Dsuvia (Sufentanil) - Uses, Dose, Side effects

Dsuvia (Sufentanil) is a very potent opioid pain medicine that is 500 times more potent than morphine is used in the management of severe pain not responding to other non-opioid pain medicines.

Sufentanil (Dsuvia) Uses:

  • Acute pain management (sublingual tablet):

    • Management of acute pain that is too severe to be treated with other methods and that necessitates the use of an opioid analgesic.
  • Limitations of use:

    • Reserved for use in patients for whom alternative pain management choices (such as nonopioid analgesics and opioid combination medications) are ineffective, poorly tolerated, or would otherwise not be sufficient.
    • Only to be administered by a health care professional in a healthcare facility (such as a hospital, surgery centre, or emergency room); not for use at home.
    • Do not administer >72 hours (has not been studied).
  • Epidural analgesia (injection):

    • For epidural administration for analgesia combined with low dose bupivacaine during labor and vaginal delivery.
  • Surgical analgesia (injection):

    • In patients who are intubated and receiving ventilation, analgesic support is necessary to maintain balanced anaesthesia.
  • Surgical anesthesia (injection):

    • In patients who are intubated and ventilated, such as during cardiovascular surgery or neurosurgical procedures while the patient is sitting, to provide the best and most favourable myocardial and cerebral oxygen balance, or when extended postoperative ventilation is anticipated. As the primary anaesthetic agent for the induction and maintenance of anaesthesia with 100% oxygen during major surgical procedures.

Sufentanil (Dsuvia) Dose in Adults

Sufentanil (Dsuvia) Dose in Acute pain management:

  • Sublingual tablet:
    • Initial: Sublingual: 30 mcg;
    • Repeat as necessary, allowing at least one hour between doses;
    • maximum dose: 360 mcg/day (12 tablets);
    • do not use for >72 hours

Note:

  • Only be administered by a healthcare professional in a context of recognised medical supervision;
  • discontinue treatment prior to discharge from a supervised setting.

Sufentanil (Dsuvia) Dose in Surgical analgesia (as a component of balanced anesthesia) when the surgery is expected to last: 1 to 2 hours:

  • IV: Total dose: 1 to 2 mcg/kg with N2 O/O2;
  • ≥75% of total dose may be administered by slow injection or infusion prior to intubation (titrate to the individual response)
  • Maintenance:

    • Incremental dosing:

      • The maker of the medication recommends giving 10 to 25 mcg as needed when movement and/or changes in vital signs point to surgical stress or a waning of analgesia.
      • May also administer doses in the range of 5 to 20 mcg as required or at 0.1 to 0.25 mcg/kg as needed.
      • The total dose should not exceed 1 mcg/kg/hour of expected surgical time.
    • Continuous infusion:

      • May also be administered in continuous infusion with the infusion rate based on the induction dose used.
      • Maximum infusion rate according to the manufacturer: at 1 mcg/kg/hour.
      • May also administer doses in the range at 0.3 to 0.9 mcg/kg/hour or at 0.5 to 1.5 mcg/kg/hour.

Sufentanil (Dsuvia) Dose in Surgical analgesia (as a component of balanced anesthesia) when the surgery is expected to last 2 to 8 hours:

  • Total dose: at 2 to 8 mcg/kg with N O/O ;
  • ≤75% of total dose may be administered by slow intravenous injection or infusion prior to intubation (titrate to individual response).
  • Maintenance:

    • Incremental dosing:

      • According to the drug manufacturer, 10 to 50 mcg may be administered as needed when movement and/or changes in vital signs indicate surgical stress or lightening of analgesia.
      • The total dose should not exceed 1 mcg/kg/hour of expected surgical time.
    • Continuous infusion:

      • May also be administered in continuous intravenous infusion with the infusion rate based on the induction dose used.
      • Maximum infusion rate according to the manufacturer: at 1 mcg/kg/hour.
      • May also administer doses in the range at 0.3 to 0.9 mcg per kg per hour or at 0.5 to 1.5 mcg per kg per hour.

Sufentanil Dose in the treatment of Surgical anesthesia:

  • Total dose: at 8 to 30 mcg/kg as a slow injection, infusion, or injection followed by infusion;
  • titrate to individual patient response.
  • Note: To address the risk of postoperative respiratory depression in patients receiving high doses of sufentanil, trained people and suitable facilities are required.
  • Maintenance:

    • Incremental dosing: at 5 to 10 mcg/kg as needed in anticipation of surgical stress
    • Continuous infusion: Base infusion rate on the induction dose so that the total dose for the procedure does not exceed at 30 mcg/kg

Sufentanil (Dsuvia) Dose in Analgesia for labor and delivery:

  • Epidural: at 10 to 15 mcg with bupivacaine 0.125% with/without epinephrine.
  • Dose can be repeated twice (for a total of 3 doses) at not less than 1-hour intervals until delivery occurs.

Sufentanil (Dsuvia) Dose in Children

Note: 

  • The dosage should be adjusted for the desired effects;
    a wide range of doses, depending on the patient's age (especially that of small infants) and the desired level of anaesthesia or analgesia;
  • use lean body weight for patients who are >20% above ideal body weight.
  • Should only be administered under the supervision of a qualified physician experienced in the use of anesthetics.

Sufentanil (Dsuvia) Dose in Cardiac surgery anesthesia:

IV:

  • Initial: 5 to 25 mcg/kg;
  • repeat the maintenance doses:
    • 1 to 5 mcg/kg/doses up to 25 to 50 mcg/dose as necessary depending on the reaction to the initial dose and as assessed by changes in vital signs indicating surgical stress or easing of anaesthesia;
    • data based on experience in cardiac surgery, which requires much higher induction and maintenance doses;
    • lower dosing may be enough for other procedures.

Dsuvia (Sufentanil) dose in the treatment of Epidural anesthesia:

  • Infants ≥3 months and Children:

    • Epidural injection: Initial bolus: at 0.2 mcg/kg followed by continuous infusion at 0.1 mcg/kg/hour in combination with ropivacaine.

Dsuvia (Sufentanil) Dose for procedural and preoperative sedation: 

  • Children ≥3 years:

    • Intranasal: at 1 to 3 mcg/kg in combination with other agents.

Pregnancy Risk Category: C

  • Neonatal withdrawal syndrome can be caused by prolonged maternal opioid use during pregnancy. If not treated and recognized promptly, it could prove to be fatal.
  • Pregnant women who require prolonged opioid therapy should be notified and ensure that the treatment is available.
  • Opioids can cross the placenta. Opioids can cross the placenta and cause birth defects, preterm births, low fetal growth, stillbirth, or other complications.
  • A pregnant woman may experience withdrawal symptoms if they are exposed to chronic opioids.
  • The syndrome of neonatal abstinence (NAS) A person exposed to opioids may experience autonomic, gastrointestinal, or neurological symptoms.
  • Opioid-dependent mothers may give birth to babies who are also opioid dependent.
  • Opioids can cause respiratory depression in neonates and psycho-physiologic side effects in newborns. Mothers who have given opioids to their babies during labor must be monitored.
  • Sufentanil should not be used during labor or right before it.
  • In labor and delivery, epidural sufentanil is administered with or without epinephrine. Pregnant women should not use intravenous epidurals or higher doses.
  • Opioids used to treat pain during childbirth may momentarily change the fetus's heart rate.
  • Long-term opioid abuse may result in lower fertility for males and women.

Sufentanil use during breastfeeding:

  • It is unknown if breast milk contains sufentanil.
  • The drug's maker advises that when deciding whether to stop or continue breastfeeding while receiving treatment, one should take into account the risks to the baby as well as the advantages for the mother.
  • The natural instinct to breastfeed in the first hours after birth may be affected by maternal opioids.
  • Women who are breastfeeding should consider a short-acting opioid like sufentanil.
  • Monitor infants breastfeeding opioid-exposed infants (Montgomery 2012).

Dsuvia dose in Kidney Disease:

  • There are no dosage adjustments provided in the drug manufacturer’s labeling.
  • Use with caution and reduce the dose as needed;
  • titrate slowly and closely monitor for signs of CNS and respiratory depression.

