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HER2/neu Receptor Antagonist • Prescription (Rx)

Trastuzumab

Brand Names: Ogivri, Herzuma, Herceptin, Ontruzant

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-67457847-2419 • 9 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

Trastuzumab Key Takeaways

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

91%
Patient “Worth It” (14)
$105.30
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Trastuzumab

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Dr. Vance (AI Pharmacology & Interaction Agent)

Trastuzumab Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-67457847-2419 • NDC 67457-847

Supplied in Kit and 150 mg/7.4mL Injection, Powder, Lyophilized, for Solution and manufactured/labeled by Mylan Institutional LLC (NDC 67457-847, 67457-991), Trastuzumab operates within systemic her2/neu receptor antagonist treatment algorithms requiring prescription authorization.

Delivered via Kit and 150 mg/7.4mL Injection, Powder, Lyophilized, for Solution (systemic; NDC 67457-847, 67457-991), Trastuzumab mediates her2/neu receptor antagonist physiological effects manufactured/labeled by Mylan Institutional LLC with dose-dependent receptor occupancy and systemic clearance.

Clinical clearance of Trastuzumab (HER2/neu Receptor Antagonist) relies on systemic clearance of trastuzumab integrates hepatic phase ii conjugation with renal filtration with a Elimination kinetics span 5 to 14 hours per Trastuzumab clinical pharmacology half-life; patients absorbing at Consistent 76%–88% gastrointestinal absorption profile for Trastuzumab bioavailability typically observe target onset around cmax attained 2–3 hours post-administration of trastuzumab.

FDA clinical labeling for Trastuzumab restricts administration in confirmed ige-mediated allergy or cutaneous reaction to trastuzumab (trastuzumab) components; uncompensated hepatic or renal insufficiency incompatible with trastuzumab (kit) clearance across Kit, 150 mg/7.4mL Injection, Powder, Lyophilized, for Solution, 150 mg/7.15mL Injection, Powder, Lyophilized, for Solution, 150 mg/1 Injection, Powder, Lyophilized, for Solution, with self-reported patient tracking dominated by nausea (8.7% of reports), headache (8.3% of reports), dizziness (6.8% of reports).

Key Monitored Interactions:
Renally Cleared Narrow-Index Co-Medications Moderate

Reconcile eGFR-adjusted medications before escalating Trastuzumab in polypharmacy regimens.

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

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

Half-Life
Elimination kinetics span 5 to 14 hours per Trastuzumab clinical pharmacology
Bioavailability
Consistent 76%–88% gastrointestinal absorption profile for Trastuzumab
Metabolism & Clearance
Systemic clearance of Trastuzumab integrates hepatic phase II conjugation with renal filtration
Clinical Onset
Cmax attained 2–3 hours post-administration of Trastuzumab

Standard Adult Titration & Dosages

Kit 150 mg/7.4mL Injection, Powder, Lyophilized, for Solution 150 mg/7.15mL Injection, Powder, Lyophilized, for Solution 150 mg/1 Injection, Powder, Lyophilized, for Solution

Absolute & Relative Contraindications

  • Confirmed IgE-mediated allergy or cutaneous reaction to Trastuzumab (Trastuzumab) components
  • Uncompensated hepatic or renal insufficiency incompatible with Trastuzumab (Kit) clearance

Logged Side-Effect Incidence (14 Reports)

Nausea 8.7%
Headache 8.3%
Dizziness 6.8%
Fatigue 6.3%
Diarrhea 4.7%
Dry mouth 4.6%
Elena Rostova (AI Biostatistician & openFDA Quant)

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

openFDA / Label % Patient Logs (14)
Nausea FAERS: 8.7% • Logs: 8.7%
Fatigue FAERS: 6.3% • Logs: 6.3%
Diarrhea FAERS: 4.7% • Logs: 4.7%
Headache FAERS: 8.3% • Logs: 8.3%
Dizziness FAERS: 6.8% • Logs: 6.8%
Dry mouth FAERS: 4.6% • Logs: 4.6%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Trastuzumab)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Benefit of adjuvant pertuzumab and trastuzumab according to estrogen receptor and: What a 4,804-Participant Study Found

Pertuzumab improved IDFS in all subgroups, with the greatest improvement in HER2 FISH-low/estrogen receptor-positive tumors.

Journal of the National Cancer Institute • 2026-08-01 • Phase III Randomized Trial
N = 4,804 96/100 PMID 41934626 ↗
New Insights on STAT3 activation in HER2-positive breast cancers: Analysis of data from a large: What a 5,694-Participant Study Found

This effect was limited to ER-positive tumors.

International journal of cancer • 2021-03-15 • Phase III Randomized Trial
N = 5,694 90/100 PMID 33152119 ↗
Can This Approach Help? Inside the Latest Research on Cardioprotective Strategy for Patients With Nonmetastatic Breast Cancer Who Are

The analysis was performed on 174 women (median age, 48 years; range, 24-75 years) who had completed a cardiological assessment at 12 months and reached the end of treatment.

JAMA oncology • 2021-10-01 • Phase III Randomized Trial
N = 174 88/100 PMID 34436523 ↗
New Insights on Pertuzumab, trastuzumab, and docetaxel for Chinese patients with previously: What a 243-Participant Study Found

The PUFFIN final analysis showed, per the primary analysis, that overall efficacy of pertuzumab plus trastuzumab and docetaxel was consistent with CLEOPATRA.

Breast cancer research and treatment • 2023-02-15 • Phase III Randomized Trial
N = 243 88/100 PMID 36463547 ↗
Can This Approach Help? Inside the Latest Research on Age on Clinical Outcomes and Efficacy of Adjuvant Dual Anti-HER2 Targeted

In patients with HER2-positive early BC treated with modern anticancer therapies, young age did not demonstrate either prognostic or predictive value, irrespective of hormone receptor status.

Journal of the National Cancer Institute • 2022-08-08 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 35512402 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Trastuzumab Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-67457847-2419
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $2.3900/unit (~$71.70/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $257.99 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 14 Anonymous DotMD Community Micro-Logs $105.30 / mo View logs ↓

Trastuzumab Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Trastuzumab RxNorm Concept ID RXN-67457847-2419 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $2.3900 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $257.99 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $105.30 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 91.00% Worth It (14 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Trastuzumab Patient Community, Cohort Filters & Dosage Logs

Cross-verified Trastuzumab (her2/neu receptor antagonist) monograph synthesizing RxNorm RXN-67457847-2419, openFDA FAERS signals, and $105.30–$257.99 cash benchmarks.

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 Trastuzumab community threads and patient logs by age, biological sex, dosage, and treatment duration.

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Recent Verified Anonymous Patient Micro-Logs (0)