Infiniti International

Nelabin 250 mg Injection contains Nelarabine, a chemotherapy medication used in the treatment of certain types of T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL). Nelarabine is a prodrug of arabinosylguanine, which is converted inside the body to an active form that inhibits DNA synthesis in cancer cells, leading to cell death.

Nelabin is available in a strength of 250 mg per vial and is typically packaged as a single-use vial for intravenous administration. The intravenous form allows for direct delivery of the medication into the bloodstream, ensuring rapid and effective action against cancer cells.

The active ingredient, Nelarabine, interferes with the growth and proliferation of cancer cells by incorporating into their DNA and halting the replication process. This mechanism of action helps to reduce the number of cancerous cells in the body, contributing to the treatment and management of T-ALL and T-LBL.

The dosage and administration schedule of Nelabin are determined by the healthcare provider based on the patient's medical condition, body surface area, and response to treatment. It is crucial to follow the prescribed regimen precisely to achieve optimal results and minimize potential side effects.

Common side effects of Nelabin may include fatigue, nausea, vomiting, diarrhea, and decreased appetite. More serious side effects can occur, such as neurotoxicity, which may present as numbness, tingling, or weakness in the extremities. Regular monitoring by the healthcare provider is essential to manage any adverse effects and adjust the treatment as necessary.

Nelabin is manufactured by MSN Laboratories, a well-known pharmaceutical company dedicated to producing high-quality medications for various medical conditions. Patients receiving Nelabin should have regular follow-ups with their healthcare provider to monitor their response to the treatment and manage any side effects.

Nelabin 250 mg Injection offers an effective treatment option for patients with T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma. Its targeted action against cancer cells helps to control the progression of these aggressive diseases, providing hope and improved outcomes for affected individuals. With its proven efficacy and reliable manufacturing, Nelabin is a trusted choice in oncology care.

Durolane 20mg Injection is a medicine used in the treatment of osteoarthritis of the knee in patients who have failed to respond adequately to conservative therapy and simple analgesics. It reduces the swelling and stiffness in the joints and improve joint function.Durolane 20mg Injection is generally administered by a doctor or a nurse. You should not self-administer this medicine at home. The dosage will depend on the the age, weight, and clinical condition of the patient as well as laboratory determinations. Get the injection for as long as the doctor has prescribed even if you get better until that doctor tells you it is alright to stop.Common side effects of this medicine include injection site reactions (such as swelling, pain, and redness), joint swelling, and pain in the joints. If the side effects get worse or bother you, or if you experience any other symptoms which you think are caused by this medicine, let your doctor know. Your doctor may help with ways to reduce or prevent these symptoms.To make sure the medicine is safe for you, let your doctor know of all the other medicines you are taking before using this medicine. If you are pregnant or breastfeeding, you should consult your doctor first before taking this medicine.

Renocel 10000IU Injection is given by injection either under the skin or into a vein which will be decided by your doctor. Usually, the injections are given by a nurse or doctor. The dose depends on your body weight and the cause of your anemia. Iron supplements both before and during treatment may make this treatment more effective. Renocel 10000IU Injection needs to be stored in a fridge but used at room temperature.

The most common side effects of taking this medicine include nausea, vomiting, fever, and increased blood pressure. It may also cause flu-like symptoms such as headache, tiredness, dizziness and aches and pains. These side effects are most common at the start of treatment but if they persist your doctor may be able to suggest ways of preventing or reducing them. Tell your doctor straight away if you get any serious side effects, including seizures (fits). Sometimes this medicine can cause serious blood clots that need urgent medical attention.

Before using Renocel 10000IU Injection you should tell your doctor if you have uncontrolled high blood pressure, heart disease, or gout (disease of joint pain). You should also tell him/her what other medicines you are taking in case they affect this treatment. Your blood pressure should be checked often during this treatment by you or your doctor. You may also need other regular medical tests to be sure this medicine is not causing harmful effects. It is not known whether this medicine will harm an unborn baby. Tell your doctor if you are pregnant, plan to become pregnant, or are breastfeeding.

• Treatment of Anemia due to cancer chemotherapy
• Treatment of Anemia due to chronic kidney disease

Aggramed Tirofiban Injection

Brand Names: Aggramed, Aggrastat (internationally known as)

Composition: Tirofiban

Strength: 0.25 mg/ml

Manufacturer: Emcure Pharmaceuticals Ltd.

