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Drug Interactions between PediaCare Smooth Melts Acetaminophen Fever Reducer/Pain Reliever and warfarin

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Moderate

warfarin acetaminophen

Applies to: warfarin and PediaCare Smooth Melts Acetaminophen Fever Reducer/Pain Reliever (acetaminophen)

MONITOR: Acetaminophen (APAP) may potentiate the hypoprothrombinemic effect of warfarin and other vitamin K antagonists, although data are somewhat conflicting and the precise mechanism of interaction has not been established. A toxic metabolite of APAP is thought to be involved by interfering with vitamin K-dependent clotting factors. The interaction has generally been associated with prolonged ingestion of relatively high APAP dosages (greater than 1.3 g/day continuously for greater than 1 week) but not with brief, intermittent exposures of average doses. Reported increases in prothrombin time or INR from most studies were often small but statistically significant, although there have been isolated case reports citing bleeding episodes and clinically significant alterations in coagulation parameters. In contrast, one retrospective study found no significant effect of APAP 2000 to 2500 mg/day on the anticoagulant effect of phenprocoumon, and another study reported no effect of APAP 4 g/day for 2 weeks on single-dose warfarin pharmacokinetics and pharmacodynamics in healthy volunteers.

MANAGEMENT: Due to the lack of safer alternatives, acetaminophen is considered the analgesic and antipyretic drug of choice for patients receiving warfarin and similar anticoagulants. However, caution is recommended during concomitant therapy, particularly if high dosages of APAP are used continuously for more than a few days, or in patients with risk factors such as ethanol consumption, old age, and malnutrition. Closer monitoring of INR may be advisable. Patients should be advised to promptly report any signs of bleeding to their physician, including pain, swelling, headache, dizziness, weakness, prolonged bleeding from cuts, increased menstrual flow, vaginal bleeding, nosebleeds, bleeding of gums from brushing, unusual bleeding or bruising, red or brown urine, or red or black stools.

References

  1. Antlitz AM, Mead JA Jr, Tolentino MA (1968) "Potentiation of oral anticoagulant therapy by acetaminophen." Curr Ther Res Clin Exp, 10, p. 501-7
  2. Boeijinga JJ, Boerstra EE, Ris P, Breimer DD, Jeletich-Bastiaanse A (1982) "Interaction between paracetamol and coumarin anticoagulants." Lancet, 1, p. 506
  3. Wells PS, Holbrook AM, Crowther NR, Hirsh J (1994) "Interactions of warfarin with drugs and food." Ann Intern Med, 121, p. 676-83
  4. Hylek EM, Heiman H, Skates SJ, Sheehan MA, Singer DE (1998) "Acetaminophen and other risk factors for excessive warfarin anticoagulation." JAMA, 279, p. 657-62
  5. Bell RB (1998) "Acetaminophen and warfarin: undesirable synergy." JAMA, 279, p. 702-3
  6. Singer DE, Skates SJ (1999) "Acetaminophen and risk factors for excess anticoagulation with warfarin." JAMA, 281, p. 37
  7. Kwan D, Bartle WR, Walker SE (1999) "The effects of acetaminophen on pharmacokinetics and pharmacodynamics of warfarin." J Clin Pharmacol, 39, p. 68-75
  8. Bagheri H, Bernhard NB, Montastruc JL (1999) "Potentiation of the acenocoumarol anticoagulant effect by acetaminophen." Ann Pharmacother, 33, p. 506
  9. Shek KL, Chan LN, Nutescu E (1999) "Warfarin-acetaminophen drug interaction revisited." Pharmacotherapy, 19, p. 1153-8
  10. Fattinger K, Frisullo R, Masche U, Braunschweig S, Meier PJ, Roos M (2002) "No clinically relevant drug interaction between paracetamol and phenprocoumon based on a pharmacoepidemiological cohort study in medical inpatients." Eur J Clin Pharmacol, 57, p. 863-7
  11. Gebauer MG, Nyfort-Hansen K, Henschke PJ, Gallus AS (2003) "Warfarin and acetaminophen interaction." Pharmacotherapy, 23, p. 109-12
View all 11 references

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Drug and food interactions

Major

acetaminophen food

Applies to: PediaCare Smooth Melts Acetaminophen Fever Reducer/Pain Reliever (acetaminophen)

GENERALLY AVOID: Chronic, excessive consumption of alcohol may increase the risk of acetaminophen-induced hepatotoxicity, which has included rare cases of fatal hepatitis and frank hepatic failure requiring liver transplantation. The proposed mechanism is induction of hepatic microsomal enzymes during chronic alcohol use, which may result in accelerated metabolism of acetaminophen and increased production of potentially hepatotoxic metabolites.

