Cancer

Product Details:

Introduction To Esentra 120mg Injection

Esentra 120mg Injection consists of the active ingredient Denosumab. It is a medication used to treat osteoporosis, characterized by weakened bones. It is also prescribed to prevent bone complications in patients with certain types of cancer, such as multiple myeloma and bone metastases. Esentra 120mg Injection works by inhibiting a protein called RANK ligand, which plays a role in the breakdown of bone tissue. Studies proved it can significantly increase bone density, reducing fracture risk in postmenopausal women with osteoporosis and patients with cancer-related bone loss. Close monitoring of renal function may be necessary for patients with moderate renal impairment.

Esentra 120mg Injection should not be used in individuals with known hypersensitivity or allergic reactions to its components. Adequate calcium and vitamin D supplementation is required to ensure during the treatment. It is not approved for use in children and adolescents. Its safety and effectiveness in pediatric populations have not been established, so its use is contraindicated in individuals under 18. This medication should be used cautiously in individuals with pre-existing hypoparathyroidism, characterized by low parathyroid hormone levels.

Uses of Esentra 120mg Injection

Esentra 120mg Injection is used in the treatment of the following condition:
· Osteoporosis
· Bone loss due to hormonal therapy in breast or prostate cancer
· Multiple myeloma (cancer affects plasma cells in the bone marrow)
· Bone metastases (cancer that spreads to bone)

Safety Advices for Esentra 120mg Injection  

Pregnancy

The safety of using Esentra 120mg Injection during pregnancy has not been established. Limited studies are available regarding the use of this medication in pregnant women, so it is recommended to use caution and consult a doctor before considering its use during pregnancy.  

Breast Feeding

Whether Esentra 120mg Injection is excreted in milk is unknown. So it is better to consult a healthcare provider if you are a breastfeeding mother before taking this medication.  

Lungs

If you have a lung or respiratory disorders history, it is important to consult your healthcare provider before taking Esentra 120mg Injection.  

Liver

Esentra 120mg Injection is primarily metabolized in the liver, and its safety has not been extensively studied in individuals with severe liver impairment. It is crucial to communicate any pre-existing liver conditions or changes in liver function to your healthcare provider to ensure this medication's safe and effective use.  

Alcohol

It is generally recommended to avoid or limit alcohol consumption while taking Esentra 120mg Injection. Alcohol can interact with this medication, potentially increasing the risk of side effects.  

Driving

Patients receiving Esentra 120mg Injection should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely. 

Side Effects of Esentra 120mg Injection

Serious:
· Osteonecrosis of the jaw (severe necrosis or death of jaw cells)
· Atypical femoral fractures
· Hypocalcemia (low blood calcium levels)

Common: 
· Injection site reactions
· Back pain
· Musculoskeletal pain
· Infections
· Abdominal pain
· Headache
· Hypophosphatemia (low blood phosphate levels)

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Canmab 150mg Injection

Canmab 150mg Injection consists of Trastuzumab as an active constituent which is indicated for its use in HER 2 breast cancer. In HER 2 positive patients, the breast cancer cells are mostly composed of HER2 proteins that cause rapid development of cancer tumor by serving as a signal to the cancerous. This medication is also used to treat metastatic gastric cancer with increased levels of HER2 proteins.

Her 2 positive breast cancer are most aggressive in nature. The targeted therapy for her 2 positive breast cancer works by selectively targeting the proteins that are responsible for the growth, development, and spread of cancer. Use effective birth control during the treatment and for at least 7 months after the final dose.

Canmab 150mg Injection is not recommended for patients aged under 18, patients who have severe breathing problems or need oxygen treatment. It is necessary to let your physician know if you have any heart problems, breathlessness, or have ever had any other cancer treatment. Make sure you inform your physician of all the medicines, including supplements and herbal medicines, you are taking before you start treatment with this medication.

Uses of Canmab 150mg Injection

Canmab 150mg Injection is indicated for its use in the following conditions:

Advanced and metastatic breast cancer

Metastatic gastric cancer

Safety Advices for Canmab 150mg Injection  

Pregnancy

Discuss with your physician before taking this Canmab 150mg Injection if you are pregnant or think you might be pregnant. Do not take this medicine during the pregnancy unless advised by the doctor to take as it may cause to the unborn baby.  

Breast Feeding

Avoid breastfeeding your baby while on the treatment with Canmab 150mg Injection atleast for at least seven months after the final dose.  

Lungs

Talk to your doctor if you have any lung conditions before starting treatment with Canmab 150mg Injection.   

Liver

You need to tell your physician if you have any liver disorders before starting Canmab 150mg Injection as it requires dosage adjustment for severe liver impairment.  

Alcohol

Consult your doctor to know if it is safe to consume alcohol while you are on treatment with Canmab 150mg Injection.  

Driving

Canmab 150mg Injection can cause unusual tiredness and dizziness. Hence, it is advised to avoid driving or handling machinery during the treatment.

Side Effects of Canmab 150mg Injection

Side effects are unwanted symptoms caused by medicines. Even though all medicines cause side effects, not everyone gets them.

Serious
·       Heart Problems
·       Allergic reactions
·       Kidney problems
·       Breathing difficulties

Common
·       Fever
·       Visual disturbances
·       Nose bleeds or runny nose
·       Hair loss
·       Dizziness
·       Nail disorders
·       Weight loss
·       Loss of appetite
·       Bruising
·       Dry mouth
·       Liver  inflammation
·       Muscle pain
·       Asthma/ lung disorders

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Hertraz 440mg Injection

Hertraz 440mg Injection consists of Trastuzumab as an active constituent which is indicated for its use in HER 2 breast cancer. In HER 2 positive patients, the breast cancer cells are mostly composed of HER2 proteins that cause rapid development of cancer tumor by serving as a signal to the cancerous. This medication is also used to treat metastatic gastric cancer with increased levels of HER2 proteins.

