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Lox 2% Lignocaine Injection 30ml
Product Brochure
Strength | 2% w/v |
Packaging Size | 30ml |
Composition | Lidocaine 2% w/v |
Brand | Xylocaine |
Manufacturer | Neon Laboratories |
Usage | As local Anesthetic |
Prescription/Non-Prescription | Prescription |
From | injection |
Country of Origin | Made in India |
Introduction :
A local anaesthetic is Xylox 2% Injection. It is used to anaesthetize or numb the surgical area during small surgical operations including dental, oral, diagnostic, or other therapeutic treatments.
Medical personnel must deliver Xylox 2% Injection. It assists in carrying out a painless treatment by momentarily numbing the surgical area and preventing pain signals from reaching the brain.
There are rarely any negative side effects associated with this medication. In some people, nevertheless, it could result in injection site reactions like pain, edoema, and redness. These are often minor and transient. Consult your doctor right away if the numbness or other side effects at the injection site persist.
It is crucial to let your doctor know if you have a heart condition or are receiving medication for a heart rhythm issue before using Xylox 2% Injection. If you are expecting or nursing a child, consult your doctor for advice. The medication may also make you feel faint. So, if you're taking medication, avoid driving or using heavy equipment.
Uses :
Local anesthesia (Numb tissues in a specific area)
Benefits :
In Local anesthesia (Numb tissues in a specific area) :
A local anaesthetic is Xylox 2% Injection. Your skin becomes numb from it. It functions by obstructing your body's nerve messages. It will lessen the discomfort that could be brought on by invasive medical procedures like surgery, needle punctures, or the placement of a catheter or breathing tube. It is often highly safe, works very quickly, and is very effective.
Side Effects :
Most side effects do not require any medical attention and disappear as your body adjusts to the medicine. Consult your doctor if they persist or if you’re worried about them.
Common side effects of Xylocaine :
Injection site reactions (pain, swelling, redness)
Dacilon 0.5mg Dactinomycin Injection
Minimum Order Quantity: 1 Vial
Product Brochure
Strength | 500 mcg |
Pack Type | Vial |
Manufacturer | Celon Laboratories Ltd |
Brand Name | Dacilon 0.5mg |
Composition | Dactinomycin Injection |
Brand | Dacilon 0.5mg |
Packaging Size | 1*1 |
Country of Origin | Made in India |
"Dacilon 0.5mg Dactinomycin Injection" is a medication used in the treatment of certain types of cancer. The active ingredient in this medication is dactinomycin, which is administered through intravenous (IV) injection. Dactinomycin is an antineoplastic (anticancer) drug that works by interfering with the DNA replication process in cancer cells, ultimately inhibiting their growth and causing cell death.
Uses:
Childhood Cancers:Dacilon 0.5mg Dactinomycin Injection is commonly used in the treatment of various childhood cancers, including:Wilms' tumor: A type of kidney cancer that primarily affects children.Rhabdomyosarcoma: A type of cancer that forms in muscle tissues and often occurs in children and young adults.Ewing's sarcoma: A rare type of bone cancer that typically affects children and adolescents.
Germ Cell Tumors:Dacilon 0.5mg Dactinomycin Injection may also be used in the treatment of certain germ cell tumors, which are cancers that develop from cells that produce eggs or sperm. It can be a part of the treatment regimen for conditions such as testicular cancer and ovarian cancer.
Other Cancers:In some cases, Dacilon 0.5mg Dactinomycin Injection may be used as part of a combination therapy for other types of cancer, such as gestational trophoblastic tumors (abnormal growth of cells inside a woman's uterus) and certain types of soft tissue sarcomas.
Side Effect:
• Nausea and vomiting• Diarrhea• Mouth sores or ulcers• Decreased appetite• Hair loss (alopecia)• Fatigue or weakness• Decreased blood cell counts (anemia, leukopenia, thrombocytopenia)• Increased risk of infection• Easy bruising or bleeding• Swelling or fluid retention (edema)• Skin changes (rash, itching)• Pain or redness at the injection site
Dosages:
If you have been prescribed Dacilon 0.5mg Dactinomycin Injection, it's essential to follow your healthcare provider's instructions carefully and only use the medication as directed. Your doctor will determine the appropriate dosage, frequency of administration, and duration of treatment for your specific situation.It's crucial to communicate openly with your healthcare provider and ask any questions you may have about the dosage or administration of the medication. If you have concerns or need further clarification, I recommend reaching out to your healthcare provider or a qualified medical professional who can provide you with accurate and personalized information.
