Details of Drug-Drug Interaction
| Drug General Information (ID: DDI30YQ4PX) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Erdafitinib | Drug Info | Magnesium gluconate | Drug Info | |||||
| Drug Type | Small molecule | Small molecule | |||||||
| Therapeutic Class | Multikinase Inhibitors | Minerals And Electrolytes | |||||||
| Structure | |||||||||
| Mechanism of Erdafitinib-Magnesium gluconate Interaction (Severity Level: Major) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Attenuated pharmacological effects (Unspecific) Click to Show/Hide Mechanism Graph | |||||||||
| Drug Name | Erdafitinib | Magnesium gluconate | |||||||
| Mechanism | Titration affected by phosphate levels | Hypophosphatemia | |||||||
| Key Mechanism Factor 1 | |||||||||
| Factor Name | Pharmacodynamics | ||||||||
| Factor Description | Reduced pharmacological effects leading to insufficient efficacy and/or treatment failure. | ||||||||
| Mechanism Description |
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| Recommended Action | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Management | The manufacturer recommends that concomitant use of erdafitinib with agents that may alter serum phosphate levels be avoided before its initial dose increase period, which is between days 14 to 21 of starting erdafitinib therapy and is based on serum phosphate levels. After the initial dose increase period, an oral phosphate binder may be appropriate in the management of patients with serum phosphate levels greater than 7 mg/dL. If concomitant use with agents known to increase serum phosphate levels is required after this initial dose increase period, close monitoring of patient tolerability and serum phosphate levels is recommended. | ||||||||
| References | |||||||||||||||||||
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| 1 | Product Information. Balversa (erdafitinib). Janssen Products, LP, Horsham, PA. | ||||||||||||||||||
