Sapropterin may increase tyrosine availability, a levodopa precursor. Neurologic events reported post-marketing in patients receiving both drugs concomitantly.
Source: NLP:sapropterin dihydrochloride
Brand names: Kuvan
Route: Oral
Contraindications
4 CONTRAINDICATIONS None. None. ( 4 )
Pregnancy & Breastfeeding
8.1 Pregnancy Risk Summary Available data from pregnancy safety studies, pharmacovigilance, and published case reports with KUVAN use during pregnancy have not identified a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes (see Data) . Uncontrolled blood phenylalanine concentrations before and during pregnancy are associated with an increased risk of adverse pregnancy outcomes and fetal adverse effects (see Clinical Considerations ) . An embryo-fetal development study with sapropterin dihydrochloride in rats using oral doses up to 3 times the maximum recommended human dose (MRHD) given during the period of organogenesis showed no effects. In a rabbit study using oral administration of sapropterin dihydrochloride during the period of organogenesis, a rare defect, holoprosencephaly, was noted at 10 times the MRHD. All pregnancies have a background risk of major birth defects, pregnancy loss, or other adverse pregnancy 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. The estimated background risk of major birth defects and miscarriage in pregnant women with PKU who maintain blood phenylalanine concentrations greater than 600 micromol/L during pregnancy is greater than the corresponding background risk for pregnant women without PKU. Clinical Considerations Disease-Associated Maternal and/or Embryo‑Fetal Risk Uncontrolled blood phenylalanine concentrations before and during pregnancy are associated with an increased risk of adverse pregnancy outcomes and fetal adverse effects. To reduce the risk of hyperphenylalaninemia-induced fetal adverse effects, blood phenylalanine concentrations should be maintained between 120 and 360 micromol/L during pregnancy and during the 3 months before conception [see Dosage and Administration 2.2) ] . Data Human Data Uncontrolled Maternal PKU Available data
8 interactions on record
Sapropterin may increase tyrosine availability, a levodopa precursor. Neurologic events reported post-marketing in patients receiving both drugs concomitantly.
Source: NLP:sapropterin dihydrochloride
May decrease endogenous BH4 levels by inhibiting dihydrofolate reductase, potentially increasing phenylalanine levels.
Source: NLP:sapropterin dihydrochloride
May decrease endogenous BH4 levels by inhibiting dihydrofolate reductase, potentially increasing phenylalanine levels.
Source: NLP:sapropterin dihydrochloride
Both sapropterin and PDE-5 inhibitors may induce vasorelaxation, potentially reducing blood pressure.
Source: NLP:sapropterin dihydrochloride
Both sapropterin and PDE-5 inhibitors may induce vasorelaxation, potentially reducing blood pressure.
Source: NLP:sapropterin dihydrochloride
May decrease endogenous BH4 levels by inhibiting dihydrofolate reductase, potentially increasing phenylalanine levels.
Source: NLP:sapropterin dihydrochloride
May decrease endogenous BH4 levels by inhibiting dihydrofolate reductase, potentially increasing phenylalanine levels.
Source: NLP:sapropterin dihydrochloride
Both sapropterin and PDE-5 inhibitors may induce vasorelaxation, potentially reducing blood pressure.
Source: NLP:sapropterin dihydrochloride