Dsuvia Dose in Liver disease:

  • There are no dosage adjustments provided in the drug manufacturer’s labeling.
  • Use with caution and reduce the dose as needed;
  • titrate slowly and closely monitor for signs of CNS and respiratory depression.

Common Side Effects of Sufentanil (Dsuvia):

  • Central nervous system:

    • Headache
  • Dermatologic:

    • Pruritus
  • Gastrointestinal:

    • Nausea

Less Common Side Effects of Sufentanil (Dsuvia):

  • Cardiovascular:

    • Hypotension
  • Central nervous system:

    • Dizziness
  • Gastrointestinal:

    • Vomiting

Rare side effects of Dsuvia (Sufentanil):

  • Cardiovascular:

    • Bradycardia
    • ECG Abnormality
    • Flushing
    • Hypertension
    • Orthostatic Hypotension
    • Oxygen Saturation Decreased
    • Peripheral Vasodilation
    • Presyncope
    • Sinus Tachycardia
    • Syncope
  • Central Nervous System:

    • Agitation
    • Anxiety
    • Confusion
    • Disorientation
    • Drowsiness
    • Drug Abuse
    • Drug Dependence
    • Euphoria
    • Hallucination
    • Insomnia
    • Lethargy
    • Memory Impairment
    • Mental Status Changes
    • Sedation
  • Dermatologic:

    • Hyperhidrosis
    • Skin Rash
  • Gastrointestinal:

    • Abdominal Distension
    • Abdominal Distress
    • Constipation
    • Decreased Gastrointestinal Motility
    • Diarrhea
    • Dyspepsia
    • Eructation
    • Flatulence
    • Gastritis
    • Hiccups
    • Intestinal Obstruction (Postoperative)
    • Oral Hypoesthesia
    • Retching
    • Upper Abdominal Pain
    • Xerostomia
  • Genitourinary:

    • Decreased Urine Output
    • Oliguria
    • Urinary Hesitancy
    • Urinary Retention
  • Hepatic:

    • Increased Liver Enzymes
    • Increased Serum Aspartate Aminotransferase
  • Neuromuscular & Skeletal:

    • Muscle Rigidity
    • Muscle Spasm
  • Ophthalmic:

    • Miosis
  • Renal:

    • Renal Failure Syndrome
  • Respiratory:

    • Apnea
    • Atelectasis
    • Bradypnea
    • Hypoventilation
    • Hypoxia
    • Respiratory Depression
    • Respiratory Distress
    • Respiratory Failure

Contraindications to Dsuvia (Sufentanil):

  • hyperresponsiveness/Hypersensitivity (eg, anaphylaxis) to sufentanil or any component of the formulation

Sublingual tablets may also be contraindicated

  • Respiratory depression is a serious problem
  • Acute or severe bronchial asthma in unmonitored settings or without resuscitative devices;
  • Paralytic ileus, suspected or known gastrointestinal obstruction

Canadian labeling: Additional contraindications not listed in the US labeling:

  • Hypersensitivity to fentanyl and other morphinomimetics
  • IV use during labor, or before clamping cord during Cesarean section
  • Patients with severe hemorhage, shock, septicemia or infection at the puncture site may require epidural administration

There is not much evidence of cross-reactivity between opioids and allergenic substances.

Cross-sensitivity can be possible due to similarities in chemical structure or pharmacologic effects.

Warnings and precautions

  • Adrenocortical Insufficiency

    • Patients with adrenal insufficiency (Addison disease) should be cautious.
    • Long-term opioid abuse can lead to secondary hypogonadism. This could cause infertility, sexual dysfunction, mood disorders, and osteoporosis.
  • Bradyarrhythmias:

    • Bradycardia can be severe; patients with bradyarrhythmias should be cautious.
  • CNS depression:

    • CNS depression can lead to mental or physical impairments.
    • Patients should be advised about tasks that require mental alertness, such as driving or operating machinery.
  • Hypotension

    • Can cause severe hypotension (including orthostatic hypertension and syncope).
    • Patients with hypovolemia, heart disease (including acute MI), and drugs that can exaggerate hypotensive effects (such as phenothiazines and general anesthetics) should be cautious.
    • After dose titration or initiation, monitor for hypotension symptoms.
    • Patients with circulatory shock should be cautious about injecting.
    • Patients with circulatory shock should not take sublingual tablets.
  • Respiratory depression [US Boxed Warning]

