Drug Interaction Report
3 potential interactions and/or warnings found for the following 2 drugs:
- gefitinib
- MagneBind 400 (calcium carbonate / magnesium carbonate)
Interactions between your drugs
calcium carbonate gefitinib
Applies to: MagneBind 400 (calcium carbonate / magnesium carbonate), gefitinib
ADJUST DOSING INTERVAL: Coadministration with drugs that elevate gastric pH such as H2-receptor antagonists and antacids may decrease the plasma concentrations of gefitinib. According to the manufacturer, the solubility of gefitinib is pH-dependent and decreases sharply between pH 4 and 6, becoming practically insoluble above pH 7. When gefitinib 250 mg was administered to healthy male volunteers (n=26) one hour following two oral 450 mg doses of ranitidine with sodium bicarbonate as needed to achieve a sustained gastric pH above 5.0, mean gefitinib peak plasma concentration (Cmax) and systemic exposure (AUC) decreased by 71% and 47%, respectively, compared to administration of gefitinib alone. High doses of short-acting antacids may have a similar effect if taken regularly in close proximity to gefitinib administration.
MANAGEMENT: The possibility of a diminished therapeutic response to gefitinib should be considered during coadministration with H2-receptor antagonists or antacids. If concomitant treatment is required, the manufacturer recommends administering gefitinib 6 hours before or 6 hours after an H2-receptor antagonist or antacid.
References (5)
- (2023) "Product Information. Iressa (gefitinib)." Astra-Zeneca Pharmaceuticals
- (2022) "Product Information. Apo-Gefitinib (gefitinib)." Apotex Inc
- (2023) "Product Information. Iressa (gefitinib)." AstraZeneca UK Ltd
- (2021) "Product Information. Iressa (gefitinib)." AstraZeneca Pty Ltd
- Tang W, Tomkinson H, Masson E (2017) "Effect of sustained elevated gastric pH levels on gefitinib exposure." Clin Pharmacol Drug Dev, 6, p. 517-23
magnesium carbonate gefitinib
Applies to: MagneBind 400 (calcium carbonate / magnesium carbonate), gefitinib
ADJUST DOSING INTERVAL: Coadministration with drugs that elevate gastric pH such as H2-receptor antagonists and antacids may decrease the plasma concentrations of gefitinib. According to the manufacturer, the solubility of gefitinib is pH-dependent and decreases sharply between pH 4 and 6, becoming practically insoluble above pH 7. When gefitinib 250 mg was administered to healthy male volunteers (n=26) one hour following two oral 450 mg doses of ranitidine with sodium bicarbonate as needed to achieve a sustained gastric pH above 5.0, mean gefitinib peak plasma concentration (Cmax) and systemic exposure (AUC) decreased by 71% and 47%, respectively, compared to administration of gefitinib alone. High doses of short-acting antacids may have a similar effect if taken regularly in close proximity to gefitinib administration.
MANAGEMENT: The possibility of a diminished therapeutic response to gefitinib should be considered during coadministration with H2-receptor antagonists or antacids. If concomitant treatment is required, the manufacturer recommends administering gefitinib 6 hours before or 6 hours after an H2-receptor antagonist or antacid.
References (5)
- (2023) "Product Information. Iressa (gefitinib)." Astra-Zeneca Pharmaceuticals
- (2022) "Product Information. Apo-Gefitinib (gefitinib)." Apotex Inc
- (2023) "Product Information. Iressa (gefitinib)." AstraZeneca UK Ltd
- (2021) "Product Information. Iressa (gefitinib)." AstraZeneca Pty Ltd
- Tang W, Tomkinson H, Masson E (2017) "Effect of sustained elevated gastric pH levels on gefitinib exposure." Clin Pharmacol Drug Dev, 6, p. 517-23
Drug and food interactions
calcium carbonate food
Applies to: MagneBind 400 (calcium carbonate / magnesium carbonate)
ADJUST DOSING INTERVAL: Administration with food may increase the absorption of calcium. However, foods high in oxalic acid (spinach or rhubarb), or phytic acid (bran and whole grains) may decrease calcium absorption.
MANAGEMENT: Calcium may be administered with food to increase absorption. Consider withholding calcium administration for at least 2 hours before or after consuming foods high in oxalic acid or phytic acid.
References (6)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Canadian Pharmacists Association (2006) e-CPS. http://www.pharmacists.ca/function/Subscriptions/ecps.cfm?link=eCPS_quikLink
- Cerner Multum, Inc. "Australian Product Information."
- Agencia Española de Medicamentos y Productos Sanitarios Healthcare (2008) Centro de información online de medicamentos de la AEMPS - CIMA. https://cima.aemps.es/cima/publico/home.html
- Mangels AR (2014) "Bone nutrients for vegetarians." Am J Clin Nutr, 100, epub
- Davies NT (1979) "Anti-nutrient factors affecting mineral utilization." Proc Nutr Soc, 38, p. 121-8
Therapeutic duplication warnings
No duplication 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.
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. |
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