Antitumor agent.
It has cytostatic action which is associated with inhibition of DNA synthesis.
In the cell it is metabolized to active diphosphate and triphosphate nucleosides.
Diphosphate nucleosides inhibit the action of ribonucleotide reductase, with the participation of which deoxynucleoside triphosphates necessary for DNA synthesis are formed in the cell, which leads to a decrease in their concentration in the cell.
Triphosphate nucleosides actively compete for inclusion in the DNA chain and can also be incorporated into RNA.
After intracellular gemcitabine metabolites are incorporated into the DNA chain, one additional nucleotide is added to its growing strands, resulting in complete inhibition of further DNA synthesis and programmed cell death.
Indications
Non-small cell lung cancer (stages IIIa-IV); advanced pancreatic carcinomas.
Active ingredient
Composition
1 ml contains:
gemcitabine 10 mg
How to take, the dosage
It is set individually, depending on the indication and stage of the disease, the state of the hematopoiesis system, the scheme of anti-tumor therapy.
Interaction
The risk and severity of leukopenia and thrombocytopenia increases after prior cytostatic therapy.
Special Instructions
It has some activity in advanced breast, ovarian, renal, bladder and prostate cancer, small cell lung cancer.
With caution it is used in patients with disorders of hematopoiesis processes; disorders of liver and/or kidney function. During the treatment period the peripheral blood picture should be controlled regularly.
In case of development of toxic hematological effect the dosage regimen should be corrected depending on the degree of leukopenia and thrombocytopenia.
Safety and effectiveness of gemcitabine in children has not been studied.
Impact on driving and operating machinery
At the time of treatment, one should refrain from potentially hazardous activities requiring increased attention and rapid psychomotor reactions.
Contraindications
Hypersensitivity to gemcitabine.
Side effects
Blood system disorders: leukopenia, thrombocytopenia, anemia.
Digestive system disorders: nausea, vomiting, diarrhea; rarely – constipation.
As to the urinary system: proteinuria, hematuria; rarely – peripheral edema; in rare cases – renal failure.
Dermatological reactions: skin rash, itching, alopecia, stomatitis; rarely – scaling, vesicular rash, eczema.
Laboratory measures: transient increase of liver transaminases activity, alkaline phosphatase, increased concentration of bilirubin in plasma.
Respiratory system disorders: rare – bronchospasm, dyspnea.
CNS and peripheral nervous system disorders: rarely – somnolence, weakness, paresthesia.
Cardiovascular system: rare – arterial hypotension, pulmonary edema; in single cases – myocardial infarction, arrhythmias.
Others: flu-like syndrome.
Similarities
Weight | 0.120 kg |
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Manufacturer | Abeve Pharma, Austria |
Medication form | concentrate for preparation of infusion solution |
Brand | Abeve Pharma |
Other forms…
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