After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration (Cmax) is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules, and the urine concentration is significantly higher than the blood concentration. It can be widely distributed in body tissues and fluids such as sputum, middle ear fluid, and vaginal secretions, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration (Cmax) is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules, and the urine concentration is significantly higher than the blood concentration. It can be widely distributed in body tissues and fluids such as sputum, middle ear fluid, and vaginal secretions, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.

Tetracycline antibiotics. This product is a broad-spectrum antibacterial agent. Many Rickettsia, Mycoplasma, Chlamydia, Spirochete, Amoeba and some Plasmodium are also sensitive to this product. Enterococcus is resistant to it. Others such as Actinomycetes, Bacillus anthracis, Listeria monocytogenes, Clostridium, Nocardia, Vibrio, Brucella, Campylobacter, Yersinia, etc. are sensitive to this product. This product has certain antibacterial activity against gonococci and meningococci, but penicillin-resistant gonococci are also resistant to oxytetracycline. Due to the widespread use of tetracyclines over the years, common clinical pathogens have serious resistance to oxytetracycline, including Gram-positive bacteria such as Staphylococcus and most Gram-negative bacteria. There is cross-resistance between different varieties of tetracycline antibiotics.

Antipyretic, anti-inflammatory, analgesic, sedative, anticonvulsant

Inhibits a variety of pathogenic microorganisms

Niuhuang Jiedu Tablets have obvious antipyretic, anti-inflammatory, analgesic, sedative and anticonvulsant effects, and have a strong inhibitory effect on a variety of pathogenic microorganisms that cause various inflammations.

Niuhuang Jiedu Tablets have obvious antipyretic, anti-inflammatory, analgesic, sedative and anticonvulsant effects, and have a strong inhibitory effect on a variety of pathogenic microorganisms that cause various inflammations.

Niuhuang Jiedu Tablets have obvious antipyretic, anti-inflammatory, analgesic, sedative and anticonvulsant effects, and have a strong inhibitory effect on a variety of pathogenic microorganisms that cause various inflammations.

Niuhuang Jiedu Tablets have obvious antipyretic, anti-inflammatory, analgesic, sedative and anticonvulsant effects, and have a strong inhibitory effect on a variety of pathogenic microorganisms that cause various inflammations.

Niuhuang Jiedu Tablets have obvious antipyretic, anti-inflammatory, analgesic, sedative and anticonvulsant effects, and have a strong inhibitory effect on a variety of pathogenic microorganisms that cause various inflammations.

Niuhuang Jiedu Tablets have obvious antipyretic, anti-inflammatory, analgesic, sedative and anticonvulsant effects, and have a strong inhibitory effect on a variety of pathogenic microorganisms that cause various inflammations.

Azithromycin is a 15-membered ring macrolide antibiotic that has antibacterial effects on a variety of Gram-positive aerobic bacteria, Gram-negative aerobic bacteria, anaerobic bacteria, sexually transmitted disease microorganisms and other microorganisms. It mainly binds to the 50S subunit of the bacterial ribosome and inhibits RNA-dependent protein synthesis.

Fluconazole is a new triazole antifungal drug with a broad-spectrum antifungal effect and can selectively inhibit fungal sterol synthesis. It is effective against Candida infection, Cryptococcus neoformans infection, Malassezia sacchari, Microsporum, Trichophyton, Epidermophyton, Blastomyces dermatitidis, Coccidioides immitis, Histoplasma capsulatum, Peyer's Chromatiaceae, and Cladosporium carinii. It has a highly selective inhibitory effect on fungal cytochrome p-450-dependent enzymes. Studies have shown that taking fluconazole has no effect on male plasma testosterone concentrations or plasma steroid concentrations in women of childbearing age, no significant effect on endogenous steroid levels or adrenocorticotropic hormone effects in healthy male volunteers, and no effect on the metabolism of antipyrine.