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lynparza olaparib tablets 150mg 56tablets per box

Description

 Indication & Scope

Olaparib Tablets (Lynparza®) is a potent oral PARP inhibitor. It blocks PARP-mediated DNA single-strand break repair, inducing synthetic lethality in tumor cells with defective homologous recombination repair (BRCA/HRD mutation) and inhibiting tumor proliferation.

  • Mechanism
    Poly (ADP-ribose) polymerase (PARP) inhibitor
  • Drug class
    Prescription oral targeted anticancer drug
  • Clinical use
    HRD/BRCA-mutated ovarian, breast and prostate cancer
Specification
Generic Name Olaparib Tablets
Brand Name Lynparza®
Ingredient Olaparib
Dosage Form Film-coated Tablets
Package 150mg*56 tablets/box
Conditions Treated Maintenance treatment for adults with BRCA-mutated advanced epithelial ovarian, fallopian tube or primary peritoneal cancer after first-line platinum chemotherapy response. Metastatic BRCA-mutated HER2-negative breast cancer
Taboos Pregnant and breastfeeding women; Patients hypersensitive to olaparib or any excipients
Place of origin Puerto Rico, United States; Gärtunavägen Södertälje, Sweden
Priscription Type Prescription Drug
Storage Conditions Sealed, store below 30°C, protected from light
Manufacturer AbbVie Limited; AstraZeneca AB
Registration Authority National Medical Products Administration (NMPA)
Approval number HJ20180049
Approval Date December 25, 2024
Shelf Life 36 months

How to use ?

Recommended Dose: Standard dosage regimen: 300 mg orally twice daily (150mg × 2 tablets each time). Take continuously until disease progression or intolerable toxicity.

 

Time: Fixed twice daily oral administration, taken with or without food.

 

Interaction: Strong CYP3A4 inhibitors significantly increase olaparib exposure, dose reduction is mandatory. Strong CYP3A4 inducers reduce drug efficacy, concurrent use forbidden.

 

Side effects: Common reactions: Anemia, neutropenia, thrombocytopenia, fatigue, nausea, vomiting, diarrhea, arthralgia, headache. Long-term risks: Myelodysplastic syndrome/acute myeloid leukemia, pneumonitis, elevated creatinine. Rare severe adverse events: Severe hypersensitivity, venous thromboembolism.

Important Notice

This product shall only be used for post-exposure rabies prophylaxis by professional medical staff. It must be applied combined with rabies vaccine and injected via wound infiltration plus intramuscular routes as specified. Do not administer intravenously or alter the dosage at will. Hypersensitivity monitoring is required throughout the whole injection process.

Packaging & Shipping

Packaging

Original manufacturer’s packaging with secure export carton. Customized export packaging is available upon request.

Shipping Methods

Express Courier (EMS, DHL, FedEx, UPS), Air Freight, and Sea Freight. Cold-chain transportation is available for products requiring temperature-controlled logistics.

Export Support

Certificate of Analysis

GMP Certificate

Commercial Invoice

Packing List & CPP

Cold Chain Logistics

Customs Documentation

Scientific and regulatory sources

1.WHO References
2.NMPA
3.FDA
4.EMA

FAQ

What is the core pharmacological classification of olaparib?

Oral PARP inhibitor targeting DNA damage repair.

Until when should patients continue olaparib maintenance treatment?

Continuous twice-daily administration until tumor progression or unendurable toxicity.

What fatal rare adverse event should patients report immediately?

New or worsening cough/dyspnea suggestive of pneumonitis.

Does food affect olaparib absorption?

No, patients can take tablets before or after meals.

Lynparza® | Olaparib Tablets | Epithelial Ovarian Cancer | DengYueRX

INN: Olaparib
Indications: Epithelial Ovarian Cancer
Dosage Form: Film-coated Tablets
Strength: 150mg/Tablet

Original price was: $887.04.Current price is: $753.98.

Low MOQ

WHO-GMP

Worldwide Delivery

Compliance and Regulatory Documents

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