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Zynlonta Side Effects

Generic name: loncastuximab tesirine

Medically reviewed by Drugs.com. Last updated on Mar 9, 2024.

Note: This document contains side effect information about loncastuximab tesirine. Some dosage forms listed on this page may not apply to the brand name Zynlonta.

Applies to loncastuximab tesirine: intravenous powder for solution.

Serious side effects of Zynlonta

Along with its needed effects, loncastuximab tesirine (the active ingredient contained in Zynlonta) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor or nurse immediately if any of the following side effects occur while taking loncastuximab tesirine:

More common

Less common

Other side effects of Zynlonta

Some side effects of loncastuximab tesirine may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

For Healthcare Professionals

Applies to loncastuximab tesirine: intravenous injection.

Hematologic

Very common (10% or more): Platelets decreased (58%), neutrophils decreased (52%), hemoglobin decreased (51%), albumin decreased (37%), neutropenia (Grade 3 or 4) (32%), thrombocytopenia (20%), anemia (12%)

Common (1% to 10%): Febrile neutropenia[Ref]

Immunologic

Common (1% to 10%): Sepsis/escherichia sepsis/septic shock

Frequency not reported: Immunogenicity[Ref]

Local

Uncommon (0.1% to 1%): Infusion site extravasation[Ref]

Musculoskeletal

Very common (10% or more): Musculoskeletal pain (e.g., musculoskeletal pain, musculoskeletal chest pain, musculoskeletal discomfort, back pain, limb discomfort, myalgia, neck pain, non-cardiac chest pain, pain in extremity) (23%)[Ref]

Metabolic

Very common (10% or more): Glucose increased (48%), edema (e.g., edema, face edema, generalized edema, peripheral edema, ascites, fluid overload, peripheral swelling, swelling, swelling face) (28%), anorexia (15%)[Ref]

Hepatic

Very common (10% or more): AST increased (37%), ALT increased (34%)[Ref]

Respiratory

Very common (10% or more): Dyspnea/dyspnea exertional (13%), pleural effusion (10%), upper respiratory tract infection (e.g., upper respiratory tract infection, upper respiratory tract congestion, nasopharyngitis, rhinitis, rhinovirus infection, sinusitis (10%)

Common (1% to 10%): Pleural effusion (Grade 3), pneumonia/pneumonitis, pleuritis[Ref]

Other

Very common (10% or more): Fatigue/asthenia/lethargy (38%)[Ref]

General

The most common (greater than 20%) adverse reactions, including laboratory abnormalities, were thrombocytopenia, increased gamma-glutamyltransferase, neutropenia, anemia, hyperglycemia, transaminase elevation, fatigue, hypoalbuminemia, rash, edema, nausea, and musculoskeletal pain.[Ref]

Cardiovascular

Common (1% to 10%): Pericarditis[Ref]

Dermatologic

Very common (10% or more): Rash (e.g., rash erythematous, rash maculopapular, rash pruritic, rash pustular, erythema, generalized erythema, dermatitis, dermatitis acneiform, dermatitis bullous, dermatitis exfoliative generalized, palmar-plantar erythrodysesthesia syndrome) (30%), pruritus (12%), photosensitivity reaction (10%)

Common (1% to 10%): Hyperpigmentation, dermatitis[Ref]

Gastrointestinal

Very common (10% or more): Nausea (23%), diarrhea (17%), abdominal pain (e.g., abdominal pain, abdominal discomfort, abdominal pain lower, abdominal pain upper) (14%), vomiting (13%), constipation (12%)

Common (1% to 10%): Pericardial effusion[Ref]

References

1. Product Information. Zynlonta (loncastuximab tesirine). ADC Therapeutics America. 2021.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.