Product Information
Olaparix 150MG (Olaparib) is a potent and selective PARP (Poly ADP-Ribose Polymerase) inhibitor indicated for patients with BRCA1 or BRCA2-mutated cancers, including ovarian, fallopian tube, primary peritoneal, breast, prostate, and pancreatic cancers. Olaparib works by blocking PARP1 and PARP2 enzymes, exploiting the DNA repair deficiency in BRCA-mutated tumour cells through the mechanism of synthetic lethality selectively inducing cancer cell death while sparing normal cells with intact DNA repair pathways. As part of Mediaid Pharmacy’s comprehensive oncology and specialty medicines portfolio, Olaparix gives patients access to this clinically proven cancer therapy at an affordable price. Olaparix 150mg is manufactured by Beacon Pharmaceuticals Ltd., Bangladesh and globally supplied by Mediaid Pharmacy with worldwide shipping.
Basic Product Information of Olaparix 150MG (Olaparib)
| Brand Name | Olaparix 150MG (Olaparib) |
| Generic Name | Olaparib INN |
| Drug Class | PARP Inhibitor (Poly ADP-Ribose Polymerase Inhibitor) |
| Available Strength | 150mg |
| Formulation | Film-Coated Tablet |
| Pack Size | 120 Tablets per Pot |
| Primary Indication | BRCA1/2-Mutated Ovarian Cancer, Breast Cancer, Prostate Cancer, and Pancreatic Cancer |
| Regulatory Approvals | USFDA Approved (Ovarian, Breast, Prostate, and Pancreatic Cancer). EMA Approved (Ovarian and Breast Cancer). |
| Originator Brand | Lynparza by AstraZeneca and MSD (Merck) |
| Manufacturer | Beacon Pharmaceuticals Ltd., Mymensingh, Bangladesh |
| Global Supplier | Mediaid Pharmacy Worldwide Shipping Available |
| Registration Date | 08/07/2021 |
| Storage Conditions | Store below 30°C in a dry place away from light and moisture. Keep out of the reach of children. |
How Olaparix 150MG (Olaparib) Works PARP Inhibition and Synthetic Lethality
Olaparib, the active ingredient in Olaparix 150MG, is a selective and potent inhibitor of Poly ADP-Ribose Polymerase enzymes PARP1 and PARP2. PARP enzymes are critical components of the base excision repair (BER) pathway the mechanism cancer cells rely upon to repair single-strand DNA breaks. In patients with germline or somatic BRCA1 or BRCA2 mutations, the homologous recombination (HR) DNA repair pathway is already defective, leaving tumour cells uniquely dependent on PARP-mediated repair for survival.
Olaparib blocks PARP1 and PARP2 activity and also traps PARP-DNA complexes at sites of single-strand DNA breaks, preventing repair and causing replication fork stalling. In BRCA-mutated cancer cells that cannot perform homologous recombination, this dual action produces irreparable double-strand DNA breaks, triggering apoptotic cancer cell death through the principle of synthetic lethality. Normal cells with intact BRCA function retain the ability to repair these breaks via homologous recombination, meaning Olaparib selectively destroys tumour cells while sparing healthy tissue. This targeted oncological mechanism underpins why Olaparix 150MG represents a precision medicine advance for BRCA-positive cancers. Mediaid Pharmacy’s oncology medicines catalogue covers a broad range of targeted therapies for multiple cancer types.
Unlike cytotoxic chemotherapy, which broadly damages all rapidly dividing cells, Olaparix exploits a specific molecular vulnerability in BRCA-deficient tumours. This selectivity translates into a clinically meaningful and well-characterised tolerability profile compared to conventional platinum-based chemotherapy regimens. In the SOLO-1 trial, Olaparib maintenance therapy demonstrated a progression-free survival (PFS) benefit of 36.0 months versus 13.8 months on placebo in newly diagnosed BRCA-mutated advanced ovarian cancer patients who achieved a complete or partial response to first-line platinum chemotherapy establishing Olaparib as the definitive standard-of-care PARP inhibitor in this setting.
Approved Indications for Olaparix 150MG (Olaparib)
Olaparix (Olaparib) 150mg is approved for the following clinical indications in adult patients with confirmed BRCA mutations:
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Ovarian, Fallopian Tube, and Primary Peritoneal Cancer Olaparib is USFDA and EMA approved as first-line maintenance therapy for adult patients with deleterious or suspected deleterious germline or somatic BRCA1/2-mutated advanced ovarian, fallopian tube, or primary peritoneal cancer who are in complete or partial response to first-line platinum-based chemotherapy. Olaparib is also approved for recurrent maintenance therapy following response to platinum-based chemotherapy, and as monotherapy in patients with germline BRCA-mutated, platinum-sensitive relapsed ovarian cancer. |
HER2-Negative BRCA-Mutated Breast Cancer USFDA and EMA approved for adult patients with deleterious or suspected deleterious germline BRCA1/2-mutated, HER2-negative locally advanced or metastatic breast cancer who have previously received chemotherapy in the neoadjuvant, adjuvant, or metastatic setting. Additionally approved as adjuvant therapy for patients with high-risk early-stage BRCA1/2-mutated HER2-negative breast cancer following standard neoadjuvant or adjuvant chemotherapy. |
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BRCA-Mutated Metastatic Prostate Cancer USFDA approved for adult patients with deleterious or suspected deleterious germline or somatic BRCA1/2-mutated metastatic castration-resistant prostate cancer (mCRPC) who have progressed following prior treatment with enzalutamide or abiraterone. Olaparib targets the homologous recombination repair deficiency that drives treatment resistance in these patients. |
BRCA-Mutated Metastatic Pancreatic Cancer USFDA approved as maintenance therapy for adult patients with deleterious or suspected deleterious germline BRCA1/2-mutated metastatic pancreatic adenocarcinoma whose disease has not progressed on at least 16 weeks of a first-line platinum-based chemotherapy regimen. Olaparib is the first PARP inhibitor approved for pancreatic cancer maintenance. |
Key Clinical Benefits of Olaparix (Olaparib) 150MG
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Oral Once-Daily Targeted Therapy Olaparix is taken orally twice daily (two 150mg tablets in the morning and two in the evening), eliminating the need for intravenous chemotherapy infusions. This convenient oral administration supports long-term maintenance therapy and improves patient quality of life compared to cytotoxic IV regimens. |
Multi-Cancer USFDA and EMA Approval Olaparib carries USFDA approval across four distinct cancer types ovarian, breast, prostate, and pancreatic and EMA approval for ovarian and breast cancers, making Olaparix one of the most comprehensively approved oncology agents available in a single oral formulation for BRCA-mutated malignancies. |
Clinically Proven Progression-Free Survival Benefit In the landmark SOLO-1 trial, Olaparib maintenance therapy achieved a median PFS of 36.0 months versus 13.8 months on placebo in newly diagnosed BRCA-mutated advanced ovarian cancer a 70% reduction in risk of disease progression or death. The OlympiAD trial confirmed significant PFS benefit in BRCA-mutated metastatic breast cancer versus standard chemotherapy. |
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Affordable Generic Alternative to Lynparza Olaparix 150mg contains the same active ingredient as Lynparza (AstraZeneca and MSD) at a substantially lower cost. Patients in developing and developed markets access the same validated PARP inhibition mechanism without the financial burden of originator pricing, improving treatment access and adherence across long-term maintenance regimens. |
Bevacizumab Combination Option for Ovarian Cancer Olaparib is approved in combination with Bevacizumab as first-line maintenance therapy for patients with HRD-positive advanced ovarian cancer following response to first-line platinum-taxane chemotherapy with Bevacizumab, expanding its utility beyond BRCA mutation status in ovarian cancer management. |
WHO-GMP and cGMP Certified Manufacturing Produced by Beacon Pharmaceuticals Ltd. under strict WHO-GMP, cGMP, and ISO-certified manufacturing standards. Every batch of Olaparix meets consistent quality, safety, and bioequivalence requirements validated for international export to Asia, Africa, Europe, and Latin America. |
How to Take Olaparix 150MG (Olaparib) Dosage Guidelines
Route of Administration: Oral taken by mouth with or without food at any consistent time of day. Tablets should be swallowed whole and not crushed, dissolved, or chewed.
