Etomidate
Etomidate is an intravenous general anesthetic used to start (induce) anesthesia and, in short procedures, to supplement weaker anesthetic agents.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 14 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Etomidate (Amidate) is an anesthetic given into a vein that puts you to sleep at the start of surgery or a short procedure, an older standby, available generically, often chosen for higher-risk patients because it barely affects heart function. Most people tolerate it well, though it can sting in the vein, brief muscle twitching (myoclonus) as you go under is common, and some feel queasy afterward. It also lowers cortisol and aldosterone, the body's stress hormones, for up to 6 to 8 hours, so it is used only to start anesthesia, never for prolonged sedation. If you feel unusually weak afterward, tell your care team.
Clinical pearls
- Etomidate has no pain-relieving effect, so it is paired with other drugs such as fentanyl, which change the dose needed.
- Mention any liver disease such as cirrhosis, since a slower-clearing liver keeps etomidate active longer than usual.
- Older adults with high blood pressure are more prone to drops in heart rate and blood pressure, so expect closer monitoring.
- It is not advised for starting anesthesia before age 10, and long elective surgery under age 3 deserves a timing discussion.
Patient information guide A plain-language walkthrough of Etomidate, written from its FDA label.
What Etomidate is used for
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Etomidate is an intravenous general anesthetic. It is used in the following ways:
- Amidate (intravenous injection) is indicated to induce general anesthesia in adults and in children older than 10 years
- Etomidate injection (intravenous) is indicated to induce general anesthesia in adults and in children older than 10 years
- Amidate (intravenous) is indicated to supplement weaker anesthetic agents — such as nitrous oxide in oxygen — during short procedures like dilation and curettage or cervical conization in adult patients
- Etomidate injection (intravenous) is similarly indicated to supplement weaker anesthetic agents during short adult procedures
- Use for induction in children under age 10 is not recommended due to insufficient data
- Supplemental use during longer procedures or in pediatric patients is not recommended
How Etomidate works
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Etomidate is a general anesthetic — it puts you into a state of unconsciousness — but it does not relieve pain on its own. When injected into a vein, it acts on the brain to produce anesthesia almost immediately, usually within one minute. It causes a temporary, proportional reduction in cerebral (brain) blood flow and brain oxygen use, and it typically lowers intracranial pressure (pressure inside the skull) for several minutes. One of its notable properties is that, at standard doses, it has very little effect on the heart and circulation, which makes it useful for patients who need careful cardiovascular management.
Etomidate also temporarily suppresses the adrenal glands' production of cortisol and aldosterone — the body's key stress hormones — for roughly 6 to 8 hours after an induction dose. This effect does not respond to ACTH (the hormone that normally triggers cortisol release), which is why prolonged or repeated dosing carries significant risk.
Etomidate dosage
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Etomidate is given only as an intravenous (IV) injection by trained anesthesia professionals in a clinical setting — it is never taken by mouth or self-administered at home. The injection is given slowly, over about 30 to 60 seconds, and the dose is carefully individualized for each patient based on body weight and other factors.
