Vinorelbine belongs to the class of medications called as antineoplastics. It prevents proliferation and maturation of cancer cells which eventually get destroyed. This injection is used to treat non-small cell lung cancer.
It is also indicated in metastatic breast cancer patients, previously treated with anthracyline andor taxane therapy.
Administration of Vinorelbine Injection should be done only by physicians experienced with cancer chemotherapeutic agents.
Blood counts are required to be taken before each dose. The dosage should be reduced or discontinued upon evidence of abnormal depression of the bone marrow.
Vinorelbine Injection is contraindicated in patients with known hypersensitivity to this drug.
In addition, this injection is contraindicated in patients who have drug-induced severe granulocytopenia or severe thrombocytopenia.
Seek immediate medical attention if you experience signs of an allergic reaction such as bronchospasm (wheezing, chest tightness, trouble breathing), hives, difficulty in breathing, fever, chills, flu symptoms, mouth and throat ulcers, bloody or black stools, pale skin, easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), rapid heart rate, rapid and shallow breathing, fainting, cough, severe constipation, stomach pain, numbness, burning, pain or tingly feeling, nausea, sweating, burning, redness, swelling or skin changes.
Epirubicin injection has strong anti tumor action by interfering with the synthesis and function of DNA. The given injection is used to treat cancers of breast, lungs, ovaries, lymph system and stomach. Epirubicin is an antineoplastic in the anthracycline class which prevents abnormal growth of tissues.
This injection is to be administered only under the supervision of your doctor. Epirubicin should be injected slowly into a vein. Do not inject into a muscle or under the skin. If this medication by coincidence leaks into the skin/muscle around the injection site, it may cause serious damage. Tell your doctor without delay if you observe redness, pain or swelling at or near the injection site.
Use of this medicine should be avoided in those are allergic to epirubicin or to any of the ingredients of the medication, allergic to other anthracycline-type medications like doxorubicin, breast-feeding, recent heart attack, heart failure, irregular heart rhythm, severe heart disease, severe liver impairment.
Epirubicin forms a complex with DNA by intercalation of its planar rings between nucleotide base pairs, with consequent inhibition of nucleic acid (DNA and RNA) and protein synthesis.Such intercalation triggers DNA cleavage by topoisomerase II, resulting in cytocidal activity. Epirubicin also inhibits DNA helicase activity, preventing the enzymatic separation of double-stranded DNA and interfering with replication and transcription
Irinotecan is used in the treatment of colorectal cancer. This injection is also given to patients having metastatic carcinoma of the colon or rectum whose disease has recurred or proceeded following initial fluorouracil-based therapy. Irinotecan is an antineoplastic enzyme inhibitor which interferes with growth and spread of cancer cells.
Before taking treatment with Irinotecan Injection, it is very important to tell your doctor if have ever experienced any allergic reaction to this drug. In addition, your doctor should know if you are pregnant or planning for pregnancy, having any other types of allergies such as foods, dyes, preservatives, or animals, non-prescription products etc.
Use of this drug is contraindicated in patients with a known hypersensitivity to this drug.
Seek medical attention if you have serious side effect such as wheezing, feeling short of breath, chest pain, dry cough, pale skin, feeling light-headed, rapid heart rate, fever, chills, body aches, flu symptoms, sores in your mouth and throat, runny nose, watery eyes, increased sweating, stomach cramps etc.
With an objective to serve clients in best possible manner, we have been betrothed in providing high quality Leuprolide Injection. This injection is ideal for the treatment of anemia. The offered injection is available in medical stores, hospitals and other similar places. The offered injection is formulated at modern processing unit by our adept professionals using high grade chemicals. In addition to this, the provided Leuprolide Injection can be bought from us in moisture proof packaging at cost effective rates.
Key Points:Longer shelf life Safe and reliable Quick acting Accurate composition
Composition- : Each 0.5ml Contains : Leuprolide Acetate 1mg
Leuprolide acts as an agonist at pituitary GnRH receptors. By interrupting the normal pulsatile stimulation and the desensitization of the GnRH receptors; it indirectly down regulates the secretion of gonadotropins luteinizing hormone (LH) and follicle-stimulating hormone (FSH) leading to hypogonadism and thus a dramatic reduction in estradiol .
|Specification-||pH range â€“ : 5.5 to 6.5
Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin releasing hormone (GnRH or LH-RH). The analog possesses greater potency than the natural hormone. It is a sterile, aqueous solution intended for subcutaneous injection.
|Indication :||Advanced prostatic carcinoma when orchidectomy or oestrogen administration is not indicated.|
|Dosage :-||SC inj., 1 mg single dose.|
|Contraindications:-||Pregnancy, in women who may become pregnant while receiving the drug, and during lactation. Sensitivity to benzyl alcohol (found in leuprolide injection). Undiagnosed abnormal vaginal bleeding. Hypersensitivity to GnRH or GnRH agonist analogs. The 30-mg depot in women.|
|Precautions:-||Patients with metastatic vertebral lesions and/or with urinary tract obstruction should be closely observed during the first few weeks of therapy. Patients with known allergies to benzyl alcohol, an ingredient of the drug's vehicle, may present symptoms of hypersensitivity, usually local, in the form of erythema and induration at the injection site.|
|Drug interaction:||Administration of leuprolide acetate in therapeutic doses results in suppression of the pituitary-gonadal system. Normal function is usually restored within 4 to 12 weeks after treatment is discontinued. Administration of leuprolide acetate in therapeutic doses results in suppression of the pituitary-gonadal system. Normal function is usually restored within 4 to 12 weeks after treatment is discontinued.|
|Adverse Effect-:||High blood pressure, ischemia, insomnia, constipation, urinating more often than usual, bone pain, loss of movement in any part of your body; swelling, rapid weight gain.|
|Storage:||: Store unopened bottles in the refrigerator. Vials can be kept at room temperature (less than 86 degrees F or 30 degrees C). Do not freeze. Protect from light.|