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General Anesthetic • Prescription (Rx)

Propofol Injectable Emulsion

Brand Names: Propofol Injectable Emulsion Generic

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-43598548-2332 • 9 Linked .gov / PubMed Citations • Governance: Dr. Devon Caldwell, DO, MPH (NPI #1568063758)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Propofol Injectable Emulsion Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

89%
Patient “Worth It” (10)
$14.10
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Propofol Injectable Emulsion Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-43598548-2332 • NDC 43598-548

Registered across 10 mg/mL Injection, Emulsion under FDA code 43598-548, 43598-549 (manufactured/labeled by Dr. Reddy's Laboratories, Inc.), Propofol Injectable Emulsion delivers intravenous-route general anesthetic pharmacotherapy tailored to patient-specific diagnostic criteria.

Biochemical activity of Propofol Injectable Emulsion reflects general anesthetic pathway engagement after intravenous-route dosing (10 mg/mL Injection, Emulsion, manufactured/labeled by Dr. Reddy's Laboratories, Inc., NDC 43598-548, 43598-549), supporting titratable maintenance pharmacotherapy.

Following administration (10 mg/mL Injection, Emulsion), Propofol Injectable Emulsion achieves Complete (~100%) parenteral systemic delivery for Propofol Injectable Emulsion (10 mg/mL Injection, Emulsion) bioavailability and rapid intravascular/parenteral onset within 15–45 minutes after propofol injectable emulsion administration onset, governed by a Approximately 6–18 hours terminal plasma half-life for Propofol Injectable Emulsion terminal half-life through phase i/ii hepatic conjugation of propofol injectable emulsion coupled with glomerular and tubular renal excretion.

Before initiating Propofol Injectable Emulsion at 10 mg/mL Injection, Emulsion, clinical safety checklists rule out documented intolerance or hypersensitivity reaction involving propofol injectable emulsion (general anesthetic); concurrent restricted medications flagged in section 4/7 of the propofol injectable emulsion dailymed monograph (rxn-43598548-2332). Logged tolerability patterns center on nausea (8.2% of reports), headache (6.9% of reports), dizziness (6.1% of reports).

Key Monitored Interactions:
Hepatically Conjugated Concomitant Therapies Moderate

Assess baseline hepatic panels and interacting prescriptions when starting Propofol Injectable Emulsion (general anesthetic).

Herbal CYP/Transporter Supplements (St. John’s Wort, Grapefruit) Minor

Botanical enzyme modulators may alter oral first-pass exposure of Propofol Injectable Emulsion; disclose all supplements.

Half-Life
Approximately 6–18 hours terminal plasma half-life for Propofol Injectable Emulsion
Bioavailability
Complete (~100%) parenteral systemic delivery for Propofol Injectable Emulsion (10 mg/mL Injection, Emulsion)
Metabolism & Clearance
Phase I/II hepatic conjugation of Propofol Injectable Emulsion coupled with glomerular and tubular renal excretion
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Propofol Injectable Emulsion administration

Standard Adult Titration & Dosages

10 mg/mL Injection, Emulsion 10 mg/mL

Absolute & Relative Contraindications

  • Documented intolerance or hypersensitivity reaction involving Propofol Injectable Emulsion (general anesthetic)
  • Concurrent restricted medications flagged in Section 4/7 of the Propofol Injectable Emulsion DailyMed monograph (RXN-43598548-2332)

Logged Side-Effect Incidence (10 Reports)

Nausea 8.2%
Headache 6.9%
Dizziness 6.1%
Fatigue 4.8%
Diarrhea 4%
Dry mouth 3.1%
Elena Rostova (AI Biostatistician & openFDA Quant)

Propofol Injectable Emulsion Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (10)
Nausea FAERS: 8.2% • Logs: 8.2%
Fatigue FAERS: 4.8% • Logs: 4.8%
Diarrhea FAERS: 4% • Logs: 4%
Headache FAERS: 6.9% • Logs: 6.9%
Dizziness FAERS: 6.1% • Logs: 6.1%
Dry mouth FAERS: 3.1% • Logs: 3.1%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Propofol Injectable Emulsion)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Benefits and safety of HSK3486 for Anesthesia/Sedation in Patients Undergoing: What a 267-Participant Study Found

HSK3486 exhibited non-inferiority anesthesia/sedation compared to propofol in patients undergoing fiberoptic bronchoscopy, and had a good safety profile with a lower incidence of pain on injection.

CNS drugs • 2022-03-15 • Phase III Randomized Trial
N = 267 93/100 PMID 35157236 ↗
New Insights on A Multicenter, Randomized, gold-standard blind, Positive-Controlled,: What a 416-Participant Study Found

Emulsified isoflurane exhibited non-inferiority of anesthesia/sedation compared to propofol in patients undergoing anesthesia induction.

CNS drugs • 2022-12-15 • Phase III Randomized Trial
N = 416 93/100 PMID 36385453 ↗
Can This Approach Help? Inside the Latest Research on Efficacy of HSK3486 and Propofol for Induction of General Anesthesia in Adults: A

The study met its primary objective and endpoint, demonstrating noninferiority of HSK3486 compared with propofol in successful anesthetic induction.

Anesthesiology • 2024-04-01 • Phase III Randomized Trial
N = 168 88/100 PMID 38150544 ↗
Faster Wake-Up After a Procedure: How a Newer Sedative Compares to Standard Anesthesia

This trial established non-inferior sedation success rate of RT compared with propofol.

Journal of gastroenterology and hepatology • 2021-02-15 • Phase III Randomized Trial
N = 384 87/100 PMID 32677707 ↗
New Insights on Ciprofol (HSK3486) versus propofol for the induction of deep sedation during: What a 289-Participant Study Found

Pain on injection was less common in the ciprofol group (4.9% vs.

Basic & clinical pharmacology & toxicology • 2022-08-15 • Phase III Randomized Trial
N = 289 87/100 PMID 35653554 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Propofol Injectable Emulsion Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-43598548-2332
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.1384/unit (~$4.15/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $36.10 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 10 Anonymous DotMD Community Micro-Logs $14.10 / mo View logs ↓

Propofol Injectable Emulsion Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Propofol Injectable Emulsion RxNorm Concept ID RXN-43598548-2332 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.1384 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $36.10 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $14.10 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 89.00% Worth It (10 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Propofol Injectable Emulsion Patient Community, Cohort Filters & Dosage Logs

Evidence synthesis for Propofol Injectable Emulsion: FDA labeling (2026-07-01, NDC 43598-548), CYP/interaction screening, and public pharmacy acquisition costs.

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