Standard Adult Dose: 300mg (two 150mg tablets) twice daily, equivalent to a total daily dose of 600mg. The standard dose applies across all approved cancer indications ovarian, breast, prostate, and pancreatic cancer.
Renal Impairment: Patients with mild renal impairment (CrCl 51–80 mL/min) do not require dose adjustment. For patients with moderate renal impairment (CrCl 31–50 mL/min), the recommended dose is reduced to 200mg (two 100mg tablets) twice daily. Olaparib is not recommended in patients with severe renal impairment (CrCl <30 mL/min) due to insufficient data.
Hepatic Impairment: No dose adjustment is required for patients with mild hepatic impairment (Child-Pugh Class A). Olaparib is not recommended in patients with moderate or severe hepatic impairment (Child-Pugh Class B or C) due to lack of safety and pharmacokinetic data.
CYP3A Inhibitor Co-Administration: The concurrent use of strong or moderate CYP3A inhibitors (such as itraconazole, clarithromycin, or fluconazole) must be avoided. If co-administration with a moderate CYP3A inhibitor is unavoidable, the Olaparib dose should be reduced to 100mg twice daily. Strong CYP3A inducers (such as rifampicin, carbamazepine, or St. John’s Wort) must be avoided as they significantly reduce Olaparib plasma concentrations and efficacy.
Dose Interruption and Reduction for Adverse Reactions: If a patient experiences haematological or non-haematological toxicity, treatment may be interrupted and then resumed at a reduced dose of 250mg (one 150mg tablet and one 100mg tablet) twice daily, and further reduced to 200mg twice daily if required.
Paediatric Use: The safety and efficacy of Olaparib in patients under 18 years of age have not been established. Use is not recommended in the paediatric population.
Clinical Monitoring Requirements During Olaparix Treatment
Regular clinical monitoring is mandatory throughout Olaparix (Olaparib) treatment. Oncologists and haematologists must monitor patients for haematological toxicities, as Olaparib commonly causes anaemia, thrombocytopenia, neutropenia, and leukopenia requiring close blood count surveillance. Monitoring parameters include Complete Blood Count (CBC) before treatment initiation, monthly for the first 12 months of treatment, and periodically thereafter; renal function assessed via serum creatinine and estimated GFR at baseline and during dose adjustment; and clinical assessment for signs of Myelodysplastic Syndrome (MDS) or Acute Myeloid Leukaemia (AML) patients who develop MDS or AML confirmed by specialist haematology evaluation must discontinue Olaparix permanently. Patients should also be monitored for signs and symptoms of Pneumonitis, a rare but potentially serious pulmonary adverse reaction requiring treatment interruption and investigation if suspected.
Drug Interactions and Important Safety Information for Olaparix
Concomitant use of Olaparix with strong or moderate CYP3A inhibitors including itraconazole, ketoconazole, clarithromycin, erythromycin, verapamil, and grapefruit or Seville orange juice must be avoided wherever possible, as CYP3A inhibition significantly increases Olaparib plasma concentrations and associated toxicity risk. If a moderate CYP3A inhibitor cannot be avoided, the Olaparib dose must be reduced to 100mg twice daily, with careful monitoring.
Strong or moderate CYP3A inducers such as rifampicin, phenytoin, carbamazepine, and St. John’s Wort must be strictly avoided during Olaparix therapy. These agents markedly decrease Olaparib plasma concentrations and are expected to substantially reduce efficacy. Patients should inform their oncologist of all medications, supplements, and herbal products before initiating Olaparix. Co-administration with other DNA-damaging agents or myelosuppressive medicines increases the risk of additive haematological toxicity and should only be considered under specialist supervision.
Side Effects and Precautions of Olaparix 150MG (Olaparib)
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Common Side Effects Anaemia (low red blood cell count) Nausea and vomiting Fatigue and asthenia Neutropenia and leukopenia Thrombocytopenia (low platelet count) Diarrhoea and abdominal pain Headache and dizziness Decreased appetite Dysgeusia (altered taste sensation) |
Serious Warnings and Precautions Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukaemia (AML) rare but serious haematological malignancies requiring permanent discontinuation if confirmed. Pneumonitis rare but potentially fatal lung inflammation. Interrupt treatment immediately if pneumonitis is suspected; discontinue permanently if confirmed. Venous Thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE) has been reported. Use with caution in patients with high thrombotic risk. Not recommended during pregnancy or breastfeeding. Effective contraception is required during treatment and for at least six months after the final dose for female patients, and for three months for male patients. Avoid concomitant use with strong or moderate CYP3A inhibitors or inducers; strong CYP3A inducers markedly reduce Olaparib plasma concentrations and efficacy. |
Who Should Use Olaparix 150MG (Olaparib)?
