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Standing risks

  • High overdose risk, use cautionconfidence medium
    Acute toxicity
    high
    View in article
  • Compulsive use risk, monitor frequencyconfidence medium
    Compulsive redosing
    high
    Dose escalation
    moderate
    View in article
  • High dependence, taper carefullyconfidence medium
    Physical dependence
    high
    Psychological dependence
    moderate
    View in article

Lethal interactions

Specific substances

  • Ketaminelethal
  • Tramadollethal

By drug class

  • Benzodiazepines, Barbiturateslethal2 mechanismsconfidence high
  • GHB, Baclofenlethal2 mechanismsconfidence high
  • GHB, GBLlethal2 mechanismsconfidence high
  • Local anestheticslethal4 mechanismsconfidence medium

Dangerous interactions

28 dangerous interactions recorded for this substance.

See the full interactions table

Contraindications

Respiratory

  • Respiratory depression or obstructive airway diseaserelative

    Pre-existing respiratory depression, severe chronic obstructive pulmonary disease, cor pulmonale, or substantially decreased respiratory reserve increases the risk of fatal respiratory arrest. Sufentanil suppresses respiratory drive via MOR activation in the pre-Bötzinger complex and parabrachial nucleus.

Neurological

  • Head injury or raised intracranial pressurerelative

    In patients with head injury, intracranial lesions, or pre-existing elevated intracranial pressure, sufentanil-induced respiratory depression can exacerbate ICP elevation via hypercapnia-mediated cerebral vasodilation. Additionally, opioid-induced miosis and sedation may obscure neurological assessment.

Psychiatric

  • Acute alcoholism or delirium tremensrelative

    Acute alcohol intoxication or delirium tremens combined with sufentanil creates additive respiratory and CNS depression risk. Standard opioid class contraindication.

Hepatic

  • Hepatic impairmentrelative

    Hepatic impairment reduces CYP3A4-mediated N-dealkylation of sufentanil to norsufentanil, decreasing clearance and increasing the risk of prolonged or excessive opioid effects including respiratory depression.

Immunological

  • Hypersensitivity to sufentanil or other opioid agonistsabsolute

    Known hypersensitivity to sufentanil citrate or any component of the formulation, or to other opioid agonists, constitutes an absolute contraindication per the FDA label.

Age

  • Neonatal populationrelative

    Neonates show markedly prolonged sufentanil elimination (t½ ~434 min vs. ~164 min in adults) due to immature hepatic CYP3A4 activity and reduced protein binding (79% vs. 93%). Dose adjustment and extended monitoring are required.

Other

  • Absence of resuscitation equipment and trained personnelabsolute

    Sufentanil must only be administered in settings with immediate access to airway management equipment, supplemental oxygen, and personnel trained in the management of respiratory depression. The FDA label restricts use to medically supervised settings.

  • Concurrent strong CYP3A4 inhibitorsrelative

    Co-administration with strong CYP3A4 inhibitors increases sufentanil plasma concentrations, potentiating all effects including respiratory depression. Dose reduction and extended monitoring are necessary.

  • Paralytic ileusrelative

    Opioids including sufentanil reduce gastrointestinal motility via peripheral MOR activation. Administration in the setting of known or suspected paralytic ileus may worsen obstruction.

  • Concurrent MAOI userelative

    Combined use of opioids with MAOIs is a general class contraindication. While sufentanil does not interact with serotonin systems (unlike meperidine or tramadol), the potential for unpredictable potentiation of CNS depression warrants avoidance. No sufentanil-specific MAOI interaction data exist.

If this is going wrong

Reducing or stopping