Her 2 positive breast cancer are most aggressive in nature. The targeted therapy for her 2 positive breast cancer works by selectively targeting the proteins that are responsible for the growth, development, and spread of cancer. Use effective birth control during the treatment and for at least 7 months after the final dose.

Hertraz 440mg Injection is not recommended for patients aged under 18, patients who have severe breathing problems or need oxygen treatment. It is necessary to let your physician know if you have any heart problems, breathlessness, or have ever had any other cancer treatment. Make sure you inform your physician of all the medicines, including supplements and herbal medicines, you are taking before you start treatment with this medication.

Uses of Hertraz 440mg Injection

Hertraz 440mg Injection is indicated for its use in the following conditions:

Advanced and metastatic breast cancer

Metastatic gastric cancer

Safety Advices for Hertraz 440mg Injection  

Pregnancy

Discuss with your physician before taking this Hertraz 440mg Injection if you are pregnant or think you might be pregnant. Do not take this medicine during the pregnancy unless advised by the doctor to take as it may cause to the unborn baby.  

Breast Feeding

Avoid breastfeeding your baby while on the treatment with Hertraz 440mg Injection atleast for at least seven months after the final dose.  

Lungs

Talk to your doctor if you have any lung conditions before starting treatment with Hertraz 440mg Injection.   

Liver

You need to tell your physician if you have any liver disorders before starting Hertraz 440mg Injection as it requires dosage adjustment for severe liver impairment.  

Alcohol

Consult your doctor to know if it is safe to consume alcohol while you are on treatment with Hertraz 440mg Injection.  

Driving

Hertraz 440mg Injection can cause unusual tiredness and dizziness. Hence, it is advised to avoid driving or handling machinery during the treatment.

Side Effects of Hertraz 440mg Injection

Side effects are unwanted symptoms caused by medicines. Even though all medicines cause side effects, not everyone gets them.

Serious
·       Heart Problems
·       Allergic reactions
·       Kidney problems
·       Breathing difficulties

Common
·       Fever
·       Visual disturbances
·       Nose bleeds or runny nose
·       Hair loss
·       Dizziness
·       Nail disorders
·       Weight loss
·       Loss of appetite
·       Bruising
·       Dry mouth
·       Liver  inflammation
·       Muscle pain
·       Asthma/ lung disorders

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Hermab 440mg Injection

Hermab 440mg Injection consists of Trastuzumab as an active constituent which is indicated for its use in HER 2 breast cancer. In HER 2 positive patients, the breast cancer cells are mostly composed of HER2 proteins that cause rapid development of cancer tumor by serving as a signal to the cancerous. This medication is also used to treat metastatic gastric cancer with increased levels of HER2 proteins.

Her 2 positive breast cancer are most aggressive in nature. The targeted therapy for her 2 positive breast cancer works by selectively targeting the proteins that are responsible for the growth, development, and spread of cancer. Use effective birth control during the treatment and for at least 7 months after the final dose.

Hermab 440mg Injection is not recommended for patients aged under 18, patients who have severe breathing problems or need oxygen treatment. It is necessary to let your physician know if you have any heart problems, breathlessness, or have ever had any other cancer treatment. Make sure you inform your physician of all the medicines, including supplements and herbal medicines, you are taking before you start treatment with this medication.

Uses Of Hermab 440mg Injection

Hermab 440mg Injection is indicated for its use in the following conditions:

Advanced and metastatic breast cancer

Metastatic gastric cancer

Safety Advices For Hermab 440mg Injection  

Pregnancy

Discuss with your physician before taking this Hermab 440mg Injection if you are pregnant or think you might be pregnant. Do not take this medicine during the pregnancy unless advised by the doctor to take as it may cause to the unborn baby.  

Breast Feeding

Avoid breastfeeding your baby while on the treatment with Hermab 440mg Injection atleast for at least seven months after the final dose.  

Lungs

Talk to your doctor if you have any lung conditions before starting treatment with Hermab 440mg Injection.   

Liver

You need to tell your physician if you have any liver disorders before starting Hermab 440mg Injection as it requires dosage adjustment for severe liver impairment.  

Alcohol

Consult your doctor to know if it is safe to consume alcohol while you are on treatment with Hermab 440mg Injection.  

Driving

Hermab 440mg Injection can cause unusual tiredness and dizziness. Hence, it is advised to avoid driving or handling machinery during the treatment.

Side Effects Of Hermab 440mg Injection

Side effects are unwanted symptoms caused by medicines. Even though all medicines cause side effects, not everyone gets them.

Serious
·       Heart Problems
·       Allergic reactions
·       Kidney problems
·       Breathing difficulties

Common
·       Fever
·       Visual disturbances
·       Nose bleeds or runny nose
·       Hair loss
·       Dizziness
·       Nail disorders
·       Weight loss
·       Loss of appetite
·       Bruising
·       Dry mouth
·       Liver  inflammation
·       Muscle pain
·       Asthma/ lung disorders

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Tarzed 440mg Injection

Tarzed 440mg Injection consists of Trastuzumab as an active constituent which is indicated for its use in HER 2 breast cancer. In HER 2 positive patients, the breast cancer cells are mostly composed of HER2 proteins that cause rapid development of cancer tumor by serving as a signal to the cancerous. This medication is also used to treat metastatic gastric cancer with increased levels of HER2 proteins.

Her 2 positive breast cancer are most aggressive in nature. The targeted therapy for her 2 positive breast cancer works by selectively targeting the proteins that are responsible for the growth, development, and spread of cancer. Use effective birth control during the treatment and for at least 7 months after the final dose.

Tarzed 440mg Injection is not recommended for patients aged under 18, patients who have severe breathing problems or need oxygen treatment. It is necessary to let your physician know if you have any heart problems, breathlessness, or have ever had any other cancer treatment. Make sure you inform your physician of all the medicines, including supplements and herbal medicines, you are taking before you start treatment with this medication.