    • Sufentanil can cause severe, life-threatening or fatal respiratory depression.
    • Monitor for signs of respiratory depression, especially when sufentanil is being administered or the dose is being increased.
    • The sedating effects that opioids can cause by carbon dioxide retention may be exacerbated by opioid-induced respiratory depression.
  • Serotonin syndrome:

    • Concurrent use of sufentanil, serotonergic medications (such as SSRIs, SNRIs, triptans, TCAs, 5-HT receptor antagonists, mirtazapine, trazodone, tramadol), and medications that interfere with serotonin metabolism has been linked to potentially fatal serotonin syndrome (SS) (eg, MAO inhibitors).
    • Pay close attention to patients' signs of SS..
      • Mental status changes (eg: agitation, hallucinations and delirium, coma).
      • autonomic instability (eg tachycardia or labile blood pressure, diaphoresis)
      • neuromuscular changes (eg, tremor, rigidity, myoclonus);
      • GI symptoms (eg, nausea, vomiting, diarrhea); and/or
      • seizures.
    • Sufentanil should be discontinued if serotonin symptoms are suspected.
  • Conditions abdominales:

    • Patients with acute abdominal conditions may not be diagnosed or treated appropriately.
    • Sublingual tablets are contraindicated in patients with GI obstruction or paralytic ileus.
  • Insufficiency of the biliary tract:

    • Patients with biliary dysfunction (including acute pancreatitis) should be cautious.
    • Opioid may cause constriction in the sphincter Oddi.
  • CNS depression and coma

    • Patients with impaired consciousness and coma should be cautious as they are more susceptible to the intracranial effects CO retention.
  • Delirium tremens:

    • Patients with delirium-tremens should be cautious when using opioids.
  • Head trauma

    • Patients with intracranial injuries, intracranial lesions or elevated intracranial Pressure (ICP) should be used with extreme caution. Exaggerated elevations of ICP could occur.
  • Hepatic impairment

    • Patients with hepatic impairment should be cautious and reduced the dosage as necessary.
  • Obesity:

    • Patients who are severely obese should be taken with caution
    • Lean body weight is recommended for patients who are >20% above their ideal body weight.
  • Prostatic hyperplasia, urinary stricture

    • Patients with prostatic hyperplasia or urinary stricture should be cautious when using opioids.
  • Psychosis:

    • Patients with toxic psychosis should be treated with caution.
  • Renal impairment

    • Patients with impaired renal function should be cautious and reduced the dosage as necessary.
  • Respiratory disease

    • Patients with COPD or cor Pulmonale significant should be monitored for respiratory depression. Preventive and titrating therapy is not recommended for patients with severe COPD.
  • Seizures:

    • Patients with seizure disorders past should be cautious.
    • This could increase the risk of or worsen preexisting seizure disorders.
  • Thyroid dysfunction:

    • Patients with thyroid dysfunction should be cautious when using opioids.

Sufentanil: Drug Interaction

Risk Factor C (Monitor therapy)

Alfuzosin

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Alizapride

May enhance the CNS depressant effect of CNS Depressants.

Amphetamines

May enhance the analgesic effect of Opioid Agonists.

Anticholinergic Agents

May enhance the adverse/toxic effect of Opioid Agonists. Specifically, the risk for constipation and urinary retention may be increased with this combination.

Aprepitant

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Beta-Blockers

Beta-Blockers may have a greater bradycardic effect when combined with opioids (anilidopiperidine). Beta-Blockers may have a greater hypotensive impact when combined with opioids (anilidopiperidine).

Blood Pressure Lowering Agents

May enhance the hypotensive effect of HypotensionAssociated Agents.

Bradycardia-Causing Agents

May intensify other bradycardia-causing agents' bradycardic effects.
Bradycardia-Causing Agents' bradycardic effect might be enhanced. In patients taking AV blocking medications, bretylium may also strengthen atrioventricular (AV) blockade

Bretylium

CNS depressants may have an enhanced CNS depressant impact.

Brimonidine (Topical)

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Brimonidine (Topical)

CNS depressants may have an enhanced CNS depressant impact.

Calcium Channel Blockers (Nondihydropyridine)

Calcium Channel Blockers may have a greater bradycardic effect when used with opioids (anilidopiperidine) (Nondihydropyridine). Anilidopiperidine, a kind of opioid, may increase the hypotensive effects of calcium channel blockers (Nondihydropyridine).

Cannabidiol

CNS depressants may have an enhanced CNS depressant impact.

Cannabis

CNS depressants may have an enhanced CNS depressant impact.

Chlorphenesin Carbamate

CNS depressants' harmful or toxic effects could be increased.

Clofazimine

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

CYP3A4 Inducers (Strong)

May decrease the serum concentration of SUFentanil.

CYP3A4 Inhibitors (Moderate)

May slow down CYP3A4 substrate metabolism (High risk with Inhibitors).

Desmopressin

Opioid Agonists may enhance the adverse/toxic effect of Desmopressin.

Diazoxide

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Dimethindene (Topical)

May enhance the CNS depressant effect of CNS Depressants.

Diuretics

Opioid Agonists may enhance the adverse/toxic effect of Diuretics. Opioid Agonists may diminish the therapeutic effect of Diuretics.

Dronabinol

May enhance the CNS depressant effect of CNS Depressants.

DULoxetine

Blood Pressure Lowering Agents may enhance the hypotensive effect of DULoxetine.

Duvelisib

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Erdafitinib

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Fosaprepitant

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Fosnetupitant

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Gastrointestinal Agents (Prokinetic)

Opioid Agonists may diminish the therapeutic effect of Gastrointestinal Agents (Prokinetic).

Herbs (Hypotensive Properties)

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Hypotension-Associated Agents

Blood Pressure Lowering Agents may enhance the hypotensive effect of Hypotension-Associated Agents.

Ivabradine

Bradycardia-Causing Agents may intensify Ivabradine's bradycardic impact.

Kava Kava

CNS depressants' harmful or toxic effects could be increased.

Lacosamide

Bradycardia-Causing Substances may intensify Lacosamide's AV-blocking effects.

Larotrectinib

May elevate CYP3A4 substrates' serum concentration (High risk with Inhibitors).

Levodopa-Containing Products

Levodopa-Containing Products' hypotensive effects may be strengthened by blood pressure-lowering medications.

Lofexidine

CNS depressants may have an enhanced CNS depressant impact. Management: Separate drug interaction monographs go into further detail about the medications indicated as exceptions to this book.

Magnesium Sulfate

CNS depressants may have an enhanced CNS depressant impact.

MetyroSINE

The sedative effects of metyroSINE may be strengthened by CNS depressants.

Midodrine

Bradycardia-Causing Agents' bradycardic effect might be enhanced.

Minocycline

May enhance the CNS depressant effect of CNS Depressants.

Molsidomine

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Nabilone

May enhance the CNS depressant effect of CNS Depressants.

Naftopidil

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Netupitant

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Nicergoline

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Nicorandil

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Nitroprusside

Blood Pressure Lowering Agents may enhance the hypotensive effect of Nitroprusside.

Palbociclib

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Pegvisomant

Opioid Agonists may diminish the therapeutic effect of Pegvisomant.

Pentoxifylline

May enhance the hypotensive effect of Blood Pressure Lowering Agents.

Phosphodiesterase 5 Inhibitors

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Piribedil

Piribedil's CNS depressing effects may be enhanced by other CNS depressants.

Pramipexole

The sedative effects of pramipexole might be enhanced by CNS depressants.

Prostacyclin Analogues

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Quinagolide

The hypotensive effects of blood pressure-lowering medications may be strengthened.

Ramosetron

Ramosetron's tendency to induce constipation may be increased by opioid agonists.

ROPINIRole

The sedative effects of CNS depressants may increase those of ROPINIRole.

Rotigotine

Rotigotine's sedative effects may be boosted by CNS depressants.

Rufinamide

CNS depressants' harmful or toxic effects could be increased. Particularly, drowsiness and lightheadedness could be worsened.