MANAGEMENT: In general, chronic alcoholics should avoid regular or excessive use of acetaminophen. Alternative analgesic/antipyretic therapy may be appropriate in patients who consume three or more alcoholic drinks per day. However, if acetaminophen is used, these patients should be cautioned not to exceed the recommended dosage (maximum 4 g/day in adults and children 12 years of age or older).

References

  1. Kaysen GA, Pond SM, Roper MH, Menke DJ, Marrama MA (1985) "Combined hepatic and renal injury in alcoholics during therapeutic use of acetaminophen." Arch Intern Med, 145, p. 2019-23
  2. O'Dell JR, Zetterman RK, Burnett DA (1986) "Centrilobular hepatic fibrosis following acetaminophen-induced hepatic necrosis in an alcoholic." JAMA, 255, p. 2636-7
  3. Seeff LB, Cuccherini BA, Zimmerman HJ, Adler E, Benjamin SB (1986) "Acetaminophen hepatotoxicity in alcoholics." Ann Intern Med, 104, p. 399-404
  4. Thummel KE, Slattery JT, Nelson SD (1988) "Mechanism by which ethanol diminishes the hepatotoxicity of acetaminophen." J Pharmacol Exp Ther, 245, p. 129-36
  5. McClain CJ, Kromhout JP, Peterson FJ, Holtzman JL (1980) "Potentiation of acetaminophen hepatotoxicity by alcohol." JAMA, 244, p. 251-3
  6. Kartsonis A, Reddy KR, Schiff ER (1986) "Alcohol, acetaminophen, and hepatic necrosis." Ann Intern Med, 105, p. 138-9
  7. Prescott LF, Critchley JA (1983) "Drug interactions affecting analgesic toxicity." Am J Med, 75, p. 113-6
  8. (2002) "Product Information. Tylenol (acetaminophen)." McNeil Pharmaceutical
  9. Whitcomb DC, Block GD (1994) "Association of acetaminopphen hepatotoxicity with fasting and ethanol use." JAMA, 272, p. 1845-50
  10. Bonkovsky HL (1995) "Acetaminophen hepatotoxicity, fasting, and ethanol." JAMA, 274, p. 301
  11. Nelson EB, Temple AR (1995) "Acetaminophen hepatotoxicity, fasting, and ethanol." JAMA, 274, p. 301
  12. Zimmerman HJ, Maddrey WC (1995) "Acetaminophen (paracetamol) hepatotoxicity with regular intake of alcohol: analysis of instances of therapeutic misadventure." Hepatology, 22, p. 767-73
View all 12 references

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Moderate

warfarin food

Applies to: warfarin

MONITOR: Vitamin K may antagonize the hypoprothrombinemic effect of oral anticoagulants. Vitamin K is a cofactor in the synthesis of blood clotting factors that are inhibited by oral anticoagulants, thus intake of vitamin K through supplements or diet can reverse the action of oral anticoagulants. Resistance to oral anticoagulants has been associated with consumption of foods or enteral feedings high in vitamin K content. Likewise, a reduction of vitamin K intake following stabilization of anticoagulant therapy may result in elevation of the INR and bleeding complications. Foods rich in vitamin K include beef liver, broccoli, Brussels sprouts, cabbage, collard greens, endive, kale, lettuce, mustard greens, parsley, soy beans, spinach, Swiss chard, turnip greens, watercress, and other green leafy vegetables. Moderate to high levels of vitamin K are also found in other foods such as asparagus, avocados, dill pickles, green peas, green tea, canola oil, margarine, mayonnaise, olive oil, and soybean oil. Snack foods containing the fat substitute, olestra, are fortified with 80 mcg of vitamin K per each one ounce serving so as to offset any depletion of vitamin K that may occur due to olestra interference with its absorption. Whether these foods can alter the effect of oral anticoagulants has not been extensively studied. One small study found that moderate consumption (1.5 servings/day) does not significantly affect the INR after one week in patients receiving long-term anticoagulation.

