Niranib 100 mg (Generic Niraparib) โ€“ Everest Pharmaceuticals

Product Name: Niranib

Generic Name: Niraparib

Brand Name: Zejula

Strength: 100mg

  • Medically Reviewes by Dr. Daria Kwaล›niewska
  • WHO-GMP standards
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Description

DK
Dr. Daria Kwaśniewska ESMO Certified Consultant Medical Oncologist
Reviewed June 2026
⚠ Prescription required. For informational purposes only. Meds For Cancer is a Named Patient Program facilitator — not a retail pharmacy. A valid oncologist prescription is mandatory before any order is processed.

Is Niranib 100 mg right for your situation?

Review these criteria with your oncologist before enquiring
✔ You may be a candidate if
  • Recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer in response to platinum-based chemotherapy
  • Need a maintenance therapy started within 8 weeks of your most recent platinum-containing regimen
  • Need a WHO-GMP generic alternative to Zejula® (GSK)
  • Hold a valid oncologist prescription
✖ May NOT be suitable if
  • Disease has not responded to platinum-based chemotherapy
  • Pre-existing myelodysplastic syndrome (MDS) or acute myeloid leukaemia (AML)
  • Pregnant, planning pregnancy, or breastfeeding
  • Severe pre-existing hypertension without medical management

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Prescription required · Named Patient Program · Worldwide shipping

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What is Niranib 100 mg?

Niranib 100 mg is a generic formulation of Niraparib — a PARP (Poly ADP-ribose Polymerase) inhibitor — manufactured by Everest Pharmaceuticals Ltd. under WHO-GMP certified conditions in Bangladesh. Each capsule contains 100 mg of niraparib tosylate monohydrate, the same active molecule found in Zejula® (GSK), and is dispensed under the Named Patient Program for patients requiring an affordable, quality-assured alternative.

Unlike olaparib, niraparib is approved for maintenance therapy regardless of BRCA mutation status — making it usable across a broader patient population, including those without a BRCA mutation.

Generic nameNiraparib
Reference brandZejula® (GSK)
ManufacturerEverest Pharmaceuticals Ltd.
StandardWHO-GMP Certified
Drug classPARP Inhibitor
Dosage formCapsule — 100 mg
Pack size30 capsules per pack
RouteOral · once daily
PrescriptionRequired — oncologist only

How Niraparib Works

PARP enzymes help cells repair single-strand DNA breaks. Cancer cells — particularly those with HRR deficiency such as BRCA mutations — rely on PARP as a critical backup repair pathway. Niraparib inhibits PARP1 and PARP2, preventing this repair and causing the accumulation of DNA damage that ultimately leads to cancer cell death.

A key distinguishing feature of niraparib is its demonstrated benefit in the maintenance setting regardless of BRCA mutation or homologous recombination deficiency (HRD) status — making it the broadest-indicated PARP inhibitor for ovarian cancer maintenance therapy. In the PRIMA trial, niraparib maintenance significantly improved progression-free survival across the overall population, including patients without HRD. NCCN guidelines list niraparib as a recommended maintenance option following response to platinum-based chemotherapy in recurrent and newly diagnosed advanced ovarian cancer. View NCCN Ovarian Cancer Guidelines →

What to Expect: First 30 Days

Niraparib has a distinct early side-effect profile compared to other PARP inhibitors — blood pressure and platelet monitoring are especially important in the first month.

  • Week 1: Nausea and fatigue are the most common early symptoms. Taking the dose at bedtime is often recommended specifically to help manage nausea.
  • Weeks 2–3: Weekly blood counts begin — particularly platelet counts, which can drop more significantly with niraparib than with other PARP inhibitors. Blood pressure monitoring also begins during this window.
  • Week 4: Weekly blood monitoring continues through the first month, transitioning to monthly checks for the remainder of the first year if counts remain stable.

Side Effects

Niraparib’s side-effect profile includes more pronounced platelet and blood pressure effects compared to other PARP inhibitors, requiring closer early monitoring.