FAQs:
1. What is Dacilon 0.5mg Dactinomycin Injection?Ans. Dacilon 0.5mg Dactinomycin Injection is a medication used in the treatment of certain types of cancer, including childhood cancers like Wilms' tumor and rhabdomyosarcoma. It contains the active ingredient dactinomycin and is administered through intravenous (IV) injection.
2. How does Dacilon 0.5mg Dactinomycin Injection work?Ans. Dacilon 0.5mg Dactinomycin Injection contains dactinomycin, an antineoplastic (anticancer) drug. Dactinomycin interferes with the DNA replication process in cancer cells, disrupting their ability to divide and grow. This leads to cell death and helps to slow down or stop the progression of cancer.
3. What types of cancer is Dacilon 0.5mg Dactinomycin Injection used for?Ans. Dacilon 0.5mg Dactinomycin Injection is commonly used in the treatment of childhood cancers like Wilms' tumor, rhabdomyosarcoma, and Ewing's sarcoma. It may also be used for certain germ cell tumors and soft tissue sarcomas.
Additional Information:
- Production Capacity: 1000
Temoside 100mg Temozolomide capsules
Minimum Order Quantity: 1 Bottle
Product Brochure
Strength | 100 mg |
Brand | Cipla |
Usage/Application | Hospital |
Packaging Type | Finished Product |
Form | Tablet |
Country of Origin | Made in India |
Temoside 100mg is a medication that contains the active ingredient temozolomide. It is available in capsule form and is primarily used in the treatment of certain types of brain tumors, particularly glioblastoma multiforme (GBM) and anaplastic astrocytoma. Temoside belongs to a class of drugs known as alkylating agents, which work by damaging the DNA of rapidly dividing cancer cells, thereby inhibiting their growth and ability to reproduce.
Uses:
Glioblastoma Multiforme (GBM): Temoside 100mg is indicated for the treatment of newly diagnosed glioblastoma multiforme (GBM) in adults. GBM is a highly aggressive and malignant brain tumor that often requires multimodal treatment approaches, including surgery, radiation therapy, and chemotherapy.
Refractory Anaplastic Astrocytoma: Temoside may also be used in the treatment of refractory anaplastic astrocytoma. Anaplastic astrocytoma is a type of brain tumor that tends to be less aggressive than GBM but can still be challenging to treat.
Adjuvant Treatment: In certain cases, Temoside may be used as part of adjuvant therapy following surgical resection and radiation therapy to help prevent or delay tumor recurrence.
Maintenance Therapy: Temoside can be used as maintenance therapy after the completion of initial treatment to help prolong the response and delay disease progression.
Side Effect:
• Nausea• Vomiting• Fatigue• Headache• Constipation• Diarrhea• Loss of appetite• Hair loss (temporary)• Changes in blood cell counts (e.g., low white blood cell count, low platelet count)• Increased susceptibility to infections• Fever
Dosages:
For Glioblastoma Multiforme (GBM):The typical recommended dosage of Temoside 100mg Temozolomide capsules for the treatment of newly diagnosed GBM may involve a "concomitant phase" and a "maintenance phase."During the concomitant phase, the typical dosage is often 75 mg/m² per day, taken orally once daily, in combination with radiation therapy. This phase usually lasts for about 6 weeks.After the concomitant phase, there is a break before starting the maintenance phase. The maintenance phase involves taking Temoside for cycles, where you take 150 mg/m² per day for 5 consecutive days, followed by a 23-day break. This cycle is repeated for a specific number of cycles.
For Refractory Anaplastic Astrocytoma:The dosing regimen for refractory anaplastic astrocytoma may differ based on individual patient factors and treatment response. It may involve taking 150 mg/m² per day for 5 consecutive days, followed by a break, similar to the maintenance phase for GBM.
Dosage Adjustment and Monitoring:Your healthcare provider will closely monitor your progress through regular check-ups, blood tests, and imaging studies to assess the response to treatment and manage any potential side effects.Dosage adjustments may be made based on your overall health, treatment response, and any side effects.
FAQs:
1. What is Temoside 100mg Temozolomide used for?Ans. Temoside 100mg Temozolomide capsules are primarily used for the treatment of certain types of brain tumors, including glioblastoma multiforme (GBM) and refractory anaplastic astrocytoma.
2. How does Temozolomide work in treating brain tumors?Ans. Temozolomide is an alkylating agent that interferes with the DNA replication process in rapidly dividing cancer cells. By damaging the DNA, it helps inhibit the growth and spread of tumor cells.
