Concomitant use of JOURNAVX with strong CYP3A inhibitors is contraindicated. Strong CYP3A inhibitors increase suzetrigine and M6-SUZ exposures, which may cause adverse reactions.
Source: NLP:suzetrigine
Brand names: Journavx
Sodium Channel Blocker · Sodium Channel Antagonists · Cytochrome P450 3A Inducers
Route: Oral
Contraindications
4 CONTRAINDICATIONS Concomitant use of JOURNAVX with strong CYP3A inhibitors is contraindicated [see Warnings and Precautions (5.1) , Drug Interactions (7.1) ] . Concomitant use with strong CYP3A inhibitors is contraindicated. ( 4 )
Pregnancy & Breastfeeding
8.1 Pregnancy Risk Summary There are no available data on the use of JOURNAVX during pregnancy to evaluate for a drug-associated risk of major birth defects, miscarriage or other adverse maternal or fetal outcomes. In animal reproduction studies in rats, effects on implantation and maintenance of pregnancy occurred at oral suzetrigine doses of ≥ 2.2-times the maximum recommended human dose (MRHD) when administered during early embryonic development or throughout organogenesis. In a pre- and postnatal development study, reduced mean gestation length and increased postnatal pup mortality were observed at maternal rat exposures of 1.6-times the MRHD and decreased rat pup body weights were observed during the period of birth to weaning at maternal exposures of 2.2-times the MRHD. No malformations were observed when suzetrigine was administered orally to rats and rabbits during the period of organogenesis at doses up to 2.2- and 5.9-times, respectively, the MRHD. The clinical relevance of these findings is unclear. The background risk of major birth defects and miscarriage in patients with moderate to severe acute pain 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. Data Animal Data Suzetrigine was administered orally to pregnant rabbits during the period of organogenesis at 50, 100, and 200 mg/kg/day (approximately 1.6-, 3.1-, and 5.9-times, respectively, the steady state MRHD exposure based on AUC). Increased post-implantation loss and lower fetal body weight were observed at 200 mg/kg/day, which is a dose that also caused maternal toxicity. No adverse embryofetal effects were observed at doses up to 100 mg/kg. Suzetrigine was administered orally to pregnant rats during the period of organogenesis at 5, 10, and 15 mg/kg/day (approximately 0
5 interactions on record
Concomitant use of JOURNAVX with strong CYP3A inhibitors is contraindicated. Strong CYP3A inhibitors increase suzetrigine and M6-SUZ exposures, which may cause adverse reactions.
Source: NLP:suzetrigine
Avoid JOURNAVX use with strong CYP3A inducers. Concomitant use results in reduced exposures of suzetrigine and M6-SUZ, which may result in reduced JOURNAVX efficacy.
Source: NLP:suzetrigine
Food or drink containing grapefruit should be avoided during treatment with JOURNAVX. Grapefruit inhibits CYP3A, increasing suzetrigine exposure.
Source: NLP:suzetrigine
Patients using hormonal contraceptives with progestins other than levonorgestrel and norethindrone should use additional nonhormonal contraceptive or alternative hormonal contraceptive during JOURNAVX use and for 28 days after discontinuation.
Source: NLP:suzetrigine
Dosage modification of sensitive CYP3A substrates may be required when initiating or discontinuing JOURNAVX. JOURNAVX is a CYP3A inducer that may reduce exposure of CYP3A substrates.
Source: NLP:suzetrigine