Acrovin Tablet 200 mg (Acyclovir)

Adult dosage

1. Treatment of herpes simplex virus infections 1) Administer acyclovir 200 mg five times a day at 4-hour intervals for 5 days; in cases of severe primary infection, treatment may be extended. 2) In severely immunocompromised patients (such as those post-bone marrow transplant) or patients with gastrointestinal absorption disorders, the dose may be increased to 400 mg per administration or changed to intravenous administration. 2. For patients with normal immune function

Children's dosage

1. Treatment of herpes simplex infections and prevention of herpes simplex infections in immunocompromised patients 1) Age 2 years and older: same as adults. 2) Under 2 years: administer half of the adult dose. 2. For children over 2 years

This medication should not be used in patients who are allergic to it or its ingredients, or who have had hypersensitivity reactions to similar drugs. Caution is required when used in patients with impaired kidney function as there may be a risk of neuropsychiatric effects. Patients with poor liver function should be administered with caution as their liver function may worsen. It should be used in infants and children only when absolutely necessary, and especially in newborns or low-birth-weight infants, caution is required as its safety has not been established. Elderly patients, who often have impaired kidney function, should be used cautiously while adjusting the dose and dosing interval as the medication may stay in the body longer and the possibility of adverse reactions increases. If symptoms such as allergic reactions or skin rashes, fever, blisters, urticaria occur while taking this medication, usage should be discontinued immediately and medical attention sought. Rarely, symptoms such as shock, consciousness disturbance, seizures, or psychiatric symptoms may appear, in which case medical personnel should be notified immediately. This medication can burden the kidneys, so it is important to ensure adequate fluid intake during the treatment period to prevent dehydration and reduce renal toxicity. Particular attention should be paid to kidney function when administering at high doses. This medication may interact with specific drugs, so if other medications are being taken, it is essential to inform a doctor or pharmacist. Women who are pregnant or may become pregnant should only use this medication when the benefits outweigh the risks, and breastfeeding women should discontinue nursing. Caution should be exercised when driving or operating hazardous machinery during treatment as consciousness disturbance may occur. In the case of overdose, serious neurological effects or renal failure may occur, so the dosage should be strictly adhered to and if abnormal symptoms appear, immediate medical attention should be sought.

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin detachment, pain in the mucous membranes of the mouth/eyes, yellowing of the skin or eyes (jaundice), sudden and severe headaches, lightning headaches, seizures, altered consciousness, visual disturbances, paralysis, significantly decreased urine output, severe general swelling accompanied by increased blood pressure, shock, anaphylactic shock,

Mild side effects

• Photosensitivity reactions
• fixed drug eruption
• rash
• fever
• blisters
• alopecia
• erythema multiforme
• consciousness disturbance
• disturbance of spatial perception
• concentration difficulties

This medication should be stored in a sealed container to avoid exposure to air and moisture, and preferably in a cool, dry place below 25 degrees Celsius. Proper storage will help maintain the medication's effectiveness.

Appearance

Light blue round tablets

Package unit

30 tablets/bottle