Also indexed as: Proloprim, Trimpex

Summary of
Interactions with Vitamins, Herbs, and Foods
In some cases, an herb or supplement may appear in more than one category, which may seem
contradictory. For clarification, read the full article for details about the summarized
interactions.
May Be Beneficial: Depletion or
interference—The medication may deplete or interfere with the absorption or
function of the nutrient. Taking these nutrients may help replenish them. |
Calcium*
Folic acid*
Magnesium*
Vitamin B12*
Vitamin B6*
Vitamin K*
|
May Be Beneficial: Side effect
reduction/prevention—Taking these supplements may help reduce the likelihood and/or
severity of a potential side effect caused by the medication. |
Bifidobacterium longum*
Folic acid
Lactobacillus acidophilus*
Lactobacillus casei*
Saccharomyces boulardii*
Saccharomyces cerevisiae*
Vitamin K*
|
May Be Beneficial: Supportive
interaction—Taking these supplements may support or otherwise help your medication
work better. |
Saccharomyces boulardii*
|
Avoid: Adverse interaction—Avoid these supplements when taking this
medication because taking them together may cause undesirable or dangerous results. |
Potassium
|
| Reduced drug
absorption/bioavailability |
None known
|
An asterisk (*) next to an item in the summary indicates that the
interaction is supported only by weak, fragmentary, and/or contradictory scientific
evidence.
Interactions with Dietary Supplements
Calcium, Magnesium, Vitamin B12
Sulfonamides, including sulfamethoxazole, can
decrease absorption of calcium, magnesium, and vitamin B12.1 This is generally not
a problem when taking sulfamethoxazole for two weeks or less. People taking sulfamethoxazole
for longer than two weeks should ask their doctor about nutrient monitoring and
supplementation.
Note: Since sulfamethoxazole is often prescribed in combination with
trimethoprim (e.g., Bactrim® or Septra®), it may be easy to associate this
interaction with trimethoprim. However, this interaction is not known to occur with
trimethoprim alone.
Folic acid, Vitamin B6, Vitamin K
Sulfonamides, including sulfamethoxazole, can
interfere with the activity of folic acid, vitamin B6, and vitamin K.2 This is
generally not a problem when taking sulfamethoxazole for two weeks or less. People taking
sulfamethoxazole for longer than two weeks should ask their doctor about nutrient monitoring
and supplementation.
Note: Since sulfamethoxazole is often prescribed in combination with
trimethoprim (e.g., Bactrim® or Septra®), it may be easy to associate this
interaction with trimethoprim. However, this interaction is not known to occur with
trimethoprim alone.
The use of multivitamin supplements
containing folic acid diminishes the occurrence of birth defects associated with trimethoprim. According
to one study,3 pregnant women who took folic acid–containing multivitamin
supplements in addition to their prescription drugs had fewer babies with heart defects and
deformities of the upper lip and mouth.
TMP/SMX has been rarely associated with
folic acid-deficiency anemia.4 This action may be due to trimethoprim-induced folic
acid depletion.5 Trimethoprim and TMP/SMX should be used with caution in patients
with folic acid deficiency, for which blood tests are available. Folic acid replacement does
not interfere with the antibacterial activity of trimethoprim6 or
TMP/SMX.7
Potassium
TMP/SMX has been reported to elevate blood potassium and other constituents of blood (creatine
and BUN).8 9 In particular, people with impaired kidney function should
be closely monitored by their prescribing doctor for these changes. People taking trimethoprim
or TMP/SMX should talk with the prescribing doctor before taking any potassium supplements or
potassium-containing products, such as No Salt®, Salt Substitute®, Lite Salt®,
and even high-potassium foods (primarily
fruit).
Probiotics
A common side effect of antibiotics is
diarrhea, which may be caused by the elimination of beneficial bacteria normally found in
the colon. Controlled studies have shown that taking probiotic microorganisms—such as
Lactobacillus casei, Lactobacillus acidophilus, Bifidobacterium
longum, or Saccharomyces boulardii—helps prevent antibiotic-induced
diarrhea.10
The diarrhea experienced by some people who take antibiotics also might be due to an
overgrowth of the bacterium Clostridium difficile, which causes a disease known as
pseudomembranous colitis. Controlled studies have shown that supplementation with harmless
yeast—such as Saccharomyces boulardii11 or Saccharomyces
cerevisiae (baker’s or brewer’s yeast)12 —helps prevent
recurrence of this infection. In one study, taking 500 mg of Saccharomyces boulardii
twice daily enhanced the effectiveness of the antibiotic vancomycin in preventing recurrent
clostridium infection.13 Therefore, people taking antibiotics who later develop
diarrhea might benefit from supplementing with saccharomyces organisms.
