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New search Medicine profile Zidovudine (AZT)

Clinical medicine profile

Zidovudine (AZT)

Antiviral / antiretroviral

POM
Evidence state Source not available Reviewed 14 Aug 2026
Route
ORAL / IV / TOPICAL
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

A traceable source link is not attached to this profile. Confirm prescribing decisions against the current SmPC and Kenya STG/EML.

01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

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.
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

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.

03 Clinical use

Use, effects & interactions

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.

Adverse effects

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

Mechanism & disposition

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…
Read complete mechanism

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.

Onset

Varies (hours–days)

Duration

Regimen-dependent; ART lifelong

Route

ORAL / IV / TOPICAL

05 Special populations

Pregnancy, lactation & diet

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.

06 Kenya market

Brands & loaded prices

From
Median
Listings1
BrandManufacturerPackObserved price
Zidovudine Tablets USP 300 mg Hetero Labs Ltd Tablet 300mg Unavailable
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; Professional class pharmacology (Antiviral / antiretroviral)
Last reviewed14 Aug 2026
EvidenceSource not available

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.