3. How should I take Temoside 100mg Temozolomide capsules?Ans. Temoside is typically taken orally, once daily, according to specific treatment cycles. The dosage and regimen will be determined by your doctor based on your medical condition and response to treatment.
Additional Information:
- Production Capacity: 1000
Hisone-5 Hydrocortisone Tablets
Product Brochure
Minimum Order Quantity | 1 Box |
Strength | 5mg |
Packaging Size | 20*10 Tablets |
Brand | Hisone |
Manufacturer | Samarth Life Sciences Pvt. Ltd |
Packaging Type | Box |
Shelf Life | 24 Months |
Usage | Severe Allergies |
From | Tablets |
Country of Origin | Made in India |
Hydrocortisone is a prescription medication, and its use should be supervised by a qualified healthcare professional.Prolonged or improper use of corticosteroids, including hydrocortisone, can lead to side effects. These may include weight gain, increased blood pressure, and an increased risk of infections.The duration of treatment and the need for gradual tapering of the medication should be determined by the healthcare provider.
Uses:
Anti-Inflammatory Action:Hydrocortisone is primarily used for its potent anti-inflammatory effects. It can be prescribed to reduce inflammation associated with various conditions.
Allergic Reactions:Hydrocortisone may be used to manage allergic reactions, including skin reactions, itching, and hives.
Skin Disorders:It is commonly prescribed for various skin conditions, such as eczema, dermatitis, and psoriasis, to reduce inflammation and alleviate symptoms.
Rheumatic Disorders:Hydrocortisone can be part of the treatment plan for rheumatic conditions, such as rheumatoid arthritis, to alleviate inflammation and pain.
Respiratory Conditions:Inhaled or systemic hydrocortisone may be prescribed to manage inflammation in the respiratory tract, such as asthma exacerbations.
Adrenal Insufficiency:Hydrocortisone is used in replacement therapy for individuals with adrenal insufficiency, a condition where the adrenal glands do not produce enough cortisol.
Autoimmune Disorders:It can be part of the treatment for certain autoimmune disorders, where the immune system is overactive and attacks healthy tissues.
Inflammatory Bowel Disease:Hydrocortisone may be used to manage inflammation in the gastrointestinal tract for individuals with conditions like Crohn's disease or ulcerative colitis.
Side Effects:
- Upset stomach
- Nausea
- Vomiting
- Increased appetite
- Weight gain
- Fluid retention and swelling (edema)
- Mood changes
Dosage:
For Inflammatory or Allergic Conditions:Typical starting dose for adults: 20 to 30 mg per day.The dosage may be divided into two or three doses per day.Dosage adjustments based on the severity of the condition and individual response.
For Replacement Therapy in Adrenal Insufficiency:Dosage varies widely based on individual patient needs.In stressful situations (illness, surgery), the dosage may be temporarily increased.
Administration:Hydrocortisone tablets are usually taken orally.The tablets should be taken with food to reduce the risk of stomach upset.
Important Considerations:Dosage adjustments may be necessary based on individual response and any observed side effects.The duration of treatment depends on the specific condition being treated.Abruptly stopping the medication without proper tapering can lead to adrenal insufficiency.
FAQs:
1. What is Hisone-5 Hydrocortisone Tablets used for?Ans. Hydrocortisone tablets are commonly used to treat various inflammatory and autoimmune conditions, allergies, and certain skin disorders.
2. How does hydrocortisone work?Ans. Hydrocortisone is a corticosteroid that works by suppressing inflammation and the immune response in the body.
3. When and how should Hisone-5 be taken?Ans. The timing and method of administration will depend on the specific instructions provided by the healthcare provider. It is typically taken with food to reduce stomach upset.
4. What is the recommended dosage for Hisone-5?Ans. The dosage can vary based on the medical condition being treated. It's essential to follow the prescribed dosage and schedule provided by the healthcare provider.
Additional Information:
- Production Capacity: 1000
Afzeta Afatinib Tablets
Minimum Order Quantity: 1 Box
Product Brochure
Prescription/Non prescription | Prescription |
Composition | Afatinib Tablets |
Brand | Afzeta |
Packaging Size | 1*30 |
Form | Tablet |
Country of Origin | Made in India |
Name and Composition:Afzeta Afatinib Tablets contain the active ingredient afatinib, available in tablet form.
Medical Uses:Afzeta is primarily used for the treatment of advanced non-small cell lung cancer (NSCLC) that has specific mutations in the epidermal growth factor receptor (EGFR) gene. These mutations drive the growth of cancer cells, and Afzeta targets them to slow down or inhibit the cancer's growth.
