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What the FDA labels say about taking them together

Digoxin and remibrutinib

Remibrutinib's FDA label of March 23, 2026 names digoxin in its drug interactions section; the digoxin labels PlainMeds reads (3) do not name remibrutinib. The remibrutinib label: “Monitor more frequently for adverse reactions when using RHAPSIDO with P-glycoprotein (P-gp) substrates where minimal concentration changes may lead to serious adverse reactions (e.g., digoxin).”

Check it at the source: the digoxin FDA label on DailyMed (effective December 5, 2024, Advanz Pharma (US) Corp.); the remibrutinib FDA label on DailyMed (effective March 23, 2026, Novartis Pharmaceuticals Corporation).

What does the digoxin label say about remibrutinib?

Digoxin's label (effective December 5, 2024) and its 2 other brand-application labels do not name remibrutinib in these sections. A label lists what its studies and reports found; it is not a complete list.

Source: FDA drug label (LANOXIN), Advanz Pharma (US) Corp., effective December 5, 2024 (SPL set d91e3646-4c63-4512-ab22-db39c085c4dc), via openFDA; the full label on DailyMed

What does the remibrutinib label say about digoxin?

Remibrutinib label, drug interactions

Monitor more frequently for adverse reactions when using RHAPSIDO with P-glycoprotein (P-gp) substrates where minimal concentration changes may lead to serious adverse reactions (e.g., digoxin).

Source: FDA drug label (RHAPSIDO), Novartis Pharmaceuticals Corporation, effective March 23, 2026 (SPL set e5e89bff-6ced-4165-acc5-fb13136b3a3d), via openFDA; the full label on DailyMed

These are the labels' own sentences. PlainMeds does not grade interactions; a pharmacist or prescriber can say what they mean for one person's medicines.

Both medicines on the record

26Digoxin generic labelers
0Remibrutinib generic labelers
DigoxinRemibrutinib
Labeled forHeart failure, Atrial fibrillationAllergies
Boxed warningNoNo
Pharmacy cost (NADAC)$0.133 per tablet 125 mcg tablet$72.46 per tablet 25 mg tablet
Shortage nowNo current entryNo current entry

Source: FDA NDC Directory, CMS NADAC of October 7, 2026 and the FDA Drug Shortage Database (FDA files October 8, 2026)

What next?