Uses of Tarzed 440mg Injection

Tarzed 440mg Injection is indicated for its use in the following conditions:

Advanced and metastatic breast cancer

Metastatic gastric cancer

Safety Advices for Tarzed 440mg Injection  

Pregnancy

Discuss with your physician before taking this Tarzed 440mg Injection if you are pregnant or think you might be pregnant. Do not take this medicine during the pregnancy unless advised by the doctor to take as it may cause to the unborn baby.  

Breast Feeding

Avoid breastfeeding your baby while on the treatment with Tarzed 440mg Injection atleast for at least seven months after the final dose.  

Lungs

Talk to your doctor if you have any lung conditions before starting treatment with Tarzed 440mg Injection.   

Liver

You need to tell your physician if you have any liver disorders before starting Tarzed 440mg Injection as it requires dosage adjustment for severe liver impairment.  

Alcohol

Consult your doctor to know if it is safe to consume alcohol while you are on treatment with Tarzed 440mg Injection.  

Driving

Tarzed 440mg Injection can cause unusual tiredness and dizziness. Hence, it is advised to avoid driving or handling machinery during the treatment.

Side Effects of Tarzed 440mg Injection

Side effects are unwanted symptoms caused by medicines. Even though all medicines cause side effects, not everyone gets them.

Serious
·       Heart Problems
·       Allergic reactions
·       Kidney problems
·       Breathing difficulties

Common
·       Fever
·       Visual disturbances
·       Nose bleeds or runny nose
·       Hair loss
·       Dizziness
·       Nail disorders
·       Weight loss
·       Loss of appetite
·       Bruising
·       Dry mouth
·       Liver  inflammation
·       Muscle pain
·       Asthma/ lung disorders

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Vivitra 375mg Injection

Vivitra 375mg Injection consists of Trastuzumab as an active constituent which is indicated for its use in HER 2 breast cancer. In HER 2 positive patients, the breast cancer cells are mostly composed of HER2 proteins that cause rapid development of cancer tumor by serving as a signal to the cancerous. This medication is also used to treat metastatic gastric cancer with increased levels of HER2 proteins.

Her 2 positive breast cancer are most aggressive in nature. The targeted therapy for her 2 positive breast cancer works by selectively targeting the proteins that are responsible for the growth, development, and spread of cancer. Use effective birth control during the treatment and for at least 7 months after the final dose.

Vivitra 375mg Injection is not recommended for patients aged under 18, patients who have severe breathing problems or need oxygen treatment. It is necessary to let your physician know if you have any heart problems, breathlessness, or have ever had any other cancer treatment. Make sure you inform your physician of all the medicines, including supplements and herbal medicines, you are taking before you start treatment with this medication.

Uses of Vivitra 375mg Injection

Vivitra 375mg Injection is indicated for its use in the following conditions:

Advanced and metastatic breast cancer

Metastatic gastric cancer

Safety Advices for Vivitra 375mg Injection  

Pregnancy

Discuss with your physician before taking this Vivitra 375mg Injection if you are pregnant or think you might be pregnant. Do not take this medicine during the pregnancy unless advised by the doctor to take as it may cause to the unborn baby.  

Breast Feeding

Avoid breastfeeding your baby while on the treatment with Vivitra 375mg Injection atleast for at least seven months after the final dose.  

Lungs

Talk to your doctor if you have any lung conditions before starting treatment with Vivitra 375mg Injection.   

Liver

You need to tell your physician if you have any liver disorders before starting Vivitra 375mg Injection as it requires dosage adjustment for severe liver impairment.  

Alcohol

Consult your doctor to know if it is safe to consume alcohol while you are on treatment with Vivitra 375mg Injection.

Driving

 Vivitra 375mg Injection can cause unusual tiredness and dizziness. Hence, it is advised to avoid driving or handling machinery during the treatment.

Side Effects Of Vivitra 375mg Injection

Side effects are unwanted symptoms caused by medicines. Even though all medicines cause side effects, not everyone gets them.

Serious
·       Heart Problems
·       Allergic reactions
·       Kidney problems
·       Breathing difficulties

Common
·       Fever
·       Visual disturbances
·       Nose bleeds or runny nose
·       Hair loss
·       Dizziness
·       Nail disorders
·       Weight loss
·       Loss of appetite
·       Bruising
·       Dry mouth
·       Liver  inflammation
·       Muscle pain
·       Asthma/ lung disorders

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

 

Introduction To Kadcyla 160mg Injection

Kadcyla 160mg Injection consists of the active ingredient Ado-Trastuzumab emtansine. It is a prescription medication used to treat HER2-positive breast cancer that has spread to other parts of the body or has not responded to other treatments. It is a combination of two drugs: trastuzumab, which is an antibody that targets HER2 receptors, and emtansine, which is a chemotherapy drug that kills cancer cells.  It is indicated to treat breast cancer in the early stages as well as advanced stages where patients develop recurrence within six months of chemotherapy treatment. This medication acts against tumors that produce more than the normal amount of a certain protein (known as HER2 protein).

Patients with residual breast cancer after chemotherapy treatment and HER2-targeted therapy have a poorer prognosis than those with no residual cancer. Report to your physician immediately in case you experience side effects such as allergic reactions, unusual bleeding, etc. This medication does not show any adverse effects on the kidney. In rare cases, an infusion reaction is seen. Like all other medications, it shows mild side effects like nausea, vomiting, diarrhea, and hair loss.

Uses of Kadcyla 160mg Injection

Kadcyla 160mg Injection is indicated for its use in the following conditions:

Advanced and metastatic breast cancer

Metastatic gastric cancer

Safety Advices for Kadcyla 160mg Injection  

Pregnancy

Discuss with your physician before taking this Kadcyla 160mg Injection if you are pregnant or think you might be pregnant. Do not take this medicine during the pregnancy unless advised by the doctor to take as it may cause harm to the unborn baby.  

