Skip to main content

What the FDA labels say about taking them together

Acalabrutinib and venetoclax

Acalabrutinib's FDA label of February 19, 2026 names venetoclax in its warnings and precautions section, and venetoclax's label names acalabrutinib too. The acalabrutinib label: “… patients treated with CALQUENCE alone and in combination with obinutuzumab or venetoclax;”

Check it at the source: the acalabrutinib FDA label on DailyMed (effective February 19, 2026, AstraZeneca Pharmaceuticals LP); the venetoclax FDA label on DailyMed (effective May 20, 2026, AbbVie Inc.).

What does the acalabrutinib label say about venetoclax?

Acalabrutinib label, warnings and precautions

Grade 3 or 4 cytopenias included absolute neutrophil count decreased (28%), absolute lymphocyte count decreased (10%), hemoglobin decreased (9%), and platelets decreased (9%) in 1,758 patients treated with CALQUENCE alone and in combination with obinutuzumab or venetoclax;

Source: FDA drug label (CALQUENCE), AstraZeneca Pharmaceuticals LP, effective February 19, 2026 (SPL set b1409184-3267-4d8c-8f17-4e01f69828b1), via openFDA; the full label on DailyMed

What does the venetoclax label say about acalabrutinib?

Venetoclax label, warnings and precautions

In patients with CLL, Grade 3 or 4 neutropenia developed in 38% of patients and Grade 4 neutropenia developed in 15% of patients when treated with VENCLEXTA in combination with acalabrutinib.

Source: FDA drug label (Venclexta), AbbVie Inc., effective May 20, 2026 (SPL set b118a40d-6b56-cee3-10f6-ded821a97018), 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

0Acalabrutinib generic labelers
0Venetoclax generic labelers
AcalabrutinibVenetoclax
Labeled forLeukemia, lymphoma and myelomaLeukemia, lymphoma and myeloma
Boxed warningNoNo
Pharmacy cost (NADAC)n/an/a
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?