Zerit is a prescription antiretroviral used in combination therapy for HIV-1. Known generically as stavudine, it belongs to the nucleoside reverse transcriptase inhibitor (NRTI) class and works by blocking the virus’s ability to replicate. While once widely used, Zerit has largely been replaced by newer, better-tolerated options in modern HIV treatment guidelines due to its risk of serious side effects such as peripheral neuropathy, pancreatitis, and lactic acidosis. It remains relevant in specific, carefully selected cases under specialist supervision. Because of its safety profile, Zerit should only be started, adjusted, or stopped under the guidance of an experienced HIV clinician.
Zerit (stavudine) is an antiretroviral medicine used as part of combination antiretroviral therapy (ART) for HIV-1 infection. As an NRTI, it mimics a natural nucleoside and blocks reverse transcriptase, the enzyme HIV uses to copy its genetic material. This reduces viral replication and helps lower the viral load when combined with other effective HIV medications.
Because of significant toxicity concerns, Zerit is no longer recommended as a preferred or alternative option in most contemporary HIV guidelines. Safer, more effective regimens have largely replaced it. In rare circumstances—such as intolerance or resistance to multiple other agents—experienced clinicians may still consider Zerit as part of a tailored regimen, always weighing risks versus benefits and monitoring closely for adverse effects.
Zerit dosing is individualized and typically weight-based in adults. Historically, adults weighing 60 kg (132 lb) or more received 40 mg twice daily, and those weighing less than 60 kg received 30 mg twice daily. In children, dosing is based on body weight or body surface area. Exact dosing, adjustments, and formulation choice (capsules versus reconstituted oral solution) should be determined by an HIV specialist.
Zerit can be taken with or without food. If you have kidney impairment, dose reductions and extended dosing intervals are often required, and dialysis patients may need supplemental dosing after sessions. Do not adjust your dose on your own. Because stavudine’s toxicity can be dose-related and exacerbated by other medicines, your prescriber will carefully balance companion drugs, individual risk factors (such as preexisting neuropathy), and lab findings before setting your regimen.
Stavudine has a well-documented risk of serious, sometimes life-threatening adverse effects. The most concerning include lactic acidosis and severe hepatomegaly with steatosis (fatty liver), which can present with profound fatigue, abdominal pain, nausea, shortness of breath, rapid breathing, and weakness. These events are more likely when Zerit is used with certain other drugs (notably didanosine) or in patients with risk factors. Immediate medical evaluation is warranted if symptoms suggesting lactic acidosis or liver injury occur.
Peripheral neuropathy—numbness, tingling, burning, or pain in the hands or feet—is another major precaution. It can be dose-limiting and may become irreversible if therapy continues despite symptoms. Risk increases with concurrent neurotoxic drugs (such as isoniazid), alcohol misuse, malnutrition, diabetes, or advanced HIV disease. Prompt reporting of neuropathy symptoms and potential dose interruption or discontinuation are essential.
Other important precautions include pancreatitis risk, dyslipidemia, insulin resistance, and lipodystrophy/lipoatrophy (fat loss in the face and limbs). Use with significant hepatic disease or active hepatitis requires caution and frequent monitoring. In pregnancy, stavudine is generally avoided, particularly in combination with didanosine, due to increased risk of life-threatening lactic acidosis. In the United States, individuals with HIV are advised not to breastfeed to prevent transmission.
Do not use Zerit if you have a known hypersensitivity to stavudine or any component of the formulation. Concomitant use with zidovudine is contraindicated because of antagonistic effects between these thymidine analogs, which can compromise antiviral efficacy.
Strong clinical caution—often amounting to practical contraindication—is warranted when considering coadministration with didanosine or hydroxyurea given the markedly increased risks of pancreatitis, hepatotoxicity, and lactic acidosis. In many cases, these combinations should be avoided altogether.
Common side effects may include headache, gastrointestinal upset (nausea, vomiting, diarrhea), fatigue, and rash. While these can be mild, persistent or worsening symptoms should be discussed with your clinician to adjust the regimen or manage side effects proactively.
Serious adverse reactions require urgent attention. These include peripheral neuropathy (burning, numbness, or pain in hands/feet), pancreatitis (severe abdominal pain radiating to the back, nausea, vomiting), lactic acidosis (deep, rapid breathing; severe weakness; abdominal discomfort), and hepatotoxicity (jaundice, dark urine, right upper quadrant pain). Body shape changes (lipoatrophy), hyperlactatemia, dyslipidemia, and insulin resistance have also been reported with stavudine and other older NRTIs. Your care team will monitor labs and clinical signs to detect problems early, and they may substitute a modern agent if toxicity emerges.