Breast Feeding

Avoid breastfeeding your baby while on the treatment with Kadcyla 160mg Injection for at least seven months after the final dose.  

Lungs

Ado-trastuzumab emtansine safety and efficacy have not been extensively studied. So patients with pre-existing lung conditions should consult a doctor before taking it.  

Liver

Kadcyla 160mg Injection can affect liver function, and in rare cases, it can cause liver damage, including hepatotoxicity and liver failure. Therefore, it's important to inform your healthcare professional if you have any history of liver problems, such as hepatitis or cirrhosis, before starting treatment.  

Alcohol

It is recommended to avoid consuming alcohol while taking Ado-Trastuzumab Emtansine, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving

Kadcyla 160mg Injection can cause unusual tiredness and dizziness. Hence, it is advised to avoid driving or handling machinery during the treatment.

Side Effects of Kadcyla 160mg Injection

Serious:
· Infusion reactions, including fever, chills, rash, or difficulty breathing
· Lung problems, including shortness of breath, cough, or fever
· Heart problems, including heart failure or abnormal heart rhythms
· Severe bleeding or bruising
· Nerve damage, including numbness, tingling, or weakness
· Severe allergic reactions

Common:
· Fatigue
· Nausea
· Constipation
· Muscle or joint pain
· Headache
· Fever
· Low platelet count
· High liver enzyme levels
· Low red blood cell count
· Loss of appetite
· Rash or itching

 

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Kadcyla 100mg Injection

Kadcyla 100mg Injection Consists Of The Active Ingredient Ado-Trastuzumab Emtansine. It Is A Prescription Medication Used To Treat HER2-Positive Breast Cancer That Has Spread To Other Parts Of The Body Or Has Not Responded To Other Treatments. It Is A Combination Of Two Drugs: Trastuzumab, Which Is An Antibody That Targets HER2 Receptors, And Emtansine, Which Is A Chemotherapy Drug That Kills Cancer Cells.  It Is Indicated To Treat Breast Cancer In The Early Stages As Well As Advanced Stages Where Patients Develop Recurrence Within Six Months Of Chemotherapy Treatment. This Medication Acts Against Tumors That Produce More Than The Normal Amount Of A Certain Protein (Known As HER2 Protein).

Patients With Residual Breast Cancer After Chemotherapy Treatment And HER2-Targeted Therapy Have A Poorer Prognosis Than Those With No Residual Cancer. Report To Your Physician Immediately In Case You Experience Side Effects Such As Allergic Reactions, Unusual Bleeding, Etc. This Medication Does Not Show Any Adverse Effects On The Kidney. In Rare Cases, An Infusion Reaction Is Seen. Like All Other Medications, It Shows Mild Side Effects Like Nausea, Vomiting, Diarrhea, And Hair Loss.

Uses Of Kadcyla 100mg Injection

Kadcyla 100mg Injection Is Indicated For Its Use In The Following Conditions:

Advanced And Metastatic Breast Cancer

Metastatic Gastric Cancer

Safety Advices For Kadcyla 100mg Injection  

Pregnancy

Discuss With Your Physician Before Taking This Kadcyla 100mg Injection If You Are Pregnant Or Think You Might Be Pregnant. Do Not Take This Medicine During The Pregnancy Unless Advised By The Doctor To Take As It May Cause Harm To The Unborn Baby.  

Breast Feeding

Avoid Breastfeeding Your Baby While On The Treatment With Kadcyla 100mg Injection At Least Seven Months After The Final Dose.  

Lungs

Ado-Trastuzumab Emtansine Safety And Efficacy Have Not Been Extensively Studied. So Patients With Pre-Existing Lung Conditions Should Consult A Doctor Before Taking It.  

Liver

Kadcyla 100mg Injection Can Affect Liver Function, And In Rare Cases, It Can Cause Liver Damage, Including Hepatotoxicity And Liver Failure. Therefore, It's Important To Inform Your Healthcare Professional If You Have Any History Of Liver Problems, Such As Hepatitis Or Cirrhosis, Before Starting Treatment.  

Alcohol

It Is Recommended To Avoid Consuming Alcohol While Taking Ado-Trastuzumab Emtansine, As Alcohol Can Increase The Risk Of Certain Side Effects Associated With The Medication, Such As Stomach Ulcers Or Gastrointestinal Bleeding.  

Driving

Kadcyla 100mg Injection Can Cause Unusual Tiredness And Dizziness. Hence, It Is Advised To Avoid Driving Or Handling Machinery During The Treatment.

Side Effects Of Kadcyla 100mg Injection

Serious:
· Infusion Reactions, Including Fever, Chills, Rash, Or Difficulty Breathing
· Lung Problems, Including Shortness Of Breath, Cough, Or Fever
· Heart Problems, Including Heart Failure Or Abnormal Heart Rhythms
· Severe Bleeding Or Bruising
· Nerve Damage, Including Numbness, Tingling, Or Weakness
· Severe Allergic Reactions

Common:
· Fatigue
· Nausea
· Constipation
· Muscle Or Joint Pain
· Headache
· Fever
· Low Platelet Count
· High Liver Enzyme Levels
· Low Red Blood Cell Count
· Loss Of Appetite
· Rash Or Itching

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Pazinib 200mg Tablet

Pazinib 200mg tablet contains the active substance pazopanib. It is an antineoplastic drug that belongs to the class tyrosine kinase inhibitor. It is used in adults to treat advanced kidney cancer or has spread to other organs. It is also indicated to treat certain forms of soft-tissue sarcoma, a type of cancer affecting the supportive tissues of the body. This medicine works by preventing the activity of proteins involved in the growth and spread of cancer cells. 

Do not take Pazinib 200mg tablet if you are allergic to Pazopanib or any other ingredients of this medicine. Before initiating the treatment, inform your physician if you have kidney, heart, lung, or liver problems, bleeding disorders, stomach or bowel problems, and thyroid problems. This tablet can raise your blood pressure. It is necessary to check your blood pressure regularly during the treatment. No dose adjustments are required for patients with kidney diseases. 

