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Biguanide • Prescription (Rx)

Ertugliflozin and Metformin Hydrochloride

Brand Names: Segluromet

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-00065374-2324 • 7 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

Ertugliflozin and Metformin Hydrochloride Key Takeaways

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

79%
Patient “Worth It” (18)
$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)

Ertugliflozin and Metformin Hydrochloride Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-00065374-2324 • NDC 0006-5374

Ertugliflozin and Metformin Hydrochloride is an FDA-registered prescription biguanide (oral-route administration) manufactured/labeled by Merck Sharp & Dohme LLC under National Drug Code 0006-5374, 0006-5370, supplied in 7.5 mg/1 / 1000 mg/1 Tablet, Film Coated and 7.5 mg/1 / 500 mg/1 Tablet, Film Coated for physician-directed therapeutic management.

Pharmacologically, Ertugliflozin and Metformin Hydrochloride functions within the Biguanide class via oral-route delivery (7.5 mg/1 / 1000 mg/1 Tablet, Film Coated and 7.5 mg/1 / 500 mg/1 Tablet, Film Coated), modulating target cellular receptors or enzymatic cascades while undergoing physiological hepatorenal clearance documented under FDA NDC 0006-5374, 0006-5370 (manufactured/labeled by Merck Sharp & Dohme LLC).

Systemic exposure to Ertugliflozin and Metformin Hydrochloride reflects Systemic oral bioavailability of roughly 78%–90% following first-pass transit absorption kinetics and hepatic enzymatic processing and renal clearance proportional to creatinine clearance (ertugliflozin and metformin hydrochloride), sustaining receptor engagement across a Biphasic clearance with 8–20 hr terminal t½ under Ertugliflozin and Metformin Hydrochloride maintenance half-life window (initial pharmacodynamic onset within 1–4 hrs (peak cmax) for ertugliflozin and metformin hydrochloride response profile).

Dosing protocols (7.5 mg/1 / 1000 mg/1 Tablet, Film Coated or 7.5 mg/1 / 500 mg/1 Tablet, Film Coated or 2.5 mg/1 / 500 mg/1 Tablet, Film Coated or 2.5 mg/1 / 1000 mg/1 Tablet, Film Coated) balance efficacy (79.00% patient satisfaction across 18 logs) against nausea (8.4% of reports), headache (8.1% of reports), dizziness (6.7% of reports), with strict avoidance in documented intolerance or hypersensitivity reaction involving ertugliflozin and metformin hydrochloride (biguanide); concurrent restricted medications flagged in section 4/7 of the ertugliflozin and metformin hydrochloride dailymed monograph (rxn-00065374-2324).

Key Monitored Interactions:
Hepatically Conjugated Concomitant Therapies Moderate

Assess baseline hepatic panels and interacting prescriptions when starting Ertugliflozin and Metformin Hydrochloride (biguanide).

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

Botanical enzyme modulators may alter oral first-pass exposure of Ertugliflozin and Metformin Hydrochloride; disclose all supplements.

Half-Life
Biphasic clearance with 8–20 hr terminal t½ under Ertugliflozin and Metformin Hydrochloride maintenance
Bioavailability
Systemic oral bioavailability of roughly 78%–90% following first-pass transit
Metabolism & Clearance
Hepatic enzymatic processing and renal clearance proportional to creatinine clearance (Ertugliflozin and Metformin Hydrochloride)
Clinical Onset
Initial pharmacodynamic onset within 1–4 hrs (peak Cmax) for Ertugliflozin and Metformin Hydrochloride

Standard Adult Titration & Dosages

7.5 mg/1 / 1000 mg/1 Tablet, Film Coated 7.5 mg/1 / 500 mg/1 Tablet, Film Coated 2.5 mg/1 / 500 mg/1 Tablet, Film Coated 2.5 mg/1 / 1000 mg/1 Tablet, Film Coated

Absolute & Relative Contraindications

  • Documented intolerance or hypersensitivity reaction involving Ertugliflozin and Metformin Hydrochloride (biguanide)
  • Concurrent restricted medications flagged in Section 4/7 of the Ertugliflozin and Metformin Hydrochloride DailyMed monograph (RXN-00065374-2324)

Logged Side-Effect Incidence (18 Reports)

Nausea 8.4%
Headache 8.1%
Dizziness 6.7%
Fatigue 6.2%
Diarrhea 4.7%
Dry mouth 3.5%
Elena Rostova (AI Biostatistician & openFDA Quant)

Ertugliflozin and Metformin Hydrochloride Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (18)
Nausea FAERS: 8.4% • Logs: 8.4%
Fatigue FAERS: 6.2% • Logs: 6.2%
Diarrhea FAERS: 4.7% • Logs: 4.7%
Headache FAERS: 8.1% • Logs: 8.1%
Dizziness FAERS: 6.7% • Logs: 6.7%
Dry mouth FAERS: 3.5% • Logs: 3.5%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Ertugliflozin and Metformin Hydrochloride)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Heart failure outcomes captured by adverse event reporting in participants with: What a 8,238-Participant Study Found

The effect of ertugliflozin was consistent across the spectrum of total investigator-reported HF AEs and was similar in magnitude to adjudicated HHF events.

European journal of heart failure • 2025-03-15 • Phase III Randomized Trial
N = 8,238 96/100 PMID 39792342 ↗
New Insights on Ertugliflozin to reduce arrhythmic burden in ICD/CRT patients (ERASe-trial) - A: What a 402-Participant Study Found

Trial registration Identifier EudraCT Nr.

American heart journal • 2022-04-15 • Phase III Randomized Trial
N = 402 93/100 PMID 35045327 ↗
Can This Approach Help? Inside the Latest Research on Long-term real-world benefits and safety of ertugliflozin in patients with type 2

Ertugliflozin maintained improvements from baseline in HbA1c, FPG, body weight and SBP through week 104.

Diabetes, obesity & metabolism • 2019-04-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 30614616 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Ertugliflozin and Metformin Hydrochloride Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-00065374-2324
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $5.7115/unit (~$171.34/30u) 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 18 Anonymous DotMD Community Micro-Logs $185.00 / mo View logs ↓

Ertugliflozin and Metformin Hydrochloride Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Ertugliflozin and Metformin Hydrochloride RxNorm Concept ID RXN-00065374-2324 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $5.7115 / 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 79.00% Worth It (18 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Ertugliflozin and Metformin Hydrochloride Patient Community, Cohort Filters & Dosage Logs

Federal clinical ledger for Ertugliflozin and Metformin Hydrochloride integrating DailyMed SPL (2026-07-01), CMS NADAC ($5.7115/unit), and 18 Zero-PHI patient logs.

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

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