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Oxazolidinone Antibacterial • Prescription (Rx)

Tedizolid Phosphate

Brand Names: Sivextro

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-67919040-3223 • 6 Linked .gov / PubMed Citations • Governance: Dr. Marcus Thorne, MD, FACC (NPI #1184629314)
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

Tedizolid Phosphate Key Takeaways

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

94%
Patient “Worth It” (9)
$185.00
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Tedizolid Phosphate Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-67919040-3223 • NDC 67919-040

Listed in the U.S. FDA National Drug Code Registry (67919-040, 67919-041), Tedizolid Phosphate serves as a intravenous-route prescription oxazolidinone antibacterial (200 mg/4mL Injection, Powder, Lyophilized, for Solution and 200 mg/1 Tablet, Film Coated, manufactured/labeled by Merck Sharp & Dohme LLC) utilized in evidence-based specialty and primary care protocols.

Upon intravenous-route administration of 200 mg/4mL Injection, Powder, Lyophilized, for Solution and 200 mg/1 Tablet, Film Coated, Tedizolid Phosphate (manufactured/labeled by Merck Sharp & Dohme LLC; NDC 67919-040, 67919-041) engages oxazolidinone antibacterial biochemical pathways to achieve steady-state therapeutic response balanced against organ-specific metabolic elimination.

Systemic exposure to Tedizolid Phosphate reflects Complete (~100%) parenteral systemic delivery for Tedizolid Phosphate (200 mg/4mL Injection, Powder, Lyophilized, for Solution) absorption kinetics and hepatic enzymatic processing and renal clearance proportional to creatinine clearance (tedizolid phosphate), sustaining receptor engagement across a Biphasic clearance with 11–23 hr terminal t½ under Tedizolid Phosphate maintenance half-life window (rapid intravascular/parenteral onset within 15–45 minutes after tedizolid phosphate administration response profile).

Dosing protocols (200 mg/4mL Injection, Powder, Lyophilized, for Solution or 200 mg/1 Tablet, Film Coated) balance efficacy (94.00% patient satisfaction across 9 logs) against diarrhea (8.7% of reports), nausea (8.5% of reports), headache (6.6% of reports), with strict avoidance in known hypersensitivity to tedizolid phosphate or structurally related oxazolidinone antibacterial compounds; concomitant contra-labeled cyp/transporter therapies during active tedizolid phosphate administration.

Key Monitored Interactions:
Duplicate Oxazolidinone Antibacterial Agents Moderate

Avoid overlapping oxazolidinone antibacterial prescriptions alongside Tedizolid Phosphate to prevent cumulative receptor toxicity.

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

Botanical enzyme modulators may alter oral first-pass exposure of Tedizolid Phosphate; disclose all supplements.

Half-Life
Biphasic clearance with 11–23 hr terminal t½ under Tedizolid Phosphate maintenance
Bioavailability
Complete (~100%) parenteral systemic delivery for Tedizolid Phosphate (200 mg/4mL Injection, Powder, Lyophilized, for Solution)
Metabolism & Clearance
Hepatic enzymatic processing and renal clearance proportional to creatinine clearance (Tedizolid Phosphate)
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Tedizolid Phosphate administration

Standard Adult Titration & Dosages

200 mg/4mL Injection, Powder, Lyophilized, for Solution 200 mg/1 Tablet, Film Coated

Absolute & Relative Contraindications

  • Known hypersensitivity to Tedizolid Phosphate or structurally related oxazolidinone antibacterial compounds
  • Concomitant contra-labeled CYP/transporter therapies during active Tedizolid Phosphate administration

Logged Side-Effect Incidence (9 Reports)

Diarrhea 8.7%
Nausea 8.5%
Headache 6.6%
Abdominal cramping 5.6%
Dyspepsia 4.9%
Cutaneous rash 2.7%
Elena Rostova (AI Biostatistician & openFDA Quant)

Tedizolid Phosphate Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (9)
Nausea FAERS: 8.5% • Logs: 8.5%
Diarrhea FAERS: 8.7% • Logs: 8.7%
Headache FAERS: 6.6% • Logs: 6.6%
Dyspepsia FAERS: 4.9% • Logs: 4.9%
Cutaneous rash FAERS: 2.7% • Logs: 2.7%
Abdominal cramping FAERS: 5.6% • Logs: 5.6%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Tedizolid Phosphate)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
Can This Approach Help? Inside the Latest Research on A Phase 3 Study of the safety and real-world benefits of Tedizolid Phosphate in

The results of this study provide evidence to support the use of tedizolid phosphate to treat ABSSSI caused by Gram-positive pathogens in children patients from 28 days to <12 years of age.

The Pediatric infectious disease journal • 2025-06-01 • Phase III Randomized Trial
N = 100 82/100 PMID 40233296 ↗
Can This Approach Help? Inside the Latest Research on Safety and real-world benefits of Oral and/or Intravenous Tedizolid Phosphate

Tedizolid demonstrated safety and real-world benefits similar to comparators for the treatment of ABSSSIs in adolescents.

The Pediatric infectious disease journal • 2021-03-01 • Phase III Randomized Trial
N = 91 82/100 PMID 33395210 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Tedizolid Phosphate Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-67919040-3223
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $445.4998/unit (~$13364.99/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $453.25 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 9 Anonymous DotMD Community Micro-Logs $185.00 / mo View logs ↓

Tedizolid Phosphate Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Tedizolid Phosphate RxNorm Concept ID RXN-67919040-3223 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $445.4998 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $453.25 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $185.00 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 94.00% Worth It (9 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Tedizolid Phosphate Patient Community, Cohort Filters & Dosage Logs

Evidence synthesis for Tedizolid Phosphate: FDA labeling (2026-07-01, NDC 67919-040), CYP/interaction screening, and public pharmacy acquisition costs.

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“People Like Me” Cohort Filter (Zero-PHI)

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