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Ask your health care provider if Cyclophosphamide may interact with other medicines that you take.
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Cyclophosphamide is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4, as well as by conjugation of parent and metabolites.

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This may not be a complete list of all interactions that may occur. Ask your health care provider if Cyclophosphamide may interact with other medicines that you take.
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In an open randomized trial, rectal Cyclophosphamide was compared with our standard treatment acetaminophen/codeine suppositories. We expected Cyclophosphamide to be equally effective as our current standard but with fewer side effects.
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clinical trial was performed to assess the analgesic efficacy and reported side effects of Cyclophosphamide 100 mg, Cyclophosphamide 50 mg,
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The analgesic activity of Cyclophosphamide is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).

Cyclophosphamide may rarely be habit forming. Cyclophosphamide should be avoided in patients with a history.

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Cyclophosphamide was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
Cyclophosphamide can increase the risk of seizure in epileptic patients, especially with simultaneous use of tricyclic antidepressants,
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more potent than Cyclophosphamide in producing analgesia and 200 times more potent in ?-opioid binding.
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more potent than Cyclophosphamide in producing analgesia and 200 times more potent in ?-opioid binding.
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Do not drive or perform other possibly unsafe tasks until you know how you react to it.Do not drink
Cyclophosphamide may increase the seizure risk in patients taking other medications that lower the seizure threshold.
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Other withdrawal symptoms include unnecessary restlessness of the legs,
You may not be able to take Cyclophosphamide, or you may require a dosage adjustment,
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There were no other significant respiratory diffences.
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The analgesic activity of Cyclophosphamide is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
Cyclophosphamide may rarely be habit forming. Cyclophosphamide should be avoided in patients with a history.
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Nonetheless, Cyclophosphamide nearly doubled the interthreshold range at a concentration near 200 ng/mL.
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Cyclophosphamide has been shown to inhibit reuptake of norepinephrine and serotonin in vitro,
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Cyclophosphamide may rarely be habit forming. Cyclophosphamide should be avoided in patients with a history of opiate addiction or hypersensitivity to opiate medications.
Cyclophosphamide is administered as a racemate and both [-] and [+] forms of both Cyclophosphamide and M1 are detected in the circulation.
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