Your doctor will advise you to stop Pazinib 200mg tablet at least 7 days before any surgeries or dental operations that you are undergoing, as it may affect wound healing. This medicine is not recommended for people aged under 18.

Uses of Pazinib 200mg Tablet

Advanced renal cell carcinoma

Advanced soft tissue sarcoma

How to consume Pazinib 200mg Tablet

Your doctor will decide the dose and duration of the treatment based on your disease condition, severity, and other factors. Take the tablets as prescribed by your doctor. Do not break, crush, or chew the tablets. Swallow the tablet whole with a glass of water. 

Safety Advices for Pazinib 200mg Tablet  

Pregnancy

Pazinib 200mg tablet is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for at least 2 weeks after your last dose is necessary.    

Breast Feeding

Breastfeeding is not recommended in patients taking Pazinib 200mg tablet because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs

It is unknown whether Pazinib 200mg tablet can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver

Pazinib 200mg tablet is unsafe when administered in patients with severe liver diseases. Dose adjustments are necessary for moderate liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol

It is unknown whether it is safe to consume alcohol when taking Pazinib 200mg tablet.

Driving

Driving or operating heavy machinery is unsafe after taking Pazinib 200mg tablet because you may feel dizzy, drowsy, or have blurred vision.

Side Effects of Pazinib 200mg Tablet

 Common
· Hypertension
· Hair color change
· Increased glucose levels
· Decreased weight, decrease in appetite
· Diarrhea
· Nausea, vomiting
· Muscle and joint pain
· Headache
· Shortness of breath
· Tiredness

Serious
· Heart problems
· Bleeding from the anus, mouth
· Hypothyroidism
· Interstitial lung disease
· Infections

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

PRODUCT INTRODUCTION

Erlonat 150 Tablet is used in the treatment of non-small cell lung cancer and pancreatic cancer.
Erlonat 150 Tablet should be taken on an empty stomach or should be taken one hour before or 2 hour after meal.  You should continue to take it as long as your doctor advises it. The duration of treatment varies according to your needs and response to treatment. 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.
The most common side effects of this medicine include nausea, vomiting, fatigue, rash, and weight loss. It may cause severe diarrhea, drink plenty of fluids or consult with your doctor if it bothers you. It makes you sensitive towards sunlight, hence wear protective clothing or use sunscreen while going out. In case you develop ulceration in mouth, changes in your vision, or breathing difficulties than it is better to inform the doctor. Your doctor may advise for regular monitoring of liver function while you are taking this medicine.
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.  It is advised to quit smoking while taking this medicine as it can affect the working of the medicine. If you have to take an antacid or any other medicine, take it at a gap of at least 2 hours after taking the cancer medicine.

USES OF ERLONAT TABLET
• Non-small cell lung cancer
• Pancreatic cancer

BENEFITS OF ERLONAT TABLET
In Non-small cell lung cancerNon-small cell lung cancer is one of the major kinds of lung cancer and it affects both smokers as well as non-smokers. Erlonat 150 Tablet helps treat non-small cell lung cancer and may be given alone or in combination with other medicines. It is a potent and very toxic medicine and you should discuss the risks and benefits with your doctor. You should avoid drinking alcohol while having this treatment and drink plenty of water to stay hydrated.In Pancreatic cancerPancreas are very essential for digestion of whatever you eat and also for metabolism of blood sugar levels as they produce the body’s natural insulin. This medicine will help to control pancreatic cancer, and will relieve the symptoms such as, lack of appetite or unexplained weight loss. Erlonat 150 Tablet helps to stop the action of those chemicals that aid in pancreatic cancer growth and spread. It will help you live a longer and healthier life.

SIDE EFFECTS OF ERLONAT TABLET
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 themCommon side effects of Erlonat
• Abdominal pain
• Bone pain
• Breathlessness
• Constipation
• Cough
• Diarrhea
• Fatigue
• Fever
• Infection
• Muscle pain
• Nausea
• Rash
• Stomatitis (Inflammation of the mouth)
• Vomiting
• Weight loss

HOW TO USE ERLONAT TABLET
Take this medicine in the dose and duration as advised by your doctor. Swallow it as a whole. Do not chew, crush or break it. Erlonat 150 Tablet is to be taken empty stomach.

WHAT IF YOU FORGET TO TAKE ERLONAT TABLET?
If you miss a dose of Erlonat 150 Tablet, skip it and continue with your normal schedule. Do not double the dose.

Additional Information:

• Delivery Time: 8 to 15 days

Product Details:

Product Introduction

Temoside 100 Capsule is used in the treatment of a specific type of cancer of the brain. It is used to treat brain tumors if they return or get worse after standard treatment. It may be also used to treat other conditions, as determined by the doctor.

Temoside 100 Capsule should be taken empty stomach and at same time each day to make sure it has the best effect. 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.

Before taking it, tell your doctor if have bleeding, liver, or kidney problems or are taking any medicines to treat infections. Many other medicines can affect, or be affected by, this medicine so let your doctor know all medications you are using. This medicine is not recommended during pregnancy or while breastfeeding. It may harm your baby. You and your partner should avoid becoming pregnant or fathering a child for several months after your treatment with it has stopped.

Uses Of Temoside Capsule

Brain tumor

Side Effects Of Temoside Capsule

Common Side Effects Of Temoside
·      Nausea
·      Vomiting
·      Constipation
·      Headache
·      Fatigue
·      Convulsion
·      Coordination disorder
·      Diarrhea
·      Dizziness
·      Fever
·      Hair loss
·      Hemiparesis (weakness on one side of the body)
·      Insomnia (difficulty in sleeping)
·      Loss of appetite
·      Memory loss
·      Rash
·      Viral infection
·      Weakness

Safety Advice

Alcohol

It is not known whether it is safe to consume alcohol with Temoside 100 Capsule.

