Thông tin thuốc gốc
Chỉ định và Liều dùng
HIV-1 infection
Adult: Given in combination w/ other antiretrovirals: As chewable or dispersible tab/soln: <60 kg: 125 mg 12 hrly or 250 mg once daily; ≥60 kg: 200 mg 12 hrly or 400 mg once daily. As delayed-release cap: 20-<25 kg: 200 mg once daily; 25-<60 kg: 250 mg once daily; ≥60 kg: 400 mg once daily.
Child: Given in combination w/ other antiretrovirals: As soln: ≥3-≤8 mth 100 mg/m2 12 hrly. >8 mth 120 mg/m2 12 hrly, not exceeding adult dose. As chewable or dispersable tab: >3 mth 240 mg/m2 daily. As delayed-release cap: >6 yr Same as adult dose.
Renal Impairment
As chewable or dispersible tab/soln:
<60 kg:
CrCl (mL/min) Dosage
<10 75 mg once daily.
10-29 100 mg once daily.
30-59 150 mg in 1-2 divided doses.
≥60 kg:
<10 100 mg once daily.
10-29 150 mg once daily.
30-59 200 mg in 1-2 divided doses.

As delayed-release cap:
<60 kg:
<10 Contraindicated.
10-59 125 mg once daily.
≥60 kg:
<30 125 mg once daily.
30-59 200 mg once daily.
Cách dùng
Should be taken on an empty stomach. Take 30 min before or 2 hr after meals.
Chống chỉ định
Hypersensitivity to didanosine. Renal (CrCl <10 mL/min) impairment (delayed-release cap). Lactation. Concomitant use w/ allopurinol, ribavirin, tenofovir, stavudine, and hydroxyurea.
Thận trọng
Patient w/ history and risk of pancreatitis, history of neuropathy, hepatomegaly. Hepatic (e.g. chronic active hepatitis) and renal impairment. Childn. Pregnancy.
Phản ứng phụ
Significant: Peripheral neuropathy, immune reconstitution syndrome, fat redistribution (e.g. central obesity, peripheral and facial wasting, breast enlargement, buffalo hump, cushingoid appearance), osteonecrosis. Rarely, retinal changes (e.g. depigmentation), optic neuritis.
Nervous: Headache, anxiety, insomnia, irritability, restlessness, seizures, fatigue, asthenia.
CV: Increased risk of MI, cardiomyopathy.
GI: Diarrhoea, nausea, vomiting, abdominal pain, anorexia, constipation, dyspepsia, dry mouth, flatulence, parotid gland enlargement, sialedenitis.
Hepatic: Hepatitis, abnormal LFT.
Endocrine: DM, hypo- and hyperglycaemia, hypertriglyceridaemia, hypercholesterolaemia, insulin resistance, hyperlactataemia, hyperuricaemia.
Haematologic: Anaemia, leucopenia, thrombocytopenia.
Musculoskeletal: Increased creatine phosphokinase, myalgia, arthralgia, myopathy, myositis, rhabdomyolysis.
Ophthalmologic: Diplopia, dry eyes, optic atrophy, blindness.
Dermatologic: Rash, alopecia, pruritus, mild erythematous macular eruption.
Immunologic: Anaphylaxis.
Others: Chills, fever, hypokalaemia, pain.
Potentially Fatal: Pancreatitis, lactic acidosis associated w/ hepatomegaly and steatosis. Rarely, noncirrhotic portal HTN, hepatic failure.
Monitor serum K, uric acid, creatinine, Hb, CBC w/ neutrophil and platelet count, CD4 cells, viral load, LFT, serum bilirubin, albumin, INR, amylase, wt gain. Monitor for signs and symptoms of peripheral neuropathy, hepatotoxicity, GI pain, and visual changes regularly during therapy. Perform dilated retinal exam every 6 mth.
Quá liều
Symptoms: Pancreatitis, peripheral neuropathy, diarrhoea, hyperuricaemia and hepatic dysfunction. Management: Supportive and symptomatic treatment. Induce emesis or perform gastric lavage.
Tương tác
Decreased plasma concentration w/ methadone. Increased plasma concentration w/ ganciclovir and valganciclovir. Decreased effects of quinolones, tetracyclines, ketoconazole w/ buffered didanosine preparations. Increased risk of pancreatitis when used w/ pentamidine. Increased bioavailability of didanosine when concomitantly used w/ antacid.
Potentially Fatal: Increased toxicity w/ allopurinol. Increased plasma concentration and risk of adverse effects (hepatic failure, peripheral neuropathy, pancreatitis, lactic acidosis) w/ ribavirin, tenofovir, stavudine, and hydroxyurea.
Food Interaction
Food decreases rate of absorption. Enhanced adverse effects w/ alcohol.
Tác dụng
Description: Didanosine is converted intracellularly to dideoxyadenosine triphosphate which inhibits HIV nucleoside reverse transcriptase, hence blocking viral DNA synthesis and suppressing HIV replication.
Absorption: Rapidly hydrolysed in the gastric acid. Reduced bioavailability w/ food. Bioavailability: 20-40%. Time to peak plasma concentration: Approx 1 hr.
Distribution: Extensive intracellular distribution. Crosses placenta and distributed into cord blood and amniotic fluid. Plasma protein binding: <5%.
Metabolism: Undergoes intracellular phosphorylation to the active metabolite, dideoxyadenosine triphosphate.
Excretion: Via urine (20% as unchanged drug). Elimination half-life: Approx 1.5 hr.
Đặc tính