Packaging: Single-use vial

Treatment: Acute Coronary Syndrome (ACS), Non-ST Elevation Myocardial Infarction (NSTEMI), Percutaneous Coronary Intervention (PCI)

Product Description:
Aggramed Tirofiban Injection contains Tirofiban, a glycoprotein IIb/IIIa inhibitor used in the management of acute coronary syndrome (ACS). It is indicated for use in patients experiencing non-ST elevation myocardial infarction (NSTEMI) or undergoing percutaneous coronary intervention (PCI). Tirofiban works by inhibiting platelet aggregation, which helps to prevent the formation of blood clots that can lead to heart attacks.

Aggramed is available in a concentration of 0.25 mg/ml and is typically packaged in single-use vials. This form allows for precise dosing and administration by healthcare professionals in a clinical setting.

Tirofiban, the active ingredient in Aggramed, blocks the glycoprotein IIb/IIIa receptors on the surface of platelets. These receptors are critical for platelet aggregation and thrombus formation. By inhibiting these receptors, Tirofiban reduces the risk of thrombotic events, thereby improving outcomes in patients with ACS.

The usual administration of Aggramed involves an initial bolus injection followed by a continuous intravenous infusion. The exact dosage and duration of treatment are determined by the healthcare provider based on the patient's clinical condition and response to therapy. It is crucial to follow the prescribed regimen to achieve the desired therapeutic effect.

Common side effects of Aggramed may include bleeding, which is the most significant risk due to its antiplatelet activity. Other side effects can include low platelet count (thrombocytopenia), headache, and dizziness. Patients receiving Aggramed should be closely monitored for signs of bleeding and other adverse effects.

Aggramed is manufactured by Emcure Pharmaceuticals Ltd., a reputable pharmaceutical company known for its commitment to quality and patient care. Regular follow-ups and monitoring by healthcare providers are essential to ensure the safety and effectiveness of the treatment.

Aggramed Tirofiban Injection offers an effective intervention for managing acute coronary syndrome and preventing thrombotic complications during percutaneous coronary interventions. Its targeted action on platelet aggregation makes it a vital tool in cardiology, helping to reduce the risk of adverse cardiovascular events and improve patient outcomes. With its reliable manufacturing and proven efficacy, Aggramed is a trusted choice in the management of ACS and related conditions.

• Ovarian cancer
• Cervical cancer
• Testicular cancer

Inclisiran 284 mg Injection contains Inclisiran, a small interfering RNA (siRNA) medication used to lower cholesterol levels in the blood. It is specifically indicated for the treatment of hypercholesterolemia, including heterozygous familial hypercholesterolemia (HeFH) and atherosclerotic cardiovascular disease (ASCVD) in adults who require additional lowering of LDL cholesterol.

Inclisiran is available in a strength of 284 mg per injection and is typically packaged as a single-use pre-filled syringe. This convenient packaging allows for easy administration, usually performed by a healthcare professional.

The active ingredient, Inclisiran, works by targeting and degrading the messenger RNA (mRNA) that encodes for the protein PCSK9 (proprotein convertase subtilisin/kexin type 9). By reducing the production of PCSK9, Inclisiran increases the number of LDL receptors on the surface of liver cells, enhancing the clearance of LDL cholesterol from the blood. This mechanism of action leads to a significant reduction in LDL cholesterol levels.

The usual dosage of Inclisiran involves an initial injection, followed by a second dose at 3 months, and subsequent doses every 6 months. This biannual dosing schedule offers a convenient and effective approach to managing cholesterol levels, especially for patients who may have difficulty adhering to daily medications.

Common side effects of Inclisiran may include injection site reactions, such as redness, pain, or swelling. These side effects are generally mild and temporary. However, any severe or persistent side effects should be reported to a healthcare provider promptly.

Inclisiran is manufactured by Novartis Pharmaceuticals, a leading global healthcare company known for its innovative treatments and commitment to improving patient outcomes. Regular monitoring of cholesterol levels and follow-ups with the healthcare provider are essential to assess the effectiveness of Inclisiran and make any necessary adjustments to the treatment plan.

