isentress
isentress Uses, Dosage, Side Effects, Food Interaction and all others data.
isentress is an antiretroviral drug produced by Merck & Co., used to treat HIV infection. It received approval by the U.S. Food and Drug Administration (FDA) on 12 October 2007, the first of a new class of HIV drugs, the integrase inhibitors, to receive such approval.
Trade Name | isentress |
Availability | Prescription only |
Generic | Raltegravir |
Raltegravir Other Names | Raltegravir |
Related Drugs | Biktarvy, Truvada, tenofovir, ritonavir, zidovudine, abacavir, emtricitabine, Complera, Atripla, Stribild |
Weight | 600mg, , 400mg, 100mg, 25mg |
Type | Film Coated Tablet, Tablet, Oral Granule For Reconstitution, Oral Tablet, Chewable |
Formula | C20H21FN6O5 |
Weight | Average: 444.4163 Monoisotopic: 444.155746017 |
Protein binding | 83% |
Groups | Approved |
Therapeutic Class | |
Manufacturer | Merck Sharp & Dohme Limited, Merck Sharp & Dohme (uk) Limited, Msd Pharmaceuticals Indian Private Ltd |
Available Country | Saudi Arabia, Canada, United Kingdom, India, United States, France, Italy, Netherlands, Portugal, Spain, Switzerland, |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
isentress is an antiretroviral agent used for the treatment of HIV infections in conjunction with other antiretrovirals.
For the treatment of HIV-1 infection in conjunction with other antiretrovirals.
isentress is also used to associated treatment for these conditions: Human Immunodeficiency Virus Type 1 (HIV-1) Infection, Post-exposure prophylaxis for occupational exposure to HIV therapy
How isentress works
isentress inhibits HIV integrase to prevent the viral genome being incorporated into the human genome. isentress is primarily metabolized by glucuronidation.
Food Interaction
- Take with or without food.
isentress Drug Interaction
Minor: etravirine, ritonavirUnknown: contained in alcoholic beverages , aspirin, lorazepam, diphenhydramine, bictegravir / emtricitabine / tenofovir alafenamide, emtricitabine / tenofovir alafenamide, omega-3 polyunsaturated fatty acids, heparin, lithium, pregabalin, acetaminophen, darunavir, cholestyramine, vitamin a topical, bioflavonoids, emtricitabine / tenofovir, cholecalciferol, bupropion
isentress Disease Interaction
Moderate: hemodialysis, liver disease, myopathy/rhabdomyolysis, PKU
Volume of Distribution
Approximately 83% bound to human plasma protein and is minimally distributed into red blood cells (blood-to-plasma partitioning ratio of 0.6).
Elimination Route
Absorbed from the gastrointestinal tract.
Half Life
9 hours
Clearance
The major mechanism of clearance of raltegravir in humans is glucuronidation mediated by UGT1A1, the renal clearance of unchanged drug is a minor pathway of elimination of raltegravir (9% of total dose).
Elimination Route
Feces and urine
Innovators Monograph
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