Consumption of large amounts of mango fruit has been associated with enhanced effects of warfarin. The exact mechanism of interaction is unknown but may be related to the vitamin A content, which may inhibit metabolism of warfarin. In one report, thirteen patients with an average INR increase of 38% reportedly had consumed one to six mangos daily 2 to 30 days prior to their appointment. The average INR decreased by 17.7% after discontinuation of mango ingestion for 2 weeks. Rechallenge in two patients appeared to confirm the interaction.

Limited data also suggest a potential interaction between warfarin and cranberry juice resulting in changes in the INR and/or bleeding complications. The mechanism is unknown but may involve alterations in warfarin metabolism induced by flavonoids contained in cranberry juice. At least a dozen reports of suspected interaction have been filed with the Committee on Safety of Medicines in the U.K. since 1999, including one fatality. In the fatal case, the patient's INR increased dramatically (greater than 50) six weeks after he started drinking cranberry juice, and he died from gastrointestinal and pericardial hemorrhage. However, the patient was also taking cephalexin for a chest infection and had not eaten for two weeks prior to hospitalization, which may have been contributing factors. Other cases involved less dramatic increases or instabilities in INR following cranberry juice consumption, and a decrease was reported in one, although details are generally lacking. In a rare published report, a 71-year-old patient developed hemoptysis, hematochezia, and shortness of breath two weeks after he started drinking 24 ounces of cranberry juice a day. Laboratory test results on admission revealed a decrease in hemoglobin, an INR greater than 18, and prothrombin time exceeding 120 seconds. The patient recovered after warfarin doses were withheld for several days and he was given packed red blood cells, fresh-frozen plasma, and subcutaneous vitamin K. It is not known if variations in the constituents of different brands of cranberry juice may affect the potential for drug interactions.

There have been several case reports in the medical literature of patients consuming grapefruit, grapefruit juice, or grapefruit seed extract who experienced increases in INR. R(+) warfarin, the less active of the two enantiomers of warfarin, is partially metabolized by CYP450 3A4. Depending on brand, concentration, dose and preparation, grapefruit juice may be considered a moderate to strong inhibitor of CYP450 3A4, thus coadministration with warfarin may decrease the clearance of R(+) warfarin. However, the clinical significance of this effect has not been established. A pharmacokinetic study found no effect on the PT or INR values of nine warfarin patients given 8 oz of grapefruit juice three times a day for one week.

A patient who was stabilized on warfarin developed a large hematoma in her calf in association with an elevated INR of 14 following consumption of approximately 3 liters of pomegranate juice in the week prior to admission. In vitro data suggest that pomegranate juice can inhibit CYP450 2C9, the isoenzyme responsible for the metabolic clearance of the biologically more active S(-) enantiomer of warfarin. In rats, pomegranate juice has also been shown to inhibit intestinal CYP450 3A4, the isoenzyme that contributes to the metabolism of R(+) warfarin.

Black currant juice and black currant seed oil may theoretically increase the risk of bleeding or bruising if used in combination with anticoagulants. The proposed mechanism is the antiplatelet effects of the gamma-linolenic acid constituent in black currants.

Soy protein in the form of soy milk was thought to be responsible for a case of possible warfarin antagonism in an elderly male stabilized on warfarin. The exact mechanism of interaction is unknown, as soy milk contains only trace amounts of vitamin K. Subtherapeutic INR values were observed approximately 4 weeks after the patient began consuming soy milk daily for the treatment of hypertriglyceridemia. No other changes in diet or medications were noted during this time. The patient's INR returned to normal following discontinuation of the soy milk with no other intervention.

An interaction with chewing tobacco was suspected in a case of warfarin therapy failure in a young male who was treated with up to 25 to 30 mg/day for 4.5 years. The inability to achieve adequate INR values led to eventual discontinuation of the chewing tobacco, which resulted in an INR increase from 1.1 to 2.3 in six days. The authors attributed the interaction to the relatively high vitamin K content in smokeless tobacco.

