Active substanceOxaliplatinOxaliplatin
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  • Dosage form: & nbsplyophilizate for solution for infusion
    Composition:

    1 bottle with the drug contains:

    active substance: oxaliplatin 50 mg and 100 mg;

    Excipients: lactose monohydrate.

    Description:

    Lyophilized powder of white color.

    Pharmacotherapeutic group:An antitumour agent, an alkylating compound
    ATX: & nbsp

    L.01.X.A   Platinum compounds

    L.01.X.A.03   Oxaliplatin

    Pharmacodynamics:

    Oxaliplatin is an antitumor drug belonging to a new class of compounds based on platinum, in which the platinum atom forms a complex bond with 1,2-diaminocyclohexane (DACG) and an oxalate group.

    Oxaliplatin has antitumor activity in various types of tumors, including colorectal cancer. It is also effective in the treatment of tumors resistant to cisplatin. The effect manifests itself regardless of the phase of the cell cycle.When used with 5-fluorouracil synergism of cytotoxic effects is observed. The mechanism of the antitumor effect of oxaliplatin is based on the cytotoxic effect and has not been fully studied. Presumably, oxaliplatinum forms inter- and intracerebral bonds with DNA, thereby inhibiting the phases of its replication and transcription.

    Pharmacokinetics:

    In vivo oxaliplatin undergoes active biotransformation and is not detected in the plasma by the end of 2 hours after administration at a dose of 130 mg / m2, with 15% of the platinum introduced in the blood, and the remaining 85% quickly distributed to the tissues or excreted by the kidneys. Platinum binds to plasma albumin and is excreted in the urine for the first 48 hours.

    By day 5, about 54% of the total dose is found in urine and less than 3% in feces. With renal insufficiency, there is a significant decrease in clearance of oxaliplatin from 17.6 ± 2.18 l / h to 9.95 ± 1.91 l / h. The effect of severe renal failure on the clearance of platinum has not been studied.

    Indications:

    - Adjuvant therapy for colorectal cancer of Stage III (Duke D) after radical resection of the primary tumor in combination with 5-fluorouracil and calcium folinate;

    - disseminated colorectal cancer (as monotherapy or combination therapy in combination with 5-fluorouracil / calcium folinate);

    - ovarian cancer (as the 2nd line of therapy).

    Contraindications:

    - Hypersensitivity to oxaliplatinum, other derivatives of platinum or other constituents of the drug;

    - myelosuppression before the first course of therapy with a neutrophil count less than 2000 / μL and / or platelets less than 100,000 / μL;

    - peripheral sensory neuropathy with functional impairment before the start of the first course of therapy;

    - marked impairment of kidney function (creatinine clearance less than 30 ml / min);

    - pregnancy and the period of breastfeeding;

    - childhood.

    Carefully:

    With violations of kidney function, severe violations of the liver.

    Dosing and Administration:

    Oxaliplatin-Filaxis is prescribed only to adults in the form of intravenous infusion for 2-6 hours.

    Hyperhydration with oxaliplatin is not required. If oxaliplatinum is used in combination with 5-fluorouracil, oxaliplatin infusion should precede the administration of 5-fluorouracil.

    Adjuvant therapy for colorectal cancer: at 85 mg / m2 1 every 2 weeks for 12 cycles (6 months).

    Treatment of metastatic colorectal cancer: at 85 mg / m2 1 every 2 weeks as a monotherapy or in combination with 5-fluorouracil.

    Treatment of ovarian cancer: 85 mg / m2 1 every 2 weeks as a monotherapy or in combination with other chemotherapeutic drugs.

    Repeated administration of oxaliplatin-Filaksis produced only when the number of neutrophils more than 1500 / mm and more than 50,000 platelets / .mu.l.

    Recommendations for dose adjustment and administration of oxaliplatin

    In hematological disorders (neutrophil count <1500 / l and / or platelet count <50,000 / ul) holding the next course deferred until restoration of laboratory parameters.

    With the development of diarrhea grade 4 toxicity (WHO scale), grade 3-4 neutropenia (neutrophil count <1000 / L), grade 3-4 thrombocytopenia (platelet count <50,000 / ul) dose oxaliplatin-Filaksis subsequent administrations must be reduced to 85 mg / m2 up to 65 mg / m2 when treating disseminated colorectal cancer and ovarian cancer; and up to 75 mg / m2 adjuvant therapy of colorectal cancer in addition to the normal decrease in dose of 5-FU in the case of their combined use.

    Patients who during infusion or within several hours after a 2-hour infusion developed acute laryngo-pharyngeal dysesthesia, following infusion of oxaliplatin-Filaksis should be performed within 6 hours.

    When pain (as a sign of neurotoxicity) lasts more than 7 days or when paresthesia without functional impairment persists until the next cycle, the subsequent dose of Oxaliplatin-Filaxis should be reduced by 25%.

    When paresthesia with functional impairment persists until the next cycle, oxaliplatin-phylaxis should be canceled; with a decrease in the severity of the symptoms of neurotoxicity after the withdrawal of oxaliplatin, one may consider resuming treatment.

    With the development of stomatitis and / or mucositis of the 2nd or more toxicity level, treatment with Oxaliplatin-Filaxis should be suspended until they stop or reduce toxicity to 1 degree.

    Patients with renal insufficiency. Data on the use of oxaliplatin in patients with severe renal impairment are not present. Due to the limited data on safety and tolerability of the drug in patients with moderate renal impairment, the benefit / risk relationship for the patient should be weighed before using the drug. Therapy in this category of patients can be initiated with the recommended dose, under careful control of kidney function.With a mild degree of impaired renal function, dosage adjustment of oxaliplatin is not required.

    Patients with hepatic failure. The change in the dosage regimen in patients with a mild or moderate form of liver failure is not required. Data on the use of oxaliplatin in patients with severe impairment of liver function are absent.

    Elderly patients. It is not necessary to correct the dosage regimen when oxaliplatin is prescribed to patients over the age of 65 (including when used in combination with 5-fluorouracil).

    Rules for the preparation and administration of a solution

    When preparing solutions and administering oxaliplatin, needles and other equipment containing aluminum can not be used.

    The drug before use is dissolved in water for injection or in a 5% solution of dextrose, to obtain a solution with a concentration of 5 mg / ml oxaliplatin (10 ml of the solvent is introduced into the 50 mg bottle, and 20 ml of the solvent into the 100 mg bottle). The reconstituted drug is immediately diluted with 250-500 ml of a 5% dextrose solution. The concentration of the resulting solution of oxaliplatin should be from 0.2 to 0.7 mg / ml; with 0.7 mg / ml - the highest concentration used in clinical practice at a dose of 85 mg / m2.

    To prepare the drug solution, only the recommended solvents should be used.

    Do not apply the drug undiluted.

    Saline solutions (sodium chloride solution) should not be used to dissolve the drug or dilute the drug solution (for the preparation of the infusion solution).

    Do not mix in the same container, do not prescribe simultaneously in one infusion system with other drugs (especially with 5-fluorouracil, basic solutions, trometamol and calcium folinate preparations containing trometamol in its composition).

    Oxaliplatin may be administered concomitantly with calcium folinate infusions. In this case, the preparations should not be mixed in one pot of infusions. Calcium folinate for infusion should be diluted with a 5% solution of dextrose, but in no case should you use solutions containing sodium chloride, or alkaline solutions.

    The prepared solution of the preparation should be transparent and should not contain undissolved particles. Otherwise, the drug solution can not be used.

    The solution of the drug is used immediately after preparation.

    The drug is intended for single use only. Unused solution of the drug should be destroyed.

    In the case of extravasation, the drug should be discontinued immediately.

    Side effects:

    The incidence of adverse reactions listed below is described in accordance with the following gradation: very often (> 1/10), often (> 1/100, ≤1 / 10); infrequently (> 1/1000, ≤1 / 100); rarely (> 1/10000, ≤1 / 1000); very rarely (≤ 1/10000), including individual messages.

