Gemcitabine (dFdC) is metabolized inside cells to its active forms, diphosphate (dFdCDP) and triphosphate (dFdCTP) nucleosides. Its mechanism involves:
Small amounts may also integrate into RNA. Gemcitabine’s incorporation into DNA causes the termination of chain growth after one additional nucleotide.
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Non-Small Cell Lung Cancer (NSCLC):
- First-line therapy: Cytogem, combined with Cisplatin, is used for patients with locally advanced (inoperable Stage IIIA or IIIB) or metastatic (Stage IV) NSCLC.
- Palliative treatment: Suitable for adult patients with locally advanced or metastatic NSCLC.
Pancreatic Cancer:
- Treats adult patients with locally advanced or metastatic adenocarcinoma of the pancreas.
- Indicated for patients with pancreatic cancer refractory to 5-FU therapy.
Bladder Cancer:
- Treats advanced bladder cancer (muscle-invasive Stage IV tumors with or without metastases) in combination with Cisplatin.
Breast Cancer:
- Used with Paclitaxel to treat metastatic breast cancer in patients who relapsed after adjuvant or neoadjuvant chemotherapy. Previous treatment should include anthracyclines unless contraindicated.
Ovarian Cancer:
- In combination with Carboplatin, treats recurrent epithelial ovarian carcinoma in patients relapsing after platinum-based therapy.
(Use only as advised by a registered physician.)
Cytogem IV Infusion works by interfering with DNA synthesis. It blocks the production of new DNA, by locking itself into the DNA strands and inhibiting any further proliferation or growth of the cell. Hence, Cytogem IV Infusion has widespread application in the field of oncology (cancer-related medicine) and chemotherapy.
Cancer is the uninhibited and uncontrolled growth of cells in the body, leading to the formation of tumors or abnormal cell clusters that can invade and damage surrounding tissues or spread to other parts of the body (metastasis).
Cytogem is a cytotoxic anti-cancer medication that is used alone or in combination with other anti-cancer drugs to treat various types of cancers, including:
No antidote is available. Overdoses may lead to myelosuppression, paresthesias, or severe rash. Patients should receive supportive care and regular blood count monitoring.
Insufficient safety and efficacy data.
Use cautiously as data on these populations are limited.
No confirmed drug interactions are reported, and no specific studies have been conducted.
Not to be used in patients with known hypersensitivity to Gemcitabine or any of its components.
Gemcitabine should not be used during pregnancy unless necessary. It is unknown if Gemcitabine is excreted in breast milk; use it with caution in breastfeeding.
Avoid in children due to limited safety data.
Store vials at 20°–25°C in the original carton, away from light. Do not refrigerate to prevent crystallization. Keep out of reach of children.
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At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.