The risk profile is amplified when Zerit is combined with certain agents, used at higher exposures due to renal impairment, or taken by individuals with preexisting neuropathy, malnutrition, or advanced HIV. Immediate reporting of alarming symptoms can prevent complications and guide a timely switch to safer alternatives.
Avoid combining Zerit with zidovudine due to antagonism. Concomitant use with didanosine significantly increases the risk of life-threatening lactic acidosis and pancreatitis and is generally avoided. Adding hydroxyurea further amplifies these toxicities and should not be done outside of exceptional, closely supervised circumstances.
Drugs that can worsen neuropathy (for example, isoniazid, vincristine, certain chemotherapies) may increase peripheral nerve toxicity when given with stavudine. Alcohol misuse compounds pancreatitis and neuropathy risk. Hepatotoxic agents, including some antituberculosis and antifungal medications, may add to liver stress and require more intensive monitoring if coadministered.
Always share a full list of prescription and nonprescription drugs, supplements, and herbal products with your HIV specialist. Because modern HIV regimens are designed to minimize interactions and toxicity, your provider will usually prefer agents with safer profiles over Zerit when possible.
If you miss a dose, take it as soon as you remember unless it is close to the time for your next scheduled dose. If it is nearly time for the next dose, skip the missed dose and resume your regular schedule. Do not double up to make up for a missed dose. Consistent adherence to your overall antiretroviral therapy is vital—contact your care team if you are missing doses due to side effects, cost, or access barriers so they can help troubleshoot.
Suspected overdose warrants immediate medical evaluation. Symptoms can overlap with known toxicities, including severe fatigue, gastrointestinal distress, rapid breathing, confusion, neuropathy, abdominal pain, and signs of liver injury. Management is supportive, with prompt discontinuation of stavudine and treatment of complications such as lactic acidosis or pancreatitis. In cases of significant renal impairment, dialysis can remove some stavudine, but clinical stabilization and monitoring of acid-base status, lactate levels, and liver and pancreatic enzymes are the priorities.
Store Zerit capsules at room temperature, typically 20°C to 25°C (68°F to 77°F), protected from excessive heat and moisture. Keep in the original container and out of reach of children. For the oral solution prepared from powder, follow the pharmacy’s instructions; many preparations require refrigeration and have a limited shelf-life after reconstitution. Do not use beyond the expiration date, and dispose of unused medicine according to pharmacist guidance or local take-back programs.
In the United States, Zerit (stavudine) is a prescription-only medication. It is not legal or safe to buy Zerit without prescription. Appropriate use requires individualized medical evaluation, drug–drug interaction review, and ongoing monitoring for side effects. Attempting to purchase antiretrovirals without licensed oversight risks treatment failure, drug resistance, and serious harm from preventable toxicities.
HealthSouth Rehabilitation Hospital of Tallahassee does not dispense or sell medications without a prescription. Instead, it offers a legal, structured pathway to care: coordinating with your infectious diseases specialist, supporting transitions of care after hospitalization or rehabilitation, assisting with medication management, and helping you navigate insurance coverage and patient assistance programs when eligible. If you do not currently have an HIV clinician, the team can help connect you to licensed providers who can evaluate you and, when appropriate, prescribe evidence-based, guideline-concordant HIV therapy. This approach keeps you safe, compliant with U.S. law, and aligned with best-practice standards in HIV care.
Zerit, the brand name for stavudine, is a nucleoside reverse transcriptase inhibitor (NRTI) that blocks HIV’s reverse transcriptase enzyme, stopping viral DNA synthesis and reducing viral replication; it’s a thymidine analog that also carries a risk of mitochondrial toxicity.
No—due to significant long-term toxicities and the availability of safer, more effective alternatives, Zerit has been phased out of most modern HIV treatment guidelines and may be unavailable in many regions.
Serious risks include lactic acidosis and severe hepatomegaly with steatosis (boxed warning), pancreatitis, and peripheral neuropathy; urgent symptoms include persistent nausea, abdominal pain, shortness of breath, unusual weakness, or tingling and numbness in hands or feet.
Common effects can include headache, nausea, diarrhea, fatigue, and changes in body fat (lipoatrophy—loss of fat in the face, arms, legs, and buttocks).
Avoid if you’ve had severe hypersensitivity to stavudine, active pancreatitis, or significant peripheral neuropathy; it should not be combined with didanosine or zidovudine due to serious toxicity and antagonism, and it’s generally not recommended in pregnancy.
Stavudine can be taken with or without food; dosing is typically twice daily and weight-based, with adjustments for kidney function—your clinician will individualize the regimen.
Take it as soon as you remember unless it’s close to your next dose; do not double up—resume your regular schedule and contact your clinician if multiple doses are missed.
Yes—lipoatrophy is strongly associated with stavudine, often noticeable in the face, limbs, and buttocks; risk increases with longer use, which is why it has largely been replaced by other NRTIs.
Yes—numbness, tingling, burning, or pain in the hands and feet can occur; dose changes or discontinuation may be needed if symptoms develop, especially if other neurotoxic drugs are used.
Clinicians typically monitor liver enzymes, lactate (if symptomatic), pancreatic enzymes if pancreatitis is suspected, kidney function for dosing, and clinical signs of neuropathy and lipoatrophy.
Avoid combining with didanosine (ddI) due to lactic acidosis and pancreatitis risk, and with zidovudine (AZT) due to antagonism; hydroxyurea markedly increases toxicity; use caution with alcohol and other neurotoxic or pancreatotoxic drugs.
It is not recommended in pregnancy due to maternal toxicity risks, especially lactic acidosis when combined with didanosine; for breastfeeding, HIV guidelines vary by region, but in settings where safe formula is available, breastfeeding is typically discouraged regardless of regimen.
Dose adjustments are required for reduced kidney function; pre-existing liver disease increases the risk of lactic acidosis and hepatic steatosis, so careful monitoring or alternative therapy is preferred.
No—stavudine has no activity against HBV; other NRTIs like tenofovir and lamivudine/emtricitabine are used when HIV/HBV coinfection is present.
Capsules are stored at room temperature; the reconstituted oral solution is typically refrigerated and used within the time frame specified by the manufacturer and pharmacist.
Alcohol can increase the risk of pancreatitis and worsen liver stress, so limiting or avoiding alcohol is advisable while on stavudine.
Look for persistent nausea, vomiting, abdominal pain, rapid or labored breathing, unusual fatigue, and muscle pain; this is a medical emergency.
Because safer, once-daily agents with superior tolerability and long-term metabolic profiles became available, and because stavudine’s mitochondrial toxicity leads to neuropathy, lipoatrophy, and lactic acidosis.
When used in an effective combination regimen, virologic suppression typically occurs within weeks to months, but due to toxicity, stavudine is rarely chosen today.
Do not stop abruptly without clinician guidance; your provider will switch you to an appropriate alternative NRTI to maintain viral suppression and minimize rebound.
Tenofovir (TDF) is preferred for first-line therapy due to once-daily dosing, potent efficacy, and a better mitochondrial toxicity profile; TDF has renal and bone risks, while Zerit is strongly linked to neuropathy and lipoatrophy.
TAF generally offers excellent efficacy with reduced kidney and bone toxicity compared with TDF, and far less mitochondrial toxicity than stavudine; TAF is favored over Zerit in modern regimens.
Both are NRTIs, but lamivudine is well tolerated, once daily, and active against hepatitis B, while stavudine is twice daily with higher rates of peripheral neuropathy, lipoatrophy, and lactic acidosis; 3TC is preferred.
Emtricitabine is generally very well tolerated, with mild side effects and HBV activity; stavudine carries significant mitochondrial toxicity and cosmetic fat loss, making FTC the safer choice.
Abacavir requires HLA-B*57:01 testing to avoid hypersensitivity and may carry cardiovascular risk in some patients, but it lacks the severe lipoatrophy and neuropathy typical of stavudine; ABC is commonly preferred when appropriate.
Zidovudine can cause anemia and neutropenia, while stavudine is more associated with lipoatrophy and neuropathy; both can cause lactic acidosis, but AZT is generally considered safer than d4T and remains an option in certain scenarios.
No—stavudine and zidovudine are thymidine analogs that antagonize each other’s antiviral activity; guidelines recommend against using them together.
No—this combination substantially increases the risk of lactic acidosis and pancreatitis, including fatal cases, especially in pregnancy, and is contraindicated.
Modern tenofovir-based backbones are once daily, potent, and better tolerated long term, with fewer mitochondrial toxicities and improved metabolic profiles compared with stavudine.
Both can cause fat loss, but the risk and severity are higher with stavudine; switching away from d4T can partially improve but may not fully reverse lipoatrophy.
Peripheral neuropathy is much more common with stavudine and didanosine than with lamivudine, emtricitabine, abacavir, or tenofovir.
In modern practice, no—its efficacy can be matched or exceeded by safer agents with simpler dosing and better long-term tolerability, which is why Zerit has been largely retired from routine use.