Inclisiran 284 mg Injection provides a groundbreaking solution for managing high cholesterol levels, particularly in patients with ASCVD and familial hypercholesterolemia. Its novel siRNA mechanism offers a new approach to cholesterol reduction, helping to reduce the risk of cardiovascular events and improve overall cardiovascular health. With its convenient dosing schedule and proven efficacy, Inclisiran represents a significant advancement in lipid management therapy.

Bleocel Bleomycin 15IU Injection

Brand Names: Bleocel, Blenoxane (widely known brand based on composition)

Composition: Bleomycin

Strength: 15 IU

Manufacturer: Celon Laboratories

Packaging: Typically available in a single-use vial

Treatment: Various types of cancer, including Hodgkin's lymphoma, non-Hodgkin's lymphoma, testicular cancer, and certain types of skin cancer

Product Description:
Bleocel Bleomycin 15IU Injection contains Bleomycin, an antineoplastic antibiotic that is used in the treatment of various types of cancer. Bleomycin works by causing breaks in DNA strands, leading to the inhibition of DNA synthesis in rapidly dividing cancer cells. It is commonly used as part of combination chemotherapy regimens for treating cancers such as Hodgkin's lymphoma, non-Hodgkin's lymphoma, testicular cancer, and certain types of skin cancer.

Common indications for Bleocel Bleomycin 15IU Injection include:

• Cancer Treatment: Used in the management of Hodgkin's lymphoma, non-Hodgkin's lymphoma, testicular cancer, and certain types of skin cancer.

Dosage and Administration:

• For Adults: The dosage and frequency of administration depend on the specific type of cancer being treated, the stage of the disease, and the patient's overall health. It is typically administered by a healthcare professional in a hospital or clinical setting.
• Administration: Bleocel is administered intravenously or intramuscularly under the supervision of an oncologist. The dosage schedule is determined based on the specific treatment protocol.

Common side effects of Bleocel Bleomycin 15IU Injection may include:

• Pulmonary toxicity (interstitial pneumonitis, pulmonary fibrosis)
• Skin reactions (hyperpigmentation, rash)
• Mucositis
• Fever and chills

Patients receiving Bleocel should be closely monitored for signs of pulmonary toxicity, which is a serious and potentially life-threatening side effect of Bleomycin.

Packaging:
Bleocel Bleomycin 15IU Injection is typically packaged in a single-use vial, intended for administration by a healthcare professional.

Bleocel Bleomycin 15IU Injection is a critical component of cancer therapy, particularly in the treatment of certain lymphomas, testicular cancer, and skin cancers. Due to its potential for serious side effects, it should only be administered under the guidance and supervision of an experienced oncologist. Regular monitoring of lung function and overall patient health is essential during treatment with Bleomycin.

• Calutide 50mg (Genric Casodex) is an anti-androgen. It works in the body by preventing the actions of androgens (male hormones)Calutide 50mg (Genric Casodex) is used together with another hormone to treat prostate cancerCalutide 50mg (Genric Casodex) may also be used for purposes not listed in this medication guide Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat
• Oral consumption permitted chemical compounds Competitive prices

• 500mg CA Cape Tablets 
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• Breast cancer

Onco Bcg 40mg Injection is administered by a healthcare professional. It is instilled directly into the bladder through the urethra. For it to be effective, you should complete the course of the vaccine. You should not discontinue even if you get better until the course is completed.

Some common side effects of this medicines include difficulty in urination, urinary tract infection, and fever. These are usually mild and go away with time. However, if they persist or get worse, you should let your doctor know.

Before receiving the vaccine, you should let your doctor if you have ever had an allergic reaction to any vaccine. Also tell your doctor if you have any problems with your heart, kidneys, or liver. Some other medicines may react with this vaccine, so let your doctor know of all the medication you are taking. Pregnant or breastfeeding should consult their doctors first before receiving this vaccine.

• Treatment of Early-stage bladder cancer

Lupride Depot 11.25mg Injection is given as an injection under the skin by a qualified medical professional.  Your doctor will decide what dose is necessary and how often you need to take it. This will depend on what you are being treated for and may change from time to time. You should take it exactly as your doctor has advised. Taking it in the wrong way or taking too much can cause very serious side effects. It may take several weeks or months for you to see or feel the benefits but do not stop taking it unless your doctor tells you to.

Decreased libido, increased sweating, fatigue, muscle weakness, and hot flashes are some very common side effects of this medicine. The long-term use of medicine may cause weakened bones and a reduction in bone mineral density. You are advised to take vitamin D and calcium supplements while taking this medicine. It might cause menstrual periods to stop for a period of 7- 12 weeks, inform your doctor if menstrual bleeding continues even during the treatment.

