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Expert perspectives

ZEJULA is the only approved 1L once-daily maintenance for patients with aOC.^1–3 Explore videos from world-leading oncologists on their experience of using ZEJULA in clinical practice.

ZEJULA in BRCAm patients

Dr Domenica Lorusso discusses ZEJULA in BRCAm patients.

WATCH HERE

ZEJULA in HRd BRCAwt patients

Dr Bradley Monk discusses ZEJULA in HRd BRCAwt patients.

WATCH HERE

Impact on patient experience

Dr Bradley Monk discusses ZEJULA patient benefits beyond efficacy.

WATCH HERE

Contact your local representative to hear more about ZEJULA.

REQUEST A REP VISIT

All imagery shown depicts hypothetical patients only.

Zejula Safety Information¹:

Contraindications:
Hypersensitivity to the active substances or to any of the excipients.

Special warnings and precautions:
Haematologic adverse reactions (thrombocytopenia, anaemia, neutropenia) have been reported. Discontinue if a patient develops severe persistent haematologic toxicity including pancytopenia that does not resolve within 28 days following interruption.
Use with caution in patients on anticoagulants and medicinal products known to reduce the thrombocyte count hypertension, hepatic impairment.

Pregnancy/contraception:
Should not be used during pregnancy or in women of childbearing potential.

Adverse Events:
Very common: Urinary Tract Infections, thrombocytopenia, anaemia, neutropenia, leukopenia, decreased appetite, insomnia.

Please refer to the local prescribing information for a more detailed safety information.

Abbreviations

1L, first-line; aOC, advanced ovarian cancer; BRCA, breast cancer susceptibility gene; BRCAm, BRCA-mutation; BRCAwt, BRCA wild-type; HRd, homologous recombination deficient.

References

Zejula Prescribing Information
Lynparza (olaparib). Summary of Product Characteristics.
Rubraca (rucaparib). Summary of Product Characteristics.

For more information, please refer to the prescribing information or contact GlaxoSmithKline via gcc.medinfo@gsk.com
To report Adverse Event/s associated with the use of GSK product/s, please contact us via
gulf.safety@gsk.com
To report quality complaint/s associated with the use of GSK product/s, please contact us via
Gulf.ProductQualityComplaints@gsk.com

Department of Pharmacovigilance & Drug Information
Directorate General of Pharmaceutical Affairs & Drug Control
Ministry of Health, Sultanate of Oman
Phone Nos. 0096822357687 / 0096822357686
Fax: 0096822358489
Email: pharma-vigil@moh.gov.om
Website: www.moh.gov.om

دائرة التيقظ و المعلومات الدوائية
المديرية العامة للصيدلة و الرقابة الدوائية
وزارة الصحة, سلطنة عمان
0096822357687 / 0096822357686 :هاتف
0096822358489 :فاكس
pharma-vigil@moh.gov.om :البريد الالكتروني
www.moh.gov.om :الموقع الالكتروني

PM-RCH-NRP-SRCH-240001 | April 2024