Mechanism of Action:Afzeta inhibits multiple receptors involved in cell growth and signaling, including EGFR and HER2. By blocking these receptors, it interferes with the signaling pathways that drive the growth and spread of cancer cells.
Uses:
Non-Small Cell Lung Cancer (NSCLC) with EGFR Mutations:Afzeta is indicated for the treatment of patients with NSCLC that has specific mutations in the epidermal growth factor receptor (EGFR) gene. These mutations are associated with the rapid growth and spread of cancer cells. Afzeta is used in cases where the cancer has progressed or recurred despite previous treatments or in patients who have not received prior EGFR-targeted therapy.
Treatment of Advanced NSCLC:Afzeta is prescribed for advanced stages of non-small cell lung cancer, particularly when the disease has metastasized (spread to other parts of the body) and has shown specific EGFR mutations.
First-Line Therapy:Afzeta can be used as a first-line treatment option for patients with NSCLC and specific EGFR mutations who have not received previous EGFR-targeted therapy.
Targeted Therapy:Afzeta is considered a targeted therapy because it specifically targets and inhibits the activity of the mutated EGFR protein, which is responsible for promoting the growth and spread of cancer cells.
Side Effect:
• Diarrhea• Skin rash or acne-like rash• Nail changes (such as discoloration or brittleness)• Mouth sores or ulcers• Dry skin• Fatigue or weakness• Loss of appetite• Nausea and vomiting• Abdominal pain or discomfort• Cough
Dosages:
Non-Small Cell Lung Cancer (NSCLC) with EGFR Mutations:The recommended dosage of Afzeta for NSCLC with EGFR mutations is usually 40 mg taken orally once daily.
Dosage Adjustments:Your doctor may adjust your dosage based on your response to treatment and any side effects you may experience.Dosage adjustments may also be necessary if you have certain medical conditions or are taking other medications.
FAQs:
1. What is Afzeta Afatinib Tablets used for?Ans. Afzeta is primarily used for the treatment of non-small cell lung cancer (NSCLC) with specific mutations in the epidermal growth factor receptor (EGFR) gene.
2. How does Afzeta work in treating lung cancer?Ans. Afzeta is a tyrosine kinase inhibitor that targets EGFR and HER2 receptors, which are involved in the growth and spread of cancer cells. By inhibiting these receptors, Afzeta slows down or inhibits the growth of cancer cells.
3. What is the recommended dosage of Afzeta Afatinib Tablets?Ans. The typical dosage for NSCLC with EGFR mutations is 40 mg taken orally once daily. Your healthcare provider will determine the appropriate dose for your specific condition.
4. What are the common side effects of Afzeta Afatinib Tablets?Ans. Common side effects may include diarrhea, skin rash, nail changes, mouth sores, fatigue, and gastrointestinal symptoms. Serious side effects such as lung problems and liver issues can also occur.
Additional Information:
- Production Capacity: 1000
Sorafenat 200mg Sorafenat Tablets
Minimum Order Quantity: 1 Bottle
Product Brochure
Manufactured By | Natco Pharma Limited |
Composition | Sorafenat Tablets |
Brand | Sorafenat 200mg |
Packaging Size | 1*120 |
Treatment | CANCER |
Country of Origin | Made in India |
Sorafenat 200mg tablets are a medication used in the treatment of certain types of cancer. The active ingredient in Sorafenat is sorafenib, which is a targeted therapy drug that belongs to a class of medications called kinase inhibitors. Kinase inhibitors work by blocking the action of specific enzymes (kinases) that are involved in the growth and spread of cancer cells.Sorafenat is primarily used for the treatment of advanced kidney cancer (renal cell carcinoma) and certain types of advanced liver cancer (hepatocellular carcinoma). It is prescribed to patients who are not candidates for surgical treatments or other forms of therapy, or for cases where the cancer has progressed despite previous treatments.
Uses:
Renal Cell Carcinoma (Kidney Cancer): Sorafenat is prescribed for the treatment of advanced renal cell carcinoma, a type of kidney cancer that has spread to other parts of the body. It works by inhibiting the growth and spread of cancer cells, as well as blocking the formation of new blood vessels that tumors need to grow.Hepatocellular Carcinoma (Liver Cancer): Sorafenat is also used in the treatment of advanced hepatocellular carcinoma, which is the most common form of primary liver cancer. It helps slow down the progression of the disease and may improve overall survival in some patients.
