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Tafasitamab Side Effects

Medically reviewed by Drugs.com. Last updated on Mar 4, 2024.

Applies to tafasitamab: intravenous powder for solution.

Serious side effects of Tafasitamab

Along with its needed effects, tafasitamab 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 tafasitamab:

More common

Other side effects of Tafasitamab

Some side effects of tafasitamab 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

Less common

For Healthcare Professionals

Applies to tafasitamab: intravenous powder for injection.

Hematologic

Very common (10% or more): Neutropenia (51%), activated partial thromboplastin time increased (46%), anemia (36%), thrombocytopenia (31%), febrile neutropenia (12%), leukopenia

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

Immunologic

Very common (10% or more): Infections (73%), Grade 3 or higher infection (30%)

Common (1% to 10%): Sepsis, hypogammaglobulinemia

Frequency not reported: Potential immunogenicity[Ref]

Local

Common (1% to 10%): Infusion related reactions (IRRs) (e.g., chills, flushing, dyspnea, hypertension)[Ref]

Musculoskeletal

Very common (10% or more): Back pain (19%), muscle spasms (15%)

Common (1% to 10%): Arthralgia, pain in extremity, musculoskeletal pain[Ref]

Metabolic

Very common (10% or more): Glucose increased (49%), calcium decreased (47%), gamma glutamyl transferase increased (34%), albumin decreased (26%), magnesium decreased (22%), anorexia (22%), urate increased (20%), phosphate decreased (20%), hypokalemia (19%), decreased appetite

Common (1% to 10%): Weight loss, C-reactive protein increased[Ref]

Genitourinary

Very common (10% or more): Urinary tract infection (e.g., urinary tract infection, Escherichia urinary tract infection, urinary tract infection bacterial, urinary tract infection enterococcal) (17%)[Ref]

Hepatic

Very common (10% or more): Aspartate aminotransferase increased (20%)

Common (1% to 10%): Hyperbilirubinemia, transaminases increased (includes ALT and/or AST increased)[Ref]

Oncologic

Common (1% to 10%): Basal cell carcinoma[Ref]

Respiratory

Very common (10% or more): Cough (26%), respiratory tract infection (e.g., lower respiratory tract infection, upper respiratory tract infection, respiratory tract infection) (24%), bronchitis (16%), dyspnea (12%), nasopharyngitis (10%), pneumonia (10%)

Common (1% to 10%): Nasal congestion, exacerbation of obstructive pulmonary disease[Ref]

Other

Very common (10% or more): Fatigue/asthenia (38%), pyrexia (24%), peripheral edema (24%)[Ref]

General

The most common adverse reactions (20% or greater) were infections, neutropenia, fatigue, asthenia, anemia, diarrhea, thrombocytopenia, cough, pyrexia, peripheral edema, respiratory tract infection, and decreased appetite.[Ref]

Nervous system

Common (1% to 10%): Headache, paresthesia, dysgeusia[Ref]

Renal

Very common (10% or more): Creatinine increased (20%)[Ref]

Dermatologic

Common (1% to 10%): Erythema, alopecia, hyperhidrosis, rash (includes different types of rash, e.g. rash, rash maculopapular, rash pruritic, rash erythematous)[Ref]

Gastrointestinal

Very common (10% or more): Diarrhea (36%), constipation (17%), nausea (15%), vomiting (15%), abdominal pain

Common (1% to 10%): Mucosal inflammation[Ref]

References

1. Product Information. Monjuvi (tafasitamab). Morphosys US. 2020.

2. Product Information. Minjuvi (tafasitamab). Incyte Biosciences UK Ltd. 2022.

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.