- Older adults may need a lower dose
- It is not intended for prolonged continuous infusion
- When used to supplement anesthesia during a short procedure, smaller follow-up doses may be given, but these are also individualized
- Other medications given during anesthesia — including fentanyl — can affect how much etomidate is needed; the care team manages this
Dosing details from the FDA-approved label
From the Etomidate prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Induction of anesthesia in adult patients and pediatric patients above the age of ten (10) years
- Varies between 0.2 mg/kg and 0.6 mg/kg of body weight, individualized in each case
- Usual dose is 0.3 mg/kg, injected over a period of 30 to 60 seconds
- Geriatric patients may require reduced doses of etomidate
- Induction of anesthesia in patients below the age of ten (10) years
- There are inadequate data to make dosage recommendations
- Such use is not recommended
- Supplementing subpotent anesthetic agents, such as nitrous oxide, during short operative procedures in adult patients
- Smaller increments of intravenous etomidate may be administered
- Dosage usually smaller than the original induction dose, must be individualized
- Insufficient data to support use for longer adult procedures or any procedures in pediatric patients; such use is not recommended
Read the label’s full dosing text
DOSAGE AND ADMINISTRATION Do not administer unless solution is clear and container is undamaged. Discard unused portion (see DOSAGE AND ADMINISTRATION ). Etomidate Injection is intended for administration only by the intravenous route (see CLINICAL PHARMACOLOGY ). The dose for induction of anesthesia in adult patients and in pediatric patients above the age of ten (10) years will vary between 0.2 mg/kg and 0.6 mg/kg of body weight, and it must be individualized in each case. The usual dose for induction in these patients is 0.3 mg/kg, injected over a period of 30 to 60 seconds. There are inadequate data to make dosage recommendations for induction of anesthesia in patients below the age of ten (10) years; therefore, such use is not recommended. Geriatric patients may require reduced doses of etomidate. Smaller increments of intravenous etomidate may be administered to adult patients during short operative procedures to supplement subpotent anesthetic agents, such as nitrous oxide. The dosage employed under these circumstances, although usually smaller than the original induction dose, must be individualized. There are insufficient data to support this use of etomidate for longer adult procedures or for any procedures in pediatric patients; therefore, such use is not recommended. The use of intravenous fentanyl and other neuroactive drugs employed during the conduct of anesthesia may alter the etomidate dosage requirements. Consult the prescribing information for all other such drugs before using. Premedication: Etomidate Injection is compatible with commonly administered pre-anesthetic medications, which may be employed as indicated. See also CLINICAL PHARMACOLOGY , ADVERSE REACTIONS , and dosage recommendations for maintenance of anesthesia. Etomidate Injection anesthesia does not significantly alter the usual dosage requirements of neuromuscular blocking agents employed for endotracheal intubation or other purposes shortly after induction of anesthesia. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. To prevent needle-stick injuries, needles should not be recapped, purposely bent, or broken by hand.
Read the full Dosage and Administration section on DailyMed →
Etomidate side effects
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The most common side effects of etomidate happen during or immediately after the injection:
Common side effects
- Pain or burning at the injection site in the vein
- Involuntary muscle movements or twitching (myoclonus) during induction
- Hiccups
- Nausea and/or vomiting after the procedure
- Brief periods of irregular or rapid breathing
- Short-lived changes in blood pressure or heart rate
- Hiccups or snoring during induction
- Brief changes in breathing — too fast, too slow, or a very short pause in breathing
- Short-term changes in blood pressure or heart rate
When to get medical help
- Call for immediate medical help if you experience severe low blood pressure or racing heart rate, which could signal a serious allergic (anaphylactoid) reaction
- Tell your care team right away if you have trouble breathing, throat tightness, or laryngospasm (airway spasm) after the injection
- Etomidate temporarily lowers the body's production of cortisol and aldosterone (stress hormones) for up to 6–8 hours — alert your care team if you feel unusually weak or unwell after your procedure
- Older adults with high blood pressure are at higher risk of cardiac depression (reduced heart function) and should be monitored closely
Serious reactions — including laryngospasm (airway spasm), severe low blood pressure, or signs of an allergic reaction — require immediate medical attention and are managed by the anesthesia team on site.
Etomidate warnings and precautions
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- Trained personnel only: Etomidate must be administered solely by clinicians trained in general anesthesia, with equipment available to manage any complications immediately.
- No prolonged infusion: Because etomidate suppresses the production of cortisol and aldosterone (vital stress hormones) for 6–8 hours after a single dose — an effect that does not respond to ACTH — it must never be given as a prolonged continuous drip. Extended hormonal suppression poses serious risks.
- Developing brain risk in young children: Anesthetic drugs that act on certain brain receptors may cause nerve-cell loss and possible long-term cognitive or behavioral effects when used in the developing brain. The vulnerable window is thought to run from the third trimester of pregnancy through roughly the first 3 years of life. Families and providers should carefully weigh the necessity and timing of elective procedures in very young children.