Ruxolitinib

Bradycardia-Causing Agents' bradycardic effect might be enhanced. Management: The Canadian product labelling for roxolitinib advises against using it in conjunction with medications that can cause bradycardia whenever feasible.

Selective Serotonin Reuptake Inhibitors

Selective serotonin reuptake inhibitors may have a worsened or more hazardous effect when taken with CNS depressants. Particularly, there may be an increased risk of psychomotor impairment.

Serotonin Modulators

Serotonin Modulators' serotonergic effects may be strengthened by opioid agonists. Serotonin syndrome might occur from this. The exception is nigroline.

Simeprevir

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Succinylcholine

May enhance the bradycardic effect of Opioid Agonists.

Terlipressin

May enhance the bradycardic effect of Bradycardia-Causing Agents.

Tetrahydrocannabinol

May enhance the CNS depressant effect of CNS Depressants.

Tetrahydrocannabinol and Cannabidiol

May enhance the CNS depressant effect of CNS Depressants.

Tofacitinib

May enhance the bradycardic effect of Bradycardia-Causing Agents.

Risk Factor D (Consider therapy modification)

Alvimopan

Opioid Agonists may enhance the adverse/toxic effect of Alvimopan. This is most notable for patients receiving long-term (i.e., more than 7 days) opiates prior to alvimopan initiation. Management: Alvimopan is contraindicated in patients receiving therapeutic doses of opioids for more than 7 consecutive days immediately prior to alvimopan initiation.

Amifostine

Blood Pressure Lowering Agents may enhance the hypotensive effect of Amifostine. Management: When amifostine is used at chemotherapy doses, blood pressure lowering medications should be withheld for 24 hours prior to amifostine administration. If blood pressure lowering therapy cannot be withheld, amifostine should not be administered.

Blonanserin

CNS Depressants may enhance the CNS depressant effect of Blonanserin.

Ceritinib

Bradycardia-Causing Agents may intensify Ceritinib's bradycardic impact. Management: If this combination cannot be avoided, continuously monitor patients' blood pressure and heart rate throughout therapy and look for any signs of symptomatic bradycardia in them. A separate monograph is dedicated to discussing exceptions.

Chlormethiazole

May enhance the CNS depressant effect of CNS Depressants. Management: Monitor closely for evidence of excessive CNS depression. The chlormethiazole labeling states that an appropriately reduced dose should be used if such a combination must be used.

CNS Depressants

May enhance the CNS depressant effect of Opioid Agonists. Management: Avoid concomitant use of opioid agonists and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug.

CYP3A4 Inhibitors (Strong)

SUFentanil serum concentration can rise. Treatment: If a powerful CYP3A4 inhibitor is started in a patient on sufentanil, consider lowering the dose and keep an eye out for any toxicities and side effects that may become more severe (eg, respiratory depression).

Droperidol

May enhance the CNS depressant effect of CNS Depressants. Management: Consider dose reductions of droperidol or of other CNS agents (eg, opioids, barbiturates) with concomitant use. Exceptions to this monograph are discussed in further detail in separate drug interaction monographs.

Flunitrazepam

CNS Depressants may enhance the CNS depressant effect of Flunitrazepam.

HYDROcodone

CNS Depressants may enhance the CNS depressant effect of HYDROcodone. Management: Avoid concomitant use of hydrocodone and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug.

Methotrimeprazine

CNS Depressants may enhance the CNS depressant effect of Methotrimeprazine. Methotrimeprazine may enhance the CNS depressant effect of CNS Depressants. Management: Reduce adult dose of CNS depressant agents by 50% with initiation of concomitant methotrimeprazine therapy. Further CNS depressant dosage adjustments should be initiated only after clinically effective methotrimeprazine dose is established.

MiFEPRIStone

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Management: Minimize doses of CYP3A4 substrates, and monitor for increased concentrations/toxicity, during and 2 weeks following treatment with mifepristone. Avoid cyclosporine, dihydroergotamine, ergotamine, fentanyl, pimozide, quinidine, sirolimus, and tacrolimus.

