π© Olaparix 50 mg
Generic Name: Olaparib
Brand Name: Olaparix
Manufacturer: Beacon Pharmaceuticals Ltd.
Dosage Form & Strength: Capsules, 50 mg
Therapeutic Class: Anticancer | PARP Inhibitor
π Indications:
Olaparix (Olaparib) is an oral targeted anticancer therapy indicated for:
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Ovarian Cancer β maintenance treatment in adult patients with BRCA-mutated, platinum-sensitive recurrent ovarian, fallopian tube, or primary peritoneal cancer.
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Breast Cancer β treatment of HER2-negative, germline BRCA-mutated metastatic breast cancer.
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Pancreatic Cancer β maintenance treatment of metastatic pancreatic adenocarcinoma with BRCA mutations.
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Prostate Cancer β metastatic castration-resistant prostate cancer (mCRPC) with HRR (homologous recombination repair) gene mutations including BRCA1/2.
π Pharmacology:
Olaparix contains Olaparib, a poly (ADP-ribose) polymerase (PARP) inhibitor.
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PARP enzymes are essential for repairing single-strand DNA breaks.
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In BRCA-mutated cells, homologous recombination repair is defective.
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Inhibition of PARP leads to accumulation of DNA damage, causing cancer cell death (synthetic lethality).
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Normal cells with intact DNA repair are less affected, making Olaparix a precision medicine for BRCA-related cancers.
π Dosage & Administration:
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Recommended Dose: 300 mg orally twice daily (total 600 mg/day).
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Since Olaparix 50 mg capsules are available, dose adjustments may be required based on patient profile.
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Swallow capsules whole; do not chew or crush.
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Continue until disease progression or unacceptable toxicity.
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Dose reductions may be necessary for toxicity management.
β οΈ Precautions & Warnings:
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Myelosuppression: Monitor complete blood counts (CBC) at baseline and monthly. May cause anemia, neutropenia, thrombocytopenia.
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MDS/AML: Rare cases of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) have been reported.
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Pneumonitis: Monitor for unexplained cough, fever, or dyspnea.
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Drug Interactions: Avoid strong CYP3A inhibitors/inducers.
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Liver & Kidney Function: Dose adjustment may be required in moderate hepatic/renal impairment.
β Contraindications:
π€° Pregnancy & Lactation:
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Pregnancy: Contraindicated β may cause fetal harm. Women of childbearing potential should use effective contraception during treatment and for 6 months after last dose.
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Breastfeeding: Not recommended during therapy and for 1 month after last dose.
βοΈ Side Effects:
Common:
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Nausea, vomiting, loss of appetite
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Fatigue, weakness
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Anemia, low blood counts
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Diarrhea or constipation
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Headache, dizziness
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Dysgeusia (altered taste)
Serious:
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Myelosuppression (anemia, neutropenia, thrombocytopenia)
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MDS/AML
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Pneumonitis
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Secondary malignancies (rare)
π§ Storage Conditions: