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Drug Interactions between didanosine and Mylocel

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

didanosine hydroxyurea

Applies to: didanosine and Mylocel (hydroxyurea)

GENERALLY AVOID: Hydroxyurea may potentiate the risk of toxicities associated with the use of didanosine (ddI), a nucleoside reverse transcriptase inhibitor (NRTI). Specifically, concurrent use of hydroxyurea and ddI, with or without stavudine (d4T), has been associated with an increased risk of pancreatitis and peripheral neuropathy, the former of which may be fatal. Although rare, the syndrome of lactic acidosis and severe hepatomegaly with steatosis (with or without pancreatitis) may also occur more frequently with the combination than with ddI alone. Investigators theorize that hydroxyurea may enhance the potency of nucleoside analogues, particularly ddI, by preferentially depleting intracellular deoxyadenosine triphosphate and, to a lesser extent, other deoxynucleoside triphosphates. This action results in increased incorporation of the active metabolites of ddI and other NRTIs into DNA synthesis and disruption of the process.

MANAGEMENT: In general, antiretroviral regimens containing ddI and hydroxyurea should probably not be prescribed if other treatment options are available. Close observation for signs and symptoms of toxicity is recommended if these drugs must be used together, particularly in patients with advanced HIV disease and/or elderly patients. Both drugs should be suspended if pancreatitis is suspected, and ddI discontinued permanently if pancreatitis is confirmed. Prompt withdrawal of these drugs is also essential in patients who develop peripheral neuropathy to avoid irreversible damage. Therapy with ddI may be reinstituted following resolution of neuropathy symptoms, but reduced dosages are recommended. Likewise, treatment should be suspended in any patient who develops clinical or laboratory findings suggestive of lactic acidosis or pronounced hepatotoxicity, and permanent discontinuation considered if the syndrome is confirmed. Patients should be advised to seek medical attention promptly if symptoms of toxicity occur such as nausea, vomiting, abdominal pain, fatigue, unexplained weight loss, tachypnea, dyspnea, motor weakness, numbness, tingling, and pain in hands and feet.

References

  1. (2002) "Product Information. Videx (didanosine)." Bristol-Myers Squibb
  2. Moore RD, Wong WME, Keruly JC, McArthur JC (2000) "Incidence of neuropathy in HIV-infected patients on monotherapy versus those on combination therapy with didanosine, stavudine and hydroxyurea." Aids, 14, p. 273-8
  3. Cepeda JA, Wilks D (2000) "Excess peripheral neuropathy in patients treated with hydroxyurea plus didanosine and stavudine for HIV infection." Aids, 14, p. 332-3
  4. Longhurst HJ, Pinching AJ (2001) "Drug points - Pancreatitis associated with hydroxyurea in combination with didanosine." Br Med J, 322, p. 81
  5. Moore RD, Keruly JC, Chaisson RE (2001) "Incidence of pancreatitis in HIV-infected patients receiving nucleoside reverse transcriptase inhibitor drugs." Aids, 15, p. 617-20
  6. Havlir DV, Gilbert PB, Bennett K, et al. (2001) "Effects of treatment intensification with hydroxyurea in HIV-infected patients with virologic suppression." AIDS, 15, p. 1379-88
  7. Coghlan ME, Sommadossi JP, Jhala NC, Many WJ, Saag MS, Johnson VA (2001) "Symptomatic lactic acidosis in hospitalized antiretroviral-treated patients with human immunodeficiency virus infection: a report of 12 cases." Clin Infect Dis, 33, p. 1914-21
  8. Cerner Multum, Inc. "UK Summary of Product Characteristics."
  9. Cerner Multum, Inc. "Australian Product Information."
View all 9 references

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Drug and food interactions

Moderate

didanosine food

Applies to: didanosine

ADJUST DOSING INTERVAL: Didanosine bioavailability is decreased when administered with food. Loss of efficacy may result.

MANAGEMENT: Didanosine should be administered in the fasting state, at least 30 minutes before or more than 2 hours after eating.

References

  1. (2002) "Product Information. Videx (didanosine)." Bristol-Myers Squibb

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Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.