Nalmefene

May diminish the therapeutic effect of Opioid Agonists. Management: Avoid the concomitant use of nalmefene and opioid agonists. Discontinue nalmefene 1 week prior to any anticipated use of opioid agonistss. If combined, larger doses of opioid agonists will likely be required.

Naltrexone

May diminish the therapeutic effect of Opioid Agonists. Management: Seek therapeutic alternatives to opioids. See full drug interaction monograph for detailed recommendations.

Obinutuzumab

May enhance the hypotensive effect of Blood Pressure Lowering Agents. Management: Consider temporarily withholding blood pressure lowering medications beginning 12 hours prior to obinutuzumab infusion and continuing until 1 hour after the end of the infusion.

Opioid Agonists

CNS Depressants may enhance the CNS depressant effect of Opioid Agonists. Management: Avoid concomitant use of opioid agonists and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug.

OxyCODONE

CNS Depressants may enhance the CNS depressant effect of OxyCODONE. Management: Avoid concomitant use of oxycodone and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug.

Perampanel

May enhance the CNS depressant effect of CNS Depressants. Management: Patients taking perampanel with any other drug that has CNS depressant activities should avoid complex and high-risk activities, particularly those such as driving that require alertness and coordination, until they have experience using the combination.

PHENobarbital

May enhance the CNS depressant effect of SUFentanil. PHENobarbital may decrease the serum concentration of SUFentanil. Management: Avoid use of sufentanil and phenobarbital when possible. Monitor for respiratory depression/sedation. Because phenobarbital is also a strong CYP3A4 inducer, monitor for decreased sufentanil efficacy and withdrawal if combined.

Primidone

May enhance the CNS depressant effect of SUFentanil. Primidone may decrease the serum concentration of SUFentanil. Management: Avoid use of sufentanil and primidone when possible. Monitor for respiratory depression/sedation. Because primidone is also a strong CYP3A4 inducer, monitor for decreased sufentanil efficacy and withdrawal if combined.

Sincalide

Drugs that Affect Gallbladder Function may diminish the therapeutic effect of Sincalide. Management: Consider discontinuing drugs that may affect gallbladder motility prior to the use of sincalide to stimulate gallbladder contraction.

Siponimod

Bradycardia-Causing Agents may intensify Siponimod's bradycardic impact. Management: Steer clear of combining siponimod with medications that can slow your heart rate.

Sodium Oxybate

CNS depressants may have an enhanced CNS depressant impact. Management: Take into account substitutes for combined use. Reduce the doses of one or more medications when simultaneous use is necessary. It is not advised to use sodium oxybate with alcoholic beverages or hypnotic sedatives.

Stiripentol

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Management: Use of stiripentol with CYP3A4 substrates that are considered to have a narrow therapeutic index should be avoided due to the increased risk for adverse effects and toxicity. Any CYP3A4 substrate used with stiripentol requires closer monitoring.

Suvorexant

CNS Depressants may enhance the CNS depressant effect of Suvorexant. Management: Dose reduction of suvorexant and/or any other CNS depressant may be necessary. Use of suvorexant with alcohol is not recommended, and the use of suvorexant with any other drug to treat insomnia is not recommended.

Tapentadol

May enhance the CNS depressant effect of CNS Depressants. Management: Avoid concomitant use of tapentadol and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug.

Zolpidem

CNS Depressants may enhance the CNS depressant effect of Zolpidem. Management: Reduce the Intermezzo brand sublingual zolpidem adult dose to 1.75 mg for men who are also receiving other CNS depressants. No such dose change is recommended for women. Avoid use with other CNS depressants at bedtime; avoid use with alcohol.

Risk Factor X (Avoid combination)

Azelastine (Nasal)

CNS Depressants may enhance the CNS depressant effect of Azelastine (Nasal).

Bromperidol

Blood Pressure Lowering Agents may enhance the hypotensive effect of Bromperidol. Bromperidol may diminish the hypotensive effect of Blood Pressure Lowering Agents.

Bromperidol

May enhance the CNS depressant effect of CNS Depressants.

Conivaptan

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Eluxadoline

Opioid Agonists may enhance the constipating effect of Eluxadoline.

Fusidic Acid (Systemic)

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Idelalisib

May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors).

Monoamine Oxidase Inhibitors

SUFentanil may make monoamine oxidase inhibitors more harmful or hazardous. Particularly, there may be an elevated risk for serotonin syndrome or opioid toxicities (such as respiratory depression or coma). Management: Due to the risk of serotonin syndrome and/or severe CNS depression, fentanyl should not be administered in conjunction with monoamine oxidase (MAO) inhibitors (or within 14 days of discontinuing an MAO inhibitor).

Opioids (Mixed Agonist / Antagonist)

May diminish the analgesic effect of Opioid Agonists. Management: Seek alternatives to mixed agonist/antagonist opioids in patients receiving pure opioid agonists, and monitor for symptoms of therapeutic failure/high dose requirements (or withdrawal in opioid-dependent patients) if patients receive these combinations.

Orphenadrine

CNS Depressants may enhance the CNS depressant effect of Orphenadrine.

Oxomemazine

May enhance the CNS depressant effect of CNS Depressants.

Paraldehyde

CNS Depressants may enhance the CNS depressant effect of Paraldehyde.

Thalidomide

CNS Depressants may enhance the CNS depressant effect of Thalidomide.

Monitoring parameters:

  • Pain relief,
  • respiratory and cardiovascular status,
  • blood pressure, and heart rate

How to administer Dsuvia (Sufentanil)?

  • IV:

    • Intermittent doses can be administered intravenously either as a slow injection, ranging from 2-10 minutes to a full infusion or as a slow injection.
    • Also available as continuous infusions
  • Oral: Sublingual tablet:

    • Only administer by a licensed health care provider in a medically supervised setting.
    • Use gloves for administering.
    • The tablet is packed in a single-dose container; keep it closed until you are ready to administer.
    • The patient should open his mouth and touch the roof of their mouth with their tongue.
    • Use the single-dose applicator to administer into sublingual space.
    • The patient must not chew or swallow the tablet.
    • Do not eat or drink for at least 10 min after administering the medication.

Mechanism of action of Dsuvia (Sufentanil):

  • The CNS binds to opioid receptors.
  • After receptor binding has occurred, the effects of opening K+ channels or inhibiting Ca++ channel are felt.
  • These mechanisms increase pain threshold and alter pain perception, inhibit ascending painful pathways; short-acting opioid; dose-related inhibition catecholamine release (upto 30 mcg/kg); controls sympathetic response to surgical stress

The onset of action:

  • Analgesia:
    • IV: in 1 to 3 minutes;
    • Epidural: in 10 minutes;
    • Sublingual tablets: ~30 minutes.

Duration:

  • Dose-dependent:
    • Anesthesia adjunct doses: IV: in 5 minutes;
    • Epidural: at 10 to 15 mcg with bupivacaine 0.125%: 1.7 hours;
    • Sublingual tablets: at ~3 hours.

Protein binding:

  • Neonates: about 79%;
  • Adults: about 91% to 93%; primarily to alpha 1-acid glycoprotein

Metabolism:

  • Primarily metabolism is hepatic and small intestine via demethylation and dealkylation

Bioavailability:

  • Sublingual tablet: ~53%

Half-life elimination (IV):

  • Neonates: 7.2 ± 2.7 hours;
  • Infants and Children (2 to 8 years): 97 ± 42 minutes;
  • Adolescents 10 to 15 years: 76 ± 33 minutes;
  • Adults: 164 minutes
  • Sublingual tablet: 2.5 ± 0.85 hours (Fisher 2018)

Time to peak:

  • Sublingual tablet: 1 hour

Excretion:

  • Urine (2% excreted as unchanged drug; 80% metabolites) within 24 hours

Clearance:

  • Children 2 to 8 years: 30.5 ± 8.8 mL/minute/kg
  • Adolescents: 12.8 ± 12 mL/minute/kg
  • Adults: 12.7 ± 0.8 mL/minute/kg

International Brands of Sufentanil:

  • Dsuvia
  • Dzuveo
  • Fentafienil
  • Sufenta
  • Sufenta Forte
  • Sufental
  • Sufentil
  • Zalviso
  • Zuftil

Sufentanil Brands Name in Pakistan:

No Brands Available in Pakistan.