Interações de Pomalidomida
Pomalidomida (Pomalyst) tem 29 interações documentadas nas bulas da FDA e nas fichas informativas que indexamos (graves: 9; moderadas: 20; leves: 0; casos em que uma bula relata não haver interação significativa: 0). Cada item abaixo cita a frase em que se baseia. Esta página de medicamento é um ponto de partida, não um veredito para a sua situação.
Interações segundo a bula
Interações graves (9)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Treatment of patients with MM with a PD-1 or PD-L1 blocking antibody in combination with a thalidomide analogue plus dexamethasone is not recommended outside of controlled clinical trials. (bula de Pomalidomida, Advertências e precauções)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Strong CYP1A2 Inhibitors: Avoid concomitant use of strong CYP1A2 inhibitors. (bula de Pomalidomida, Interações medicamentosas)
Interações moderadas (20)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
Females must commit either to abstain continuously from heterosexual sexual intercourse or to use 2 methods of reliable birth control, beginning 4 weeks prior to initiating treatment with POMALYST, during therapy, during dose interruptions, and continuing for 4 weeks following discontinuation of POMALYST therapy. (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
Patients with known risk factors, including prior thrombosis, may be at greater risk, and actions should be taken to try to minimize all modifiable factors (e.g., hyperlipidemia, hypertension, smoking). (bula de Pomalidomida, Advertências e precauções)
In Trial 2, where anticoagulant therapies were mandated, thromboembolic events occurred in 8.0% of patients treated with POMALYST and low dose-dexamethasone (Low-dose Dex), and 3.3% of patients treated with high-dose dexamethasone. (bula de Pomalidomida, Advertências e precauções)
Verifique Pomalidomida com tudo o que você toma. Adicione sua lista completa; todos os pares são verificados de uma vez.
Abrir no verificadorNão é aconselhamento médico. A gravidade reflete a redação da bula, não as suas circunstâncias. Um alerta “grave” pode ser rotina sob supervisão, e um “leve” pode ser importante em doses altas. Pergunte a um farmacêutico.