    On the part of the hematopoiesis system: very often - anemia, leukopenia, neutropenia, thrombocytopenia, lymphopenia; often - febrile neutropenia (including grade 3-4), sepsis against neutropenia; rarely - hemolytic anemia, immune thrombocytopenia.

    On the part of the digestive system: very often - nausea, vomiting, diarrhea, stomatitis, mucositis, abdominal pain, constipation, loss of appetite, increased levels of alkaline phosphatase activity of "liver" enzymes, bilirubin, lactate dehydrogenase; often - dyspepsia, gastroesophageal reflux, hiccough; infrequently - intestinal obstruction; rarely - colitis, including cases of pseudomembranous colitis.

    From the central and peripheral nervous system: very often - peripheral sensory neuropathy, sensitivity disorders, headache, asthenia; often - dizziness, meningism, depression, insomnia; infrequent - increased nervousness; rarely - dysarthria.Neurotoxicity is a dose-limiting factor. Often the symptoms of sensory neuropathy are provoked by cold. The duration of these symptoms, which are usually docked in the interval between courses, increases depending on the total dose of oxaliplatin. Functional disorders in the form of difficulty in performing precise movements are possible consequences of sensory damage. The risk of functional disorders for a total dose of about 850 mg / m2 (10 cycles) is about 10%, reaching 20% ​​in the case of a total dose of 1020 mg / m2 (12 cycles). In most cases, neurologic symptoms are weakened or they completely stop. However, in 3% of patients 3 years after the end of treatment, either stable localized paresthesias of moderate intensity (2.3%) or paresthesia, affecting functional activity (0.5%) were observed.

    On the background of treatment with oxaliplatin, acute neurosensory manifestations were noted, which usually occurred within a few hours after the administration of the drug and were most often provoked by exposure to cold. They were characterized by transient paresthesia, dysesthesia or hypoesthesia, rarely (1-2%) with an acute syndrome of laryngeal dysaesthesia.The latter manifested itself as a subjective feeling of dysphagia and dyspnea without objective signs of respiratory distress syndrome (cyanosis or hypoxia), or spasm of the larynx, or bronchospasm (without stridor or wheezing). Also observed were such phenomena as spasm of the jaw, dysesthesia of the tongue, dysarthria and a feeling of pressure in the chest. Usually, these symptoms were quickly stopped both without the use of drug therapy, and with the administration of antihistamines and bronchodilators. Increasing the infusion time during subsequent cycles of oxaliplatin therapy can reduce the incidence of this syndrome.

    From the musculoskeletal system: very often - back pain; often - arthralgia, pain in the bones.

    On the part of the respiratory system: very often - cough, shortness of breath; often - rhinitis, infections of the upper respiratory tract; rarely - pulmonary fibrosis.

    From the side of the cardiovascular system: often - chest pain, thrombophlebitis of deep veins, thromboembolism of pulmonary arteries.

    From the urinary system: often - hematuria, dysuria.

    From the skin and skin appendages: very often - alopecia, skin rashes; often - peeling of the skin of the palms and feet, erythematous rashes, excessive sweating, changes from the nails.

    On the part of the organs of sight and hearing: often - conjunctivitis, visual impairment; rarely - transient reduction in visual acuity, loss of visual fields, decreased hearing, neuritis of the auditory nerve

    Allergic reactions: rarely (with monotherapy) or often (in combination with 5-fluorouracil +/- calcium folinate) can have bronchospasm, angioedema, hypotension and anaphylactic shock. Often there have been cases of allergic manifestations, such as a rash (especially hives), conjunctivitis or rhinitis.

    Local reactions: with extravasation of the drug - pain and inflammatory reactions at the site of administration.

    From the laboratory indicators: very often: hypokalemia, hyponatremia, hyperglycemia; often - increasing the level of creatinine.

    Other: very often - increased body temperature, increased fatigue, weight gain, taste disorders.