Chemical Structure Image

Source: National Center for Biotechnology Information. PubChem Database. Didanosine, CID=135398739, https://pubchem.ncbi.nlm.nih.gov/compound/Didanosine (accessed on Jan. 21, 2020)

Bảo quản
Tab/Oral Soln: Store between 15-30°C. Cap: Store at 25°C.
Phân loại MIMS
Phân loại ATC
J05AF02 - didanosine ; Belongs to the class of nucleoside and nucleotide reverse transcriptase inhibitors. Used in the systemic treatment of viral infections.
Anon. Didanosine. Lexicomp Online. Hudson, Ohio. Wolters Kluwer Clinical Drug Information, Inc. https://online.lexi.com. Accessed 21/02/2017.

Buckingham R (ed). Didanosine. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 21/02/2017.

Joint Formulary Committee. Didanosine. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 21/02/2017.

McEvoy GK, Snow EK, Miller J et al (eds). Didanosine. AHFS Drug Information (AHFS DI) [online]. American Society of Health-System Pharmacists (ASHP). https://www.medicinescomplete.com. Accessed 21/02/2017.

Videx EC Capsule, Delayed Release (Bristol-Myers Squibb Company). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/. Accessed 21/02/2017.

Videx Powder, For Solution (Bristol-Myers Squibb Company). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/. Accessed 21/02/2017.

Thông báo miễn trừ trách nhiệm: Thông tin này được MIMS biên soạn một cách độc lập dựa trên thông tin của Didanosine từ nhiều nguồn tài liệu tham khảo và được cung cấp chỉ cho mục đích tham khảo. Việc sử dụng điều trị và thông tin kê toa có thể khác nhau giữa các quốc gia. Vui lòng tham khảo thông tin sản phẩm trong MIMS để biết thông tin kê toa cụ thể đã qua phê duyệt ở quốc gia đó. Mặc dù đã rất nỗ lực để đảm bảo nội dung được chính xác nhưng MIMS sẽ không chịu trách nhiệm hoặc nghĩa vụ pháp lý cho bất kỳ yêu cầu bồi thường hay thiệt hại nào phát sinh do việc sử dụng hoặc sử dụng sai các thông tin ở đây, về nội dung thông tin hoặc về sự thiếu sót thông tin, hoặc về thông tin khác. © 2021 MIMS. Bản quyền thuộc về MIMS. Phát triển bởi MIMS.com
  • Videx
  • Videx EC
Register or sign in to continue
Asia's one-stop resource for medical news, clinical reference and education
Sign up for free
Already a member? Sign in