The dangers of taking metronidazole while breastfeeding

The dangers of taking metronidazole while breastfeeding

Subacute pericoronitis is an inflammation of the soft tissue around the tooth when the wisdom tooth (third molar) is incompletely erupted or impacted. The clinical symptoms are mainly hematoma, swelling, erosion or blind bag with pus. Artificial bezoar metronidazole capsules have a good effect on the treatment of subacute pericoronitis of wisdom teeth. So, can I take artificial bezoar metronidazole capsules during breastfeeding? What are the harms of taking metronidazole while breastfeeding?

Ornidazole is a nitroimidazole compound, which has a strong killing effect on Trichomonas and also has a killing effect on anaerobic fermentation microorganisms. Ornidazole is a nitroimidazole compound, which has a strong killing effect on Trichomonas and also has a killing effect on anaerobic fermentation microorganisms. Taking ornidazole while breastfeeding may cause digestive system reactions: such as nausea, vomiting, loss of appetite, abdominal distension, diarrhea, metallic taste in the mouth, etc. Breast milk can have an impact on the fetus. It is recommended that you do not take this type of medicine during the breastfeeding period. You can use other medicines instead, preferably those with some herbal ingredients, and use them under the guidance of a doctor.

The harm of taking ornidazole and feeding breast milk. The usage of artificial bezoar metronidazole capsules is for oral administration. Take 2 pills at a time, 3 times a day; for children, take 1 pill at a time, 3 times a day.

Ornidazole can pass through the embryo and quickly enter the fetal circulatory system. Animal experiments have found that oral administration is not toxic to the fetus. There have been no sufficient and rigorous comparative observations on the effects of metronidazole on the fetus, so pregnant women are prohibited from using it. The concentration of ornidazole in breast milk is similar to that in blood. Animal experiments have shown that this product is carcinogenic to young children, so it is not suitable for use during breastfeeding. If you must take medicine, you should stop breastfeeding and resume breastfeeding 24 to 48 hours after the treatment is completed.

Do not drink alcoholic beverages during the medication period, as it can cause accumulation of hydrogen bromide in the body, affecting the oxidation process of ethanol and causing disulfiram-like reactions. Patients may experience abdominal cramps, nausea, vomiting, headaches, red cheeks, etc. Patients with decreased liver function test results have slowed metabolism of this product, and the drug and its compounds tend to accumulate in the body. Dosage should be reduced and blood drug concentrations should be monitored. This product can be continuously eliminated from gastric acid. Some people who have a gastric tube inserted for suction to relieve pressure may experience a decrease in blood drug concentration. During blood analysis, this product and its compounds are rapidly eliminated, so no dose reduction is required when using this product. For patients with Pseudomonas aeruginosa infection and renal mechanical dysfunction, the dosing interval should be increased from 8 hours to 12 hours. When treating vaginal mycoses, sexual partners need to be treated at the same time.

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