Sufentanil

{{DrugProjectFormSinglePage |authorTag=Chetan Lokhande, M.B.B.S [1] |genericName=Sufentanil |aOrAn=a |drugClass=analgesic opioid |indication=analgesia in labor, epidural; adjunct, general anesthesia |adverseReactions=cardiovascular: bradyarrhythmia (3% to 9% ), hypotension (3% to 9% ), dermatologic: pruritus (25% ), gastrointestinal: nausea (3% to 9% ), vomiting (3% to 9% ), musculoskeletal: muscle rigidity, chest wall (3% to 9% ), neurologic: somnolence (3% to 9% ) |blackBoxWarningTitle=TITLE |blackBoxWarningBody=Condition Name: (Content) |fdaLIADAdult=* Dosage should be individualized

• Analgesia in labor, epidural; adjunct: (epidural use) 10-15 mcg sufentanil administered with 10 mL bupivacaine 0.125% with or without epinephrine; may repeat twice at not less than 1 hr intervals until delivery; max 3 doses
• General anesthesia: primary anesthetic agent, 8-30 mcg/kg IV with 100% oxygen and a muscle relaxant, then 0.5-10 mcg/kg as needed in response to signs of lightening of anesthesia; max 30 mcg/kg/procedure
• General anesthesia: analgesic adjunct to balanced general anesthesia, 1-8 mcg/kg IV (approximately 1 mcg/kg/hr of estimated surgical duration); 75% given prior to intubation, then incrementally as 10-50 mcg IV as needed in response to signs of lightening of analgesia

|offLabelAdultGuideSupport=There is limited information about Off-Label Guideline-Supported Use of Sufentanil in adult patients. |offLabelAdultNoGuideSupport=There is limited information about Off-Label Non–Guideline-Supported Use of Sufentanil in adult patients. |fdaLIADPed=* General anesthesia: cardiovascular surgery (age under 12 yr) 10-25 mcg/kg with 100% oxygen, additional doses up to 25-50 mcg for maintenance of anesthesia |offLabelPedGuideSupport=There is limited information about Off-Label Guideline-Supported Use of Sufentanil in pediatric patients. |offLabelPedNoGuideSupport=There is limited information about Off-Label Non–Guideline-Supported Use of Sufentanil in pediatric patients. |contraindications=* Sufentanil is contraindicated in patients with known hypersensitivity to the drug or known intolerance to other opioid agonists. |warnings=* Sufentanil should be administered only by persons specifically trained in the use of intravenous and epidural anesthetics and management of the respiratory effects of potent opioids.

• An opioid antagonist, resuscitative and intubation equipment and oxygen should be readily available.
• Prior to catheter insertion, the physician should be familiar with patient conditions (such as infection at the injection site, bleeding diathesis, anticoagulant therapy, etc.) which call for special evaluation of the benefit versus risk potential.

Intravenous use

• Intravenous administration or unintentional intravascular injection during epidural administration of Sufentanil may cause skeletal muscle rigidity, particularly of the truncal muscles. The incidence and severity of muscle rigidity is dose related. Administration of Sufentanil may produce muscular rigidity with a more rapid onset of action than that seen with fentanyl. Sufentanil may produce muscular rigidity that involves the skeletal muscles of the neck and extremities. As with fentanyl, muscular rigidity has been reported to occur or recur infrequently in the extended postoperative period. The incidence of muscular rigidity associated with intravenous Sufentanil can be reduced by: 1) administration of up to 1/4 of the full paralyzing dose of a non-depolarizing neuromuscular blocking agent just prior to administration of Sufentanil at dosages of up to 8 mcg/kg, 2) administration of a full paralyzing dose of a neuromuscular blocking agent following loss of consciousness when Sufentanil is used in anesthetic dosages (above 8 mcg/kg) titrated by slow intravenous infusion, or, 3) simultaneous administration of Sufentanil and a full paralyzing dose of a neuromuscular blocking agent when Sufentanil is used in rapidly administered anesthetic dosages (above 8 mcg/kg).
• The neuromuscular blocking agents used should be compatible with the patient's cardiovascular status. Adequate facilities should be available for postoperative monitoring and ventilation of patients administered Sufentanil. It is essential that these facilities be fully equipped to handle all degrees of respiratory depression.

|clinicalTrials=* The most common adverse reactions of opioids are respiratory depression and skeletal muscle rigidity, particularly of the truncal muscles. Sufentanil may produce muscular rigidity that involves the skeletal muscles of the neck and extremities. See Clinical Pharmacology, Warnings And Precautions on the management of respiratory depression and skeletal muscle rigidity. Urinary retention has been associated with the use of epidural opioids but was not reported in the clinical trials of epidurally administered Sufentanill due to the use of indwelling catheters. The incidence of urinary retention in patients without urinary catheters receiving epidural Sufentanil is unknown; return of normal bladder activity may be delayed.

• The following adverse reaction information is derived from controlled clinical trials in 320 patients who received intravenous Sufentanil during surgical anesthesia and in 340 patients who received epidural Sufentanil plus bupivacaine 0.125% for analgesia during labor and is presented below. Based on the observed frequency, none of the reactions occurring with an incidence less than 1% were observed during clinical trials of epidural Sufentanil used during labor and delivery (N=340).
• In general cardiovascular and musculoskeletal adverse experiences were not observed in clinical trials of epidural Sufentanilnil. Hypotension was observed 7 times more frequently in intravenous trials than in epidural trials. The incidence of central nervous system, dermatological and gastrointestinal adverse experiences was approximately 4 to 25 times higher in studies of epidural use in labor and delivery.
• Probably Causally Related: Incidence Greater than 1% - Derived from clinical trials (See preceding paragraph)

• Cardiovascular: bradycardia, hypertension, hypotension.
• Musculoskeletal: chest wall rigidity.

• Central Nervous System: somnolence.
• Dermatological: pruritus (25%).
• Gastrointestinal: nausea, vomiting.
• Probably Causally Related: Incidence Less than 1% - Derived from clinical trials (Adverse events reported in post-marketing surveillance, not seen in clinical trials, are italicized.)
• Body as a whole: anaphylaxis.
• Cardiovascular: [[arrhythmia[[, tachycardia, cardiac arrest.
• Central Nervous System: chills.
• Dermatological: erythema.
• Musculoskeletal: skeletal muscle rigidity of neck and extremities.
• Respiratory: apnea, bronchospasm, postoperative respiratory depression.
• Miscellaneous: intraoperative muscle movement.

|FDAPregCat=C |useInPregnancyFDA=* Sufentanil has been shown to have an embryocidal effect in rats and rabbits when given in doses 2.5 times the upper human intravenous dose for a period of 10 days to over 30 days. These effects were most probably due to maternal toxicity (decreased food consumption with increased mortality) following prolonged administration of the drug.

• No evidence of teratogenic effects have been observed after administration of Sufentanil in rats or rabbits.

|useInLaborDelivery=* The use of epidurally administered Sufentanil in combination with bupivacaine 0.125% with or without epinephrine is indicated for labor and delivery. (See Indications and Usage and Dosage and Administration sections.) Sufentanil is not recommended for intravenous use or for use of larger epidural doses during labor and delivery because of potential risks to the newborn infant after delivery. * In clinical trials, one case of severe fetal bradycardia associated with maternal hypotension was reported within 8 minutes of maternal administration of Sufentanilnil 15 mcg plus bupivacaine 0.125% (10 mL total volume). |useInNursing=* It is not known whether Sufentanil is excreted in human milk. Because fentanyl analogs are excreted in human milk, caution should be exercised when Sufentanil is administered to a nursing woman. |useInPed=* The safety and efficacy of intravenous Sufentanil in pediatric patients as young as 1 day old undergoing cardiovascular surgery have been documented in a limited number of cases. The clearance of Sufentanil in healthy neonates is approximately one-half that in adults and children. The clearance rate of Sufentanil can be further reduced by up to a third in neonates with cardiovascular disease, resulting in an increase in the elimination half-life of the drug. |useInRenalImpair=* In patients with liver or kidney dysfunction, Sufentanil should be administered with caution due to the importance of these organs in the metabolism and excretion of Sufentanil |useInHepaticImpair=* In patients with liver or kidney dysfunction, Sufentanil should be administered with caution due to the importance of these organs in the metabolism and excretion of Sufentanil |overdose=* Overdosage is manifested by an extension of the pharmacological actions of Sufentanil (see CLINICAL PHARMACOLOGY) as with other potent opioid analgesics. The most serious and significant effect of overdose for both intravenous and epidural administration of Sufentanil is respiratory depression. Intravenous administration of an opioid antagonist such as naloxone should be employed as a specific antidote to manage respiratory depression. The duration of respiratory depression following overdosage with Sufentanil may be longer than the duration of action of the opioid antagonist. Administration of an opioid antagonist should not preclude more immediate countermeasures. In the event of overdosage, oxygen should be administered and ventilation assisted or controlled as indicated for hypoventilation or apnea. A patent airway must be maintained, and a nasopharyngeal airway or endotracheal tube may be indicated. If depressed respiration is associated with muscular rigidity, a neuromuscular blocking agent may be required to facilitate assisted or controlled respiration. Intravenous fluids and vasopressors for the treatment of hypotension and other supportive measures may be employed. |drugBox=

Sufentanil
Systematic (IUPAC) name
N-[4-(Methoxymethyl)-1-(2-thiofuran-2-ylethyl)-4-piperidyl]-N-phenylpropanamide
Identifiers
CAS number	56030-54-7
ATC code	N01AH03
PubChem	41693
DrugBank	DB00708
Chemical data
Formula	Template:OrganicBox atomTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBox
Mol. mass	386.552 g/mol
SMILES	eMolecules & PubChem
Physical data
Melt. point	97 °C (207 °F)
Pharmacokinetic data
Bioavailability	?
Metabolism	?
Half life	162 minutes
Excretion	?
Therapeutic considerations
Pregnancy cat.	C(US)
Legal status	Controlled (S8)(AU) Class A(UK) Schedule II(US)
Routes	IV, IM, SubQ, epidural, intrathecal, transdermal patch (in clinical trials)

|mechAction=* Sufentanil is an opioid analgesic. When used in balanced general anesthesia, Sufentanil has been reported to be as much as 10 times as potent as fentanyl. When administered intravenously as a primary anesthetic agent with 100% oxygen, Sufentanil is approximately 5 to 7 times as potent as fentanyl.

• Assays of histamine in patients administered Sufentanil have shown no elevation in plasma histamine levels and no indication of histamine release.

(See dosage chart for more complete information on the intravenous use of Sufentanil.) |structure=* SUFENTA® (sufentanil citrate) is a potent opioid analgesic chemically designated as N-[4-(methyoxymethyl)-1-[2-(2-thienyl)ethyl]-4-piperidinyl]-N-phenylpropanamide:2-hydroxy-1,2,3-propanetricarboxylate (1:1) with a molecular weight of 578.68. The structural formula of SUFENTA is:

This image is provided by the National Library of Medicine.

• SUFENTA is a sterile, preservative free, aqueous solution containing sufentanil citrate equivalent to 50 mcg per mL of sufentanil base for intravenous and epidural injection. The solution has a pH range of 3.5 to 6.0.

|PD=

Intravenous use

• At intravenous doses of up to 8 mcg/kg, Sufentanil is an analgesic component of general anesthesia; at intravenous doses ≥8 mcg/kg, Sufentanil produces a deep level of anesthesia. Sufentanil produces a dose related attenuation of catecholamine release, particularly norepinephrine.
• At intravenous dosages of ≥8 mcg/kg, Sufentanil produces hypnosis and anesthesia without the use of additional anesthetic agents. A deep level of anesthesia is maintained at these dosages, as demonstrated by EEG patterns. Dosages of up to 25 mcg/kg attenuate the sympathetic response to surgical stress. The catecholamine response, particularly norepinephrine, is further attenuated at doses of Sufentanil of 25 to 30 mcg/kg, with hemodynamic stability and preservation of favorable myocardial oxygen balance.
• Sufentanil has an immediate onset of action, with relatively limited accumulation. Rapid elimination from tissue storage sites allows for relatively more rapid recovery as compared with equipotent dosages of fentanyl. At dosages of 1 to 2 mcg/kg, recovery times are comparable to those observed with fentanyl; at dosages of >2 to 6 mcg/kg, recovery times are comparable to enflurane, isoflurane and fentanyl. Within the anesthetic dosage range of 8 to 30 mcg/kg of Sufentanil, recovery times are more rapid compared to equipotent fentanyl dosages.
• The vagolytic effects of pancuronium may produce a dose dependent elevation in heart rate during Sufentanil-oxygen anesthesia. The use of moderate doses of pancuronium or of a less vagolytic neuromuscular blocking agent may be used to maintain a stable lower heart rate and blood pressure during Sufentanil-oxygen anesthesia. The vagolytic effects of pancuronium may be reduced in patients administered nitrous oxide with Sufentanil.
• Preliminary data suggest that in patients administered high doses of Sufentanil, initial dosage requirements for neuromuscular blocking agents are generally lower as compared to patients given fentanyl or halothane, and comparable to patients given enflurane.
• Bradycardia is infrequently seen in patients administered Sufentanil-oxygen anesthesia. The use of nitrous oxide with high doses of Sufentanil may decrease mean arterial pressure, heart rate and cardiac output.
• Sufentanil at 20 mcg/kg has been shown to provide more adequate reduction in intracranial volume than equivalent doses of fentanyl, based upon requirements for furosemide and anesthesia supplementation in one study of patients undergoing craniotomy. During carotid endarterectomy, Sufentanil-nitrous oxide/oxygen produced reductions in cerebral blood flow comparable to those of enflurane-nitrous oxide/oxygen. During cardiovascular surgery, Sufentanil-oxygen produced EEG patterns similar to fentanyl-oxygen; these EEG changes were judged to be compatible with adequate general anesthesia.
• The intraoperative use of Sufentanil at anesthetic dosages maintains cardiac output, with a slight reduction in systemic vascular resistance during the initial postoperative period. The incidence of postoperative hypertension, need for vasoactive agents and requirements for postoperative analgesics are generally reduced in patients administered moderate or high doses of Sufentanil as compared to patients given inhalation agents.
• Skeletal muscle rigidity is related to the dose and speed of administration of Sufentanil. This muscular rigidity may occur unless preventative measures are taken (see Warnings).
• Decreased respiratory drive and increased airway resistance occur with Sufentanil. The duration and degree of respiratory depression are dose related when Sufentanil is used at sub-anesthetic dosages. At high doses, a pronounced decrease in pulmonary exchange and apnea may be produced.

Epidural use in Labor and Delivery

• Onset of analgesic effect occurs within approximately 10 minutes of administration of epidural doses of Sufentanil and bupivacaine. Duration of analgesia following a single epidural injection of 10 to 15 mcg Sufentanil and bupivacaine 0.125% averaged 1.7 hours.
• During labor and vaginal delivery, the addition of 10 to 15 mcg Sufentanil to 10 mL 0.125% bupivacaine provides an increase in the duration of analgesia compared to bupivacaine without an opioid. Analgesia from 15 mcg Sufentanil plus 10 mL 0.125% bupivacaine is comparable to analgesia from 10 mL of 0.25% bupivacaine alone. Apgar scores of neonates following epidural administration of both drugs to women in labor were comparable to neonates whose mothers received bupivacaine without an opioid epidurally.

|PK=

Intravenous use

• The pharmacokinetics of intravenous Sufentanil can be described as a three-compartment model, with a distribution time of 1.4 minutes, redistribution of 17.1 minutes and elimination half-life of 164 minutes in adults. The elimination half-life of Sufentanil is shorter (e.g. 97 +/- 42 minutes) in infants and children, and longer in neonates (e.g. 434 +/- 160 minutes) compared to that of adolescents and adults. The liver and small intestine are the major sites of biotransformation. Approximately 80% of the administered dose is excreted within 24 hours and only 2% of the dose is eliminated as unchanged drug. Plasma protein binding of Sufentanil, related to the alpha acid glycoprotein concentration, was approximately 93% in healthy males, 91% in mothers and 79% in neonates.

Epidural use in Labor and Delivery

• After epidural administration of incremental doses totaling 5 to 40 mcg Sufentanil during labor and delivery, maternal and neonatal Sufentanil plasma concentrations were at or near the 0.05 to 0.1 ng/mL limit of detection, and were slightly higher in mothers than in their infants.

|howSupplied=

• SUFENTA (Sufentanil Citrate Injection, USP) is supplied as a sterile aqueous preservative-free solution for intravenous and epidural use as:

NDC 11098-050-01 50 mcg/mL sufentanil base, 1 mL ampules in packages of 10

NDC 11098-050-02 50 mcg/mL sufentanil base, 2 mL ampules in packages of 10

NDC 11098-050-05 50 mcg/mL sufentanil base, 5 mL ampules in packages of 10

|storage=

• Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]. PROTECT FROM LIGHT.

U.S. Patent No. 3,998,834

MAY 1995, SEPTEMBER 1995

TAYLOR PHARMACEUTICALS

AN AKORN COMPANY

Decatur, IL 62522

SFA0N

Rev. 07/07

|alcohol=Alcohol-Sufentanil interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication. }} {{#subobject:

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