Drug Interaction Report
1 potential interaction and/or warning found for the following 2 drugs:
- Pemrydi RTU (pemetrexed)
- sodium phosphate p32
Interactions between your drugs
sodium phosphate p32 PEMEtrexed
Applies to: sodium phosphate p32, Pemrydi RTU (pemetrexed)
MONITOR: The concomitant use of bone marrow depressants and sodium phosphate P-32 may have additive myelosuppressive effects.
MANAGEMENT: Patients should be monitored for excessive bone marrow suppression during treatment with sodium phosphate P-32. Sodium phosphate P-32 should not be used as part of a sequential treatment with a chemotherapeutic agent. Dose reductions of the other bone marrow depressants may be necessary. The manufacturer's labeling should be consulted for more specific recommendations for each agent involved. Patients should be advised to contact their physician if they develop signs and symptoms of myelosuppression such as pallor, dizziness, fatigue, lethargy, fainting, easy bruising or bleeding, or signs of infection such as fever, chills, sore throat, body aches, and other influenza-like symptoms.
References (1)
- AnazaoHealth Corporation (2023) P32 sodium phosphate - p32 sodium phosphate solution https://dailymed.nlm.nih.gov/dailymed/fda/fdaDrugXsl.cfm?setid=735f92e3-cc92-4d9b-afe8-f935a685ee78&type=display
Drug and food interactions
No alcohol/food interactions were found with the drugs in your list. However, this does not necessarily mean no food interactions exist. Always consult your healthcare provider.
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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Further information
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