Olaparix is indicated for adult patients diagnosed with BRCA1 or BRCA2-mutated cancers specifically advanced or recurrent ovarian, fallopian tube, or primary peritoneal cancer; HER2-negative locally advanced or metastatic breast cancer; metastatic castration-resistant prostate cancer (mCRPC); and metastatic pancreatic adenocarcinoma as detailed in the approved indications above. All patients must undergo validated BRCA mutation testing using an approved companion diagnostic before initiating Olaparib, as treatment is indicated only for those with confirmed deleterious or suspected deleterious germline or somatic BRCA1/2 mutations. Olaparix is prescribed exclusively by oncologists and specialist physicians with expertise in managing hereditary cancers and targeted oncology therapies. A full pre-treatment medical assessment including complete blood count (CBC), renal function, hepatic function, and BRCA biomarker testing is mandatory before initiating therapy. For patients whose treatment plans extend across multiple oncology agents, Mediaid Pharmacy’s oncology specialty medicines portfolio provides a comprehensive range of targeted cancer therapies to support multidisciplinary oncology management.
Manufacturer: Beacon Pharmaceuticals Ltd., Bangladesh
Beacon Pharmaceuticals Ltd. is a leading pharmaceutical manufacturer based in Mymensingh, Bangladesh and the number one oncology and specialty medicine company in the country. Beacon was the first company in Bangladesh to export cancer drugs and currently exports to markets across Asia, Africa, Europe, and Latin America. With more than 200 generic drugs and 65 oncology products in its portfolio, Beacon operates under strict WHO-GMP, cGMP, and ISO-certified manufacturing standards. Olaparix 150MG (Olaparib) is one of Beacon’s internationally recognised precision oncology products, offering a high-quality, bioequivalent, and affordable alternative to Lynparza by AstraZeneca and MSD at a fraction of the originator cost. Every batch exported by Beacon meets the quality benchmarks required for approval in regulated international markets.
Global Supplier: Mediaid Pharmacy Worldwide Shipping for Olaparix (Olaparib)
Mediaid Pharmacy is a trusted global supplier of specialty, autoimmune, and oncology medications. Olaparix (Olaparib) 150mg is available through Mediaid Pharmacy with reliable worldwide shipping to South Asia, the Middle East, Africa, Europe, and beyond. Our team provides full order support including pricing, availability confirmation, documentation, and delivery tracking. Contact Mediaid Pharmacy directly via WhatsApp, phone, or WeChat for enquiries.
Why Choose Olaparix (Olaparib) from Mediaid Pharmacy?
Olaparix represents a clinically proven advance in precision oncology for patients with BRCA-mutated cancers. As the generic bioequivalent of Lynparza by AstraZeneca and MSD, Olaparix delivers the same active ingredient Olaparib with the same validated PARP1 and PARP2 inhibition mechanism and synthetic lethality in BRCA-deficient tumours, at a dramatically more affordable price point. Manufactured by the internationally trusted Beacon Pharmaceuticals Ltd. under WHO-GMP and cGMP standards, and distributed globally by Mediaid Pharmacy with worldwide shipping, Olaparix gives patients and oncologists access to high-quality targeted cancer therapy without the financial barrier of brand-name pricing. For patients whose comprehensive treatment plans also require additional targeted therapies or supportive cancer medicines, Mediaid Pharmacy’s oncology medicines section provides a comprehensive range of specialty oncology products sourced from verified manufacturers. For any patient or oncologist seeking a proven, affordable, and globally accessible Olaparib treatment option, Olaparix from Mediaid Pharmacy is the trusted choice.
Frequently Asked Questions About Olaparix 150MG (Olaparib)
What is Olaparix 150MG (Olaparib) used for?
