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ROCURONIUM(rocuronium bromide injection)
2014-01-20 18:30:07 来源: 作者: 【 】 浏览:396次 评论:0
HIGHLIGHTS OF PRESCRIBING INFORMATION
These highlights do not include all the information needed to use rocuronium bromide injection safely and effectively. See full prescribing information for rocuronium bromide injection.
Rocuronium bromide injection for intravenous use
Initial U.S. Approval: 1994


 

 

RECENT MAJOR CHANGES

 

Warnings and Precautions, Anaphylaxis (5.2)      11/2010

 

INDICATIONS AND USAGE

 

Rocuronium bromide injection is a nondepolarizing neuromuscular blocking agent indicated as an adjunct to general anesthesia to facilitate both rapid sequence and routine tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation. (1)

 

DOSAGE AND ADMINISTRATION

 

To be administered only by experienced clinicians or adequately trained individuals supervised by an experienced clinician familiar with the use, actions, characteristics, and complications of neuromuscular blocking agents. (2)

  • Individualize the dose for each patient. (2)
  • Peripheral nerve stimulator recommended for determination of drug response and need for additional doses, and to eva luate recovery. (2)
  • Tracheal intubation: Recommended initial dose is 0.6 mg/kg. (2.1)
  • Rapid sequence intubation: 0.6 to 1.2 mg/kg. (2.2)
  • Maintenance doses: Guided by response to prior dose, not administered until recovery is evident. (2.3)
  • Continuous infusion: Initial rate of 10 to 12 mcg/kg/min. Start only after early evidence of spontaneous recovery from an intubating dose. (2.4)
 

DOSAGE FORMS AND STRENGTHS

 
  • 5 mL multiple dose vials containing 50 mg rocuronium bromide injection (10 mg/mL). (3)
  • 10 mL multiple dose vials containing 100 mg rocuronium bromide injection (10 mg/mL). (3)
 

CONTRAINDICATIONS

 
  • Hypersensitivity (e.g., anaphylaxis) to rocuronium bromide or other neuromuscular blocking agents. (4)
 

WARNINGS AND PRECAUTIONS

 
  • Appropriate Administration and Monitoring: Use only if facilities for intubation, mechanical ventilation, oxygen therapy, and an antagonist are immediately available. (5.1)
  • Anaphylaxis: Severe anaphylaxis has been reported. Consider cross-reactivity among neuromuscular blocking agents. (5.2)
  • Need for Adequate Anesthesia: Must be accompanied by adequate anesthesia or sedation. (5.3)
  • Residual Paralysis: Consider using a reversal agent in cases where residual paralysis is more likely to occur. (5.4)
 

ADVERSE REACTIONS

 

Most common adverse reactions (2%) are transient hypotension and hypertension. (6.1)

To report SUSPECTED ADVERSE REACTIONS, contact Sagent Pharmaceuticals, Inc. at 1-866-625-1618 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

 

DRUG INTERACTIONS

 
  • Succinylcholine: Use before succinylcholine has not been studied. (7.11)
  • Nondepolarizing muscle relaxants: Interactions have been observed. (7.7)
  • Enhanced rocuronium bromide activity possible: Inhalation anesthetics (7.3), certain antibiotics (7.1), quinidine (7.10), magnesium (7.6), lithium (7.4), local anesthetics (7.5), procainamide (7.8)
  • Reduced rocuronium bromide activity possible: Anticonvulsants. (7.2)
 

USE IN SPECIFIC POPULATIONS

 
  • Labor and Delivery: Not recommended for rapid sequence induction in patients undergoing Cesarean section. (8.2)
  • Not recommended for rapid sequence intubation in pediatric patients. (8.4)

Due to Organon USA Inc.'s marketing exclusivity rights, this drug product is not approved with certain pediatric use information. Labeling with additional information on pediatric use is approved for Organon USA Inc.'s rocuronium bromide injection. (8.4)


See 17 for PATIENT COUNSELING INFORMATION

Revised: 07/2011

FULL PRESCRIBING INFORMATION: CONTENTS*
*
Sections or subsections omitted from the full prescribing information are not listed