Treatment with antibiotics also commonly leads to an overgrowth of yeast (Candida
albicans) in the vagina (candida
vaginitis) and the intestines (sometimes referred to as “dysbiosis”).
Controlled studies have shown that Lactobacillus acidophilus might prevent candida
vaginitis.14
Vitamin
K
Several cases of excessive bleeding have been reported in people who take
antibiotics.15 16 17 18 This side effect may be
the result of reduced vitamin K activity and/or reduced vitamin K production by bacteria in
the colon. One study showed that people who had taken broad-spectrum antibiotics had lower
liver concentrations of vitamin K2 (menaquinone), though vitamin K1 (phylloquinone) levels
remained normal.19 Several antibiotics appear to exert a strong effect on vitamin K
activity, while others may not have any effect. Therefore, one should refer to a specific
antibiotic for information on whether it interacts with vitamin K. Doctors of natural medicine
sometimes recommend vitamin K supplementation to people taking antibiotics. Additional
research is needed to determine whether the amount of vitamin K1 found in some multivitamins
is sufficient to prevent antibiotic-induced bleeding. Moreover, most multivitamins do not
contain vitamin K.
References:1. Holt GA. Food & Drug Interactions. Chicago: Precept
Press, 1998, 248–49, 250–1.
2. Holt GA. Food & Drug Interactions. Chicago: Precept
Press, 1998, 248–49, 251–2.
3. Hernández-Díaz S, Werler MM, Walker AM, Mitchell AA. Folic
acid antagonists during pregnancy and the risk of birth defects. New Engl J Med
2000;343:1608–14.
4. Sahai J. Urinary tract infections. In Applied Therapeutics: The
Clinical Use of Drugs, 6th ed. Vancouver, WA: Applied Therapeutics, 1995, 63–6.
5. Kahn SB, Fein SA, Brodsky I. Effects of trimethoprim on folate
metabolism in man. Clin Pharmacol Ther 1968;9:550–60.
6. Threlkeld DS, ed. Systemic Anti-Infectives, Miscellaneous
Anti-Infectives, Trimethoprim. In Facts and Comparisons Drug Information. St. Louis,
MO: Facts and Comparisons, Aug 1992, 408–a.
7. Sahai J. Urinary tract infections. In Applied Therapeutics: The
Clinical Use of Drugs, 6th ed. Vancouver, WA: Applied Therapeutics, 1995, 63–6.
8. Alappan R, Perazella MA, Buller GK. Hyperkalemia in hospitalized
patients treated with trimethoprim-sulfamethoxazole. Ann Intern Med
1996;124:316–20.
9. Perazella MA. Drug-induced hyperkalemia: Old culprits and new
offenders. Am J Med 2000;109:307–14 [review].
10. Elmer GW, Surawicz CM, McFarland LV. Biotherapeutic agents. A
neglected modality for the treatment and prevention of selected intestinal and vaginal
infections. JAMA 1996;275:870–6 [review].
11. Elmer GW, Surawicz CM, McFarland LV. Biotherapeutic agents. A
neglected modality for the treatment and prevention of selected intestinal and vaginal
infections. JAMA 1996;275:870–6 [review].
12. Schellenberg D, Bonington A, Champion CM, et al. Treatment of
Clostridium difficile diarrhoea with brewer’s yeast. Lancet
1994;343:171–2.
13. Surawicz CM, Elmer GW, Speelman P, et al. Prevention of
antibiotic-associated diarrhea by Saccharomyces boulardii: A prospective study.
Gastroenterol 1989;96:981–8.
14. Elmer GW, Surawicz CM, McFarland LV. Biotherapeutic agents. A
neglected modality for the treatment and prevention of selected intestinal and vaginal
infections. JAMA 1996;275:870–6 [review].
15. Suzuki K, Fukushima T, Meguro K, et al. Intracranial hemorrhage in an
infant owing to vitamin K deficiency despite prophylaxis. Childs Nerv Syst
1999;15:292–4.
16. Huilgol VR, Markus SL, Vakil NB. Antibiotic-induced iatrogenic
hemobilia. Am J Gastroenterol 1997;92:706–7.
17. Bandrowsky T, Vorono AA, Borris TJ, Marcantoni HW. Amoxicllin-related
postextraction bleeding in an anticoagulated patient with tranexamic acid rinses. Oral
Surg Oral Med Oral Pathol Oral Radiol Endod 1996;82:610–2.
18. Kaiser CW, McAuliffe JD, Barth RJ, Lynch JA. Hypoprothrombinemia and
hemorrhage in a surgical patient treated with cefotetan. Arch Surg
1991;126:524–5.
19. Conly J, Stein K. Reduction of vitamin K2 concentration in human
liver associated with the use of broad spectrum antimicrobials. Clin Invest Med
1994;17:531–9.