Interaksi Lumateperon dan Suvoreksant

Lumateperon dan Suvoreksant: kedua label peresepan menguraikan interaksi yang biasanya memerlukan pemantauan, perubahan dosis, atau pemberian jarak antardosis.

Moderat

Biasanya dapat dikelola dengan pemantauan atau perubahan dosis. Beri tahu apoteker Anda bahwa Anda menggunakan keduanya.

Apa kata label FDA

Dari label Suvoreksant (BELSOMRA) · berlaku sejak 2025-03-10

Moderat

CNS Depressant Effects and Daytime Impairment: Risk of impaired alertness and motor coordination, including impaired driving; risk increases with dose; caution patients taking 20 mg against next-day driving and other activities requiring complete mental alertness ( 5.1 ).

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Prescribers should monitor for somnolence and CNS depressant effects, but impairment can occur in the absence of symptoms, and may not be reliably detected by ordinary clinical exam (i.e., less than formal testing of daytime wakefulness and/or psychomotor performance).

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Co-administration with other CNS depressants (e.g., benzodiazepines, opioids, tricyclic antidepressants, alcohol) increases the risk of CNS depression.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Dosage adjustments of BELSOMRA and of concomitant CNS depressants may be necessary when administered together because of potentially additive effects.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

The risk of next-day impairment, including impaired driving, is increased if BELSOMRA is taken with less than a full night of sleep remaining, if a higher than the recommended dose is taken, if co-administered with other CNS depressants, or if co-administered with other drugs that increase blood levels of BELSOMRA.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed

Dari label Lumateperon (CAPLYTA) · berlaku sejak 2025-06-20

Moderat

Strong CYP3A4 inhibitors: Recommended dosage is 10.5 mg once daily.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Moderat

Moderate CYP3A4 inhibitors: Recommended dosage is 21 mg once daily.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Moderat

Moderate or Strong CYP3A4 Inhibitors* Prevention or Management Reduce the CAPLYTA dosage when used concomitantly with moderate or strong CYP3A4 inhibitors [see Dosage and Administration ( 2.2 ) ].

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Moderat

Clinical Impact Concomitant use of CAPLYTA with moderate or strong CYP3A4 inhibitors increases lumateperone exposure [see Clinical Pharmacology ( 12.3 ) ] , which may increase the risk of adverse reactions.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Tanpa interaksi

…interactions with adjunctive SSRI/SNRIs in MDD were observed in CAPLYTA clinical trials, CAPLYTA’s moderate serotonin transporter (SERT) activity may increase the risk of SRI-associated adverse reactions (e.g., serotonin syndrome, hyponatremia). * See www.fda.gov/CYPandTransporterInteractingDrugs for examples of CYP3A4 Inducers and Moderate or Strong CYP3A4 Inhibitors

Interaksi obatberdasarkan golongan obatLihat label di DailyMed

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