Olaparix 150mg (Olaparib) is a PARP inhibitor used to treat BRCA1 or BRCA2-mutated cancers. Approved indications include: advanced ovarian, fallopian tube, and primary peritoneal cancer (first-line maintenance, recurrent maintenance, and monotherapy in platinum-sensitive relapsed disease); HER2-negative locally advanced or metastatic breast cancer with germline BRCA1/2 mutations; high-risk early-stage BRCA-mutated HER2-negative breast cancer (adjuvant); BRCA-mutated metastatic castration-resistant prostate cancer; and BRCA-mutated metastatic pancreatic adenocarcinoma (maintenance). Olaparib works by blocking PARP enzymes and trapping PARP-DNA complexes, inducing lethal DNA damage in BRCA-deficient cancer cells through synthetic lethality.
What is the correct dose of Olaparix (Olaparib)?
The standard dose of Olaparix is 300mg (two 150mg tablets) taken twice daily once in the morning and once in the evening for a total daily dose of 600mg. Olaparix tablets are taken orally with or without food and should be swallowed whole. For patients with moderate renal impairment (CrCl 31–50 mL/min), the dose is reduced to 200mg twice daily. If moderate CYP3A inhibitors cannot be avoided, the dose is reduced to 100mg twice daily. Always follow your prescribing oncologist’s exact dosing instructions.
What strength and pack size is Olaparix (Olaparib) available in?
Olaparix is available as 150mg film-coated tablets supplied in a pot of 120 tablets. The 150mg tablet strength is taken as two tablets twice daily to achieve the standard 300mg twice-daily dose. The 120-tablet pot provides a one-month supply at the standard dosing regimen, supporting convenient dispensing for long-term maintenance therapy.
Is Olaparix the same as Lynparza (Olaparib by AstraZeneca)?
Yes. Olaparix is the generic equivalent of Lynparza. Both products contain the same active ingredient Olaparib in the same 150mg film-coated tablet dosage form. Olaparix is manufactured by Beacon Pharmaceuticals Ltd. in Bangladesh under WHO-GMP-certified conditions and delivers the same clinical mechanism of PARP1 and PARP2 inhibition and synthetic lethality in BRCA-mutated tumour cells as Lynparza, at a significantly lower cost. This makes Olaparix a financially accessible long-term maintenance treatment option for patients worldwide.
What are the side effects of Olaparix (Olaparib)?
Common side effects of Olaparix include anaemia, nausea, vomiting, fatigue, neutropenia, thrombocytopenia, diarrhoea, headache, decreased appetite, and dysgeusia (altered taste). Serious but less frequent risks include Myelodysplastic Syndrome (MDS), Acute Myeloid Leukaemia (AML), pneumonitis, and venous thromboembolism (VTE). Routine CBC monitoring is mandatory during treatment. Always consult your oncologist for a complete individual risk-benefit assessment before and during treatment.
Does Olaparix require a BRCA test before treatment?
Yes. All patients must have a confirmed deleterious or suspected deleterious BRCA1 or BRCA2 mutation detected by an approved validated companion diagnostic before initiating Olaparix therapy. BRCA testing may be performed on blood (germline testing) or tumour tissue (somatic testing) depending on the cancer indication. Your oncologist will arrange appropriate biomarker testing prior to prescribing Olaparix.
Is Olaparix (Olaparib) safe during pregnancy or while breastfeeding?
No. Olaparix is not recommended during pregnancy or breastfeeding due to potential embryotoxic and teratogenic risks. Female patients of childbearing potential must use highly effective contraception during the full course of Olaparix treatment and for at least six months after the final dose. Male patients with female partners of childbearing potential must use effective contraception during treatment and for three months after the final dose. Consult your oncologist before starting treatment if you are pregnant, planning to become pregnant, or currently breastfeeding.
Can I order Olaparix 150MG (Olaparib) online with worldwide shipping?
Yes. Mediaid Pharmacy supplies Olaparix (Olaparib) 150mg to patients and healthcare providers globally with worldwide shipping. Contact Mediaid Pharmacy via WhatsApp, phone, or WeChat at +8801773428128, or send an email enquiry to info@mediaidpharmacy.com for pricing, stock availability, and delivery details for your country.
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