Long-Term Administration: The most frequent adverse events reported in a clinical trial for the prevention of recurrences with continuous administration of 400 mg (two 200-mg capsules) 2 times daily for 1 year in 586 patients treated with acyclovir tablets were nausea (4.8%) and diarrhea (2.4%).
Each 400 mg tablet of acyclovir contains 400 mg of acyclovir, USP and the inactive ingredients colloidal silicone dioxide, magnesium stearate, microcrystalline cellulose, pregelatinized starch, and sodium starch glycolate. Acyclovir, USP is a white crystalline powder with the molecular formula C 8 H 11 N 5 O 3 and a molecular weight of 225. The
Each 400-mg tablet of acyclovir contains 400 mg of acyclovir and the inactive ingredients corn starch, microcrystalline cellulose, magnesium stearate, and sodium starch glycolate. Acyclovir is a white, crystalline powder with the molecular formula C 8 H 11 N 5 O 3 and a molecular weight of 225. The maximum solubility in water at 37°C is 2.5 mg/mL.
• Komposisi: Acyclovir 200 mg • Golongan: Obat keras • Perlu resep: Ya • Rute obat: Oral • Kemasan: Tablet 200 Mg x 50 x 1. Indikasi. Herpes zoster, varicella zoster, herpes simpleks, cacar air, dan campak. Komposisi. Acyclovir. Dosis • Herpes simpleks - Dewasa dan anak >2 tahun: 5 kali sehari 200 mg. Konsumsi obat setiap 4 jam sekali.
Dosage in adults. Treatment of herpes simplex infections: 200 mg Aciclovir should be taken five times daily at approximately four hourly intervals omitting the night time dose. Treatment should continue for 5 days, but in severe initial infections this may have to be extended.
Daftar Harga Agustus 2023-2 - Free download as PDF File (.pdf), Text File (.txt) or read online for free. 60 ml 48 5,750 TABLET ACIFAR 200 MG Acyclovir 200 mg
Acyclovir is a synthetic nucleoside analogue active against herpes viruses. Acyclovir capsules and tablets are formulations for oral administration. Each 200 mg capsule contains 200 mg of VIROLOGY. Mechanism of Antiviral Action - Acyclovir is a synthetic purine nucleoside analogue with in vitro and in vivo inhibitory activity against herpes