1 INDICATIONS AND USAGE

2 DOSAGE AND ADMINISTRATION

2.1 Dose for Tracheal Intubation

2.2 Rapid Sequence Intubation

2.3 Maintenance Dosing

2.4 Use by Continuous Infusion

2.5 Dosage in Specific Populations

2.6 Preparation for Administration of Rocuronium Bromide Injection

3 DOSAGE FORMS AND STRENGTHS

4 CONTRAINDICATIONS

5 WARNINGS AND PRECAUTIONS

5.1 Appropriate Administration and Monitoring

5.2 Anaphylaxis

5.3 Need for Adequate Anesthesia

5.4 Residual Paralysis

5.5 Long-Term Use in an Intensive Care Unit

5.6 Malignant Hyperthermia (MH)

5.7 Prolonged Circulation Time

5.8 QT Interval Prolongation

5.9 Conditions/Drugs Causing Potentiation of, or Resistance to, Neuromuscular Block

5.10 Incompatibility with Alkaline Solutions

5.11 Increase in Pulmonary Vascular Resistance

5.12 Use In Patients with Myasthenia

5.13 Extravasation

6 ADVERSE REACTIONS

6.1 Clinical Trials Experience

6.2 Postmarketing Experience

7 DRUG INTERACTIONS

7.1 Antibiotics

7.2 Anticonvulsants

7.3 Inhalation Anesthetics

7.4 Lithium Carbonate

7.5 Local Anesthetics

7.6 Magnesium

7.7 Nondepolarizing Muscle Relaxants

7.8 Procainamide

7.9 Propofol

7.10 Quinidine

7.11 Succinylcholine

8 USE IN SPECIFIC POPULATIONS

8.1 Pregnancy

8.2 Labor and Delivery

8.4 Pediatric Use

8.5 Geriatric Use

8.6 Patients with Hepatic Impairment

8.7 Patients with Renal Impairment

10 OVERDOSAGE

11 DESCRIPTION

12 CLINICAL PHARMACOLOGY

12.1 Mechanism of Action

12.2 Pharmacodynamics

12.3 Pharmacokinetics

13 NONCLINICAL TOXICOLOGY

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

14 CLINICAL STUDIES

14.1 Adult Patients

14.2 Geriatric Patients

14.3 Pediatric Patients

16 HOW SUPPLIED/STORAGE AND HANDLING

17 PATIENT COUNSELING INFORMATION

 


FULL PRESCRIBING INFORMATION

 

 

1 INDICATIONS AND USAGE

Rocuronium bromide injection is indicated for inpatients and outpatients as an adjunct to general anesthesia to facilitate both rapid sequence and routine tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.

 

2 DOSAGE AND ADMINISTRATION

Rocuronium bromide injection is for intravenous use only. This drug should only be administered by experienced clinicians or trained individuals supervised by an experienced clinician familiar with the use, actions, characteristics, and complications of neuromuscular blocking agents. Doses of rocuronium bromide injection should be individualized and a peripheral nerve stimulator should be used to monitor drug effect, need for additional doses, adequacy of spontaneous recovery or antagonism, and to decrease the complications of overdosage if additional doses are administered.

The dosage information which follows is derived from studies based upon units of drug per unit of body weight. It is intended to serve as an initial guide to clinicians familiar with other neuromuscular blocking agents to acquire experience with rocuronium bromide.

In patients in whom potentiation of, or resistance to, neuromuscular block is anticipated, a dose adjustment should be considered [see Dosage and Administration (2.5), Warnings and Precautions (5.9, 5.12), Drug Interactions (7.2, 7.3, 7.4, 7.5, 7.6, 7.8, 7.10), and Use in Specific Populations (8.6)].

 

2.1 Dose for Tracheal Intubation

The recommended initial dose of rocuronium bromide injection, regardless of anesthetic technique, is 0.6 mg/kg. Neuromuscular block sufficient for intubation (80% block or greater) is attained in a median (range) time of 1 (0.4-6) minute(s) and most patients have intubation completed within 2 minutes. Maximum blockade is achieved in most patients in less than 3 minutes. This dose may be expected to provide 31 (15-85) minutes of clinical relaxation under opioid/nitrous oxide/oxygen anesthesia. Under halothane, isoflurane, and enflurane anesthesia, some extension of the period of clinical relaxation should be expected [see Drug Interactions (7.3)].

