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Trichopol (Metronidazole)

Trichopol is an oral antiprotozoal and antibacterial. It is thought to work by entering the bacterial cell, acting on some components of the cell, and destroying the bacteria. Treating certain infections caused by bacteria or amoebas. It may also be used for other conditions as determined by your doctor.

Other names for this medication:
Metronidazole, Flagyl, Acuzole, Aldezol, Aldezole, Amodis, Amrizole, Anabact, Anaerobex, Anamet, Anazol, Arilin, Aristogyl, Bemetrazole, Biatron, Birodogyl, Clont, Colpofilin, Deflamon, Diazole, Dumozol, Efloran, Elyzol, Entizol, Etron, Filmet, Fladex, Fladystin, Flagenase, Flagicure, Flagystatin, Flagystatine, Flazol, Flazole, Flegyl, Florazole, Geloderm, Ginkan, Gynotran, Klion, Klont, Medazol, Metazol, Metazole, Metco, Metrazol, Metrin, Metris, Metrocream, Metrocreme, Metroderme, Metrogel, Metrogyl, Metrol, Metrolag, Metrolotion, Metrolyl, Metronex, Metronid, Metronidazol, Metronidazolum, Metronide, Metropast, Metrosa, Metrosil, Metroson, Metrovax, Metrozin, Metrozine, Metrozol, Metrozole, Metryl, Metsina, Nalox, Negazole, Nidagel, Nidagyl, Nidazol, Nidazole, Nizole, Noritate, Norzol, Orvagil, Padet, Polibiotic, Repligen, Rhodogil, Riazole, Robaz, Rodogyl, Rosalox, Rosasol, Rosazol, Rosiced, Rozamet, Rozex, Stomorgyl, Suanatem, Supplin, Tolbin, Trichazole, Trichex, Trichodazol, Trichopol, Trichozole, Tricodazol, Triconex, Trikozol, Unigyl, Vagilen, Vagimid, Vandazole, Vertisal, Zidoval,

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A multienzyme complex that catalyzes the anthranilate synthetase, phosphoribosylanthranilate (PRA) isomerase, and indoleglycerolphosphate (InGP) synthetase reactions was produced in vitro when extracts from a tryp-1 mutant and a tryp-2 mutant of Neurospora crassa were mixed. The clinical scene investigator academy: the power of staff nurses improving patient and organizational outcomes. Findings indicated that these students tended to see experiential learning in terms of clinical learning and learning through working in the wards and community settings. The results expressed in accordance with the criteria defined by the European group on malignant hyperthermia, coupled with a histoenzymatic study, defined three of the subjects as HMN (negative) and one subject as HM (c) (equivocal or intermediate). We found that purified PON1 is as a mixture of at least two states, and that the absence of HPBP favors homo-oligomerization of PON1 into state(s) of higher molecular size.

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