MANAGEMENT: Intake of vitamin K through supplements or diet should not vary significantly during oral anticoagulant therapy. The diet in general should remain consistent, as other foods containing little or no vitamin K such as mangos and soy milk have been reported to interact with warfarin. Some experts recommend that continuous enteral nutrition should be interrupted for one hour before and one hour after administration of the anticoagulant dose and that enteral formulas containing soy protein should be avoided. Patients should also consider avoiding or limiting the consumption of cranberry juice or other cranberry formulations (e.g., encapsulated dried cranberry powder), pomegranate juice, black currant juice, and black currant seed oil.

References

  1. Andersen P, Godal HC (1975) "Predictable reduction in anticoagulant activity of warfarin by small amounts of vitamin K." Acta Med Scand, 198, p. 269-70
  2. Westfall LK (1981) "An unrecognized cause of warfarin resistance." Drug Intell Clin Pharm, 15, p. 131
  3. Lee M, Schwartz RN, Sharifi R (1981) "Warfarin resistance and vitamin K." Ann Intern Med, 94, p. 140-1
  4. Zallman JA, Lee DP, Jeffrey PL (1981) "Liquid nutrition as a cause of warfarin resistance." Am J Hosp Pharm, 38, p. 1174
  5. Griffith LD, Olvey SE, Triplett WC (1982) "Increasing prothrombin times in a warfarin-treated patient upon withdrawal of ensure plus." Crit Care Med, 10, p. 799-800
  6. Kempin SJ (1983) "Warfarin resistance caused by broccoli." N Engl J Med, 308, p. 1229-30
  7. Watson AJ, Pegg M, Green JR (1984) "Enteral feeds may antagonise warfarin." Br Med J, 288, p. 557
  8. Walker FB (1984) "Myocardial infarction after diet-induced warfarin resistance." Arch Intern Med, 144, p. 2089-90
  9. Howard PA, Hannaman KN (1985) "Warfarin resistance linked to enteral nutrition products." J Am Diet Assoc, 85, p. 713-5
  10. Karlson B, Leijd B, Hellstrom K (1986) "On the influence of vitamin K-rich vegetables and wine on the effectiveness of warfarin treatment." Acta Med Scand, 220, p. 347-50
  11. Pedersen FM, Hamberg O, Hess K, Ovesen L (1991) "The effect of dietary vitamin K on warfarin-induced anticoagulation." J Intern Med, 229, p. 517-20
  12. Parr MD, Record KE, Griffith GL, et al. (1982) "Effect of enteral nutrition on warfarin therapy." Clin Pharm, 1, p. 274-6
  13. Wells PS, Holbrook AM, Crowther NR, Hirsh J (1994) "Interactions of warfarin with drugs and food." Ann Intern Med, 121, p. 676-83
  14. O'Reilly RA, Rytand DA (1980) ""Resistance" to warfarin due to unrecognized vitamin K supplementation." N Engl J Med, 303, p. 160-1
  15. Kazmier FJ, Spittell JA Jr (1970) "Coumarin drug interactions." Mayo Clin Proc, 45, p. 249-55
  16. Chow WH, Chow TC, Tse TM, Tai YT, Lee WT (1990) "Anticoagulation instability with life-threatening complication after dietary modification." Postgrad Med J, 66, p. 855-7
  17. MacLeod SM, Sellers EM (1976) "Pharmacodynamic and pharmacokinetic drug interactions with coumarin anticoagulants." Drugs, 11, p. 461-70
  18. Sullivan DM, Ford MA, Boyden TW (1998) "Grapefruit juice and the response to warfarin." Am J Health Syst Pharm, 55, p. 1581-3
  19. Harrell CC, Kline SS (1999) "Vitamin K-supplemented snacks containing olestra: Implication for patients taking warfarin." Jama J Am Med Assn, 282, p. 1133-4
  20. Beckey NP, Korman LB, Parra D (1999) "Effect of the moderate consumption of olestra in patients receiving long-term warfarin therapy." Pharmacotherapy, 19, p. 1075-9
  21. Monterrey-Rodriguez J (2002) "Interaction between warfarin and mango fruit." Ann Pharmacother, 36, p. 940-1
  22. Cambria-Kiely JA (2002) "Effect of soy milk on warfarin efficacy." Ann Pharmacother, 36, p. 1893-6
  23. MHRA. Mediciines and Healthcare products Regulatory Agency. Committee on Safety of Medicines (2003) Possible interaction between warfarin and cranberry juice. http://medicines.mhra.gov.uk/ourwork/monitorsafequalmed/currentproblems/currentproblems.htm
  24. Suvarna R, Pirmohamed M, Henderson L (2003) "Possible interaction between warfarin and cranberry juice." BMJ, 327, p. 1454
  25. Kuykendall JR, Houle MD, Rhodes RS (2004) "Possible warfarin failure due to interaction with smokeless tobacco." Ann Pharmacother, 38, p. 595-7
  26. Grant P (2004) "Warfarin and cranberry juice: an interaction?" J Heart Valve Dis, 13, p. 25-6
  27. Rindone JP, Murphy TW (2006) "Warfarin-cranberry juice interaction resulting in profound hypoprothrombinemia and bleeding." Am J Ther, 13, p. 283-4
  28. Brandin H, Myrberg O, Rundlof T, Arvidsson AK, Brenning G (2007) "Adverse effects by artificial grapefruit seed extract products in patients on warfarin therapy." Eur J Clin Pharmacol, 63, p. 565-70
  29. Agencia EspaƱola de Medicamentos y Productos Sanitarios Healthcare (2008) Centro de informaciĆ³n online de medicamentos de la AEMPS - CIMA. https://cima.aemps.es/cima/publico/home.html
  30. Griffiths AP, Beddall A, Pegler S (2008) "Fatal haemopericardium and gastrointestinal haemorrhage due to possible interaction of cranberry juice with warfarin." J R Soc Health, 128, p. 324-6
  31. Guo LQ, Yamazoe Y (2004) "Inhibition of cytochrome P450 by furanocoumarins in grapefruit juice and herbal medicines." Acta Pharmacol Sin, 25, p. 129-36
  32. Hamann GL, Campbell JD, George CM (2011) "Warfarin-cranberry juice interaction." Ann Pharmacother, 45, e17
  33. Jarvis S, Li C, Bogle RG (2010) "Possible interaction between pomegranate juice and warfarin." Emerg Med J, 27, p. 74-5
  34. Roberts D, Flanagan P (2011) "Case report: Cranberry juice and warfarin." Home Healthc Nurse, 29, p. 92-7
  35. Ge B, Zhang Z, Zuo Z (2014) "Updates on the clinical evidenced herb-warfarin interactions." Evid Based Complement Alternat Med, 2014, p. 957362
  36. Wohlt PD, Zheng L, Gunderson S, Balzar SA, Johnson BD, Fish JT (2009) "Recommendations for the use of medications with continuous enteral nutrition." Am J Health Syst Pharm, 66, p. 1438-67
  37. Bodiford AB, Kessler FO, Fermo JD, Ragucci KR (2013) "Elevated international normalized ratio with the consumption of grapefruit and use of warfarin." SAGE Open Med Case Rep, p. 1-3
View all 37 references