A lower dose of rocuronium bromide (0.45 mg/kg) may be used. Neuromuscular block sufficient for intubation (80% block or greater) is attained in a median (range) time of 1.3 (0.8-6.2) minute(s), and most patients have intubation completed within 2 minutes. Maximum blockade is achieved in most patients in less than 4 minutes. This dose may be expected to provide 22 (12-31) minutes of clinical relaxation under opioid/nitrous oxide/oxygen anesthesia. Patients receiving this low dose of 0.45 mg/kg who achieve less than 90% block (about 16% of these patients) may have a more rapid time to 25% recovery, 12 to 15 minutes.

A large bolus dose of 0.9 or 1.2 mg/kg can be administered under opioid/nitrous oxide/oxygen anesthesia without adverse effects to the cardiovascular system [see Clinical Pharmacology (12.2)].

 

2.2 Rapid Sequence Intubation

In appropriately premedicated and adequately anesthetized patients, rocuronium bromide 0.6 to 1.2 mg/kg will provide excellent or good intubating conditions in most patients in less than 2 minutes [see Clinical Studies (14.1)].

 

2.3 Maintenance Dosing

Maintenance doses of 0.1, 0.15, and 0.2 mg/kg rocuronium bromide, administered at 25% recovery of control T1 (defined as 3 twitches of train-of-four), provide a median (range) of 12 (2-31), 17 (6-50), and 24 (7-69) minutes of clinical duration under opioid/nitrous oxide/oxygen anesthesia [see Clinical Pharmacology (12.2)]. In all cases, dosing should be guided based on the clinical duration following initial dose or prior maintenance dose and not administered until recovery of neuromuscular function is evident. A clinically insignificant cumulation of effect with repetitive maintenance dosing has been observed [see Clinical Pharmacology (12.2)].

 

2.4 Use by Continuous Infusion

Infusion at an initial rate of 10 to 12 mcg/kg/min of rocuronium bromide injection should be initiated only after early evidence of spontaneous recovery from an intubating dose. Due to rapid redistribution [see Clinical Pharmacology (12.3)] and the associated rapid spontaneous recovery, initiation of the infusion after substantial return of neuromuscular function (more than 10% of control T1) may necessitate additional bolus doses to maintain adequate block for surgery.

Upon reaching the desired level of neuromuscular block, the infusion of rocuronium bromide injection must be individualized for each patient. The rate of administration should be adjusted according to the patient's twitch response as monitored with the use of a peripheral nerve stimulator. In clinical trials, infusion rates have ranged from 4 to 16 mcg/kg/min.

Inhalation anesthetics, particularly enflurane and isoflurane, may enhance the neuromuscular blocking action of nondepolarizing muscle relaxants. In the presence of steady-state concentrations of enflurane or isoflurane, it may be necessary to reduce the rate of infusion by 30% to 50%, at 45 to 60 minutes after the intubating dose.

Spontaneous recovery and reversal of neuromuscular blockade following discontinuation of rocuronium bromide infusion may be expected to proceed at rates comparable to that following comparable total doses administered by repetitive bolus injections [see Clinical Pharmacology (12.2)].

Infusion solutions of rocuronium bromide injection can be prepared by mixing rocuronium bromide injection with an appropriate infusion solution such as 5% glucose in water or lactated Ringers [see Dosage and Administration (2.6)]. These infusion solutions should be used within 24 hours of mixing. Unused portions of infusion solutions should be discarded.

Infusion rates of rocuronium bromide injection can be individualized for each patient using the following tables for 3 different concentrations of rocuronium bromide solution as guidelines:

TABLE 1: Infusion Rates Using Rocuronium Bromide Injection (0.5 mg/mL)*

* 50 mg rocuronium bromide in 100 mL solution

Patient Weight Drug Delivery Rate (mcg/kg/min)
(kg) (lbs) 4 5 6 7 8 9 10 12 14 16
Infusion Delivery Rate (mL/hr)
10 22 4.8 6 7.2 8.4 9.6 10.8 12 14.4 16.8 19.2
15 33 7.2 9 10.8 12.6 14.4 16.2 18 21.6 25.2 28.8
20 44 9.6 12 14.4 16.8 19.2 21.6 24 28.8 33.6 38.4
25 55 12 15 18 21 24 27 30 36 42 48
35 77 16.8 21 25.2 29.4 33.6
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