American Diabetes Association logoResearch presented recently at the American Diabetes Association (ADA) 77th Scientific Sessions in San Diego warned that clinicians managing blood glucose levels in critically ill children should ascertain that they are not treating false elevations of blood glucose caused by acetaminophen interaction.

The researchers from Boston and Philadelphia determined that after acetaminophen is administered, clinicians should wait between 2.4 and 3.7 hours to avoid treating falsely elevated blood glucose levels. Peak concentrations of acetaminophen were found to be higher when measured by continuous glucose monitor (CGM) devices when administered intravenously vs. enterally or rectally.

Acetaminophen and Stevens-Johnson Syndrome

Besides causing elevated blood glucose levels in children, acetaminophen has been linked to other serious illnesses, including Stevens-Johnson Syndrome (SJS), a life-threatening and extremely painful condition.

Symptoms of SJS include:

  • Cough
  • Headache
  • Rash
  • Blisters
  • Widespread damage to the surface of the skin

Stevens-Johnson Syndrome typically requires hospitalization and in some cases can even result in death. In 2013, the U.S. Food and Drug Administration (FDA) issued a warning directing the makers of acetaminophen products to intensify their warnings about Stevens-Johnson Syndrome and advising patients who develop symptoms of the skin disease to stop taking acetaminophen and seek immediate medical attention. The warning came after the FDA its own Adverse Event Reporting System, identifying 107 cases of adverse skin reactions between 1969 and 2012 that were connected to acetaminophen.

Acetaminophen has also been linked to toxic epidermal necrolysis (TEN) and acute generalized exanthematous pustulosis (AGEP). While AGEP usually resolves within two weeks of stopping the medication, TEN usually requires hospitalization and can be fatal. A serious skin reaction can occur at any time, even in those who have taken acetaminophen previously without incident, and there is no way of predicting who might be most at risk.

Free Case Evaluation

More About CSS

Other Dangerous Drugs News

  • Researchers in a lab conducting various tests.
    Published On: March 13, 2026

    Research suggests Dupixent (dupilumab) may be linked to an increased risk of cutaneous T-cell lymphoma (CTCL). Learn what studies show, how CTCL may be misdiagnosed as eczema, and the legal options for patients diagnosed with lymphoma after taking Dupixent.

  • Gavel, scales of justice on files on a table signifying a lawsuit being filed.
    Published On: December 26, 2025

    Childers, Schlueter & Smith has filed the first Dupixent lawsuit in Georgia, alleging a link between the eczema drug and cutaneous T-cell lymphoma (CTCL). The complaint highlights questions about risk disclosure.

  • Doctor working on virtual touch screen presses abbreviation: FDA. Food and Drug Administration ( FDA ) Department Service Medical Concept.
    Published On: December 23, 2025

    A recent FDA-approved label change now warns of brain meningioma risks linked to Depo-Provera. This update explains what changed, why lawsuits are being filed, and what the warning may mean for women diagnosed with brain tumors.

  • male patient at dentist office getting anesthesia injection
    Published On: February 6, 2025

    While Suboxone helps fight opioid addiction, it’s now at the center of a growing legal battle over severe, preventable dental harm not disclosed to patients for years.

  • A lawyer present a woman with legal paperwork
    Published On: January 24, 2025

    Women across the U.S. are filing lawsuits against Pfizer after a major study linked long-term use of Depo-Provera to a fivefold increase in the risk of developing brain tumors known as meningiomas.

  • closeup of a young woman getting a depo-provera birth control injection from a doctor with a syringe.
    Published On: October 29, 2024

    Women diagnosed with meningiomas after using Depo-Provera may be eligible for financial compensation, as lawsuits claim Pfizer failed to warn about the potential risk of brain tumors.