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Moderate

warfarin food

Applies to: warfarin

MONITOR: Enhanced hypoprothrombinemic response to warfarin has been reported in patients with acute alcohol intoxication and/or liver disease. The proposed mechanisms are inhibition of warfarin metabolism and decreased synthesis of clotting factors. Binge drinking may exacerbate liver impairment and its metabolic ability in patients with liver dysfunction. The risk of bleeding may be increased. Conversely, reductions in INR/PT have also been reported in chronic alcoholics with liver disease. The proposed mechanism is that continual drinking of large amounts of alcohol induces the hepatic metabolism of anticoagulants. Effects are highly variable and significant INR/PT fluctuations are possible.

MANAGEMENT: Patients taking oral anticoagulants should be counseled to avoid large amounts of ethanol, but moderate consumption (one to two drinks per day) are not likely to affect the response to the anticoagulant in patients with normal liver function. Frequent INR/PT monitoring is recommended, especially if alcohol intake changes considerably. It may be advisable to avoid oral anticoagulant therapy in patients with uncontrollable drinking problems. Patients should be advised to promptly report any signs of bleeding to their doctor, including pain, swelling, headache, dizziness, weakness, prolonged bleeding from cuts, increased menstrual flow, nosebleeds, bleeding of gums from brushing, unusual bleeding or bruising, red or brown urine, or red or black stools.

