Para-aminosalicylic acid isoniazid tablets
Function and Efficacy
This product is a chemical synthesis of isoniazid (INH) and para-aminosalicylic acid (PAS). INH is mainly effective against mycobacteria in the growth and reproduction period. Its mechanism of action has not yet been elucidated, and it may inhibit the synthesis of mycolic acid (myolic acid) of sensitive bacteria and cause cell wall rupture. PAS effectively delays and blocks the acetylation process of INH in the body. Therefore, this product can maintain a higher and longer INH concentration in the blood and reduce liver toxicity. After taking equal amounts of INH and this product, it was found that the INH blood concentration was only 0.03 mg/L in 12 hours, while this product still had 2.6 mg/L. The INH blood concentration was 0 in 14 hours, while this product was still as high as 2 mg/L, which was twice the MIC. This not only enhances the bactericidal effect of the drug, but also delays the development of bacterial resistance. Clinically, it has been confirmed that in combined treatment with other anti-tuberculosis drugs, the anti-tuberculosis efficacy of this product is significantly better than that of INH; and the incidence of adverse reactions such as gastrointestinal reactions, liver damage and low white blood cells is significantly lower than that of INH. Animal experiments show that for artificially infected mice, the anti-tuberculosis efficacy of this crystal is about 5 times that of INH, and the therapeutic effect of this crystal at 10 mg/kg per day is significantly better than the physical mixture of INH (20 mg/kg per day) and PAS (200 mg/kg per day).
Ingredients
Isoniazid-para-aminosalicylate
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| PasiniazidIngredients |
This product is a chemical synthesis of isoniazid (INH) and para-aminosalicylic acid (PAS). INH is mainly effective against mycobacteria in the growth and reproduction period, and may inhibit the synthesis of mycolic acid (myolic acid) of sensitive bacteria and cause cell wall rupture. PAS effectively delays and blocks the acetylation process of INH in the body, can maintain a higher and longer INH concentration in the blood, and reduces the toxicity to the liver. Clinically confirmed, in combination with other anti-tuberculosis drugs, the anti-tuberculosis efficacy of this product is significantly better than INH, while the incidence of adverse reactions such as gastrointestinal reactions, liver function damage and leukopenia is significantly lower than that of INH. Animal experiments show that for artificially infected mice, the anti-tuberculosis efficacy of this product is about 5 times that of INH. More |
2066-89-9 | 5 |
Appearance
This product is a film-coated tablet.
Indication
It is used in combination with other anti-tuberculosis drugs to treat various types of pulmonary tuberculosis, endobronchial tuberculosis and extrapulmonary tuberculosis. It can also be used as a protective drug for tuberculosis-related surgeries, and can also be used to prevent tuberculosis infection and recurrence during long-term or high-dose corticosteroid and immunosuppressive therapy.
Usage and Dosage
Oral. For treatment combined with other anti-tuberculosis drugs, adults: 10-20 mg/kg per day, children: depending on individual needs, it can be increased to 20-40 mg/kg per day, taken all at once. For prevention, 10-15 mg/kg per day, taken all at once.
Adverse Reactions
Occasionally, adverse reactions such as dizziness, headache, insomnia, fever, rash, nausea, fatigue, jaundice, peripheral neuritis, optic neuritis and hematocytopenia may occur.
Precautions
1. It is contraindicated for patients with mental illness and epilepsy. 2. It is contraindicated for patients with severe liver dysfunction.
Special Population Medication
Precautions for children: This experiment has not been conducted and there is no reliable reference. Precautions for pregnancy and lactation: Use with caution in pregnant and lactating women. Precautions for the elderly: This experiment has not been conducted and there is no reliable reference.
Drug Interactions
Not yet clear.
Storage
Keep away from light, sealed and stored in a dry place.
Packaging Specification
0.1g
Validity Period
Tentative 24 months
Manufacturer
Guangzhou Baiyunshan Pharmaceutical Co., Ltd. Guangzhou Baiyunshan Pharmaceutical General
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Founded in:
1973-07-01 -
Address:
No. 88, Yunxiang Road, Tonghe Street, Baiyun District, Guangzhou -
Tax NO.:
91440101714253245D -
Registered Funds:
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Website:
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Email: