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Drug Interactions between axicabtagene ciloleucel and foscarbidopa / foslevodopa

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Moderate

axicabtagene ciloleucel foslevodopa

Applies to: axicabtagene ciloleucel and foscarbidopa / foslevodopa

Consumer information for this interaction is not currently available.

MONITOR: Polyneuropathy has been reported during treatment with levodopa/carbidopa combinations, and concurrent use of other medications that are also associated with this adverse effect may potentiate the risk and/or severity of nerve damage. Polyneuropathy has most commonly been observed in patients receiving levodopa/carbidopa by continuous intestinal infusion, with a frequency of up to 5.8% in clinical trials. Cases were generally consistent with axonal polyneuropathy, manifested as sensory or sensorimotor neuropathies, with subacute or chronic onset. Reported symptoms primarily included numbness, tingling, decreased sensation, weakness, and pain in the legs, hands, feet, and extremities. Many of these patients had deficiencies in folic acid, vitamin B12 and vitamin B6 as well as elevated homocysteine levels. However, there was insufficient information to determine the potential role of vitamin deficiencies in the etiology of neuropathy associated with the treatment. It is also unknown whether there is a causal relationship between polyneuropathy and treatment with levodopa/carbidopa combinations.

MANAGEMENT: Before initiating treatment with enteral formulations of levodopa/carbidopa, the manufacturers recommend evaluating patients for history or signs of polyneuropathy and known risk factors such as diabetes mellitus, hypothyroidism, or concomitant use of other medications associated with polyneuropathy. For patients with preexisting polyneuropathy, the benefits of treatment should be carefully weighed against the potential risks, including the potential for impaired mobility. Plasma concentrations of vitamin B12, vitamin B6, homocysteine, methylmalonic acid, and folic acid should be obtained at baseline and at regular intervals during treatment. Patients who develop symptoms of peripheral neuropathy and low plasma concentrations of vitamin B6 and/or vitamin B12, or elevated homocysteine or methylmalonic acid concentrations, may benefit from vitamin supplementation. Physicians should carefully evaluate if a dose adjustment is warranted and assess the benefit versus risk of continued treatment.

Drug and food interactions

Moderate

foslevodopa food

Applies to: foscarbidopa / foslevodopa

Alcohol can increase the nervous system side effects of foslevodopa such as dizziness, drowsiness, and difficulty concentrating. Some people may also experience impairment in thinking and judgment. You should avoid or limit the use of alcohol while being treated with foslevodopa. You may experience reduced effectiveness of foslevodopa in the presence of foods or enteral (tube) feedings with a high protein content. This may make the symptoms of Parkinson's disease worse. Talk with your doctor or nutrition counselor about the best foods to eat while you are taking this medication. Contact your doctor if your condition changes.

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.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.