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A ENCARNAÇÃO DE AMENÓFIS

นักเขียน: Adnan_Baahdra
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What is A ENCARNAÇÃO DE AMENÓFIS

อ่านนิยาย A ENCARNAÇÃO DE AMENÓFIS โดย ผู้เขียน Adnan_Baahdra ที่เผยแพร่บน WebNovel....

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When Golden Finger Meets Salted Fish

System 223 is a new system that has just left the factory, and it can’t wait to bind the host on the first day it leaves the factory. However, before it showed its talents and led the host to the pinnacle of life, the host directly stepped on the end of life because of the short-term stagnation of binding it. Helpless, the disheveled 223 had no choice but to take its host who had just died in a car accident to choose a new plane, and properly chose a little white tiger that had just passed away for the host to possess. “Ding, system 223 has been loaded. This system has its own game upgrade system, foundation building in January, golden pill in March, and Nascent Soul in a year is not a dream! I wish the host an early ascension and reach the pinnacle of life!!!” Jiang Mo who was inexplicably bound: “…” Jiang Mo, who had just received the memory of the white tiger inheritance: How tiring is it to cut monsters, and the cultivation base of the gods and beasts increases even when they sleep. It’s not as good as this, the foundation building once, the golden elixir twice, and the Nascent Soul three times all depend on dreams! System: … Is there such a good thing? I’m afraid it’s not really a dream, is it?! So how long are you going to sleep? Jiang Mo: Ten years and eight years are not too short, and a hundred years and a thousand years are not too long. System: Unable to unbind, I choose to shut down. However, Jiang Mo couldn’t sleep for hundreds of thousands of years after all, because she, who is the ultimate face control, soon met a stunning beauty… Who is willing to ignore a kitten lying down on the porcelain? —————————————————— The novel is not mine, I am just editing the MTL version If you want you can support me on: ko-fi.com/mitake55760

Mitak_E · หนังสือและวรรณกรรม
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32 Chs

Pregnancy prevention

Postinor 2 Description 0.75 mg levonorgestrel in each tablet. Excipients/Inactive Ingredients: silica colloidal anhydrous, magnesium stearate, potato starch, talc, maize starch, lactose monohydrate. Action Pharmacotherapeutic Group: Sex hormones and modulators of the genital system, Emergency contraceptives. ATC Code: G03A Efficacy: It was estimated from the results of an earlier clinical study, that 750 micrograms of levonorgestrel (taken as two 750 microgram doses with a 12 hour interval) prevents 85% of expected pregnancies. Efficacy appears to decline with time of start of treatment after intercourse (95% within 24 hours, 85% 24-48 hours, 58% if started between 48 and 72 hours). Results from a recent clinical study showed that two 750 microgram tablets of levonorgestrel taken at the same time (and within 72 hours of unprotected sex) prevented 84% of expected pregnancies. There was no difference between pregnancy rates in case of women who were treated on the third or the fourth day after the unprotected act of intercourse (p>0.2).There is limited and inconclusive data on the effect of high body weight/high BMI on the contraceptive efficacy. In three WHO studies no trend for a reduced efficacy with increasing body weight/BMI was observed (Table 1), whereas in the two other studies (Creinin et al., 2006 and Glasier et al., 2010) a reduced contraceptive efficacy was observed with increasing body weight or BMI (Table 2). Both meta-analyses excluded intake later than 72 hours after unprotected intercourse (i.e. off-label use of levonorgestrel) and women who had further acts of unprotected intercourse. (See the recommended regimen, levonorgestrel is not expected to induce significant modification of blood clotting factors, and lipid and carbohydrate metabolism. Paediatric population: A prospective observational study showed that out of 305 treatments with levonorgestrel emergency contraceptive tablets, seven women became pregnant resulting in an overall failure rate of 2.3%. The failure rate in women under 18 years (2.6% or 4/153) was comparable to the failure rate in women 18 years and over (2.0% or 3/152).Pharmacokinetics: Orally administered levonorgestrel is rapidly and almost completely absorbed. The results of a pharmacokinetic study carried out with 16 healthy women showed that following ingestion of 1.5 mg levonorgestrel maximum drug serum levels of 18.5 ng/ml were found at 2 hours. After reaching maximum serum levels, the concentration of levonorgestrel decreased with a mean elimination half-life of about 26 hours.Levonorgestrel is not excreted in unchanged form but as metabolites. Levonorgestrel metabolites are excreted in about equal proportions with urine and faeces. The biotransformation follows the known pathways of steroid metabolism, the levonorgestrel is hydroxylated in the liver and the metabolites are excreted as glucuronide conjugates. No pharmacologically active metabolites are known.

Stephen_Moses_6913 · แอคชั่น
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