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Praziquantel and its metabolites are mainly excreted renally; within 24 h after a single oral dose, 70 to 80% is found in urine, but less than 0.1% as the unchanged drug. Praziquantel is metabolized through the cytochrome P450 pathway via CYP3A4 .
Thus, it is important to have repeated schistosomiasis testing of the stool and/or urine around 4–6 weeks after praziquantel therapy. [19] Treatment of praziquantel may be repeated to ensure complete elimination of the parasite. [19]
Praziquantel, however, is often the preferred treatment. [2] It is given by mouth and used as a single dose. [2] Common side effects include sleepiness, headache, nausea, diarrhea, and reddish urine. [1] It is typically not recommended during pregnancy, if possible. [1] Seizures may occur and therefore caution is recommended in people with ...
Schistosoma japonicum is an important parasite and one of the major infectious agents of schistosomiasis.This parasite has a very wide host range, infecting at least 31 species of wild mammals, including nine carnivores, 16 rodents, one primate (human), two insectivores and three artiodactyls and therefore it can be considered a true zoonosis.
Schistosomiasis was first reported in the Mekong River's Lower Basin region in 1957, from Laotian island of Khong to Cambodian province of Kratié, specifically. [2] It was believed that the cause of these cases was Schistosoma japonicum until 1978, when Neotricula aperta was discovered and it was determined that the Schistosome was a unique species, Schistosoma mekongi. [2]
Ozempic and other GLP-1 agonist medications might interfere with birth control and give certain patients a fertility boost, say doctors.
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The distinct symptom for urogenital schistosomiasis is blood in the urine (haematuria), which is often associated with frequent urination, painful micturition, and discomfort in the groin. In endemic regions, haematuria is so widespread that it is thought a natural sign of puberty for boys, and is confused with menses in girls. [37]
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