Before taking this medicine, inform your doctor if you have a history of drinking alcohol, smoking, and osteoporosis. Many other medicines can affect, or be affected by, this medicine so let your healthcare team know all medications you are using. This medicine is not recommended during pregnancy or while breastfeeding. The use of effective contraception by both males and females during treatment is important to avoid pregnancy.

• Prostate cancer
• Endometriosis
• Uterine fibroids
• Precocious puberty (premature puberty)
• Female infertility

Luprodex Depot 3.75mg Injection is given as an injection under the skin by a qualified medical professional.  Your doctor will decide what dose is necessary and how often you need to take it. This will depend on what you are being treated for and may change from time to time. You should take it exactly as your doctor has advised. Taking it in the wrong way or taking too much can cause very serious side effects. It may take several weeks or months for you to see or feel the benefits but do not stop taking it unless your doctor tells you to.

Decreased libido, increased sweating, fatigue, muscle weakness, and hot flashes are some very common side effects of this medicine. The long-term use of medicine may cause weakened bones and a reduction in bone mineral density. You are advised to take vitamin D and calcium supplements while taking this medicine. It might cause menstrual periods to stop for a period of 7- 12 weeks, inform your doctor if menstrual bleeding continues even during the treatment.

Before taking this medicine, inform your doctor if you have a history of drinking alcohol, smoking, and osteoporosis. Many other medicines can affect, or be affected by, this medicine so let your healthcare team know all medications you are using. This medicine is not recommended during pregnancy or while breastfeeding. The use of effective contraception by both males and females during treatment is important to avoid pregnancy.

• Prostate cancer
• Endometriosis
• Uterine fibroids
• Precocious puberty (premature puberty)
• Female infertility

Luprodex 22.5mg Injection is given as an injection under the skin by a qualified medical professional.  Your doctor will decide what dose is necessary and how often you need to take it. This will depend on what you are being treated for and may change from time to time. You should take it exactly as your doctor has advised. Taking it in the wrong way or taking too much can cause very serious side effects. It may take several weeks or months for you to see or feel the benefits but do not stop taking it unless your doctor tells you to.

Decreased libido, increased sweating, fatigue, muscle weakness, and hot flashes are some very common side effects of this medicine. The long-term use of medicine may cause weakened bones and a reduction in bone mineral density. You are advised to take vitamin D and calcium supplements while taking this medicine. It might cause menstrual periods to stop for a period of 7- 12 weeks, inform your doctor if menstrual bleeding continues even during the treatment.

Before taking this medicine, inform your doctor if you have a history of drinking alcohol, smoking, and osteoporosis. Many other medicines can affect, or be affected by, this medicine so let your healthcare team know all medications you are using. This medicine is not recommended during pregnancy or while breastfeeding. The use of effective contraception by both males and females during treatment is important to avoid pregnancy.

• Prostate cancer
• Endometriosis
• Uterine fibroids
• Precocious puberty (premature puberty)
• Female infertility

5 Flucel 500mg Injection contains the active ingredient as Fluorouracil. It belongs to a class of drugs called antimetabolites, which interfere with the genetic material (DNA and RNA) synthesis of rapidly dividing cancer cells, leading to their death. It is commonly used to treat breast, colorectal, stomach, esophagus, and pancreatic cancers. It can be administered in different ways, including through injection or as a cream. 

Like all other anticancer medication, 5 Flucel 500mg Injection can cause side effects. Common side effects are nausea, vomiting, diarrhea, mouth sores, hair loss, and an increased risk of infection. However, not all patients will experience these side effects, and the severity of the side effects can vary from person to person.  No specific foods need to be avoided when receiving 5 Flucel 500mg Injection, but alcohol, spicy or acidic foods, citrus fruits and juices, and high-fiber foods may worsen some side effects, such as nausea, vomiting, mouth sores, and gastrointestinal problems. Patients should consider avoiding or limiting these foods during treatment. Inform your physician before starting this treatment if you have undergone surgery in the last 30 days or are following a controlled sodium diet.

• Myelodysplastic syndrome
• Blood cancer

• Non-small cell lung cancer
• Malignant pleural mesothelioma

• Osteoporosis
• Hypercalcemia