Lamtidine
Lamtidine is a fictional antiviral medication used primarily in the treatment of viral infections such as Hepatitis B and HIV/AIDS. It is a nucleoside analog reverse transcriptase inhibitor (NRTI) that works by inhibiting the reverse transcriptase enzyme, which is essential for the replication of certain viruses.
Mechanism of Action[edit | edit source]
Lamtidine is a synthetic analog of deoxycytidine. It is phosphorylated intracellularly to its active triphosphate form, which competes with the natural substrate, deoxycytidine triphosphate, for incorporation into viral DNA. Once incorporated, it causes chain termination, thereby inhibiting viral replication.
Pharmacokinetics[edit | edit source]
Lamtidine is well absorbed from the gastrointestinal tract, with an oral bioavailability of approximately 80%. It is widely distributed throughout the body and has a low protein binding of about 10%. The drug is metabolized in the liver and has an elimination half-life of approximately 12 hours. It is primarily excreted through the kidneys.
Clinical Uses[edit | edit source]
Lamtidine is indicated for the treatment of chronic Hepatitis B infection and as part of combination therapy for HIV/AIDS. It is often used in conjunction with other antiretroviral agents to enhance efficacy and reduce the risk of resistance development.
Adverse Effects[edit | edit source]
Common side effects of Lamtidine include headache, nausea, and fatigue. Serious adverse effects may include lactic acidosis, hepatomegaly with steatosis, and pancreatitis. Patients should be monitored for signs of liver dysfunction and metabolic abnormalities.
Drug Interactions[edit | edit source]
Lamtidine may interact with other medications that are metabolized by the liver. Caution should be exercised when co-administering with drugs that induce or inhibit hepatic enzymes.
Contraindications[edit | edit source]
Lamtidine is contraindicated in patients with known hypersensitivity to the drug or any of its components. It should be used with caution in patients with pre-existing liver disease.
Also see[edit | edit source]
- Antiviral drug
- Nucleoside analog
- Reverse transcriptase inhibitor
- Hepatitis B treatment
- HIV/AIDS management
Drugs for HIV Infection, in the Subclass Antiretroviral Agents
- Fusion Inhibitors (HIV)
- Integrase Inhibitors (HIV)
- Nonnucleoside Reverse Transcriptase Inhibitors (HIV)
- Nucleoside Analogues (HIV)
- Protease Inhibitors (HIV)
HCV NS5A Inhibitors
HCV NS5B Inhibitors (Polymerase inhibitors)
- Asunaprevir, Boceprevir, Glecaprevir, Grazoprevir, Paritaprevir, Simeprevir, Telaprevir, Voxilaprevir
Combination Therapies
Drugs for Herpes Virus
- infections (HSV), CMV, others
Acyclovir, Cidofovir, Famciclovir, Foscarnet, Ganciclovir, Valacyclovir, Valganciclovir
Drugs for Influenza
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Contributors: Prab R. Tumpati, MD