    Overdose:

    Symptoms: myelosuppression, neurotoxicity, diarrhea, nausea, vomiting.

    Antidote to oxaliplatinum is not known.

    Treatment: hematological control and symptomatic therapy.

    Interaction:

    Significant changes in the binding of oxaliplatin to plasma proteins with simultaneous use with erythromycin, salicylates, granisetron, paclitaxel, valproic acid have not been noted.

    The drug is incompatible with alkaline solutions or solutions containing chlorides. When interacting with aluminum, it is possible to form a precipitate and reduce the activity of oxaliplatin.

    Special instructions:

    Oxaliplatin-Filaxis should be used only under the supervision of an oncologist who has experience with antitumor drugs.

    Regularly (once a week), as well as before each injection of Oxaliplatin-Filaxis, it is necessary to monitor the peripheral blood elements and the renal and hepatic function.

    Before the beginning of each cycle of therapy with Oxaliplatin-Filaxis, a neurologic examination should be performed to determine signs of neurotoxicity. Patients should be informed about the possibility of persistent symptoms of peripheral sensory neuropathy after the end of the course of treatment. Localized mild paresthesias with functional disorders can last up to 3 years after the end of treatment according to the adjuvant treatment regimen.

    When respiratory symptoms appear (dry cough, dyspnoea, wheezing, or pulmonary infiltrate detection during X-ray examination),treatment with oxaliplatin-Filaksis should be suspended to preclude the presence of interstitial pneumonitis. Symptoms such as dehydration, paralytic ileus, intestinal obstruction, hypokalemia, metabolic acidosis and renal failure may be due to severe diarrhea or vomiting, especially when using the drug-Filaksis Oxaliplatin in combination with 5-fluorouracil.

    Patients with allergic reactions to other platinum compounds in the anamnesis should be monitored for allergic symptoms. In the case of reaction to Oksaliplatin- Filaksis similar anaphylactic, infusion should be interrupted immediately and appoint appropriate symptomatic treatment. Further application Filaksis Oxaliplatin-drug in the case of allergic reactions is contraindicated.

    In the case of extravasation, the infusion should be stopped immediately and local symptomatic treatment started. The remaining dose of the drug should be injected into another vein. Women and men during treatment and for 6 months after treatment with oxaliplatin should use reliable methods of contraception.

    When using Oxaliplatin-Filaxis, all the usual instructions for the use of cytotoxic drugs should be observed. If Oxaliplatin-Filaxis hits the skin or mucous membranes, they should be washed immediately and thoroughly with water.

    Form release / dosage:

    Liofilizate for the preparation of a solution for infusions, 50 mg and 100 mg.

    Packaging:

    For 50 mg of the drug in bottles of light-protective glass with a lid of bromobutyl under an aluminum run-off and a lid of the type flip-off. 1 bottle (50 mg) is placed in a cardboard box of cardboard for consumer packaging brand chromium or chromium-ersatz together with instructions for use or 2, 3, 5 bottles (50 mg) placed in a plastic pallet, then in a cardboard pack of cardboard for consumer packaging brand chrome or chrome-ersatz together with instructions for use.

    For 100 mg of the drug in bottles of light-protective glass with a lid of bromobutyl under an aluminum run-off and a lid of type flip-off 1 bottle (100 mg) is placed in a cardboard box of cardboard for consumer packaging brand chromium or chromium-ersatz together with instructions for use or 2, 3 bottles (100 mg) placed in a plastic pallet,then in a cardboard pack of cardboard for consumer packaging brand chrome or chromium-ersatz together with instructions for use.

    Storage conditions:

    Store in a dark place at a temperature of 15-25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    Do not use after the expiration date printed on the package.
    Terms of leave from pharmacies:On prescription
    Registration number:LSR-000614/09
    Date of registration:02.02.2009
    Expiration Date:Unlimited
    The owner of the registration certificate:CEFARMA, LLC CEFARMA, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp23.05.2017
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