Perraud J, Stadler J, Kessedjian M J, Monro A M
Toxicology. 1984 Feb 14;30(1):59-63. doi: 10.1016/0300-483x(84)90062-3.
Reproductive toxicology studies were conducted in rabbits and rats given piroxicam, a non-steroidal anti-inflammatory agent (NSAI), orally at 2, 5 and 10 mg/kg/day. In teratology studies there was neither drug-related embryotoxicity nor teratogenicity. As piroxicam, like other NSAI, affects parturition in rats and leads to a progressive toxicity in lactating females, standard protocols were modified: dams of the female fertility study were treated from 2 weeks prior to mating until day 6 of gestation and females of the post-natal toxicity study were treated from parturition until day 12 of lactation. No other adverse effects on reproduction, fertility and postnatal development were observed.
在给予兔和大鼠口服非甾体抗炎药(NSAI)吡罗昔康,剂量分别为2、5和10毫克/千克/天的情况下进行了生殖毒理学研究。在致畸学研究中,未发现与药物相关的胚胎毒性或致畸性。由于吡罗昔康与其他NSAI一样,会影响大鼠的分娩并导致哺乳期雌性大鼠出现进行性毒性,因此对标准方案进行了修改:雌性生育力研究中的母鼠从交配前2周开始治疗,直至妊娠第6天;产后毒性研究中的雌性大鼠从分娩开始治疗,直至哺乳第12天。未观察到对生殖、生育力和产后发育的其他不良影响。