Drug Interactions between Avelox and didanosine
This report displays the potential drug interactions for the following 2 drugs:
- Avelox (moxifloxacin)
- didanosine
Interactions between your drugs
didanosine moxifloxacin
Applies to: didanosine and Avelox (moxifloxacin)
ADJUST DOSING INTERVAL: Concomitant administration with didanosine buffered tablets or pediatric oral solution may reduce the oral bioavailability of moxifloxacin and other quinolone antibiotics. The mechanism is reduced quinolone absorption due to chelation with metallic cations from buffering agents and antacids used in certain formulations of didanosine. In 12 healthy volunteers, administration of an antacid containing aluminum hydroxide-magnesium hydroxide (900 mg-600 mg/10 mL dose) 4 hours before, simultaneously, and 2 hours after a single 400 mg dose of moxifloxacin reduced the relative bioavailability of moxifloxacin by 23%, 60%, and 26%, respectively. The pharmacokinetics of moxifloxacin have not been studied in combination with the various didanosine formulations, but significant reductions in bioavailability have been reported for ciprofloxacin, another quinolone, in interaction studies with didanosine.
MANAGEMENT: Moxifloxacin should be administered at least 4 hours before or 8 hours after didanosine buffered tablets or pediatric oral solution, and patients should be monitored for potentially decreased antimicrobial efficacy during concomitant therapy. Didanosine buffered powder for oral solution, which uses a citrate-phosphate buffer, and the delayed-release capsules, which are not buffered, are not expected to cause this interaction.
References (9)
- Polk RE (1989) "Drug-drug interactions with ciprofloxacin and other fluoroquinolones." Am J Med, 87, s76-81
- Marchbanks CR (1993) "Drug-drug interactions with fluoroquinolones." Pharmacotherapy, 13, s23-8
- (2002) "Product Information. Videx (didanosine)." Bristol-Myers Squibb
- Sahai J, Gallicano K, Oliveras L, Khaliq S, Hawley-Foss N, Garber G (1993) "Cations in the didanosine tablet reduce ciprofloxacin bioavailability." Clin Pharmacol Ther, 53, p. 292-7
- Deppermann KM, Lode H (1993) "Fluoroquinolones: interaction profile during enteral absorption." Drugs, 45 Suppl 3, p. 65-72
- Knupp CA, Barbhaiya RH (1997) "A multiple-dose pharmacokinetic interaction study between didanosine (videx(r)) and ciprofloxacin (cipro(r)) in male subjects seropositive for HIV but asymptomatic." Biopharm Drug Dispos, 18, p. 65-77
- (2001) "Product Information. Avelox (moxifloxacin)." Bayer
- Stass H, Bottcher MF, Ochmann K (2001) "Evaluation of the influence of antacids and H2 antagonists on the absorption of moxifloxacin after oral administration of a 400mg dose to healthy volunteers." Clin Pharmacokinet, 40 Suppl 1, p. 39-48
- Damle BD, Mummaneni V, Kaul S, Knupp C (2002) "Lack of Effect of Simultaneously Administered Didanosine Encapsulated Enteric Bead Formulation (Videx EC) on Oral Absorption of Indinavir, Ketoconazole, or Ciprofloxacin." Antimicrob Agents Chemother, 46, p. 385-91
Drug and food interactions
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
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.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
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. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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