Zuvitrex – Methotrexate Inj 50 mg

Methotrexate (formerly Amethopterin) is an antimetabolite used in the treatment of certain neoplastic diseases, severe psoriasis, and adult rheumatoid arthritis.

Chemically methotrexate is N-[4-[[(2,4-diamino-6-pteridinyl) methyl]methylamino]benzoyl]-L-glutamic acid.

The structural formula is:

Methotrexate is indicated in the treatment of choriocarcinoma, chorioadenomadestruens and molahydatidosa. In molahydatidosa primary therapy consists of the evacuation of the uterus. Methotrexate is used in prophylactic therapy. In the treatment of low-risk trophoblastic tumors, methotrexate is used as a single agent. It is indicated in Psoriasis and Rheumatoid arthritis.

n the treatment of high-risk trophoblastic tumors methotrexate is applied as a part of the multidrug regimen. Methotrexate is used in a normal dose or high dose as a single agent or as part of a multidrug regimen in the treatment of acute lymphoblastic leukemia. (CNS Leukemia and maintenance therapy), osteosarcoma Hodgkin’s lymphoma, Burkitt lymphoma, advanced cancer of the head and the neck, invasive tumors of the bladder, and in advanced stages of mycosis fungoides.

The dose of methotrexate to be given, the frequency of dosing, the total dose and the combination with other cytostatic drugs and/or folinic acid are subject to frequent modification as our knowledge improves. Methotrexate should be only applied by Physician’s experience in the area.

Head and Neck Cancer :

Methotrexate at a dose of 40mg/m2 body surface area is given at weekly intervals, until progression. This dosage is used without folinic acid therapy.

Trophoblastic Toumours :

The treatment of trophoblastic tumors has to be strictly supervised by as assigned committee of exports, In patients with non-metastatic and low risk metastatic trophoblastic tumors a methotrexate dose of 15 to 30 mg daily isadministared orally or intramuscularly for 5 days. A repeat course may be given after a period of one or more weeks. Three to five courses are usually employed. Patients with high risk trophoblastic tumours are often trated with a combination therapy, including 300 mg methotrexate/m2 body surface. followed by folinic acid therapy the therapy has to be evaluated on the basis of hCG (Human Chorinic gonadotropin) plasma concentrations.

Leukemia :

Methotrexate is used as part of the maintenance therap, in acute lymphoblastic leukemia at a dose of 15-30 mg/m2 orally, intramuscularly or intravenously once a week.

Psoriasis :

The treatment of psoriasis in women should start immediately following a menstrual period. Once week prior rointiation of methotrexate therapy a testdose of 5-10 mg is given parenterally to detect idiosyncratic reactions of the patients. In adults weekly dosage schedule of 10-25 mg orally intramus- cularly or intravenously is used. In most patients an improvement occurs usually within 4 week and an optimal results is reached in 2-3 months. Discontinuation of the methotrexate treatment gives relapse symptoms within 2 weeks to 6 months. After optional clinical result has been reached the dose should be reduced to the lowest possible with the longest intermediate time span possible. Conventational topical therapy should be restarted as soon as possible.

RheunmatoidArthritis :

A single test dose of methotrexate may be given prior to initiation of therapy to detect possible sensitivity to adverse effect to the drugs. A weekly regimen is used. The recommended starting dosage schedule, is either a) single oral dosage of 7.5 mg once weekly or b) an oral dose of 2.5 mg at 12 hours intervals for three dosages given as a course once weekly. Althrough an upward gradual modification in either the single or divided dosage schedule may be done foroptimisation of response, the total dosage usually should not exceed beyond 20 mg per week so as to avoid severe toxicity particularly bone marrow suppression associated with. After the optimum response is achived the dose in each schedule should be preferably reduced to the lowest possible effective dose. The response, whicj is apparent by between 3-6 weeks may continue for three months or more. The optimal duration of therapy is not known. However limited response for at least 2 years with continued therapy. On discontimuation of therapy arthritis usually worsens within a span of 3-6 weeks.

or Intrathecal Use :

LEUKEMIA MENINGENEAL

IMPORTANT NOTE : Only preservative free methotrexate dilute with preservative free 0.9% Sodium Chloride Injection, USP or other suitable medium to a concentration of 1 mg / ml should be used for intrathecal administration.

Following intrathecal dosing regiments based on patient age

n the treatment of menigeal leukemia, intrathecal (IT) methotrexate may be administered at intervals of 2 to 5 days. Caution should be excercised as IT methorexate administered at intervals of less than once week may increase subacute toxicity. IT methotrexate should be given until the cell count of the CSF returns to normal, and then one additional dose. IT methotrexate adds significantly to the systemic methotrexate drug level. therefore, concurrent systemic antileukemic therapy should be appropriately adjusted.

DOSE MODIFICATIONS :

When the leukocyte count or thrombocyte count is decreased on the first day of treatment the dose of methotrexate, in case of a standard therapy with 40mg/m2 body surface, should be adapted according to the following scheme, the lowest value determines the reduction. %of Normal doseeucocuytes count / mm3hrombocytes

If the number of leukocytes is 2500-35000/mm3 and or the number of thrombocytes is 75000-125000 it is preferred to discontinue the treatment for once week. If the blood count has shown a recovery, the treatment can be continued. If the blood count is not recovered, a dose reductions can be applied .

Methotrexate should not be given to patients with a creatinine clearance less than 60ml./min. Therapy with high dose methotrexate should be postponed in case of in case of liver toxicity.

ROUTE OF ADMINISTRATION

For intramuscular, intravenous & intrathecal use.

• Keep out of reach of children.
• Do not exceed recommended dose.
• Keep in cool dry place. Protect from light

During methotrexatetherapy and until at least three months after treatment with methothotrexate contraceptive precautions should be taken by female as well as male patients. While in general a low dose of methogerxate is applied in the treatment of psoriasis, as compared to the doses used in antineoplastic therapy, intoxication and death may occur. Patients should be fully informed on the risks of methotrexate therapy and should be instructed to report any manifestation of toxicity immediately. The simultaneous use of methotrexate and other potentially hepatotoxic drugs or alcohol should be avoided.

Non-steroidal anti inflammatory drugs should not be administrated prior to or concomitantly with the high doses of methotrexate. NSAIDs with high dose methotrexate therapy has been reported to elevate and prolong seru methotrexate levels, resulting in deaths from severe hematologic and gastrointestinal toxicity. Oral antibiotics such as tetracycline, chloramphenicol and non absorbable broad spectrum antibiotics may increase intestinal absorption of methotrexate or interfere with the enterohepatic circulation by inhibiting bowel flora and suppressing metabolism of the drug by bacteria.