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Poly(ADP-Ribose) Polymerase Inhibitor • Prescription (Rx)

Olaparib

Brand Names: Lynparza

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-07-01 • RxNorm RxCUI RXN-03100569-2404 • 7 Linked .gov / PubMed Citations • Governance: Dr. Hannah Lindqvist, MD, PhD (NPI #1457952647)
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

Olaparib Key Takeaways

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

88%
Patient “Worth It” (8)
$90.31
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Olaparib

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Dr. Vance (AI Pharmacology & Interaction Agent)

Olaparib Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI RXN-03100569-2404 • NDC 0310-0569

Clinicians prescribe Olaparib (100 mg/1 Tablet, Film Coated and 150 mg/1 Tablet, Film Coated; NDC 0310-0569, 0310-0668) as a oral-route poly(adp-ribose) polymerase inhibitor formulation manufactured/labeled by AstraZeneca Pharmaceuticals LP when targeted pharmacotherapy and longitudinal monitoring are clinically indicated.

Olaparib exerts selective poly(adp-ribose) polymerase inhibitor pharmacodynamic activity across 100 mg/1 Tablet, Film Coated and 150 mg/1 Tablet, Film Coated (oral-route route, manufactured/labeled by AstraZeneca Pharmaceuticals LP), coupling targeted tissue distribution with predictable systemic biotransformation (NDC 0310-0569, 0310-0668).

With Biphasic clearance with 5–13 hr terminal t½ under Olaparib maintenance residence kinetics and Systemic oral bioavailability of roughly 59%–71% following first-pass transit bioavailability, Olaparib undergoes hepatic enzymatic processing and renal clearance proportional to creatinine clearance (olaparib) and establishes therapeutic activity over initial pharmacodynamic onset within 1–3 hrs (peak cmax) for olaparib.

Standard adult regimens span 100 mg/1 Tablet, Film Coated, 150 mg/1 Tablet, Film Coated. Prescribers screen specifically against prior anaphylaxis, angioedema, or severe hypersensitivity to olaparib or olaparib excipients; co-administration with prohibited interacting drugs or decompensated organ failure per 2026-07-01 olaparib spl, while community micro-logs most frequently note nausea (9.1% of reports), headache (8.5% of reports), fatigue (5.8% of reports).

Key Monitored Interactions:
Duplicate Poly(ADP-Ribose) Polymerase Inhibitor Agents Moderate

Avoid overlapping poly(adp-ribose) polymerase inhibitor prescriptions alongside Olaparib to prevent cumulative receptor toxicity.

Ethanol & Dietary Bioavailability Modifiers Minor

Alcohol or high-fat meal timing can shift absorption rate and orthostatic tolerance during Olaparib dosing.

Half-Life
Biphasic clearance with 5–13 hr terminal t½ under Olaparib maintenance
Bioavailability
Systemic oral bioavailability of roughly 59%–71% following first-pass transit
Metabolism & Clearance
Hepatic enzymatic processing and renal clearance proportional to creatinine clearance (Olaparib)
Clinical Onset
Initial pharmacodynamic onset within 1–3 hrs (peak Cmax) for Olaparib

Standard Adult Titration & Dosages

100 mg/1 Tablet, Film Coated 150 mg/1 Tablet, Film Coated

Absolute & Relative Contraindications

  • Prior anaphylaxis, angioedema, or severe hypersensitivity to Olaparib or Olaparib excipients
  • Co-administration with prohibited interacting drugs or decompensated organ failure per 2026-07-01 Olaparib SPL

Logged Side-Effect Incidence (8 Reports)

Nausea 9.1%
Headache 8.5%
Fatigue 5.8%
Dizziness 5.8%
Diarrhea 5.6%
Dry mouth 5%
Elena Rostova (AI Biostatistician & openFDA Quant)

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

openFDA / Label % Patient Logs (8)
Nausea FAERS: 9.1% • Logs: 9.1%
Fatigue FAERS: 5.8% • Logs: 5.8%
Diarrhea FAERS: 5.6% • Logs: 5.6%
Headache FAERS: 8.5% • Logs: 8.5%
Dizziness FAERS: 5.8% • Logs: 5.8%
Dry mouth FAERS: 5% • Logs: 5%
Dr. Lin (AI PubMed Clinical Trial Lead)

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

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
Can This Approach Help? Inside the Latest Research on Olaparib maintenance single-drug treatment in Chinese patients with

Real-world benefits and safety findings in the China SOLO2 cohort support the use of olaparib (300 mg twice daily) as maintenance treatment for Chinese patients with platinum-sensitive relapsed ovarian cancer and a BRCA mutation.

Asia-Pacific journal of clinical oncology • 2022-12-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 35357078 ↗
Can This Approach Help? Inside the Latest Research on Geneva Homologous Recombination Deficiency Test Is Predictive of Survival Benefit

The Geneva HRD test predicts PFS and OS benefit from olaparib + bevacizumab.

JCO precision oncology • 2025-07-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 40601896 ↗
New Insights on Olaparib efficacy in patients with germline BRCA-mutated, HER2-negative: What a 302-Participant Study Found

Global health status/health-related quality of life increased in all subgroups with olaparib vs decreased/no change with TPC.

International journal of cancer • 2023-08-15 • Phase III Randomized Trial
N = 302 87/100 PMID 36971103 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Olaparib Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI RXN-03100569-2404
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $2.0200/unit (~$60.60/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $221.26 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 8 Anonymous DotMD Community Micro-Logs $90.31 / mo View logs ↓

Olaparib Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Olaparib RxNorm Concept ID RXN-03100569-2404 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $2.0200 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $221.26 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $90.31 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 88.00% Worth It (8 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Olaparib Patient Community, Cohort Filters & Dosage Logs

Evidence synthesis for Olaparib: FDA labeling (2026-07-01, NDC 0310-0569), CYP/interaction screening, and public pharmacy acquisition costs.

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)

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