Drug interactions between WARFARIN and many antimicrobials

Questions often come up about how to handle alerts for drug interactions between warfarin and many antimicrobials....
Abdelwahab Ward, BS Pharm, PharmD

Questions often come up about how to handle alerts for drug interactions between warfarin and many antimicrobials. The risk of an interaction varies, but it can be significant, especially when the antimicrobial affects warfarin metabolism. For more details, see Table (1) below. Follow these rules of thumb...

  • TMP/SMX (Septazole, Septrin) and metronidazole (Flagyl) are the worst culprits.
    • Suggest trying to avoid them. They can significantly raise INR and increase bleeding risk 2- to 4-fold, especially in the elderly. Suggest an alternative, such as nitrofurantoin (Uvamin Retard) or plain trimethoprim instead of TMP/SMX for urinary tract infections or vaginal clindamycin instead of oral metronidazole for bacterial vaginosis.
      • If TMP/SMX or metronidazole is needed, recommend monitoring INR closely and possibly lowering the warfarin dose 25% to 40% in patients at high bleeding risk.
  • For other antimicrobials: Suggest monitoring INR about 5 days after starting the drug and then again after it's stopped. Explain that interactions are more likely with azole antifungals, quinolones, most macrolides or doxycycline. On the other hand, interactions are less likely with amoxicillin, azithromycin, oral cephalosporins or 3 days or less of a quinolone. Keep in mind that INR changes are also more likely if the patient is acutely ill. Explain that infection and changes in diet can also affect INR.
  • Rifampin is a different story. It can increase warfarin metabolism and LOWER the INR and it takes several weeks to see the full effect. Recommend checking INR weekly for several weeks when starting rifampin and possibly increasing the warfarin dose by 25% to 50%.

Table (1). Warfarin, antimicrobials drug interaction
Drug Class Effect on Warfarin/Mechanism Recommendations/Comments
Azole antifungals
Fluconazole (Diflucan)
Itraconazole (Sporanox), Ketoconazole (Nizoral), Miconazole (Miconaz), Posaconazole, Voriconazole (Vfend)		 Increased response due to inhibition of warfarin metabolism. Increased INR also reported with intravaginal and topical miconazole. INR can be increased significantly with single doses of fluconazole.

Dose-related interaction, but can be seen with lower doses.


Monitor INR when therapy started, stopped, or dose changed. Some clinicians consider empirically lowering the warfarin dose by about 25%.
Cephalosporins Second- and third-generation cephalosporins might increase the effect of warfarin by inhibiting the production of vitamin K-dependent clotting factors and other mechanisms. Oral cephalosporins such as cefaclor, cefixime, cefpodoxime, cefuroxime have generally not been shown to interact with warfarin.


Avoid use of cefotetan. It can increase INR directly.


Consider monitoring INR when therapy started or stopped.
Fluoroquinolones
Ciprofloxacin (Cipro)
Gemifloxacin, Levofloxacin (Tavanic), Moxifloxacin (Avelox), Norfloxacin, Ofloxacin		 Increased response possibly due to inhibition of warfarin metabolism, displacement of warfarin from protein binding sites, or disruption of intestinal flora that contribute to vitamin K synthesis. Increase in INR is typically seen within first week of quinolone therapy.


Monitor INR when any fluoroquinolone started or stopped.
Griseofulvin Decreased response possibly due to induced hepatic metabolism. Effect on warfarin is gradual. Maximum effect might not be seen for several weeks or more.
Monitor INR when therapy started, stopped, or dose changed. Continue to monitor until INR stable.
Isoniazid Increased response possibly due to inhibition of warfarin metabolism. Slow INH acetylators are at greatest risk.Monitor INR when therapy started, stopped, or dose changed.
Macrolides
Azithromycin (Zithromax), Clarithromycin, Erythromycin		 Macrolides can increase the effect of warfarin through inhibition of hepatic metabolism of warfarin.
(Azithromycin affects warfarin by an unknown mechanism).		 Increased INR reported with all macrolides. Strongest evidence with erythromycin. Increased INR reported with ophthalmic erythromycin.

Monitor INR when any macrolide is started or stopped.
Metronidazole(Flagyl) Increased response caused by inhibition of metabolism of warfarin. Avoid use if possible. Metronidazole can dramatically increase INR. Topical preparations are less of a problem due to minimal systemic absorption.

If used, monitor INR closely when therapy started or stopped. Some clinicians consider empirically lowering the warfarin dose by 25% to 40%.
Penicillins High doses of IV penicillins increase the risk of warfarin-associated bleeding by inhibiting platelet function. Oral amoxicillin and amoxicillin/clavulanic acid may increase the risk of bleeding with warfarin.


Exception: Decreased response seen with dicloxacillin and nafcillin possibly due to enhanced metabolism of warfarin.		 Oral penicillin G or V and ampicillin do not appear to interact with warfarin.
Monitor INR several days after start of dicloxacillin or nafcillin, and again after treatment ends. Effects might persist for weeks after dicloxacillin or nafcillin is discontinued.

For high-dose IV penicillins and amoxicillin or amoxicillin/clavulanic acid, monitor INR when therapy started or stopped.
Rifampin
 Decreased response due to increased hepatic clearance of warfarin. Avoid use if possible.
Effect usually seen within one to three weeks after starting rifampin.

If used, monitor INR closely for at least two weeks when therapy is started, stopped, or dose is changed. Some clinicians consider empirically increasing the dose of warfarin by 25% to 50%.

It can take more than a month after rifampin is stopped for warfarin metabolism to normalize. Check INR at least weekly until stable.
SulfonamidesSulfamethoxazole Increased effect resulting from reduced warfarin clearance, displacement of warfarin from protein binding sites, alterations in gut flora. Increased INR reported with TMP/SMX, sulfamethoxazole, sulfisoxazole. (Including with 3-day courses of TMP/SMX for acute cystitis).
Avoid use if possible. A case study showed a more than three-fold increase in INR after six days of concomitant therapy with TMP/SMX. Increased risk of bleeding may be especially significant in the elderly.

If used, monitor INR when therapy is started or stopped. Some clinicians consider empirically lowering the warfarin dose by 25% to 50%.
Telithromycin
 Increased effect likely due to reduced hepatic metabolism of warfarin. Monitor INR closely when telithromycin is started or stopped. A case report noted an increase in INR over the first five days of concomitant therapy.
Tetracyclines
Doxycycline, Minocycline, Tetracycline		 Increased response due to unknown mechanisms. Increased INR seen with doxycycline and tetracycline.


Monitor INR when therapy with any tetracycline is started or stopped.

Sensitivity of patients to drug interactions can vary in terms of magnitude of response, time of onset, and duration of interaction’s effect. Some clinicians recommend checking INR about five days after start of interacting drug, and then adjusting warfarin dose as needed. Prolonged fever can increase sensitivity to warfarin by enhancing the breakdown of vitamin K-dependent clotting factors. Factors that increase the risk of bleeding in warfarin patients include advanced age, history of GI bleeding, hypertension, cerebrovascular disease, severe heart disease, concurrent use of interacting drugs, alcohol abuse, liver disease, and renal insufficiency.

References

Abdelwahab Ward, BS Pharm, PharmD