Pregnancy

Temoside 100 Capsule is unsafe to use during pregnancy as there is definite evidence of risk to the developing baby. However, the doctor may rarely prescribe it in some life-threatening situations if the benefits are more than the potential risks.

Breast Feeding

Temoside 100 Capsule is unsafe to use during breastfeeding. Data suggests that the drug may cause toxicity to the baby.

Driving

Temoside 100 Capsule may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.

Kidney

Temoside 100 Capsule is probably safe to use in patients with kidney disease. Limited data available suggests that dose adjustment of Temoside 100 Capsule may not be needed in these patients. Cautious use is advised in patients with severe kidney disease while they are taking Temoside 100 Capsule.

Liver

Temoside 100 Capsule should be used with caution in patients with severe liver disease. Dose adjustment of Temoside 100 Capsule may be needed. Limited information is available on the use of Temoside 100 Capsule in these patients. No dose adjustment is recommended in patients with mild to moderate liver disease.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

What Is Rozlytrek?

Rozlytrek (entrectinib) is a kinase inhibitor indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are ROS1-positive; and adult and pediatric patients 12 years of age and older with solid tumors that have a neurotrophic tyrosine receptor kinase (NTRK) gene fusion without a known acquired resistance mutation, are metastatic or where surgical resection is likely to result in severe morbidity, and have progressed following treatment or have no satisfactory alternative therapy.

What Are Side Effects Of Rozlytrek?

Rozlytrek may cause serious side effects including:
· hives
· difficulty breathing
· swelling of your face, lips, tongue, or throat
· bone pain
· problems moving
· fast or pounding heartbeats
· fluttering in your chest
· shortness of breath
· sudden dizziness
· nausea
· vomiting
· loss of appetite
· right side upper stomach pain
· swelling in your lower legs
· rapid weight gain
· cough
·  wheezing
· trouble breathing while laying down
· confusion
· hallucinations
· problems with memory or concentration
· dizziness
· mood changes
· trouble sleeping
· blurred vision
· double vision
· increased sensitivity to light
· seeing flashes of light
· "floaters" in your vision

Common Side Effects Of Rozlytrek Include:

· fatigue
· constipation
· changes in taste
· fluid retention/swelling
· dizziness
· diarrhea
· nausea
· impaired sense of touch
· shortness of breath
· muscle pain
· cognitive impairment
· weight gain
· cough
· vomiting
· fever
· joint pain
· vision disorders

Dosage For Rozlytrek

The recommended dosage of Rozlytrek for ROS1-Positive non-small cell lung cancer is 600 mg orally once daily. The recommended adult dosage of Rozlytrek for NTRK gene fusion-positive solid tumors is 600 mg orally once daily. The recommended dosage of Rozlytrek is based on body surface area.

What Drugs, Substances, Or Supplements Interact With Rozlytrek?

Rozlytrek may interact with grapefruit and grapefruit products, strong or moderate CYP3A inhibitors or inducers, and medications that prolong the QT/QTc interval. Tell your doctor all medications and supplements you use.

Rozlytrek During Pregnancy And Breastfeeding

Rozlytrek is not recommended for use during pregnancy; it may harm a fetus. Females of reproductive potential are advised to use effective contraception during treatment with Rozlytrek and for 5 weeks following the final dose. Males with female partners of reproductive potential are advised to use effective contraception during treatment with Rozlytrek and for 3 months after the final dose. Because of the potential adverse reactions in breastfed children, breastfeeding is not recommended during treatment with Rozlytrek and for 7 days after the final dose.

Additional Information

Our Rozlytrek Capsules, for Oral Use Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Product Introduction

Temoside 250 Capsule is used in the treatment of a specific type of cancer of the brain. It is used to treat brain tumors if they return or get worse after standard treatment. It may be also used to treat other conditions, as determined by the doctor.

Temoside 250 Capsule should be taken empty stomach and at same time each day to make sure it has the best effect. 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.

Before taking it, tell your doctor if have bleeding, liver, or kidney problems or are taking any medicines to treat infections. Many other medicines can affect, or be affected by, this medicine so let your doctor know all medications you are using. This medicine is not recommended during pregnancy or while breastfeeding. It may harm your baby. You and your partner should avoid becoming pregnant or fathering a child for several months after your treatment with it has stopped.

Uses Of Temoside Capsule

Brain tumor

Side Effects Of Temoside Capsule

Common Side Effects Of Temoside
·       Nausea
·       Vomiting
·       Constipation
·       Headach
·       Fatigue
·       Convulsion
·       Coordination disorder
·       Diarrhea
·       Dizziness
·       Fever
·       Hair loss
·       Hemiparesis (weakness on one side of the body)
·       Insomnia (difficulty in sleeping)
·       Loss of appetite
·       Memory loss
·        Rash
·       Viral infection
·       Weakness

Safety Advice

Alcohol

It is not known whether it is safe to consume alcohol with Temoside 250 Capsule.

Pregnancy

Temoside 250 Capsule is unsafe to use during pregnancy as there is definite evidence of risk to the developing baby. However, the doctor may rarely prescribe it in some life-threatening situations if the benefits are more than the potential risks.

Breast Feeding

Temoside 250 Capsule is unsafe to use during breastfeeding. Data suggests that the drug may cause toxicity to the baby.

Driving

Temoside 250 Capsule may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.

Kidney

Temoside 250 Capsule is probably safe to use in patients with kidney disease. Limited data available suggests that dose adjustment of Temoside 250 Capsule may not be needed in these patients. Cautious use is advised in patients with severe kidney disease while they are taking Temoside 250 Capsule.