- Older adults with high blood pressure: Elderly patients — particularly those with hypertension — face a higher risk of drops in heart rate and blood pressure (cardiac depression) with etomidate.
- Liver disease: In patients with cirrhosis, etomidate stays active in the body roughly twice as long as in healthy individuals.
Etomidate interactions
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Etomidate is given in a controlled medical setting, so your anesthesia team manages interactions directly. The key ones to know about include:
- Fentanyl and other neuroactive drugs: These can reduce how much etomidate is needed and may shorten recovery time — your care team will adjust doses accordingly
- Neuromuscular blocking agents (drugs that relax muscles for breathing tube placement): etomidate does not significantly change the dose needed for these, but they are always used together under close supervision
- Pre-anesthetic (premedication) drugs: Common premedications are generally compatible with etomidate, but the full medication list must be reviewed before your procedure
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Etomidate
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- Allergy to etomidate: Etomidate is contraindicated (must not be used) in anyone with a known hypersensitivity (allergic reaction) to it — tell your team about any prior reactions
- Children under 10: Etomidate is not recommended for induction of anesthesia in this age group due to insufficient safety data
- Young children and pregnancy: Because of the potential for anesthetic drugs to affect the developing brain, parents and pregnant women should discuss the timing of any elective procedures with their doctor
- Older adults, especially with high blood pressure: Greater risk of drops in blood pressure, heart rate, and cardiac output — dose adjustments and close monitoring are needed
- Liver disease (cirrhosis): The drug is cleared more slowly, meaning effects may last longer
- Severe trauma or very low blood volume: The cardiovascular response to etomidate in these situations is not well established — full disclosure of your condition to the care team is essential
Etomidate overdose
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An overdose of etomidate can occur if it is injected too rapidly or in repeated doses. Too fast an injection can cause a drop in blood pressure. If an overdose is suspected, the drug is stopped immediately, the airway is secured (with a breathing tube if necessary), and oxygen with assisted breathing is provided as needed.
What Etomidate does in the body
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Etomidate produces unconsciousness rapidly — usually within one minute — but provides no pain relief on its own. It causes a temporary 20–30% reduction in cerebral (brain) blood flow and a proportional reduction in brain oxygen use, and it typically lowers intracranial pressure (pressure inside the skull) for several minutes. At standard doses, it has little to no effect on the heart, cardiac output, or circulation, making it particularly useful in patients with cardiovascular disease. It also temporarily suppresses cortisol and aldosterone production by the adrenal glands for roughly 6 to 8 hours, an effect that does not respond to the body's normal hormonal signals.
How your body processes Etomidate
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After a single intravenous dose, etomidate takes effect within about one minute, and unconsciousness typically lasts only 3 to 5 minutes at a standard dose — making recovery relatively quick. The drug is rapidly broken down (metabolized) in the liver; the main breakdown product is excreted in the urine, with about 75% of the dose eliminated in the first day. The elimination half-life — the time it takes the body to clear half the drug — is roughly 75 minutes in healthy adults. In patients with liver disease (cirrhosis), both the volume of distribution and the half-life are approximately doubled, meaning the drug stays active longer. Older adults also clear etomidate more slowly than younger adults.
How to store Etomidate
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Store at 20 to 25°C (68 to 77°F).
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Etomidate
5 supplements and herbal products have documented interactions with Etomidate in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 1
- Moderate · 4
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Etomidate: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Etomidate — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is etomidate, and why did my doctor choose it for my procedure?
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Will I feel anything during the injection, and what should I expect right after?
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I heard this drug affects your stress hormones — should I be worried?
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Is etomidate safe for children?
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I'm older and have high blood pressure — is etomidate safe for me?
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What should I tell my care team before I receive etomidate?
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Is Etomidate available over the counter?
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When was Etomidate first available?
