PYRUKYND may affect CYP2B6 substrates with narrow therapeutic index. Avoid concomitant use.
Source: NLP:mitapivat
Brand names: Aqvesme
Pyruvate Kinase Activator · Pyruvate Kinase Activators · Cytochrome P450 3A Inducers · Cytochrome P450 2B6 Inducers · Cytochrome P450 2C8 Inducers · Cytochrome P450 2C9 Inducers · Cytochrome P450 2C19 Inducers · UGT1A1 Inducers · P-Glycoprotein Inhibitors
Route: Oral
FDA Black Box Warning
WARNING: HEPATOCELLULAR INJURY AQVESME can cause serious hepatocellular injury. Measure liver laboratory tests (ALT, AST, alkaline phosphatase, and total bilirubin with fractionation) at baseline and every 4 weeks for 24 weeks and then as clinically indicated. Avoid use of AQVESME in patients with cirrhosis. Discontinue AQVESME if hepatic injury is suspected [see Warnings and Precautions ( 5.1 )] . Because of the risk of hepatocellular injury, AQVESME is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the AQVESME REMS [see Warnings and Precautions ( 5.2 )] . WARNING: HEPATOCELLULAR INJURY See full prescribing information for complete boxed warning. AQVESME can cause serious hepatocellular injury. Measure liver laboratory tests (ALT, AST, alkaline phosphatase, and total bilirubin with fractionation) at baseline and every 4 weeks for 24 weeks and then as clinically indicated. Avoid use of AQVESME in patients with cirrhosis. Discontinue AQVESME if hepatocellular injury is suspected. ( 5.1 ) AQVESME is available only through a restricted program called the AQVESME REMS. ( 5.2 )
Contraindications
4 CONTRAINDICATIONS None. None. ( 4 )
Pregnancy & Breastfeeding
8.1 Pregnancy Risk Summary Available data from clinical trials of AQVESME are insufficient to evaluate for a drug-associated risk of major birth defects, miscarriage or other adverse maternal or fetal outcomes. In animal reproduction studies, mitapivat orally administered twice daily to pregnant rats and rabbits during organogenesis was not teratogenic at exposures up to 9.9- and 2.4‑fold the human exposure associated with the MRHD, respectively. Mitapivat administered orally to pregnant rats twice daily during organogenesis through lactation did not result in adverse developmental effects at doses up to 9.9 times the MRHD ( see Data) . The estimated background risk of major birth defects for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Clinical Considerations Disease-Associated Maternal Risk Transfusion requirements in thalassemia patients are increased during pregnancy. Pregnant women with transfusion-dependent thalassemia are considered high risk, with their major complications being cardiac in origin, including cardiac dysrhythmia, right ventricular dysfunction, and cardiac failure, reported in 1.1% to 15.6%. Pregnant women with non-transfusion-dependent thalassemia need to be monitored and treated for risk of thrombosis, especially those who are splenectomized or infrequently transfused. Patients with non-transfusion-dependent thalassemia may develop a need for regular transfusions during pregnancy, and in such patients the risk of alloimmunization should be carefully evaluated. All pregnant women with thalassemia should be closely monitored for iron overload. Data Animal Data In an embryo-fetal development study in rats, mitapivat was administered at doses of 5, 10, 25, and 100 mg/kg twice daily by oral
6 interactions on record
PYRUKYND may affect CYP2B6 substrates with narrow therapeutic index. Avoid concomitant use.
Source: NLP:mitapivat
PYRUKYND may affect P-gp substrates with narrow therapeutic index. Avoid concomitant use.
Source: NLP:mitapivat
Co-administration decreases mitapivat plasma concentrations, reducing efficacy of PYRUKYND. Avoid concomitant use.
Source: NLP:mitapivat
Co-administration increases mitapivat plasma concentrations, increasing risk of adverse reactions. Avoid concomitant use.
Source: NLP:mitapivat
PYRUKYND induces CYP3A, decreasing concentrations of sensitive substrates with narrow therapeutic index. Avoid concomitant use.
Source: NLP:mitapivat
PYRUKYND induces CYP3A, decreasing systemic concentrations of this hormonal contraceptive. Monitor for loss of contraceptive efficacy or use non-hormonal alternatives.
Source: NLP:mitapivat