Suworeksant i Triazolam: interakcja
Suworeksant i Triazolam: obie etykiety FDA opisują to połączenie najsilniejszymi sformułowaniami, takimi jak przeciwwskazanie, ostrzeżenie w ramce lub zalecenie, aby go unikać.
Nie łączyć bez zaleceń lekarza przepisującego leki. Poniższe sformułowania z etykiety to najsilniejsze, jakich używa FDA.
Co mówią etykiety FDA
Źródło: etykieta leku Triazolam · obowiązuje od 2026-07-10
• Effects on Driving and Operating Heavy Machinery : Patients receiving triazolam should be cautioned against driving or operating heavy machinery, as well as avoiding concomitant use with alcohol and other CNS depressant drugs.
Strong CYP 3A Inhibitors Triazolam is contraindicated in patients receiving strong inhibitors of CYP 3A such as ketoconazole, itraconazole, nefazodone, ritonavir, indinavir, nelfinavir, saquinavir, and lopinavir [see Contraindications (4) , Drug Interactions (7.1) ] .
Prevention or management Do not administer triazolam with a strong CYP3A4 inhibitor [see Contraindications (4) , Warnings and Precautions (5.8) ].
The use of alcohol and other central nervous system (CNS) depressants with sedative-hypnotics appears to increase the risk, as well as doses exceeding the maximum recommended dose.
Although behaviors such as sleep-driving may occur with sedative-hypnotics alone at recommended dosages, the use of alcohol and other central nervous system (CNS) depressants with sedative-hypnotics appears to increase the risk of such behaviors, as does the use of sedative-hypnotics at doses exceeding the maximum recommended dose.
Źródło: etykieta leku Suworeksant (BELSOMRA) · obowiązuje od 2025-03-10
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 ).
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).
Co-administration with other CNS depressants (e.g., benzodiazepines, opioids, tricyclic antidepressants, alcohol) increases the risk of CNS depression.
Dosage adjustments of BELSOMRA and of concomitant CNS depressants may be necessary when administered together because of potentially additive effects.
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.
Więcej leków niż te dwa? Interakcje się kumulują. Całą listę można sprawdzić jednocześnie; pozostaje ona w przeglądarce.
Otwórz w wyszukiwarceTo nie jest porada medyczna. Interaction Checker cytuje tekst etykiet FDA i karty informacyjne NIH. To, czy interakcja ma znaczenie w konkretnym przypadku, zależy od dawek, pory przyjmowania, czynności nerek i wątroby oraz innych schorzeń. Należy to potwierdzić u farmaceuty lub lekarza przepisującego leki.