Drug Interactions between estradiol and Fe C
This report displays the potential drug interactions for the following 2 drugs:
- estradiol
- Fe C (ascorbic acid/carbonyl iron)
Interactions between your drugs
ascorbic acid estradiol
Applies to: Fe C (ascorbic acid/carbonyl iron) and estradiol
Ascorbic acid may increase the serum levels of estrogens in oral contraceptives. The mechanism may be due to decreased metabolism of the estrogen by competitive inhibition involving ascorbic acid. Consider monitoring the patient more closely for estrogen-related side effects if ascorbic acid is coadministered.
References (4)
- Back DJ, Breckenridge AM, MacIver M, L'e Orme M, Purba H Rowe PH (1981) "Interaction of ethinyloestradiol with ascorbic acid in man." Br Med J, 282, p. 1516
- Morris JC, Beeley L, Ballantine N (1981) "Interaction of ethinyloestradiol with ascorbic acid in man." Br Med J, 283, p. 503
- Briggs MH (1981) "Megadose vitamin C and metabolic effects of the pill." Br Med J, 283, p. 1547
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
Drug and food interactions
carbonyl iron food
Applies to: Fe C (ascorbic acid/carbonyl iron)
ADJUST DOSING INTERVAL: Concomitant use of some oral medications may reduce the bioavailability of orally administered iron, and vice versa.
Food taken in conjunction with oral iron supplements may reduce the bioavailability of the iron. However, in many patients intolerable gastrointestinal side effects occur necessitating administration with food.
MANAGEMENT: Ideally, iron products should be taken on an empty stomach (i.e., at least 1 hour before or 2 hours after meals), but if this is not possible, administer with meals and monitor the patient more closely for a subtherapeutic effect. Some studies suggest administration of iron with ascorbic acid may enhance bioavailability. In addition, administration of oral iron products and some oral medications should be separated whenever the bioavailability of either agent may be decreased. Consult the product labeling for specific separation times and monitor clinical responses as appropriate.
References (2)
- "Product Information. Feosol (ferrous sulfate)." SmithKline Beecham
- (2021) "Product Information. Accrufer (ferric maltol)." Shield Therapeutics
estradiol food
Applies to: estradiol
Coadministration with grapefruit juice may increase the bioavailability of oral estrogens. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall induced by certain compounds present in grapefruits. In a small, randomized, crossover study, the administration of ethinyl estradiol with grapefruit juice (compared to herbal tea) increased peak plasma drug concentration (Cmax) by 37% and area under the concentration-time curve (AUC) by 28%. Based on these findings, grapefruit juice is unlikely to affect the overall safety profile of ethinyl estradiol. However, as with other drug interactions involving grapefruit juice, the pharmacokinetic alterations are subject to a high degree of interpatient variability. Also, the effect on other estrogens has not been studied.
References (2)
- Weber A, Jager R, Borner A, et al. (1996) "Can grapefruit juice influence ethinyl estradiol bioavailability?" Contraception, 53, p. 41-7
- Schubert W, Eriksson U, Edgar B, Cullberg G, Hedner T (1995) "Flavonoids in grapefruit juice inhibit the in vitro hepatic metabolism of 17B-estradiol." Eur J Drug Metab Pharmacokinet, 20, p. 219-24
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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