Pharm
Zidovudine
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Zidovudine
, Retrovir, ZDV, AZT
See Also
Anti-Retroviral Therapy
Nucleoside Reverse Transcriptase Inhibitor
Indications
HIV Infection
Replaced in the U.S. by other
nRTI
s
Mechanism
Nucleoside Reverse Transcriptase Inhibitor
Thymidine analogue
Interferes with viral reverse transcriptase and elongation of the viral DNA chain (as with other
nRTI
s)
Pharmacokinetics
Well absorbed from the
Gastrointestinal Tract
Glucuronidase added in the liver
Excreted by the
Kidney
Crosses the blood-brain barrier and the placenta
Efficacy
Delays the progression to
AIDS
and late HIV
Increases
CD4 Count
s
Suppresses viral replication in mild HIV (CD4 200-500)
Resistance develops 6 months into therapy
Dosing
Taken as part of combination therapy with other
Antiretroviral
s
Not to be used as HIV monotherapy (including in pregnancy)
Adult (or child weight >30 kg)
Zidovudine 300 mg orally twice daily OR
Zidovudine 1 mg/kg IV over 1 hour every 4 hours
Pregnancy - Prevention of vertical transmission
First, starting at 14 weeks gestation: Take 100 mg orally five times daily until labor
Peripartum, during labor
Load 2 mg/kg total body weight IV over 1 hour
Maintain 1 mg/kg/hour until
Umbilical Cord
clamped
Child (age >=4 weeks and weight >=4 kg)
Weight 4 to 9 kg: 4 mg/kg orally twice daily
Weight 9 to 30 kg: 9 mg/kg orally twice daily
Weight >30 kg: 300 mg orally twice daily (adult dosing)
Infant - Prevention of vertical transmission
Start within 12 hours of delivery
Continue until age 6 weeks (four weeks if maternal sustained viral suppression on HAART)
Original FDA approved protocol
Give 2 mg/kg (using syringe with 0.1 ml markers) orally every 6 hours
Alternatively, give 1.5 mg/kg IV over 30 min every 6 hours
Off Label dosing
Gestational age
>35 weeks: Give 4 mg orally twice daily
See other references for dosing
Gestational age
<35 weeks
Renal Dosing
(Adults with
Creatinine Clearance
<15 ml/min or
Hemodialysis
)
Take 100 mg orally every 8 hours OR
Take 300 mg orally once daily OR
Give 1 mg/kg IV every 6 to 8 hours
Adverse effects
Gene
ral
See
nRTI
for adverse effects attributed to the class
Toxicity limits use as first-line
nRTI
(other agents are preferred)
Short term
Headache
Myalgia
Malaise
Fatigue
Insomnia
Nausea
or
Vomiting
Bloating
Dyspepsia
Long term
Nail and
Oral Mucosa Hyperpigmentation
Myopathy
Adverse Effects
Major Toxicities
Hepatitis
Myopathy
Bone Marrow
suppression
Anemia
(Macrocytosis) (7% late, 1.8% early)
Leukopenia
(
Neutropenia
) (37% late, 4% early)
Management of toxicity
Interrupt treatment
Results in reversal of
Anemia
and
Neutropenia
Specific Therapy
Anemia
: Give
Erythropoietin
Neutropenia
: Give growth factors
Persistent
Anemia
or
Neutropenia
Change therapy
Safety
Avoid in
Lactation
Pregnancy
Alternative
nRTI
in pregnancy
Pregnancy registry exists
Monitoring
Advanced disease:
Complete Blood Count
each month
Early disease:
Complete Blood Count
every 2-3 months
Drug Interactions
CMV Prophylaxis agents (
Ganciclovir
or
Valganciclovir
)
Increased
Bone Marrow
suppression risk
Nevirapine
Increased
Granulocytopenia
risk (esp. children)
Resources
Zidovudine (DailyMed)
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ca9f0c57-fc8b-4da4-a987-0fc52b7fd4f4
References
Hamilton (2020) Tarascon Pocket Pharmacopoeia
(1998) Med Lett Drugs Ther 40(1041):115 [PubMed]
(2009) Treat Guidel Med Lett 7(78): 11-22 [PubMed]
Reust (2011) Am Fam Physician 83(12): 1443-51 [PubMed]
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