Rifaximin Tablets
Function and Efficacy
This product is a rifamycin derivative and the first non-aminoglycoside intestinal antibiotic. This product has a strong effect and a broad antibacterial spectrum. This product has good antibacterial activity against Staphylococcus aureus, Staphylococcus epidermidis and Streptococcus faecalis among Gram-positive aerobic bacteria, and against Salmonella, Escherichia coli, Shigella and Yersinia enterocolitica among Gram-negative aerobic bacteria. This product has high antibacterial activity against Proteus, Clostridium difficile among Gram-positive anaerobic bacteria, and Bacteroides among Gram-negative anaerobic bacteria. When using this product, there is no need to use intestinal antispasmodics (such as lopramamide, etc.) or intestinal adsorbents (such as white clay, pectin, etc.). This product acts quickly, and diarrhea will no longer occur after 2 days, and abdominal cramps, headaches, nausea, and vomiting symptoms will disappear quickly. This product is not absorbed and maintains extremely high concentrations in the intestine, but does not exist in other organs. This product is superior to neomycin, streptomycin and other aminoglycoside antibiotics in the following features: ① This product does not damage hearing function; ② It does not cause renal damage; ③ Parasitic normal flora, especially non-pathogenic enteric bacteria Escherichia coli, quickly relocate to the intestines to avoid repeated infection; ④ Intestinal mucosal inflammation may tend to disappear. Mucosal inflammation is a contraindication to the use of topical aminoglycosides, because the inflammation may be aggravated after medication.
Ingredients
Rifaximin. Chemical name: 4-deoxy-4-methylpyridinium [1,2-1,2] imidazole well [5,4-cyclo] rifamycin SV.
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| RifaximinIngredients |
This product is a rifamycin derivative and is the first non-aminoglycoside intestinal antibiotic. It has good antibacterial activity against Staphylococcus aureus, Staphylococcus epidermidis and Streptococcus faecalis among Gram-positive aerobic bacteria, and against Salmonella, Escherichia coli, Shigella and Yersinia enterocolitica among Gram-negative aerobic bacteria. This product has high antibacterial activity against Proteus, Clostridium difficile among Gram-positive anaerobic bacteria, and Bacteroides among Gram-negative anaerobic bacteria. This product is not absorbed and maintains extremely high concentrations in the intestine, while it does not exist in other organs. When using this product, there is no need to use intestinal antispasmodics (such as lopramamide, etc.) or intestinal adsorbents (such as white clay, pectin, etc.). This product acts quickly, and diarrhea will no longer occur after 2 days, and abdominal cramps, headaches, nausea, and vomiting symptoms will disappear quickly. This product is superior to neomycin, streptomycin and other aminoglycoside antibiotics in the following features: ① It does not damage hearing function; ② It does not cause renal damage; ③ The parasitic normal flora, especially the non-pathogenic intestinal bacteria Escherichia coli, quickly relocate to the intestines to avoid repeated infection; ④ Intestinal mucositis may tend to disappear. More |
80621-81-4 | 36 |
Appearance
This product is a film-coated tablet, which appears orange-red or brick-red after removing the coating.
Indication
Acute and chronic intestinal infections caused by Gram-positive and negative, aerobic and anaerobic bacteria, diarrhea syndrome, diarrhea caused by changes in intestinal flora (enterocolitis, antibiotic-induced enterocolitis, traveler's diarrhea), preoperative and postoperative intestinal preventive medication, high blood ammonia, portal encephalitis, and hepatic coma.
Usage and Dosage
Diarrhea: Adults and children over 12 years old take 200 mg orally, once every 6 to 8 hours, 10 to 15 mg/(kg.d); children aged 6 to 12 years old, 1 to 2 spoons every 6 to 8 hours; children aged 2 to 6 years old, 1 spoon every 6 to 8 hours. The method of preparing the oral suspension is to add water to the mark on the bottle, shake vigorously to moisten the powder. Add the rest of the water and shake vigorously again. Store at room temperature. This suspension is stable within 7 days.
Adverse Reactions
1. Headaches have been reported in the central nervous system. 2. Metabolic/secretory system Patients with hepatic encephalopathy may experience weight loss and a slight increase in serum potassium and serum sodium concentrations after taking this drug. 3. Common gastrointestinal symptoms are abdominal distension, abdominal pain, nausea and vomiting. The incidence of the above symptoms is less than 1%. 4. Long-term use of large doses of the skin may cause mycosis fungoides in a very small number of patients. 5. There are reports that other drugs may cause foot edema. 6. Some patients may experience nausea after taking the drug (usually after the first dose), but the symptoms can subside quickly. Long-term use of large doses may cause mycosis fungoides in a very small number of patients.
Precautions
The following patients are contraindicated: 1. Those who are allergic to this drug or rifamycin; 2. Those with intestinal obstruction; 3. Those with severe intestinal ulcerative lesions
Special Population Medication
Precautions for children: It is recommended that children under 6 years old should not take this drug. For the method of taking this drug for children 6 years old and above, please refer to [Usage and Dosage]. Precautions for pregnancy and lactation: 1. Effects of the drug on pregnancy: This drug has no teratogenic effect in animal experiments. However, the safety and effectiveness of the drug for pregnant women are still unclear. Therefore, pregnant women need to weigh the pros and cons before taking the drug. 2. Effects of the drug on lactation: Only a very small amount of this drug is absorbed after oral administration, and the concentration in breast milk is also very low. Precautions for the elderly: It is still unclear.
Drug Interactions
Less than 1% of an oral dose of rifaximin is absorbed from the gastrointestinal tract, so rifaximin is unlikely to cause systemic problems due to drug interactions.
Storage
Sealed, store in a dark and dry place.
Packaging Specification
0.1g
Validity Period
24 months
Manufacturer
Sichuan Mingxing Pharmaceutical Co., Ltd.
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Founded in:
2001-12-28 -
Address:
No. 1 Mingyue West Road, Suining Economic and Technological Development Zone -
Tax NO.:
915109007348810707 -
Registered Funds:
228.75 million yuan -
Email: