Select your primary concerns below. The tool will recommend which protease inhibitors may be most appropriate for your situation based on information from the article.
This is for informational purposes only. Always consult your HIV specialist before making treatment decisions.
Choosing the right protease inhibitor for HIV can feel like navigating a maze of pills, doses, and side‑effects. If you’ve landed on this page, you probably want to know how Indinavir measures up against the other options on the market and whether an alternative might suit your lifestyle or health needs better.
Indinavir is a synthetic protease inhibitor that blocks the HIV‑1 protease enzyme, preventing the virus from maturing into an infectious form. Sold under the brand name Crixivan, it was one of the first drugs in the class and remains a viable choice for many patients.
Key attributes:
Common side‑effects include kidney stones, high bilirubin, and a metallic taste. Because it’s cleared through the kidneys, patients with chronic kidney disease often need to switch to a drug that isn’t so renal‑heavy.
Even though Indinavir works well for many, several practical issues push clinicians and patients to consider other protease inhibitors:
Below is a side‑by‑side look at the most frequently prescribed alternatives.
Drug | Dosing Frequency | Key Metabolism | Renal Clearance | Common Side‑effects | Typical Cost (US$ per month) |
---|---|---|---|---|---|
Indinavir | 3× daily | CYP3A4 | 80% unchanged | Kidney stones, hyperbilirubinemia | ≈$300 |
Saquinavir | 2× daily (soft‑gel) or 3× daily (tablet) | CYP3A4 | Minimal | Diarrhea, nausea, rash | ≈$250 |
Lopinavir/ritonavir | 2× daily | CYP3A4 (boosted) | Low | GI upset, hyperlipidemia | ≈$400 |
Atazanavir | 1× daily (with food) or 2× daily (unboosted) | CYP3A4 (boosted with ritonavir) | Low | Jaundice, indirect hyperbilirubinemia | ≈$350 |
Darunavir | 1-2× daily (boosted) | CYP3A4 (boosted) | Low | Rash, metabolic changes | ≈$380 |
If you’ve experienced any of the following, it’s worth a chat with your HIV specialist:
Switching early can keep your viral load suppressed and protect your kidneys.
Saquinavir entered the market shortly after Indinavir. It’s available as a soft‑gel capsule that can be taken twice daily, simplifying the schedule. Because it’s not heavily excreted by the kidneys, it’s gentler on renal function.
Saquinavir’s biggest drawback is its reliance on a high‑fat meal for optimal absorption, which can be inconvenient for people watching their diet. It also has a higher propensity for drug‑interaction warnings, especially with statins.
Lopinavir/ritonavir combines two protease inhibitors in a single pill. Ritonavir acts as a “booster,” slowing the metabolism of lopinavir so the drug stays in the body longer. This lets patients stick to a twice‑daily regimen.
While the combo is potent, it often raises cholesterol and triglycerides, which can be a concern for patients with cardiovascular risk. It also has a distinctive taste that some find off‑putting.
Atazanavir is known for its once‑daily dosing when paired with ritonavir. It’s praised for causing fewer metabolic disturbances compared with lopinavir/ritonavir.
The trade‑off is a higher chance of developing indirect hyperbilirubinemia, which can cause yellowing of the skin. Usually it’s harmless, but it can be cosmetically concerning for some patients.
Darunavir is a newer, high‑potency protease inhibitor that works well against many resistant HIV strains. Dosed once or twice daily depending on the boost, it gives flexibility.
Side‑effects are generally mild, but the drug does interact with a broad range of medications, so a thorough medication review is essential before starting.
Talk to your provider about your lifestyle, lab results, and any side‑effects you’ve noticed. A tailored regimen can keep your viral load undetectable and your quality of life high.
Yes, most ibuprofen‑type NSAIDs are fine, but avoid high‑dose aspirin because it can increase bleeding risk when combined with other antiretrovirals.
Absolutely - aim for at least 2‑3liters per day. Hydration helps flush the drug and reduces stone formation.
Studies show that patients on once‑daily regimens have higher adherence rates, which translates to lower viral rebound risk.
Regular kidney function tests, urine analysis for crystals, and liver enzymes are key. Your doctor will schedule these every 3‑6months.
Usually a short overlap isn’t needed, but your clinician may stagger the change to keep viral suppression steady.
I am a pharmaceutical specialist passionate about advancing healthcare through innovative medications. I enjoy delving into current research and sharing insights to help people make informed health decisions. My career has enabled me to collaborate with researchers and clinicians on new therapeutic approaches. Outside of work, I find fulfillment in writing and educating others about key developments in pharmaceuticals.
Ted Whiteman, October 16, 2025
Wow, reading this feels like a trip through a pharmacy maze that never ends. Three doses a day? Who signed up for that schedule? I gotta say, the stone thing sounds like a horror movie subplot. If you can handle the water intake, maybe it's not the worst option. Still, I’d question why anyone would stay on a drug that makes you chase the bathroom.