Acyclovir Tablets
Function and Efficacy
Antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase to inhibit viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells. There are reports of carcinogenicity in in vitro cell transformation assays, but no evidence of carcinogenicity has been found in animal experiments. Some animal experiments show that high concentrations of drugs can cause mutations, but there is no evidence of chromosomal changes. The carcinogenic and mutagenic effects of this product are still unclear. High-dose injection can cause testicular atrophy and reduced sperm count in animals. The drug can pass through the placenta, and animal experiments have confirmed that it has no effect on the embryo.
Ingredients
Acyclovir
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| AcyclovirIngredients |
Antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase and inhibiting viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells. More |
59277-89-3 | 50 |
Appearance
This product is white tablets.
Indication
1. Herpes simplex virus infection: used for the initial and recurrent cases of genital herpes virus infection. For recurrent cases, this product can be taken orally for prevention. 2. Herpes zoster: used for the treatment of herpes zoster in people with normal immune function and mild cases in people with immunodeficiency. 3. Treatment of chickenpox in people with immunodeficiency.
Usage and Dosage
Oral. 1 Genital herpes for the first time and mucocutaneous herpes simplex in immunocompromised patients: The usual dose for adults is 0.2g (2 tablets) once, 5 times a day, for 10 days; or 0.4g (4 tablets) once, 3 times a day, for 5 days; recurrent infection is 0.2g (2 tablets) once, 5 times a day, for 5 days; chronic suppressive therapy for recurrent infection is 0.2g (2 tablets) once, 3 times a day, for 6 months, and the dose can be increased to 5 times a day if necessary, 0.2g (2 tablets) once, for 6 to 12 months. 2 Herpes zoster: The usual dose for adults is 0.8g (8 tablets) once, 5 times a day, for 7 to 10 days. For the dosage of adult patients with renal insufficiency, please refer to the instructions. 3 Varicella: Children over 2 years old are treated with 20mg/kg of body weight once, 4 times a day, for 5 days, and treatment begins immediately when symptoms appear. The usual dose for children and adults over 40kg is 0.8g (8 tablets) once, 4 times a day, for 5 days.
Adverse Reactions
Occasionally, dizziness, headache, joint pain, nausea, vomiting, diarrhea, stomach discomfort, loss of appetite, thirst, leukocytopenia, slight increase in proteinuria and urea nitrogen, skin itching, etc. may occur. Acne, insomnia, and menstrual disorders may occur occasionally with long-term administration.
Precautions
It is contraindicated for those who are allergic to this product.
Special Population Medication
Precautions for children: The dosage for children under 2 years old has not been determined. Precautions for pregnancy and lactation: The drug can pass through the placenta. Although animal experiments have confirmed that it has no effect on the embryo, pregnant women still need to weigh the pros and cons of using the drug. The concentration of the drug in breast milk is 0.6 to 4.1 times the blood concentration. Although no abnormalities have been found in infants, breastfeeding women should use it with caution. Precautions for the elderly: Due to the decline of physiological renal function, the dosage and medication interval of this product need to be adjusted.
Drug Interactions
1. Combination with zidovudine can cause nephrotoxicity, manifested as deep lethargy and fatigue. 2. Competitive inhibition of organic acid secretion with probenecid. Combination with probenecid can slow down the excretion of this product, prolong the half-life, and accumulate the drug in the body.
Storage
Keep tightly closed in a cool, dry place.
Packaging Specification
0.1g
Validity Period
36 months
Manufacturer
Livzon (GROUP) Pharmaceutical FACTORY
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Founded in:
1989-11-26 -
Address:
No. 38 Chuangye North Road, Jinwan District, Zhuhai City -
Tax NO.:
91440400617489061P -
Registered Funds:
450 million yuan -
Website:
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Email: