Sufentanil
 Sufentanil Citrate

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|Sufentanil Sufentanil Citrate

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Sufentanil


Generic Name: Sufentanil citrate
Dosage Form: Injection, usp cii

Sufentanil Description

Sufentanil Citrate Injection, USP is a sterile, nonpyrogenic, aqueous solution for intravenous and epidural injection. Each mL contains Sufentanil citrate equivalent to 50 mcg (0.05 mg) of Sufentanil in Water for Injection. pH 3.5–6.0; citric acid added, if needed, for pH adjustment. Contains no preservative. Sufentanil Citrate is a potent opioid analgesic chemically designated as N-[4-(methoxymethyl)-1-[2-(2-thienyl)ethyl]-4-piperidinyl]-N-phenylpropanamide 2-hydroxy-1,2,3-propanetricarboxylate (1:1) with the following structural formula:

Sufentanil - Clinical Pharmacology

Pharmacology

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 citrate 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 Citrate Injection.)

Pharmacodynamics

Intravenous Use

At intravenous doses 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≥ 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 25-30 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 1-2 mcg/kg, recovery times are comparable to those observed with fentanyl; at dosages > 2-6 mcg/kg, recovery times are comparable to en???urane, iso???urane and fentanyl. Within the anesthetic dosage range of 8-30 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. 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 en???urane.

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 ???ow comparable to those of en???urane-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 10-15 mcg Sufentanil and bupivacaine 0.125% averaged 1.7 hours.

During labor and vaginal delivery, the addition of 10-15 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.

Pharmacokinetics

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 an 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 alpha1 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 5-40 mcg Sufentanil during labor and delivery, maternal and neonatal Sufentanil plasma concentrations were at or near the 0.05-0.1 ng/mL limit of detection, and were slightly higher in mothers than in their infants.

Clinical Studies

Epidural Use In Labor And Delivery

Epidural Sufentanil was tested in 340 patients in two (one single-center and one multi-center) double-blind, parallel studies. Doses ranged from 10 to 15 mcg Sufentanil and were delivered in a 10 mL volume of 0.125% bupivacaine with and without epinephrine 1:200,000. In all cases, Sufentanil was administered following a dose of local anesthetic to test proper catheter placement. Since epidural opioids and local anesthetics potentiate each other, these results may not re???ect the dose or ef???cacy of epidural Sufentanil by itself.

Individual doses of 10-15 mcg Sufentanil plus bupivacaine 0.125% with epinephrine provided analgesia during the ???rst stage of labor with a duration of 1-2 hours. Onset was rapid (within 10 minutes). Subsequent doses (equal dose) tended to have shorter duration. Analgesia was profound (complete pain relief) in 80% to 100% of patients and a 25% incidence of pruritus was observed. The duration of initial doses of Sufentanil plus bupivacaine with epinephrine is approximately 95 minutes, and of subsequent doses, 70 minutes.

There are insuf???cient data to critically evaluate neonatal neuromuscular and adaptive capacity following recommended doses of maternally administered epidural sufentanil with bupivacaine. However, if larger than recommended doses are used for combined local and systemic analgesia, e.g., after administration of a single dose of 50 mcg epidural Sufentanil during delivery, then impaired neonatal adaption to sound and light can be detected for 1 to 4 hours and if a dose of 80 mcg is used, impaired neuromuscular coordination can be detected for more than 4 hours.

Indications and Usage for Sufentanil

Sufentanil Citrate Injection is indicated for intravenous administration in adults and pediatric patients:

– as an analgesic adjunct in the maintenance of balanced general anesthesia in patients who are intubated and ventilated.

– as a primary anesthetic agent for the induction and maintenance of anesthesia with 100% oxygen in patients undergoing major surgical procedures; in patients who are intubated and ventilated, such as cardiovascular surgery or neurosurgical procedures in the sitting position; to provide favorable myocardial and cerebral oxygen balance or when extended postoperative ventilation is anticipated.

Sufentanil Citrate Injection is indicated for epidural administration as an analgesic combined with low dose bupivacaine, usually 12.5 mg per administration, during labor and vaginal delivery.

SEE DOSAGE AND ADMINISTRATION SECTION FOR MORE COMPLETE INFORMATION ON THE USE OF SUFENTANIL.

Contraindications

Sufentanil Citrate Injection is contraindicated in patients with known hypersensitivity to the drug or known intolerance to other opioid agonists.

Warnings

Sufentanil CITRATE INJECTION 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 citrate 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 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.

Precautions

General

The initial dose of Sufentanil should be appropriately reduced in elderly and debilitated patients. The effect of the initial dose should be considered in determining supplemental doses.

Vital signs should be monitored routinely.

Nitrous oxide may produce cardiovascular depression when given with high doses of Sufentanil (see CLINICAL PHARMACOLOGY).

Bradycardia has been reported infrequently with sufentanil-oxygen anesthesia and has been responsive to atropine.

Respiratory depression caused by opioid analgesics can be reversed by opioid antagonists such as naloxone. Because the duration of respiratory depression produced by sufentanil may last longer than the duration of the opioid antagonist action, appropriate surveillance should be maintained. As with all potent opioids, profound analgesia is accompanied by respiratory depression and diminished sensitivity to CO2 stimulation which may persist into or recur in the postoperative period. Respiratory depression may be enhanced when Sufentanil is administered in combination with volatile inhalational agents and/or other central nervous system depressants such as barbiturates, tranquilizers and other opioids. Appropriate postoperative monitoring should be employed to ensure that adequate spontaneous breathing is established and maintained prior to discharging the patient from the recovery area. Respiration should be closely monitored following each administration of an epidural injection of sufentanil.

Proper placement of the needle or catheter in the epidural space should be veri???ed before Sufentanil is injected to assure that unintentional intravascular or intrathecal administration does not occur. Unintentional intravascular injection of Sufentanil could result in a potentially serious overdose, including acute truncal muscular rigidity and apnea. Unintentional intrathecal injection of the full sufentanil/bupivacaine epidural doses and volume could produce effects of high spinal anesthesia including prolonged paralysis and delayed recovery. If analgesia is inadequate, the placement and integrity of the catheter should be veri???ed prior to the administration of any additional epidural medications. Sufentanil should be administered epidurally by slow injection.

Neuromuscular Blocking Agents

The hemodynamic effects and degree of skeletal muscle relaxation required should be considered in the selection of a neuromuscular blocking agent. High doses of pancuronium may produce increases in heart rate during sufentanil-oxygen anesthesia. Bradycardia and hypotension have been reported with other muscle relaxants during sufentanil-oxygen anesthesia; this effect may be more pronounced in the presence of calcium channel and/or beta blockers. Muscle relaxants with no clinically signi???cant effect on heart rate (at recommended doses) would not counteract the vagotonic effect of sufentanil; therefore, a lower heart rate would be expected. Rare reports of bradycardia associated with the concomitant use of succinylcholine and Sufentanil have been reported.

Interaction With Calcium Channel And Beta Blockers

The incidence and degree of bradycardia and hypotension during induction with Sufentanil may be greater in patients on chronic calcium channel and beta blocker therapy. (See Neuromuscular Blocking Agents.)

Interaction With Other Central Nervous System Depressants

Both the magnitude and duration of central nervous system and cardiovascular effects may be enhanced when Sufentanil is administered to patients receiving barbiturates, tranquilizers, other opioids, general anesthetics or other CNS depressants. In such cases of combined treatment, the dose of Sufentanil and/or these agents should be reduced.

The use of benzodiazepines with Sufentanil during induction may result in a decrease in mean arterial pressure and systemic vascular resistance.

Head Injuries

Sufentanil may obscure the clinical course of patients with head injuries.

Impaired Respiration

Sufentanil should be used with caution in patients with pulmonary disease, decreased respiratory reserve or potentially compromised respiration. In such patients, opioids may additionally decrease respiratory drive and increase airway resistance. During anesthesia, this can be managed by assisted or controlled respiration.

Impaired Hepatic Or Renal Function

In patients with liver or kidney dysfunction, Sufentanil citrate should be administered with caution due to the importance of these organs in the metabolism and excretion of sufentanil.

Carcinogenesis, Mutagenesis, Impairment Of Fertility

No long-term animal studies of Sufentanil have been performed to evaluate carcinogenic potential. The micronucleus test in female rats revealed that single intravenous doses of Sufentanil as high as 80 mcg/kg (approximately 2.5 times the upper human intravenous dose) produced no structural chromosome mutations. The AmesSalmonella typhimurium metabolic activating test also revealed no mutagenic activity. See Animal Toxicology for reproduction studies in rats and rabbits.

Pregnancy

Teratogenic Effects—Pregnancy Category C.

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 citrate in rats or rabbits.

Labor and Delivery

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.) 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 Sufentanil 15 mcg plus bupivacaine 0.125% (10 mL total volume).

Nursing Mothers

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 citrate is administered to a nursing woman.

Pediatric Use

The safety and ef???cacy 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.

Animal Toxicology

The intravenous LD50 of Sufentanil is 16.8 to 18.0 mg/kg in mice, 11.8 to 13.0 mg/kg in guinea pigs and 10.1 to 19.5 mg/kg in dogs. Reproduction studies performed in rats and rabbits given doses up to 2.5 times the upper human intravenous dose for a period of 10 to over 30 days revealed high maternal mortality rates due to decreased food consumption and anoxia, which preclude any meaningful interpretation of the results. Epidural and intrathecal injections of sufentanil in dogs and epidural injections in rats were not associated with neurotoxicity.

Adverse Reactions

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 Sufentanil 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. 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 sufentanil. 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*

*Incidence 3% to 9%

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*

*Incidence 0.3 to 1%

Drug Abuse and Dependence

Sufentanil Citrate Injection is a Schedule II controlled drug substance that can produce drug dependence of the morphine type and therefore has the potential for being abused.

Overdosage

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 speci???c 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 ???uids and vasopressors for the treatment of hypotension and other supportive measures may be employed.

Sufentanil Dosage and Administration

The dosage of Sufentanil should be individualized in each case according to body weight, physical status, underlying pathological condition, use of other drugs, and type of surgical procedure and anesthesia. In obese patients (more than 20% above ideal total body weight), the dosage of Sufentanil should be determined on the basis of lean body weight. Dosage should be reduced in elderly and debilitated patients (see PRECAUTIONS).

Vital signs should be monitored routinely.

Because the clearance of Sufentanil is reduced in neonates, especially those with cardiovascular disease, the dose of Sufentanil should be reduced accordingly (see PRECAUTIONS).

Intravenous Use

Sufentanil citrate may be administered intravenously by slow injection or infusion 1) in doses up to 8 mcg/kg as an analgesic adjunct to general anesthesia and 2) in doses ≥ 8 mcg/kg as a primary anesthetic agent for induction and maintenance of anesthesia (see Dosage Range Chart). If benzodiazepines, barbiturates, inhalation agents, other opioids or other central nervous system depressants are used concomitantly, the dose of sufentanil and/or these agents should be reduced (see PRECAUTIONS). In all cases, dosage should be titrated to individual patient response.

Usage In Children

For induction and maintenance of anesthesia in pediatric patients less than 12 years of age undergoing cardiovascular surgery, an anesthetic dose of 10-25 mcg/kg administered with 100% oxygen is generally recommended. Supplemental dosages of up to 25-50 mcg are recommended for maintenance, based on response to initial dose and as determined by changes in vital signs indicating surgical stress or lightening of anesthesia.

Premedication

The selection of preanesthetic medications should be based upon the needs of the individual patient.

Neuromuscular Blocking Agents

The neuromuscular blocking agent selected should be compatible with the patient’s condition, taking into account the hemodynamic effects of a particular muscle relaxant and the degree of skeletal muscle relaxation required (see CLINICAL PHARMACOLOGY, WARNINGS and PRECAUTIONS).

ADULT DOSAGE RANGE CHART for Intravenous use (expressed as sufentanil)
ANALGESIC COMPONENT TO GENERAL ANESTHESIA TOTAL DOSAGE REQUIREMENTS OF 1 MCG/KG/HR OR LESS ARE RECOMMENDED
TOTAL DOSAGE MAINTENANCE DOSAGE
ANALGESIC DOSAGES
Incremental or Infusion
1–2 mcg/kg (expected duration of anesthesia 1–2 hours). Approximately 75% or more of the total Sufentanil dosage may be administered prior to intubation by either slow injection or infusion titrated to individual patient response. Dosages in this range are generally administered with nitrous oxide/oxygen in patients undergoing general surgery in which endotracheal intubation and mechanical ventilation are required.
Incremental
10–25 mcg (0.2–0.5 mL) may be administered in increments as needed when movement and/or changes in vital signs indicate surgical stress or lightening of analgesia. Supplemental dosages should be individualized and adjusted to the remaining operative time anticipated.
Infusion
Sufentanil citrate may be administered as an intermittent or continuous infusion as needed in response to signs of lightening of analgesia. In absence of signs of lightening of analgesia, infusion rates should always be adjusted downward until there is some response to surgical stimulation. Maintenance infusion rates should be adjusted based upon the induction dose of Sufentanil so that the total dose does not exceed 1 mcg/kg/hr of expected surgical time. Dosage should be individualized and adjusted to the remaining operative time anticipated.
ANALGESIC DOSAGES
Incremental or Infusion
2-8 mcg/kg (expected duration of anesthesia 2–8 hours). Approximately 75% or less of the total calculated Sufentanil dosage may be administered by slow injection or infusion prior to intubation, titrated to individual patient response. Dosages in this range are generally administered with nitrous oxide/oxygen in patients undergoing more complicated major surgical procedures in which endotracheal intubation and mechanical ventilation are required. At dosages in this range, Sufentanil has been shown to provide some attenuation of sympathetic reflex activity in response to surgical stimuli, provide hemodynamic stability and provide relatively rapid recovery.
Incremental
10–50 mcg (0.2–1 mL) may be administered in increments as needed when movement and/or changes in vital signs indicate surgical stress or lightening of analgesia. Supplemental dosages should be individualized and adjusted to the remaining operative time anticipated.  
Infusion
Sufentanil citrate may be administered as an intermittent or continuous infusion as needed in response to signs of lightening of analgesia. In absence of signs of lightening of analgesia, infusion rates should always be adjusted downward until there is some response to surgical stimulation. Maintenance infusion rates should be adjusted based upon the induction dose of Sufentanil so that the total dose does not exceed 1 mcg/kg/hr of expected surgical time. Dosage should be individualized and adjusted to the remaining operative time anticipated.
ANESTHETIC DOSAGES
Incremental or Infusion
8–30 mcg/kg (anesthetic doses). At this anesthetic dosage range, Sufentanil is generally administered as a slow injection, as an infusion or as an injection followed by an infusion. Sufentanil with 100% oxygen and a muscle relaxant has been found to produce sleep at dosages ≥ 8 mcg/kg and to maintain a deep level of anesthesia without the use of additional anesthetic agents. The addition of N2O to these dosages will reduce systolic blood pressure. At dosages in this range of up to 25 mcg/kg, catecholamine release is attenuated. Dosages of 25–30 mcg/kg have been shown to block sympathetic response including catecholamine release. High doses are indicated in patients undergoing major surgical procedures in which endotracheal intubation and mechanical ventilation are required, such as cardiovascular surgery and neurosurgery in the sitting position with maintenance of favorable myocardial and cerebral oxygen balance. Postoperative observation is essential and postoperative mechanical ventilation may be required at the higher dosage range due to extended postoperative respiratory depression. Dosage should be titrated to individual patient response.
Incremental
Depending on the initial dose, maintenance doses of 0.5–10 mcg/kg may be administered by slow injection in anticipation of surgical stress such as incision, sternotomy or cardiopulmonary bypass.
Infusion
Sufentanil citrate may be administered by continuous or intermittent infusion as needed in response to signs of lightening of anesthesia. In the absence of lightening of anesthesia, infusion rates should always be adjusted downward until there is some response to surgical stimulation. The maintenance infusion rate for sufentanil should be based upon the induction dose so that the total dose for the procedure does not exceed 30 mcg/kg.

In patients administered high doses of sufentanil, it is essential that quali???ed personnel and adequate facilities are available for the management of postoperative respiratory depression.

Also see WARNINGS and PRECAUTIONS sections.

For purposes of administering small volumes of Sufentanil Citrate Injection accurately, the use of a tuberculin syringe or equivalent is recommended.

EPIDURAL USE IN LABOR AND DELIVERY
Proper placement of the needle or catheter in the epidural space should be veri???ed before Sufentanil citrate is injected to assure that unintentional intravascular or intrathecal administration does not occur. Unintentional intravascular injection of Sufentanil could result in a potentially serious overdose, including acute truncal muscular rigidity and apnea. Unintentional intrathecal injection of the full sufentanil-bupivacaine epidural doses and volume could produce effects of high spinal anesthesia, including prolonged paralysis and delayed recovery. If analgesia is inadequate, the placement and integrity of the catheter should be veri???ed prior to the administration of any additional epidural medications. Sufentanil should be administered by slow injection. Respiration should be closely monitored following each administration of an epidural injection of sufentanil.
DOSAGE FOR LABOR AND DELIVERY
The recommended dosage is Sufentanil 10–15 mcg administered with 10 mL bupivacaine 0.125% with or without epinephrine. Sufentanil and bupivacaine should be mixed together before administration. Doses can be repeated twice (for a total of three doses) at not less than one hour intervals until delivery.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

How is Sufentanil Supplied

Sufentanil Citrate Injection, USP, equivalent to 50 mcg (0.05 mg) Sufentanil per mL, is available in the following:

1 mL (50 mcg) DOSETTE ampuls packaged in 10s (NDC 10019-050-43)

2 mL (100 mcg) DOSETTE ampuls packaged in 10s (NDC 10019-050-21)

5 mL (250 mcg) DOSETTE ampuls packaged in 10s (NDC 10019-050-06)

Storage

PROTECT FROM LIGHT: Keep covered in carton until time of use.

Store at 20˚-25˚C (68˚-77˚F), excursions permitted to 15˚-30˚C (59˚-86˚F) [see USP Controlled Room Temperature].

Baxter and Dosette are trademarks of Baxter International Inc., or its subsidiaries.

Manufactured by

Baxter Healthcare Corporation

Deerfield, IL 60015 USA

For Product Inquiry 1 800 ANA DRUG (1-800-262-3784)

MLT-7/1.0


Sufentanil Citrate (Sufentanil Citrate)
PRODUCT INFO
Product Code 10019-050 Dosage Form INJECTION
Route Of Administration INTRAVENOUS, EPIDURAL DEA Schedule
INGREDIENTS
Name (Active Moiety) Type Strength
Sufentanil citrate (sufentanil) Active 0.05 MILLIGRAM  In 1 MILLILITER
water Inactive  
citric acid Inactive  
IMPRINT INFORMATION
Characteristic Appearance Characteristic Appearance
Color Score
Shape Symbol
Imprint Code Coating
Size
PACKAGING
# NDC Package Description Multilevel Packaging
1 10019-050-43 10 AMPULE In 1 PACKAGE contains a AMPULE
1 1 MILLILITER In 1 AMPULE This package is contained within the PACKAGE (10019-050-43)
2 10019-050-21 10 AMPULE In 1 PACKAGE contains a AMPULE
2 2 MILLILITER In 1 AMPULE This package is contained within the PACKAGE (10019-050-21)
3 10019-050-06 10 AMPULE In 1 PACKAGE contains a AMPULE
3 5 MILLILITER In 1 AMPULE This package is contained within the PACKAGE (10019-050-06)

Revised: 02/2006





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Typical mistypes for Sufentanil Sufentanil Citrate
aufentanil sufentanil citrate, zufentanil sufentanil citrate, xufentanil sufentanil citrate, dufentanil sufentanil citrate, eufentanil sufentanil citrate, wufentanil sufentanil citrate, syfentanil sufentanil citrate, shfentanil sufentanil citrate, sjfentanil sufentanil citrate, sifentanil sufentanil citrate, s8fentanil sufentanil citrate, s7fentanil sufentanil citrate, sudentanil sufentanil citrate, sucentanil sufentanil citrate, suventanil sufentanil citrate, sugentanil sufentanil citrate, sutentanil sufentanil citrate, surentanil sufentanil citrate, sufwntanil sufentanil citrate, sufsntanil sufentanil citrate, sufdntanil sufentanil citrate, sufrntanil sufentanil citrate, suf4ntanil sufentanil citrate, suf3ntanil sufentanil citrate, sufebtanil sufentanil citrate, sufemtanil sufentanil citrate, sufejtanil sufentanil citrate, sufehtanil sufentanil citrate, sufenranil sufentanil citrate, sufenfanil sufentanil citrate, sufenganil sufentanil citrate, sufenyanil sufentanil citrate, sufen6anil sufentanil citrate, sufen5anil sufentanil citrate, sufentznil sufentanil citrate, sufentsnil sufentanil citrate, sufentwnil sufentanil citrate, sufentqnil sufentanil citrate, sufentabil sufentanil citrate, sufentamil sufentanil citrate, sufentajil sufentanil citrate, sufentahil sufentanil citrate, sufentanul sufentanil citrate, sufentanjl sufentanil citrate, sufentankl sufentanil citrate, sufentanol sufentanil citrate, sufentan9l sufentanil citrate, sufentan8l sufentanil citrate, sufentanik sufentanil citrate, sufentanip sufentanil citrate, sufentanio sufentanil citrate, sufentanil aufentanil citrate, sufentanil zufentanil citrate, sufentanil xufentanil citrate, sufentanil dufentanil citrate, sufentanil eufentanil citrate, sufentanil wufentanil citrate, sufentanil syfentanil citrate, sufentanil shfentanil citrate, sufentanil sjfentanil citrate, sufentanil sifentanil citrate, sufentanil s8fentanil citrate, sufentanil s7fentanil citrate, sufentanil sudentanil citrate, sufentanil sucentanil citrate, sufentanil suventanil citrate, sufentanil sugentanil citrate, sufentanil sutentanil citrate, sufentanil surentanil citrate, sufentanil sufwntanil citrate, sufentanil sufsntanil citrate, sufentanil sufdntanil citrate, sufentanil sufrntanil citrate, sufentanil suf4ntanil citrate, sufentanil suf3ntanil citrate, sufentanil sufebtanil citrate, sufentanil sufemtanil citrate, sufentanil sufejtanil citrate, sufentanil sufehtanil citrate, sufentanil sufenranil citrate, sufentanil sufenfanil citrate, sufentanil sufenganil citrate, sufentanil sufenyanil citrate, sufentanil sufen6anil citrate, sufentanil sufen5anil citrate, sufentanil sufentznil citrate, sufentanil sufentsnil citrate, sufentanil sufentwnil citrate, sufentanil sufentqnil citrate, sufentanil sufentabil citrate, sufentanil sufentamil citrate, sufentanil sufentajil citrate, sufentanil sufentahil citrate, sufentanil sufentanul citrate, sufentanil sufentanjl citrate, sufentanil sufentankl citrate, sufentanil sufentanol citrate, sufentanil sufentan9l citrate, sufentanil sufentan8l citrate, sufentanil sufentanik citrate, sufentanil sufentanip citrate, sufentanil sufentanio citrate, sufentanil sufentanil xitrate, sufentanil sufentanil vitrate, sufentanil sufentanil fitrate, sufentanil sufentanil ditrate, sufentanil sufentanil cutrate, sufentanil sufentanil cjtrate, sufentanil sufentanil cktrate, sufentanil sufentanil cotrate, sufentanil sufentanil c9trate, sufentanil sufentanil c8trate, sufentanil sufentanil cirrate, sufentanil sufentanil cifrate, sufentanil sufentanil cigrate, sufentanil sufentanil ciyrate, sufentanil sufentanil ci6rate, sufentanil sufentanil ci5rate, sufentanil sufentanil citeate, sufentanil sufentanil citdate, sufentanil sufentanil citfate, sufentanil sufentanil cittate, sufentanil sufentanil cit5ate, sufentanil sufentanil cit4ate, sufentanil sufentanil citrzte, sufentanil sufentanil citrste, sufentanil sufentanil citrwte, sufentanil sufentanil citrqte, sufentanil sufentanil citrare, sufentanil sufentanil citrafe, sufentanil sufentanil citrage, sufentanil sufentanil citraye, sufentanil sufentanil citra6e, sufentanil sufentanil citra5e, sufentanil sufentanil citratw, sufentanil sufentanil citrats, sufentanil sufentanil citratd, sufentanil sufentanil citratr, sufentanil sufentanil citrat4, sufentanil sufentanil citrat3, ufentanil sufentanil citrate, sfentanil sufentanil citrate, suentanil sufentanil citrate, sufntanil sufentanil citrate, sufetanil sufentanil citrate, sufenanil sufentanil citrate, sufentnil sufentanil citrate, sufentail sufentanil citrate, sufentanl sufentanil citrate, sufentani sufentanil citrate, sufentanil sufentanil citrate, sufentanil sufentanil citrate, sufentanil ufentanil citrate, sufentanil sfentanil citrate, sufentanil suentanil citrate, sufentanil sufntanil citrate, sufentanil sufetanil citrate, sufentanil sufenanil citrate, sufentanil sufentnil citrate, sufentanil sufentail citrate, sufentanil sufentanl citrate, sufentanil sufentani citrate, sufentanil sufentanilcitrate, sufentanil sufentanil itrate, sufentanil sufentanil ctrate, sufentanil sufentanil cirate, sufentanil sufentanil citate, sufentanil sufentanil citrte, sufentanil sufentanil citrae, sufentanil sufentanil citrat, usfentanil sufentanil citrate, sfuentanil sufentanil citrate, suefntanil sufentanil citrate, sufnetanil sufentanil citrate, sufetnanil sufentanil citrate, sufenatnil sufentanil citrate, sufentnail sufentanil citrate, sufentainl sufentanil citrate, sufentanli sufentanil citrate, sufentani l sufentanil citrate, sufentanil sufentanil citrate, sufentanil s ufentanil citrate, sufentanil usfentanil citrate, sufentanil sfuentanil citrate, sufentanil suefntanil citrate, sufentanil sufnetanil citrate, sufentanil sufetnanil citrate, sufentanil sufenatnil citrate, sufentanil sufentnail citrate, sufentanil sufentainl citrate, sufentanil sufentanli citrate, sufentanil sufentani lcitrate, sufentanil sufentanilc itrate, sufentanil sufentanil ictrate, sufentanil sufentanil ctirate, sufentanil sufentanil cirtate, sufentanil sufentanil citarte, sufentanil sufentanil citrtae, sufentanil sufentanil citraet, ssufentanil sufentanil citrate, suufentanil sufentanil citrate, suffentanil sufentanil citrate, sufeentanil sufentanil citrate, sufenntanil sufentanil citrate, sufenttanil sufentanil citrate, sufentaanil sufentanil citrate, sufentannil sufentanil citrate, sufentaniil sufentanil citrate, sufentanill sufentanil citrate, sufentanil sufentanil citrate, sufentanil sufentanil citrate, sufentanil ssufentanil citrate, sufentanil suufentanil citrate, sufentanil suffentanil citrate, sufentanil sufeentanil citrate, sufentanil sufenntanil citrate, sufentanil sufenttanil citrate, sufentanil sufentaanil citrate, sufentanil sufentannil citrate, sufentanil sufentaniil citrate, sufentanil sufentanill citrate, sufentanil sufentanil citrate, sufentanil sufentanil ccitrate, sufentanil sufentanil ciitrate, sufentanil sufentanil cittrate, sufentanil sufentanil citrrate, sufentanil sufentanil citraate, sufentanil sufentanil citratte, sufentanil sufentanil citratee, etc.



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