Side Effect:
• Fatigue or weakness• Diarrhea• Nausea and vomiting• Loss of appetite• Abdominal pain or discomfort• Hand-foot skin reaction (palmar-plantar erythrodysesthesia), causing redness, swelling, and pain on the palms of hands and soles of feet• Rash or skin changes• Hair thinning or changes in hair color• High blood pressure (hypertension)• Changes in taste
Dosages:
Renal Cell Carcinoma (Kidney Cancer):The typical starting dosage for advanced renal cell carcinoma is often 400mg (two tablets of Sorafenat 200mg) taken orally once daily, either with or without food.Your doctor may adjust the dosage based on your response to treatment and any side effects you experience.
Hepatocellular Carcinoma (Liver Cancer):For advanced hepatocellular carcinoma, the recommended dosage is usually 400mg (two tablets of Sorafenat 200mg) taken orally once daily, either with or without food.Dosage adjustments may be made by your doctor based on your individual situation.
FAQs:
1. What is Sorafenat 200mg used for?Ans. Sorafenat 200mg tablets are used to treat advanced renal cell carcinoma (kidney cancer) and advanced hepatocellular carcinoma (liver cancer) when other treatment options are not suitable or have been ineffective.
2. How does Sorafenat work?Ans. Sorafenat is a targeted therapy that works by inhibiting specific enzymes and pathways involved in the growth and spread of cancer cells. It blocks the formation of new blood vessels that tumors need to grow and helps control the progression of the disease.
3. How should I take Sorafenat 200mg tablets?Ans. Take Sorafenat exactly as prescribed by your healthcare provider. The usual dose is 400mg (two tablets) taken orally once daily, with or without food. Do not adjust the dosage without consulting your doctor.
4. What are the common side effects of Sorafenat?Ans. Common side effects may include fatigue, diarrhea, nausea, vomiting, hand-foot skin reaction, rash, high blood pressure, changes in taste, and hair thinning. Your doctor will monitor you for these and other potential side effects.
Additional Information:
- Production Capacity: 1000
Endace 40 Megestrol Acetate Tablets
Minimum Order Quantity: 1 Stripe
Product Brochure
Strength | 40 mg |
Pack Size | 1*10 Tablet |
Pack Type | Box |
Brand Name | Endace 40 |
Manufacturer | Samarth Life Sciences Pvt Ltd |
Country of Origin | Made in India |
Endace 40 Megestrol Acetate Tablets are a medication used in the treatment of certain medical conditions, often related to hormonal imbalances or cancer. Megestrol acetate is the active ingredient in Endace 40, and it belongs to a class of drugs known as progestins. These drugs have various effects on the body, including regulating hormone levels and affecting the growth of certain cells.
Uses:
Breast Cancer: Endace 40 Megestrol Acetate Tablets may be used in the treatment of advanced breast cancer, particularly in postmenopausal women with hormone receptor-positive tumors. It is often considered when other treatments have not been effective.Endometrial Cancer: Megestrol acetate is sometimes prescribed as a part of therapy for endometrial cancer, which affects the lining of the uterus. It may be used in combination with other treatments or as a palliative option for advanced cases.Cachexia and Anorexia: In cancer patients, especially those with advanced disease or undergoing chemotherapy, Endace 40 Megestrol Acetate Tablets may be used to help manage cachexia (severe weight loss and muscle wasting) and anorexia (loss of appetite).HIV-Related Weight Loss: Megestrol acetate can be prescribed to manage significant weight loss and wasting syndrome in individuals with HIV/AIDS.Palliative Care: In palliative care settings, Megestrol acetate may be used to improve appetite, promote weight gain, and enhance overall quality of life in patients with advanced cancer or other debilitating conditions.
Side Effect:
• Weight gain• Fluid retention• Increased appetite• Mood changes (e.g., depression, anxiety)• Changes in menstrual periods• Hot flashes• Nausea• Vomiting
Dosages:
For Breast Cancer or Endometrial Cancer:The typical recommended dosage of Endace 40 Megestrol Acetate Tablets for the treatment of advanced breast cancer or endometrial cancer may range from 40 mg to 320 mg per day, taken orally in divided doses.
For Cachexia and Anorexia:The dosage for managing weight loss and appetite in cancer patients may range from 800 mg to 1,000 mg per day, taken orally in divided doses.
Dosage Adjustment and Monitoring:Your healthcare provider will closely monitor your progress through regular check-ups and may adjust the dosage based on your response and any potential side effects.Dosage adjustments may be made gradually to achieve the desired effect while minimizing side effects.
FAQs:
1. What is Endace 40 Megestrol Acetate used for?Ans. Endace 40 Megestrol Acetate Tablets are primarily used for the treatment of certain types of cancer, including advanced breast cancer and endometrial cancer. They are also prescribed to manage symptoms such as weight loss and loss of appetite in cancer patients and individuals with HIV/AIDS.
2. How does Megestrol Acetate work in treating cancer and related symptoms?Ans. Megestrol acetate is a synthetic progestin that may have anti-cancer effects in hormone-sensitive tumors. It can also help improve appetite, promote weight gain, and manage symptoms of cachexia and anorexia.
3. How should I take Endace 40 Megestrol Acetate Tablets?Ans. Endace 40 Megestrol Acetate Tablets are typically taken orally with or without food, as directed by your doctor. The dosage and treatment plan will depend on your specific medical condition and response to the medication.
4. What are the common side effects of Endace 40 Megestrol Acetate?Ans. Common side effects may include weight gain, fluid retention, increased appetite, mood changes, changes in menstrual periods, and nausea. Your doctor will monitor you for these and other potential side effects.
Additional Information:
- Production Capacity: 1000
Geftinat 250mg Gefitinib Tablets
Minimum Order Quantity: 1 Bottle
Product Brochure
Strength | 250 mg |
Packaging Type | Box |
Brand | Geftinat 250mg |
Usage/Application | Hospital |
Form | Tablet |
Country of Origin | Made in India |
Introduction:
Geftinat 250mg Gefitinib Tablets is a medication used in the treatment of non-small cell lung cancer (NSCLC) that is driven by specific genetic mutations in the epidermal growth factor receptor (EGFR) gene. It is classified as a tyrosine kinase inhibitor, which targets and inhibits the growth of cancer cells by blocking certain signaling pathways. Here is an introduction to Geftinat 250mg Gefitinib Tablets.
Uses:
Locally Advanced NSCLC with EGFR Mutations: Geftinat is indicated for the treatment of locally advanced NSCLC (non-small cell lung cancer) with specific EGFR gene mutations.
Metastatic NSCLC with EGFR Mutations: Geftinat is used to treat metastatic NSCLC (non-small cell lung cancer) with the same specific EGFR mutations.
First-Line Treatment: Geftinat may be prescribed as a first-line treatment for patients with NSCLC and EGFR mutations. It can be used alone or in combination with other therapies, depending on the specific treatment plan.
Maintenance Therapy: In some cases, Geftinat may be recommended as maintenance therapy after the initial treatment to help control the progression of the cancer.
Side Effect:
• Skin Rash or Acne-like Eruptions
• Diarrhea
• Nausea
• Vomiting
• Fatigue
• Decreased Appetite
• Dry Skin
• Nail Changes (such as brittleness)
• Mouth Sores or Ulcers
Dosages:
For Non-Small Cell Lung Cancer (NSCLC) with EGFR Mutations:
The typical dosage of Geftinat for NSCLC with EGFR mutations is 250 mg taken orally once daily.
Geftinat is usually taken on an empty stomach, at least one hour before or two hours after a meal.
The tablets should be swallowed whole with water and not crushed or split.
Dosage Adjustment and Administration:
Your oncologist will determine the most appropriate dosage and treatment plan based on your specific genetic mutations, overall health, and treatment goals.
Regular follow-up appointments, genetic testing, and other assessments will be conducted to assess the effectiveness of the treatment and make any necessary adjustments.
FAQs:
1. What is Geftinat 250mg Gefitinib Tablet used for?
Ans. Geftinat is primarily used to treat non-small cell lung cancer (NSCLC) that has specific epidermal growth factor receptor (EGFR) gene mutations.
2. How does Geftinat work in cancer treatment?
Ans. Geftinat is a tyrosine kinase inhibitor that targets and inhibits the activity of the EGFR protein, which is overexpressed in some cancer cells. By blocking EGFR signaling, the medication slows down the growth and spread of cancer cells.
3. How is Geftinat 250mg Gefitinib Tablet taken?
Ans. Geftinat is taken orally as a tablet. It is usually taken on an empty stomach, at least one hour before or two hours after a meal.
4. Can Geftinat be used for other types of cancer?
Ans. Geftinat is specifically approved for the treatment of NSCLC with EGFR mutations. Its use for other types of cancer may be considered on a case-by-case basis by your oncologist.
Additional Information:
- Production Capacity: 1000