The management of
anticoagulant therapy is an important component of the treatment of various disease
states. Maintaining the narrow therapeutic range required for the safe and
effective use of warfarin is essential to avoid suboptimal dosing and adverse
events. Numerous drug interactions with warfarin are present due to alterations
in absorption, distribution, and metabolism.
The severity of interactions with warfarin varies greatly and dictates
very different recommendations for management and monitoring. In the most
insignificant interactions, no change in dosage or monitoring is necessary, whereas
some interactions require a significant empiric reduction in warfarin dosage
and close monitoring of INR.
Reports of the
interaction between acetaminophen and warfarin are sparse and generally have small
sample sizes. Prospective studies have
associated acetaminophen with elevated INR values in patients receiving warfarin
with previously stable INR values. In these patients, elevations in INR
generally occurred with the administration of acetaminophen 2–4 g/day for several days and returned to the therapeutic
range within days of discontinuing the acetaminophen. One troublesome aspect of
the interaction between acetaminophen and warfarin is the wide availability and
use of acetaminophen. One study identified that 18.5% of a large number of patients taking warfarin also used acetaminophen-containing products. The presence of acetaminophen in a patient’s
drug regimen may be neglected unintentionally as it is present in countless
combination over-the-counter and prescription products.
Mechanism of interaction
Warfarin is
available as a racemic mixture of R and S-enantiomers. Both R- and S-warfarin
are metabolized by various hepatic enzymes to inactive metabolites.
Interactions that increase S-warfarin, which has 3-fold higher potency, are known
to increase the anticoagulant effect, whereas the resulting effects of
interactions that solely increase R-warfarin are controversial (eg.
ciprofloxacin inhibits metabolism of R-warfarin but generally does not affect
the INR). S-warfarin is predominantly
metabolized by CYP2C9 and minimally by CYP3A4, and R-warfarin is
metabolized by CYP3A4 and CYP1A2, and minimally by CYP2C19. Acetaminophen undergoes
metabolism primarily by glucuronidation and sulfation with up to 15% metabolized
by CYP1A2, CYP2E1, and CYP3A4. Acetaminophen does not interact directly with warfarin
metabolism at CYP2C9 but has been observed to inhibit CYP3A4 in vitro. This is a suggested mechanism of the
interaction with acetaminophen, as acetaminophen interacts with both
enantiomers at CYP3A4 and the R-warfarin at CYP1A2. Additional components of the interaction include
the observation that R-warfarin has been seen to inhibit CYP2C9 in vitro,
potentially increasing the concentration of S-warfarin.
If acetaminophen is
necessary at doses near or greater than 2 g/day for more than 1 day, extra attention
to the INR may be prudent. Extra care should be taken in patients susceptible
to fluctuations in INR, such as geriatric patients or those at high risk for bleeding
or who have a history of significant bleeding.
Take away points:
- Some patients are likely to be susceptible to increases in INR due to a warfarin-acetaminophen interaction
- Acetaminophen ≥2 g/day for multiple days has been repeatedly shown to elevate the INR in those on warfarin
- Acetaminophen is present in many over-the-counter products a person might not mention at first during a medication history
- Some medications that inhibit CYP2C9 with serious impact on the INR are: amiodarone, fluconazole (Diflucan) capecitabine (Xeloda), sulfamethoxazole/trimethoprim (Bactrim), fluvoxamine (Luvox), metronidazole (Flagyl), voriconazole (VFEND)
References:
Hughes GJ, Patel PN, Saxena N. Effect of Acetaminophen on International Normalized
Ratio in Patients Receiving Warfarin Therapy.
Pharmacotherapy
2011;31(6):591-7.
photo by sun dazed
photo by sun dazed
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