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Who makes Etomidate?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Etomidate on HelloPharmacist
Etomidate forms and strengths (how it comes)
Etomidate is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Injection
How this form is used
- Amidate is used intravenously to induce (start) general anesthesia in adults and children over age 10
- Amidate is used intravenously to supplement weaker anesthetic agents such as nitrous oxide during short procedures like dilation and curettage or cervical conization in adult patients
- Etomidate injection is used intravenously to induce general anesthesia in adults and children over age 10
- Etomidate injection is used intravenously to supplement weaker anesthetic agents during short operative procedures in adult patients
- Amidate and Etomidate injection are given only by intravenous injection by trained anesthesia professionals — never by prolonged continuous infusion
- The solution should be inspected before use; do not administer if it is not clear or if the container is damaged, and discard any unused portion
- Amidate dosing is individualized and injected slowly; older adults may require a reduced dose
- Other anesthetic or neuroactive drugs used alongside Amidate or Etomidate may affect the required dose — the full medication list must be reviewed by the care team
Etomidate on the U.S. market: products, makers and brands
How Etomidate appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
12 companies list 24 Etomidate product records with the FDA, mostly as injection; the earliest marketing or approval year on record is 1982. Brand names on the directory include Amidate; the rest are generics.
Also listed with the FDA, not a patient dose form: Powder (3) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Etomidate is used (Medicaid data)
A general measure of how commonly Etomidate is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Etomidate is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Etomidate prescribed? Of the 1,601 medications we measure, Etomidate ranks #1,304 by Medicaid prescriptions — more than 19% of them.
Utilization by Etomidate product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
10 ML etomidate 2 MG/ML Injection Most dispensed
Summed across the 6 of 33 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1654006
20 ML etomidate 2 MG/ML Injection
Summed across the 3 of 28 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1654008
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Etomidate, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 9 of 61 listed Etomidate NDCs with Medicaid activity.
Compare Etomidate products
A representative set of FDA-listed product records for Etomidate — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Injection | ||||
| 2 mg/mL | Intravenous | Armas Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Caplin Steriles Limited × 2 listings | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Civica, Inc. × 2 listings | ANDA | View NDC → |
| 20 mg/10 mL | Intravenous | Eugia US LLC | ANDA | View NDC → |
| 40 mg/20 mL | Intravenous | Eugia US LLC | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Fosun Pharma USA Inc × 2 listings | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Fresenius Kabi USA, LLC × 2 listings | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Henry Schein, Inc. | NDA | View NDC → |
| 2 mg/mL | Intravenous | HF Acquisition Co LLC, DBA HealthFirst | ANDA | View NDC → |
| 40 mg/20 mL | Intravenous | HF Acquisition Co LLC, DBA HealthFirst | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Hikma Pharmaceuticals USA Inc. × 4 listings | ANDA | View NDC → |
| 2 mg/mL | Intravenous | Hospira, Inc. | NDA | View NDC → |
| 2 mg/mL | Intravenous | Mylan Institutional LLC × 2 listings | ANDA | View NDC → |
Showing 24 of 24 products — FDA National Drug Code Directory. See every product, package size and price: browse all 24 Etomidate NDCs →
Etomidate side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Etomidate — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Etomidate in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Etomidate FDA approval history
How Etomidate went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Etomidate recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Etomidate recalls since July 2021.
✅No Etomidate recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 4177 1 dose form · 2 strengths
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Dose form (SCDF) Injection RxCUI 1653759In current FDA listingsClinical drug / strength (SCD) 10 ML etomidate 2 MG/MLRxCUI 165400620 ML etomidate 2 MG/MLRxCUI 1654008
Look up RxCUI 4177 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Etomidate supply and shortage status
Whether Etomidate is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
Etomidate brand names
Etomidate is sold under one brand name in the FDA directory — Amidate. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Etomidate: manufacturers and labelers
12 companies list Etomidate products with the FDA. By number of product records, the largest are Hikma Pharmaceuticals USA Inc., Armas Pharmaceuticals Inc., Caplin Steriles Limited. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Etomidate drug class (RxNorm)
Etomidate belongs to the General Anesthetic class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Etomidate page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Hospira, Inc. is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →