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INN monograph

Zidovudine (AZT)

Antiviral / antiretroviral · POM

POM

Verified · Updated 01 Aug 2026 · Source: Local active-ingredient clinical extract; Professional class pharmacology (Antiviral / antiretroviral)

Class
Antiviral / antiretroviral
Schedule
POM
Route
ORAL / IV / TOPICAL
Onset
Varies (hours–days)
Duration
Regimen-dependent; ART lifelong
Pregnancy
ART is essential in preg...
Renal
Dose-adjust renally clea...
High-alert
No

Kenya market

Wholesale / list prices where loaded

From
Median
Brands
3

Risk first

Contraindications

  • Hypersensitivity (abacavir HLA-B*5701 positive — absolute for abacavir).
  • Agent-specific organ failure thresholds.
  • Never dual-count duplicate NRTIs inappropriately.

Precautions

  • Adherence critical for ART to prevent resistance.
  • Screen HLA-B*5701 before abacavir.
  • Monitor renal bone parameters with TDF.
  • IRIS after ART initiation.
  • Aciclovir: hydrate to reduce crystalluria.

Point of care

Dosing

Adult

Asymptomatic disease - initially 500mg to be increased as the disease progresses to 1.5g daily. Symptomatic disease 200mg every 4hrs. If tolerance is poor - 100mg every six hours. Children over 3months -180mg/m2 every 6hrs. I.V inf. - 2.5mg/kg every 4 hrs (for less than 2 weeks.

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Dose-adjust renally cleared NRTIs; TDF nephrotoxicity monitoring.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.

Hepatic

Several agents hepatotoxic; monitor with HBV/HCV co-infection.

Safety

Drug interactions

Open checker →
  • Use national HIV guidelines for first-line combinations.
  • Do not cease ART without plan.
  • For HSV/VZV: early therapy improves outcomes
  • dose by IBW/renal function for IV aciclovir.

Safety

Adverse effects

  • Agent-specific: GI, rash, CNS (efavirenz), hyperbilirubinaemia (atazanavir), renal/bone (TDF), anaemia (ZDV), hypersensitivity (ABC).

Use

Indications

  • HIV in adults and children with progressive or advance immunodeficiency.
  • (T-helper cell counts of less than 500/mm3).
  • Used in combination with other ARVs.
  • Clinical selection for Zidovudine (AZT) should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Antiviral / antiretroviral.
  • Confirm site-specific dose, duration and monitoring before prescribing.

Pharmacology

Mode of action

Nucleoside reverse transcriptase inhibitors [NRTIs] that are converted by cellular cells’ enzymes to active phosporylated metabo-lites that inhibit viral reverse transcriptase and viral DNA synthesis.

Nucleoside reverse transcriptase inhibitor…
Full mechanism text

Nucleoside reverse transcriptase inhibitors [NRTIs] that are converted by cellular cells’ enzymes to active phosporylated metabo-lites that inhibit viral reverse transcriptase and viral DNA synthesis.

ADME

Pharmacokinetics & PD

Onset Varies (hours–days)
Duration Regimen-dependent; ART lifelong
Route ORAL / IV / TOPICAL

Kenya

Brands & prices

3 listed
Brand Company Pack KES
Retrovir GlaxoSmithkline Standard Commercial Pack
Zidocos Cosmos Limited. Standard Commercial Pack
Zidovudine Independent / Registered Supplier Standard Commercial Pack

Special populations

Pregnancy & lactation

Pregnancy

ART is essential in pregnancy for maternal health and PMTCT — use preferred regimens per Kenya NASCOP guidance.

Lactation

Follow national HIV infant feeding + maternal ART guidance.

Diet

Food & alcohol

  • Food
  • Food

Trust

Sources & disclaimer

Source: Local active-ingredient clinical extract; Professional class pharmacology (Antiviral / antiretroviral)

Last reviewed: 01 Aug 2026

Decision support only — not a substitute for clinical judgment, product SmPC, or Kenya STG/EML.

Kenya Verified Health Registry