Amidate (etomidate)
Intravenous Anesthetics Intravenous Vial (Ml)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Generic name: etomidate
Drug class: Intravenous Anesthetics
Therapeutic class: Anesthetics
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Amidate
Indications
The following indications are listed for Amidate:
- Administration Of General Anesthesia
- General Anesthesia Adjunct
Also known as: Adjunct General Anesthesia.
Dosing
No dosing information is available for this tab.
No dosing information is available for this tab.
| Drug label | Dosing type | Instructions |
|---|---|---|
| Amidate 20 Mg/10 Ml Vial | Maintenance | Inject 0.3 mg/kg by intravenous route once. |
| Amidate 40 Mg/20 Ml Vial | Maintenance | Inject 0.3 mg/kg by intravenous route once. |
| Drug label | Dosing type | Instructions |
|---|---|---|
| Etomidate 20 Mg/10 Ml Vial | Maintenance | Inject 0.3 mg/kg by intravenous route once. |
| Etomidate 40 Mg/20 Ml Vial | Maintenance | Inject 0.3 mg/kg by intravenous route once. |
Drug interactions
There is no enhanced messaging for this drug.
There are no contraindication interactions for this drug.
Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
Agents That May Cause Respiratory Depression/Sodium Oxybate
SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
MECHANISM OF ACTION: Oxybate by itself may be associated with severe somnolence or respiratory depression. Concurrent use with other CNS depressants may further increase the risk for respiratory depression or loss of consciousness.(1-3)
CLINICAL EFFECTS: Concurrent use of sodium oxybate and sedative hypnotics or alcohol may further increase the risk for profound sedation, respiratory depression, coma, and/or death.(1,2) Fatalities have been reported.(3)
PREDISPOSING FACTORS: Based upon FDA evaluation of deaths in patients taking sodium oxybate, risk factors may include: use of multiple drugs which depress the CNS, more rapid than recommended oxybate dose titration, exceeding the maximum recommended oxybate dose, and prescribing for unapproved uses such as fibromyalgia, insomnia or migraine. Note that in oxybate clinical trials for narcolepsy 78% - 85% of patients were also receiving concomitant CNS stimulants.(1-3)
PATIENT MANAGEMENT: Avoid use of concomitant opioids, benzodiazepines, sedating antidepressants, sedating antipsychotics, general anesthetics, or muscle relaxants, particularly when predisposing risk factors are present. If combination use is required, dose reduction or discontinuation of one or more CNS depressants should be considered. If short term use of an opioid or general anesthetic is required, consider interruption of sodium oxybate treatment.(1,2) Respiratory depression can occur at any time during opioid therapy, especially during therapy initiation and following dosage increases. The risk of opioid-related overdose or overdose-related death is increased with higher opioid doses, and this risk persists over the course of therapy. Consider these risks when using concurrently with other agents that may cause CNS depression.(4) Discuss opioid reversal agents (e.g., naloxone, nalmefene) with all patients when prescribing or renewing an opioid analgesic or medicine to treat opioid use disorder (OUD). Consider prescribing an opioid reversal agent (e.g., naloxone, nalmefene) to patients prescribed medicines to treat OUD or opioid analgesics who are at increased risk of opioid overdose (such as those taking CNS depressants) and when a patient has household members/close contacts at risk for accidental overdose. Discuss the options for obtaining an opioid reversal agent (e.g., prescription, over-the-counter, or as part of a community-based program).(5)
DISCUSSION: The FDA evaluated sodium oxybate postmarket fatal adverse event reports from the FDA Adverse Event Reporting System(AERS)and from the manufacturer. Although report documentation was not always optimal or complete, useful information was obtained. Factors which may have contributed to fatal outcome: concomitant use of one or more drugs which depress the CNS, more rapid than recommended oxybate dose titration, exceeding the maximum recommended oxybate dose, and prescribing for unapproved uses such as fibromyalgia, insomnia or migraine. Many deaths occurred in patients with serious psychiatric disorders such as depression and substance abuse. Other concomitant diseases may have also contributed to respiratory and CNS depressant effects of oxybate.(3)
Moderate Interaction: Assess the risk to the patient and take action as needed.
Anesthesia Agents/Glp-1 Receptor Agonists
SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed.
MECHANISM OF ACTION: GLP-1 receptor agonists can cause delayed gastric emptying.(1,2)
CLINICAL EFFECTS: Gastric contents may remain in the stomach after preoperative fasting, which could increase the risk of regurgitation and aspiration.(1,2)
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: The American Society of Anesthesiologists (ASA) recommends the following for patients receiving elective procedures: - For patients on daily dosing, consider holding GLP-1 agonists on the day of the procedure. For patients on weekly dosing, consider holding GLP-1 agonists a week prior to the procedure. - Consult an endocrinologist for patients taking GLP-1 agonists for diabetes management if the GLP-1 agonist is held longer than the dosing schedule to avoid hyperglycemia. - For patients requiring urgent or emergent procedures, proceed and treat the patient as 'full stomach.'(3)
DISCUSSION: In one case report, a 31-year-old patient taking semaglutide followed preoperative fasting guidelines but food residue was discovered upon endoscopy, leading to cancellation of the surgical procedure.(4) In a case report, a semaglutide-treated patient experienced regurgitation upon induction of general anesthesia despite a 20 hour preoperative fasting period. The patient received semaglutide two days before the scheduled procedure.(5) A case report of a 42-year-old patient after fasting for 18 hours showed substantial gastric content upon endoscopy. The patient experienced intraoperative pulmonary aspiration of gastric contents which were suctioned from the trachea and bronchi using bronchoscopy.(6)
Contraindications
There is no enhanced messaging for this drug.
There are no contraindication contraindications for this drug.
- Adrenocortical insufficiency
- Hypotension
There are no moderate contraindications for this drug.
Adverse reactions
There is no enhanced messaging for this drug.
More Frequent
- Nausea
- Vomiting
Rare or Very Rare
- Bradycardia
- Bradypnea
- Hypertension
- Hyperventilation
- Hypotension
- Hypoventilation
- Laryngismus
- Tachycardia
- Tachypnea
More Frequent
- Injection site sequelae
- Involuntary muscle movement
Rare or Very Rare
- Hiccups
- Snoring
Precautions
No enhanced messaging available.
No enhanced messaging available.
No enhanced messaging available.
No enhanced messaging available.
No enhanced messaging available.
ICD codes
| Code | Type | Description |
|---|---|---|
| Administration of general anesthesia | ||
| 3E030FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral vein, open approach |
| 3E033FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral vein, percutaneous approach |
| 3E040FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central vein, open approach |
| 3E043FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central vein, percutaneous approach |
| 3E050FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral artery, open approach |
| 3E053FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral artery, percutaneous approach |
| 3E060FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central artery, open approach |
| 3E063FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central artery, percutaneous approach |
| General anesthesia adjunct | ||
| 3E030FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral vein, open approach |
| 3E033FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral vein, percutaneous approach |
| 3E040FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central vein, open approach |
| 3E043FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central vein, percutaneous approach |
| 3E050FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral artery, open approach |
| 3E053FZ | ICD10PCS | Introduction of intracirculatory anesthetic into peripheral artery, percutaneous approach |
| 3E060FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central artery, open approach |
| 3E063FZ | ICD10PCS | Introduction of intracirculatory anesthetic into central artery, percutaneous approach |
ICD code information from First Databank (FDB).
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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