Last reviewed · How we verify

Initial remifentanil effect-site concentration

Tri-Service General Hospital · FDA-approved active Small molecule

Initial remifentanil effect-site concentration is a Opioid agonist Small molecule drug developed by Tri-Service General Hospital. It is currently FDA-approved for Intraoperative analgesia and sedation during general anesthesia, Postoperative analgesia in monitored anesthesia care settings.

Remifentanil is a potent synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce rapid analgesia and sedation.

Remifentanil is a potent synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce rapid analgesia and sedation. Used for Intraoperative analgesia and sedation during general anesthesia, Postoperative analgesia in monitored anesthesia care settings.

At a glance

Generic nameInitial remifentanil effect-site concentration
SponsorTri-Service General Hospital
Drug classOpioid agonist
TargetMu-opioid receptor (μ-OR)
ModalitySmall molecule
Therapeutic areaAnesthesia and Analgesia
PhaseFDA-approved

Mechanism of action

Remifentanil activates mu-opioid receptors, which inhibit pain signal transmission and promote sedation through effects on the brainstem and spinal cord. It is characterized by rapid onset and offset due to its ester structure, which allows quick metabolism by non-specific plasma and tissue esterases. The 'effect-site concentration' refers to the measured or modeled concentration at the site of drug action (brain), used to guide dosing in anesthesia.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Initial remifentanil effect-site concentration

What is Initial remifentanil effect-site concentration?

Initial remifentanil effect-site concentration is a Opioid agonist drug developed by Tri-Service General Hospital, indicated for Intraoperative analgesia and sedation during general anesthesia, Postoperative analgesia in monitored anesthesia care settings.

How does Initial remifentanil effect-site concentration work?

Remifentanil is a potent synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce rapid analgesia and sedation.

What is Initial remifentanil effect-site concentration used for?

Initial remifentanil effect-site concentration is indicated for Intraoperative analgesia and sedation during general anesthesia, Postoperative analgesia in monitored anesthesia care settings.

Who makes Initial remifentanil effect-site concentration?

Initial remifentanil effect-site concentration is developed and marketed by Tri-Service General Hospital (see full Tri-Service General Hospital pipeline at /company/tri-service-general-hospital).

What drug class is Initial remifentanil effect-site concentration in?

Initial remifentanil effect-site concentration belongs to the Opioid agonist class. See all Opioid agonist drugs at /class/opioid-agonist.

What development phase is Initial remifentanil effect-site concentration in?

Initial remifentanil effect-site concentration is FDA-approved (marketed).

What are the side effects of Initial remifentanil effect-site concentration?

Common side effects of Initial remifentanil effect-site concentration include Respiratory depression, Hypotension, Bradycardia, Muscle rigidity, Nausea and vomiting.

What does Initial remifentanil effect-site concentration target?

Initial remifentanil effect-site concentration targets Mu-opioid receptor (μ-OR) and is a Opioid agonist.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing