Drug Guide
Didanosine
Classification
Therapeutic: Antiretroviral agent for HIV infection
Pharmacological: Nucleoside Reverse Transcriptase Inhibitor (NRTI)
FDA Approved Indications
- Treatment of HIV-1 infection in combination with other antiretroviral agents
Mechanism of Action
Didanosine is a nucleoside analog that inhibits HIV reverse transcriptase, leading to termination of viral DNA elongation during reverse transcription.
Dosage and Administration
Adult: Typically 250 mg once daily on an empty stomach (at least 30 minutes before or 2 hours after meals). Dosage may vary based on patient weight and clinical response.
Pediatric: Dosage varies based on body weight; usually 250 mg/m² once daily. Precise dosing must be individualized.
Geriatric: No specific dosage adjustment solely based on age; however, renal function should be monitored.
Renal Impairment: Dose adjustments are required in renal impairment; typically, the interval is prolonged.
Hepatic Impairment: No specific dosage adjustment; caution due to potential accumulation.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed in body fluids and tissues.
Metabolism: Primarily hydrolyzed in tissues; minimal metabolism.
Excretion: Mostly excreted unchanged in urine.
Half Life: Approximately 4-6 hours.
Contraindications
- Known hypersensitivity to didanosine or any components of the formulation
Precautions
- Lactic acidosis and hepatic failure can occur, especially in pregnant women, women of childbearing age, and obese patients. Caution in patients with pre-existing pancreatitis or hepatic disease, including hepatitis B or C. Monitor for peripheral neuropathy, pancreatitis, and hepatic toxicity.
Adverse Reactions - Common
- Headache (Common)
- Nausea (Common)
- Diarrhea (Common)
- Peripheral neuropathy (Less common)
Adverse Reactions - Serious
- Pancreatitis (Rare)
- Lactic acidosis with hepatomegaly (Rare)
- Hepatic failure (Rare)
- Severe hypersensitivity reactions (Rare)
Drug-Drug Interactions
- Allopurinol - may increase didanosine levels.
- Zidovudine - potential antagonism in effect.
- Alcohol - enhances lactic acidosis risk.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor clinical response, check for signs of pancreatitis (abdominal pain, nausea), liver function tests, serum amylase, and serum lactate levels.
Diagnoses:
- Risk for infection related to HIV status
- Risk for lactic acidosis
Implementation: Administer on an empty stomach, instruct about adherence. Monitor for adverse effects.
Evaluation: Assess viral load reduction and CD4 counts; monitor for adverse reactions.
Patient/Family Teaching
- Take medication exactly as prescribed, preferably on an empty stomach.
- Report symptoms of pancreatitis (severe abdominal pain), lactic acidosis (weakness, nausea, fast breathing), or hepatic symptoms.
- Do not abruptly stop medication.
- Use contraception as advised; discuss pregnancy considerations.
Special Considerations
Black Box Warnings:
- Lactic acidosis and severe hepatomegaly with steatosis, which can be fatal, have been reported. Use with caution.
Genetic Factors: No specific genetic testing required.
Lab Test Interference: May interfere with certain laboratory tests, including those for lactic acid levels.
Overdose Management
Signs/Symptoms: Severe nausea, vomiting, pancreatitis, hepatic failure.
Treatment: Supportive care; no specific antidote. Hemodialysis may be considered in severe cases to remove drug.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F), away from moisture and light.
Stability: Stable within expiration date when stored properly.