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Stavudine

Antiretroviral

Also known as d4T

Antiretroviral
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
7 major
SEVERE in our sources
PREGNANCY
Manufacturer advises use only if potential benefit outweighs risk.
FDA category + note
Top interactionssee all 8
  • BexaroteneSevereDatabaseDDInter
  • DidanosineSevereDatabaseDDInter
  • LeflunomideSevereDatabaseDDInter
  • LomitapideSevereDatabaseDDInter

Mechanism

Stavudine is a nucleoside reverse transcriptase inhibitor (NRTI). It is a pyrimidine nucleoside analog that, upon intracellular phosphorylation, becomes an active metabolite. This active form competitively inhibits HIV reverse transcriptase and can be incorporated into the viral DNA chain, leading to premature chain termination and inhibition of viral replication.

Indications

HIV infection in combination with other antiretroviral drugs when no suitable alternative available and when prescribed for shortest period possibleHIV infection (in combination regimens)

Dosing

Adult
Adult (body-weight up to 60 kg): 30 mg every 12 hours, to be taken preferably at least 1 hour before food. Adult (body-weight 60 kg and above): 40 mg every 12 hours, to be taken preferably at least 1 hour before food.
Renal adjustment
Use half normal dose every 12 hours if eGFR 25–50 mL/minute/1.73 m2. Use half normal dose every 24 hours if eGFR less than 25 mL/minute/1.73 m2.

Pharmacokinetics

Half-life
1.5 hr

Contraindications

  • Excessive alcohol intake
  • History of pancreatitis
  • History of peripheral neuropathy
  • Lactic acidosis (especially when used in combination with didanosine)
  • Hepatomegaly
  • Hepatitis
  • Other risk factors for liver disease and hepatic steatosis (including obesity and alcohol abuse)

Side effects

Common
Abnormal dreamsDepressionDrowsinessDyspepsiaHyperlactacidaemiaLipoatrophyNerve disordersParaesthesiaPeripheral neuropathyThinking abnormalAnxietyAppetite decreasedArthralgiaEmotional lability
Serious
  • Lactic acidosis (associated with hepatomegaly and hepatic steatosis)
  • Progressive hepatomegaly
  • Rapid deterioration of liver function
  • Peripheral neuropathy (requiring switch to another antiretroviral if develops)
  • Gynaecomastia
  • Hepatic disorders
  • Myalgia
  • Diabetes mellitus
  • Hyperglycaemia
  • Muscle weakness
  • Thrombocytopenia
  • peripheral neuropathy (frequent)
  • lipodystrophy
  • lactic acidosis
  • pancreatitis (rarely)

Pregnancy & lactation

Pregnancy

Manufacturer advises use only if potential benefit outweighs risk.

Drug interactions

Bexarotene
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Didanosine
Severe
Database

Increased peripheral neuropathy and lactic acidosis.

Should not be combined.

Source: DDInter

Leflunomide
Severe
Database

Clinical effect not specified

Source: DDInter

Lomitapide
Severe
Database

Clinical effect not specified

Source: DDInter

Mipomersen
Severe
Database

Clinical effect not specified

Source: DDInter

Pexidartinib
Severe
Database

Clinical effect not specified

Source: DDInter

Teriflunomide
Severe
Database

Clinical effect not specified

Source: DDInter

Zidovudine
Moderate
Database

Reduced efficacy of both drugs.

Should not be used concomitantly.

Source: DDInter

4 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Other Antiretroviral drugs

Ask House about Stavudine

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Sources: KD Tripathi 7e, Katzung, BNF, Harriet Lane·Verified: 2026-05-10 · House clinical team