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Diagnostic Dye • Prescription (Rx)

Fluorescein Sodium

Brand Names: Glostrips, Dry Eye Test

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2019-12-23 • RxNorm RxCUI RXN-51801009-2030 • 9 Linked .gov / PubMed Citations • Governance: Dr. Priya Nair, MD, FAAD (NPI #1295730425)
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

Fluorescein Sodium Key Takeaways

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

92%
Patient “Worth It” (10)
$113.80
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Fluorescein Sodium

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Dr. Vance (AI Pharmacology & Interaction Agent)

Fluorescein Sodium Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-51801009-2030 • NDC 51801-009

INDICATIONS For staining the anterior segment of the eye in disclosing corneal injury, in applanation tonometry and when fitting contact lenses.

As an active diagnostic dye moiety (Nomax Inc.), Fluorescein Sodium modulates physiological signaling proportional to .6 mg/1 Strip exposure and hepatorenal clearance (SPL 2019-12-23).

With Approximately 3–8 hours terminal plasma half-life for Fluorescein Sodium residence kinetics and Estimated 77%–89% oral systemic absorption for Fluorescein Sodium bioavailability, Fluorescein Sodium undergoes phase i/ii hepatic conjugation of fluorescein sodium coupled with glomerular and tubular renal excretion and establishes therapeutic activity over peak plasma concentration (tmax) reached 1–3 hours post-dose for fluorescein sodium.

Standard adult regimens span .6 mg/1 Strip, .12 mg/1 Strip, 1 mg/mg Strip, 1 mg/1 Strip. Prescribers screen specifically against severe drug-induced hypersensitivity to fluorescein sodium or inactive tablet/vehicle binders; prohibited co-prescriptions or physiological states specified in fda spl 2019-12-23 for fluorescein sodium, while community micro-logs most frequently note nausea (7.8% of reports), headache (7.8% of reports), dizziness (5.4% of reports).

Key Monitored Interactions:
Hepatically Conjugated Concomitant Therapies Moderate

Assess baseline hepatic panels and interacting prescriptions when starting Fluorescein Sodium (diagnostic dye).

Gastric pH-Altering Agents (PPIs & H2 Blockers) Minor

Shifts in intragastric pH can modestly influence dissolution kinetics of oral Fluorescein Sodium dosage forms.

Half-Life
Approximately 3–8 hours terminal plasma half-life for Fluorescein Sodium
Bioavailability
Estimated 77%–89% oral systemic absorption for Fluorescein Sodium
Metabolism & Clearance
Phase I/II hepatic conjugation of Fluorescein Sodium coupled with glomerular and tubular renal excretion
Clinical Onset
Peak plasma concentration (Tmax) reached 1–3 hours post-dose for Fluorescein Sodium

Standard Adult Titration & Dosages

.6 mg/1 Strip .12 mg/1 Strip 1 mg/mg Strip 1 mg/1 Strip

Absolute & Relative Contraindications

  • Severe drug-induced hypersensitivity to Fluorescein Sodium or inactive tablet/vehicle binders
  • Prohibited co-prescriptions or physiological states specified in FDA SPL 2019-12-23 for Fluorescein Sodium

Logged Side-Effect Incidence (10 Reports)

Nausea 7.8%
Headache 7.8%
Dizziness 5.4%
Fatigue 4.5%
Diarrhea 3.8%
Dry mouth 3%
Elena Rostova (AI Biostatistician & openFDA Quant)

Fluorescein Sodium Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (10)
Nausea FAERS: 7.8% • Logs: 7.8%
Fatigue FAERS: 4.5% • Logs: 4.5%
Diarrhea FAERS: 3.8% • Logs: 3.8%
Headache FAERS: 7.8% • Logs: 7.8%
Dizziness FAERS: 5.4% • Logs: 5.4%
Dry mouth FAERS: 3% • Logs: 3%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Fluorescein Sodium)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Benefits and safety of the Long-Acting Diquafosol Ophthalmic Solution DE-089C in: What a 337-Participant Study Found

The real-world benefits and safety of DE-089C administered three times daily at half the dosage of DQS in patients with dry eye were confirmed in this study.

Advances in therapy • 2022-08-15 • Phase III Randomized Trial
N = 337 93/100 PMID 35716319 ↗
New Insights on Vision-Related Quality of Life in Geographic Atrophy: Association with: What a 856-Participant Study Found

In this cohort, VR-QoL is most strongly associated with minimum eye-level GA extent within the central 2.50-mm region within an individual.

Ophthalmology • 2026-08-15 • Phase III Randomized Trial
N = 856 87/100 PMID 42031134 ↗
New Insights on NOV03 for Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland: What a 620-Participant Study Found

In this randomized controlled trial of patients with DED associated with MGD, NOV03 significantly reduced both signs and symptoms of DED compared with hypotonic saline control.

American journal of ophthalmology • 2023-08-15 • Phase III Randomized Trial
N = 620 87/100 PMID 36948372 ↗
New Insights on NOV03 for Dry Eye Disease Associated with Meibomian Gland Dysfunction: Results of: What a 303-Participant Study Found

In patients with DED associated with MGD, NOV03 demonstrated statistically significant and clinically meaningful improvements versus hypotonic saline in signs and symptoms of DED and was well tolerated.

Ophthalmology • 2023-05-15 • Phase III Randomized Trial
N = 303 87/100 PMID 36574848 ↗
New Insights on Disease Activity and Therapeutic Response to Pegcetacoplan for Geographic Atrophy: What a 897-Participant Study Found

Deep learning-based OCT analysis objectively identifies and quantifies PR and RPE degeneration in GA.

Ophthalmology • 2025-02-15 • Phase III Randomized Trial
N = 897 87/100 PMID 39151755 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Fluorescein Sodium Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-51801009-2030
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $2.6000/unit (~$78.00/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $278.81 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 10 Anonymous DotMD Community Micro-Logs $113.80 / mo View logs ↓

Fluorescein Sodium Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Fluorescein Sodium RxNorm Concept ID RXN-51801009-2030 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $2.6000 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $278.81 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $113.80 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 92.00% Worth It (10 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Fluorescein Sodium Patient Community, Cohort Filters & Dosage Logs

Deterministic Fluorescein Sodium reference combining NIH RxNorm (RXN-51801009-2030), Medicaid NADAC ($2.6000/unit), and anonymous cohort outcomes (92% Worth It).

15-Second Anonymous Micro-Log (Zero-PHI Architecture)

Share your real dosage and monthly out-of-pocket cost—no account, email, or IP stored.

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

Filter Fluorescein Sodium community threads and patient logs by age, biological sex, dosage, and treatment duration.

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