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Truseltiq Side Effects

Generic name: infigratinib

Medically reviewed by Drugs.com. Last updated on Jun 16, 2024.

Note: This document provides detailed information about Truseltiq.

Applies to infigratinib: oral capsules Side Effects associated with infigratinib. Some dosage forms listed on this page may not apply specifically to the brand name Truseltiq.

Applies to infigratinib: oral capsules.

Side effects include:

Most common (≥20%) adverse reactions include nail toxicity, stomatitis, dry eye, fatigue, alopecia, palmar-plantar erythrodysesthesia syndrome, arthralgia, dysgeusia, constipation, abdominal pain, dry mouth, eyelash changes, diarrhea, dry skin, decreased appetite, blurred vision, and vomiting.

Most common laboratory abnormalities (≥20%) include increased creatinine, increased phosphate, decreased phosphate, increased alkaline phosphatase, decreased hemoglobin, increased lipase, increased calcium, decreased lymphocytes, decreased sodium, increased triglycerides, increased ALT/AST, increased urate, decreased platelets, decreased leukocytes, decreased albumin, increased bilirubin, and decreased potassium.

For healthcare professionals

Applies to infigratinib: oral capsule.

General adverse events

Serious adverse reactions in 2% or more patients included infections, anemia, pyrexia, abdominal pain, hypercalcemia, and sepsis. Fatal adverse reactions occurred in 1 (0.9%) patient. Adverse reactions requiring permanent discontinuation in 1% or more patients were blood creatinine increased, fatigue, subretinal fluid, and calcinosis.[Ref]

Musculoskeletal

Ocular

Metabolic

Hepatic

Respiratory

Nervous system

Renal

Cardiovascular

Dermatologic

Gastrointestinal

Hematologic

References

1. (2021) "Product Information. Truseltiq (infigratinib)." QED Therapeutics Inc

Further information

Truseltiq side effects can vary depending on the individual. 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.