References

  1. Breckenridge A (1975) "Clinical implications of enzyme induction." Basic Life Sci, 6, p. 273-301
  2. Karlson B, Leijd B, Hellstrom K (1986) "On the influence of vitamin K-rich vegetables and wine on the effectiveness of warfarin treatment." Acta Med Scand, 220, p. 347-50
  3. Udall JA (1970) "Drug interference with warfarin therapy." Clin Med, 77, p. 20-5
  4. (2001) "Product Information. Coumadin (warfarin)." DuPont Pharmaceuticals
  5. Havrda DE, Mai T, Chonlahan J (2005) "Enhanced antithrombotic effect of warfarin associated with low-dose alcohol consumption." Pharmacotherapy, 25, p. 303-7
  6. Cerner Multum, Inc. "UK Summary of Product Characteristics."
  7. Canadian Pharmacists Association (2006) e-CPS. http://www.pharmacists.ca/function/Subscriptions/ecps.cfm?link=eCPS_quikLink
  8. Pharmaceutical Society of Australia (2006) APPGuide online. Australian prescription products guide online. http://www.appco.com.au/appguide/default.asp
View all 8 references

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Moderate

warfarin food

Applies to: warfarin

MONITOR: Multivitamin preparations containing vitamin K may antagonize the hypoprothrombinemic effect of oral anticoagulants in some patients. Vitamin K1 in its active, reduced form serves as a cofactor in the generation of functional clotting factors, during which it becomes oxidized. It is reactivated in a process that is inhibited by oral anticoagulants, thus intake of additional vitamin K through supplements or diet can reverse the action of oral anticoagulants. Although the amount of vitamin K in over-the-counter multivitamin preparations is generally well below the dose thought to affect anticoagulation, there have been isolated case reports of patients stabilized on warfarin whose INR decreased following initiation of a multivitamin supplement and returned to therapeutic levels upon cessation of the multivitamin. Increases in warfarin dosage were required in some cases when the multivitamin was continued. One patient whose warfarin dosage was increased developed a subcapsular hematoma in her right kidney two weeks after she discontinued the multivitamin without informing her physician. Her INR was 13.2 and she was treated with vitamin K and fresh frozen plasma. It is possible that patients with low vitamin K status may be particularly susceptible to the interaction. Investigators have shown that vitamin K deficiency can cause an oversensitivity to even small increases in vitamin K intake. In one study where warfarin-stabilized patients were given a multivitamin tablet containing 25 mcg of vitamin K1 daily for 4 weeks, subtherapeutic INRs occurred in 9 of 9 patients with low vitamin K1 levels (<1.5 mcg/L) and only 1 of 7 patients with normal vitamin K1 levels (>4.5 mcg/L). INR decreased by a median of 0.51 and warfarin dosage had to be increased by 5.3% in patients with low vitamin K1 levels, whereas INR and warfarin dosage did not change significantly in patients with normal vitamin K1 levels. The prevalence of vitamin K deficiency may be small, but significant in the anticoagulated population. In a survey of 179 consecutive ambulatory patients on stable warfarin therapy attending an anticoagulation clinic, 22 (12.3%) were found to have vitamin K1 deficiency (<0.1 ng/mL).

MANAGEMENT: The potential for multivitamin supplements containing even low levels of vitamin K to affect anticoagulation should be recognized. In particular, elderly and/or malnourished patients may require more frequent monitoring of INR following the initiation or discontinuation of a multivitamin supplement, and the anticoagulant dosage adjusted as necessary.

References

  1. Kurnik D, Loebstein R, Rabinovitz H, Austerweil N, Halkin H, Almog S (2004) "Over-the-counter vitamin K1-containing multivitamin supplements disrupt warfarin anticoagulation in vitamin K1-depleted patients. A prospective, controlled trial." Thromb Haemost, 92, p. 1018-24
  2. Kumik D, Lubetsky A, Loebstein R, Almog S, Halkin H (2003) "Multivitamin supplements may affect warfarin anticoagulation in susceptible patients." Ann Pharmacother, 37, p. 1603-6
  3. Ducharlet KN, Katz B, Leung S (2011) "Multivitamin supplement interaction with warfarin therapy." Australas J Ageing, 30, p. 41-2

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Therapeutic duplication warnings

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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.