When switching from mitoxantrone to fingolimod, consider duration and mode of action to avoid unintended additive immunosuppressive effects.
Source: NLP:fingolimod
Brand names: Mitoxantrone
Route: Intravenous
FDA Black Box Warning
WARNING Mitoxantrone Injection, USP (concentrate) should be administered under the supervision of a physician experienced in the use of cytotoxic chemotherapy agents. Mitoxantrone Injection, USP (concentrate) should be given slowly into a freely flowing intravenous infusion. It must never be given subcutaneously, intramuscularly, or intra-arterially. Severe local tissue damage may occur if there is extravasation during administration. (See ADVERSE REACTIONS, General, Cutaneous and DOSAGE AND ADMINISTRATION, Preparation and Administration Precautions ). NOT FOR INTRATHECAL USE. Severe injury with permanent sequelae can result from intrathecal administration. (See WARNINGS, General ) Except for the treatment of acute nonlymphocytic leukemia, mitoxantrone therapy generally should not be given to patients with baseline neutrophil counts of less than 1,500 cells/mm 3 . In order to monitor the occurrence of bone marrow suppression, primarily neutropenia, which may be severe and result in infection, it is recommended that frequent peripheral blood cell counts be performed on all patients receiving mitoxantrone. Cardiotoxicity: Congestive heart failure (CHF), potentially fatal, may occur either during therapy with mitoxantrone or months to years after termination of therapy. Cardiotoxicity risk increases with cumulative mitoxantrone dose and may occur whether or not cardiac risk factors are present. Presence or history of cardiovascular disease, radiotherapy to the mediastinal/pericardial area, previous therapy with other anthracyclines or anthracenediones, or use of other cardiotoxic drugs may increase this risk. In cancer patients, the risk of symptomatic CHF was estimated to be 2.6% for patients receiving up to a cumulative dose of 140 mg/m 2 . To mitigate the cardiotoxicity risk with mitoxantrone, prescribers should consider the following: All Patients: • All patients should be assessed for cardiac signs and symptoms by history, physical examination, and ECG prior to st
Contraindications
CONTRAINDICATIONS Mitoxantrone is contraindicated in patients who have demonstrated prior hypersensitivity to it.
Pregnancy & Breastfeeding
Pregnancy (see WARNINGS ).
9 interactions on record
When switching from mitoxantrone to fingolimod, consider duration and mode of action to avoid unintended additive immunosuppressive effects.
Source: NLP:fingolimod
Prolonged immune effects drug requiring consideration of duration and mode of action to avoid additive immunosuppressive effects when switching to fingolimod.
Source: NLP:fingolimod hcl
BCRP substrate whose exposure may be altered by velpatasvir and voxilaprevir inhibition. Coadministration is not recommended.
Source: NLP:sofosbuvir, velpatasvir, and voxilaprevir
BCRP substrate; eltrombopag may increase exposure. Monitor closely for signs of excessive exposure.
Source: NLP:eltrombopag
BCRP substrate; monitor for excessive exposure and consider dose reduction if appropriate.
Source: NLP:eltrombopag olamine
Prolonged immune effects drug; consider duration and mode of action to avoid additive immunosuppressive effects when switching to TASCENSO ODT.
Source: NLP:fingolimod lauryl sulfate
Concomitant use may cause additive immunosuppressive effects. Consider duration and mode of action when switching from mitoxantrone to OCREVUS.
Source: NLP:ocrelizumab
Concomitant use may increase risk of additive immunosuppressive effects due to prolonged immune effects of mitoxantrone. Consider duration and mode of action when switching to ocrelizumab.
Source: NLP:ocrelizumab and hyaluronidase
Teriflunomide may increase exposure of mitoxantrone. Consider reducing dose and monitor patients closely.
Source: NLP:teriflunomide