaccination response
77 fants of women who had received two doses of albendazole rose by 59 g (95% CI 19-98), and infant mort
78 g treatment with a single dose of ivermectin-albendazole, some of these defects were reversed, with m
79 as significantly higher with oxantel pamoate-albendazole than with mebendazole (31.2% vs. 11.8%, P=0.
85 strategy of biannual mass administration of albendazole to eliminate lymphatic filariasis in areas w
86 es in IFN-gamma were significant only in the albendazole-treated A. lumbricoides infection group (P =
87 ls of IL-2 were significantly greater in the albendazole-treated group compared with the placebo grou
88 ated antigen 4 (CTLA-4) on CD4(+) T cells of albendazole-treated individuals, -0.060 [-0.107 to -0.01
89 After adjustment for sex, age, and region, albendazole-treated refugees were less likely than untre
91 o effect on infectious disease incidence for albendazole treatment (malaria [hazard ratio 0.95, 95% C
93 hes the magnitude of this response, and that albendazole treatment prior to vaccination was able to p
94 infants of mothers with hookworm infection, albendazole treatment reduced interleukin-5 (geometric m
98 were noted between targeted and nontargeted albendazole treatments for the variables measured at eac
103 antimalarials when malaria-positive whereas albendazole was given in a targeted (n = 467; treatment
105 emia, combined treatment with ivermectin and albendazole was more effective than treatment with iverm
106 ficacy and safety profile of oxantel pamoate-albendazole when used in the treatment of T. trichiura i
107 include diethylcarbamazine, ivermectin, and albendazole, which are used mostly in combination to red
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