Common · Usually Manageable

  • Nausea and vomiting
  • Fatigue
  • Constipation
  • Decreased appetite
  • Headache
  • Insomnia
  • Dry mouth or altered taste

Serious · Report Immediately

  • Thrombocytopenia (low platelet count)
  • Myelodysplastic syndrome (MDS) / acute myeloid leukaemia (AML)
  • Severe hypertension or hypertensive crisis
  • Pneumonitis (lung inflammation)
  • Posterior reversible encephalopathy syndrome (PRES) — rare
⚠ Call your doctor immediately if you experience:
  • Unusual bruising, bleeding gums, or blood in stool or urine (possible low platelets)
  • Severe headache, confusion, or vision changes (possible severe hypertension or PRES)
  • New or worsening breathlessness, dry cough, or fever

How to Take Niranib 100 mg

Standard dose: 300 mg (three 100 mg capsules) once daily, with or without food. Some patients with lower body weight or platelet counts may start at a reduced dose — follow your oncologist’s specific prescription.

  • 1
    Once daily, at approximately the same time each day — not twice daily. Bedtime dosing can help manage nausea.
  • 2
    Swallow capsules whole with water. Do not chew or crush.
  • 3
    If you vomit or miss a dose, do not take an additional dose — resume at your next scheduled time.
  • 4
    Monitor blood pressure regularly as advised by your oncologist — niraparib can cause hypertension.
  • 5
    Storage: below 30°C, protected from moisture, light, and out of reach of children. Do not use if exposed to temperatures above 40°C.

Caregiver Guidance

  • Watch for bleeding or bruising — niraparib can cause significant platelet drops. Unusual bruising, bleeding gums, or blood in urine/stool should be reported promptly.
  • Track weekly blood pressure and blood counts — especially during the first month, when monitoring is most frequent.
  • Confirm once-daily dosing — niraparib is taken once a day, not twice. Help establish a consistent bedtime routine to support adherence and manage nausea.

If the Medicine Stops Working

Resistance to niraparib, similar to other PARP inhibitors, can develop through restoration of homologous recombination repair function or through other compensatory DNA repair mechanisms. If disease progression is detected on routine imaging or tumour marker monitoring, your oncologist will reassess treatment options — which may include a switch to chemotherapy, a different targeted therapy, or enrolment in a clinical trial, depending on your prior treatment history and disease status.

Frequently Asked Questions

Do I need a BRCA test before starting Niranib?
Unlike olaparib, niraparib is approved as maintenance therapy regardless of BRCA mutation status. This means it can be prescribed for a broader range of patients who have responded to platinum-based chemotherapy, even without a confirmed BRCA mutation. Your oncologist will still confirm the appropriate clinical setting before prescribing.
Is Niranib taken once or twice daily?
Niranib is taken once daily — three 100 mg capsules (300 mg total) at approximately the same time each day. This is different from olaparib, which is taken twice daily. Bedtime dosing is often recommended to help manage nausea.
Why is blood pressure monitoring important with Niranib?
Niraparib carries a notable risk of hypertension, including severe cases, more so than some other PARP inhibitors. Regular blood pressure monitoring, especially in the early months, allows your care team to detect and manage rising blood pressure before it becomes a serious problem.
How soon after chemotherapy should I start Niranib?
Treatment with niraparib should generally start no later than 8 weeks after your most recent platinum-containing chemotherapy regimen. Your oncologist will time this carefully to maximise the maintenance benefit.
What blood monitoring will I need?
Complete blood counts are monitored weekly for the first month of treatment, then monthly for the next 11 months, and periodically thereafter. This monitors for thrombocytopenia (low platelets), anaemia, and neutropenia, which require dose adjustment if detected.
How do I order Niranib through Meds For Cancer?
Contact us via WhatsApp (+880 130 449 8958) or email (info@medsforcancer.com) with your oncologist’s prescription. Our team will verify the prescription, confirm availability and pricing for your country, and arrange secure international shipping under the Named Patient Program.
🛡 Named Patient Program — Regulatory Framework

Meds For Cancer operates as a Named Patient Program (NPP) facilitator. Under this framework, WHO-GMP certified medicines are made available to individual patients with a confirmed medical need and a valid oncologist prescription, in countries where the branded product is unavailable or unaffordable.

This service does not constitute retail pharmacy dispensing. A prescription review is mandatory before any order is processed.

Clinical References
  • Gonzalez-Martin A, et al. Niraparib in patients with newly diagnosed advanced ovarian cancer (PRIMA). NEJM 2019;381:2391–2402.
  • Mirza MR, et al. Niraparib maintenance therapy in platinum-sensitive recurrent ovarian cancer (NOVA). NEJM 2016;375:2154–2164.
  • NCCN Clinical Practice Guidelines in Oncology: Ovarian Cancer. V3.2026.
  • Moore KN, et al. Niraparib monotherapy for late-line treatment of ovarian cancer (QUADRA). Lancet Oncol 2019;20:636–648.

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