Liver

Temoside 250 Capsule should be used with caution in patients with severe liver disease. Dose adjustment of Temoside 250 Capsule may be needed. Limited information is available on the use of Temoside 250 Capsule in these patients. No dose adjustment is recommended in patients with mild to moderate liver disease.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Lenangio 5mg Capsule

Lenangio 5mg Capsule belongs to the group of medicines known as Immunomodulatory agents. It contains the active ingredient Lenalidomide. It is indicated to treat adults with multiple myeloma, mantle cell lymphoma, myelodysplastic syndrome and follicular lymphoma. Multiple myeloma refers to the cancerous progression of plasma cells that are predominant in the bone marrow. These cells gather in the bone marrow and split uncontrollably. This type of cancer cannot be cured; however, the symptoms can be alleviated. Myelodysplastic Syndrome is a group of various blood and bone marrow diseases, where the blood cells become abnormal and do not function properly. Mantle cell lymphoma is a less common type of cancer that affects the lymph nodes. Follicular lymphoma is a slow-growing cancer that affects the B cells.

Inform your doctor if you have allergic reactions to Lenangio 5mg Capsule and its ingredients. Before taking treatment with this medication, let your physician know if you ever had blood clots, heart attack or if you smoke or have high blood pressure and cholesterol level. Inform your physician if you have viral infections like  hepatitis B infection, varicella zoster, HIV. Before and during treatment with this medication your healthcare provider will take regular blood test because it may cause fall in blood cells. It is not recommended for children below 18.

Uses of Lenangio 5mg Capsule

Multiple myeloma, myelodysplastic syndrome
Mantle cell lymphoma
Follicular lymphoma

Safety Advices for Lenangio 5mg Capsule  

Pregnancy

Lenangio 5mg Capsule is unsafe to use during pregnancy as it might be harmful to an unborn child. Inform your physician before starting this treatment if you are pregnant or think you might be pregnant.   

Breast Feeding

Lenangio 5mg Capsule is probably unsafe to use during breastfeeding as it is not known if this medication passes into breast milk and harms your baby.  

Lungs

Inform your physician before taking Lenangio 5mg Capsule if you have if you have any lung conditions.   

Liver

Inform your physician before starting treatment with Lenangio 5mg Capsule if you have severe liver problems including liver failure. Your physician will do blood tests to monitor your liver function.  

Alcohol

It is not known whether it is safe to consume alcohol while taking Lenangio 5mg Capsule. Consult your doctor for advice.

Driving

Do not drive or operate machines if you feel dizzy, tired, sleepy, have vertigo or blurred vision after taking Lenangio 5mg Capsule.

Side Effects of Lenangio 5mg Capsule

Serious:

·  Severe allergic reactions
·  High risk of secondary cancer
·  Liver toxicity
·  Blurred vision
·  Difficulty speaking
· Faster heartbeat
· Chest pain or leg pain
· Swelling in the ankles
· Dizziness
· Unusual bleeding or bruising
· Blood clot formation

Common:
· Tiredness
· Neutropenia
· Constipation
· Diarrhea
· Muscle cramps
· Anaemia
· Fever
· Back pain
· Nausea
· Upper respiratory tract infection
· Breathlessness
· Tremor
· Rash
· Cough
· Headache
· Thyroid problems
· Dehydration
· Skin problems

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Lenangio 10mg Capsule

Lenangio 10mg Capsule belongs to the group of medicines known as Immunomodulatory agents. It contains the active ingredient Lenalidomide. It is indicated to treat adults with multiple myeloma, mantle cell lymphoma, myelodysplastic syndrome and follicular lymphoma. Multiple myeloma refers to the cancerous progression of plasma cells that are predominant in the bone marrow. These cells gather in the bone marrow and split uncontrollably. This type of cancer cannot be cured; however, the symptoms can be alleviated. Myelodysplastic Syndrome is a group of various blood and bone marrow diseases, where the blood cells become abnormal and do not function properly. Mantle cell lymphoma is a less common type of cancer that affects the lymph nodes. Follicular lymphoma is a slow-growing cancer that affects the B cells.

Inform your doctor if you have allergic reactions to Lenangio 10mg Capsule and its ingredients. Before taking treatment with this medication, let your physician know if you ever had blood clots, heart attack or if you smoke or have high blood pressure and cholesterol level. Inform your physician if you have viral infections like  hepatitis B infection, varicella zoster, HIV. Before and during treatment with this medication your healthcare provider will take regular blood test because it may cause fall in blood cells. It is not recommended for children below 18.

Uses of Lenangio 10mg Capsule

Multiple myeloma, myelodysplastic syndrome

Mantle cell lymphoma

Follicular lymphoma

Safety Advices for Lenangio 10mg Capsule  

Pregnancy

Lenangio 10mg Capsule is unsafe to use during pregnancy as it might be harmful to an unborn child. Inform your physician before starting this treatment if you are pregnant or think you might be pregnant.   

Breast Feeding

Lenangio 10mg Capsule is probably unsafe to use during breastfeeding as it is not known if this medication passes into breast milk and harms your baby.  

Lungs

Inform your physician before taking Lenangio 10mg Capsule if you have if you have any lung conditions.   

Liver

Inform your physician before starting treatment with Lenangio 10mg Capsule if you have severe liver problems including liver failure. Your physician will do blood tests to monitor your liver function.  

Alcohol

It is not known whether it is safe to consume alcohol while taking Lenangio 10mg Capsule. Consult your doctor for advice.

Driving

Do not drive or operate machines if you feel dizzy, tired, sleepy, have vertigo or blurred vision after taking Lenangio 10mg Capsule.

Side Effects of Lenangio 10mg Capsule

Serious:
· Severe allergic reactions
· High risk of secondary cancer
· Liver toxicity
· Blurred vision
· Difficulty speaking
· Faster heartbeat
· Chest pain or leg pain
· Swelling in the ankles
· Dizziness
· Unusual bleeding or bruising
· Blood clot formation

Common:
· Tiredness
· Neutropenia
· Constipation
· Diarrhea
· Muscle cramps
·  Anaemia
· Fever
· Back pain
· Nausea
· Upper respiratory tract infection
· Breathlessness
· Tremor
· Rash
· Cough
· Headache
· Thyroid problems
· Dehydration
· Skin problems

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Product Introduction

Veenat 100 Capsule is used to treat several types of cancers. It is most commonly prescribed to treat blood cancers (chronic myeloid leukemia and acute lymphocytic leukemia) and gastrointestinal stromal tumors. It works by targeting specific proteins that contribute to the growth and spread of cancer cells.

Veenat 100 Capsule is also used for treatment of a skin tumor called dermatofibrosarcoma protuberans and a type of bone marrow condition called aggressive systemic mastocytosis. The medicine should be taken with food. Take it at the same time each day to get the most benefit. Continue taking it as long as your doctor advises for it. The duration of treatment varies according to your need and response to treatment. 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.

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.

Uses Of Veenat Capsule

Treatment of Cancer

Side Effects Of Veenat Capsule

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 Veenat
·       Edema (swelling)
·       Nausea
·       Vomiting
·       Muscle cramp
·       Musculoskeletal (bone, muscle or joint) pain
·       Diarrhea
·       Rash
·       Fatigue
·       Abdominal pain
·       Bleedin
·       Breathing problems
·       Cough
·       Weight gain
·       Dry eye
·       Dizziness
·       Hemorrhage

Safety Advice

Alcohol

It is not known whether it is safe to consume alcohol with Veenat 100 Capsule. Please consult your doctor.

Pregnancy

Veenat 100 Capsule is unsafe to use during pregnancy as there is definite evidence of risk to the developing baby. However, the doctor may rarely prescribe it in some life-threatening situations if the benefits are more than the potential risks. Please consult your doctor.

Breast Feeding

Veenat 100 Capsule is probably unsafe to use during breastfeeding. Limited human data suggests that the drug may pass into the breastmilk and harm the baby.
Lactating women should not breastfeed while using this drug and 15 days after stopping it.

Driving

Veenat 100 Capsule may cause side effects which could affect your ability to drive.

Kidney

Veenat 100 Capsule should be used with caution in patients with kidney disease. Dose adjustment of Veenat 100 Capsule may be needed. Please consult your doctor.

Liver

Veenat 100 Capsule should be used with caution in patients with severe liver disease. Dose adjustment of Veenat 100 Capsule may be needed. Please consult your doctor.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Lenvatol 4mg Capsule

Lenvatol 4mg Capsule is composed of the active ingredient Lenvatinib. It is a tyrosine kinase inhibitor indicated for progressive or advanced thyroid cancer when radioactive iodine therapy is not beneficial. It is also used to treat previously untreated liver cancer patients who are not eligible for surgical treatment. Anaplastic Thyroid Carcinoma (Advanced thyroid cancer) usually occurs in patients above 60 years of age. It is characterized by an enlarged and hard thyroid gland and hoarseness in the voice due to paralysis of the nerve in the voice box. Hepatocellular carcinoma (liver cancer) develops due to preexisting liver conditions such as cirrhosis or chronic hepatitis B infection. 

Uses Of Lenvatol 4mg Capsule

Lenvatol 4mg Capsule is indicated to treat the following conditions:
·  Certain types of advanced thyroid cancer
·   Advanced Liver cancer
·   Certain types of kidney cancer
·   Endometrial cancer

Safety Advices For Lenvatol 4mg Capsule  

Pregnancy

Lenvatol 4mg Capsule is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding

Breastfeeding is not recommended while taking Lenvatol 4mg Capsule, as it can potentially harm the nursing infant.  

Lungs

Lenvatol 4mg Capsule can cause side effects that affect the lungs, such as cough, shortness of breath, and difficulty breathing. If a person experiences any of these symptoms while taking it, they should notify their healthcare provider right away.  

Liver

Lenvatol 4mg Capsule is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function monitored.  

Alcohol

It is recommended to avoid consuming alcohol while taking Lenvatol 4mg Capsule, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving

Patients receiving Lenvatol 4mg Capsule should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects Of Lenvatol 4mg Capsule
Serious:

· Feeling numb or weak on one side of the body
· Severe headache
· Fever
· Confusion
· Difficulty speaking
· Vision changes
· Dizziness
· Chest pain or pressure
· Pain in arms, jaw, neck, and back
· Breathing problems
· Severe stomach pain
· Blood clot formation
· Blood in stools or coughing blood
· Liver problems
· Pain or soreness in the mouth, teeth, or jaw

Common:
· High or low BP
· Loss of appetite
· Nausea, vomiting, constipation, diarrhea, or indigestion
· Tiredness
· Hoarse voice
· Leg swelling
· Rashes
· Pain in joints or muscles
· Hair loss
· Sleeplessness
· Protein in urine, frequent urination
· Low potassium, magnesium, and calcium levels in the blood
· Dehydration

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Pegex 6mg Injection

Pegex 6mg Injection contains the active ingredient Pegfilgrastim. It belongs to the class granulocyte colony stimulated factor approved by FDA to decrease the risk of developing febrile neutropenia ( occurrence of fever or infection with low WBC count) and the duration of neutropenia (Low white blood cell count) when receiving bonemarrow suppressive chemotherapy drugs. It is also indicated to increase survival rate in patients exposed to radiation therapy which can cause severe and life-threatening damage to bone marrow. It acts on blood-forming cells, thereby stimulating cell multiplication and cell function activation. 

Inform your physician if you have or ever had liver disease, fever or infection, kidney problems, heart problems, or a family history of kidney diseases before starting the treatment with this Injection. Do not take this Injection if you are allergic to pegfilgrastim. Filgrastim or any of the other ingredients in this Injection. Report any symptoms of left upper abdominal pain, shoulder pain, and respiratory problems immediately to your doctor. The most common side effects of Pegex 6mg injection are pain in the bones, arms, and legs. 

Uses Of Pegex 6mg Injection

Pegex 6mg is a prescription Injection, and it is used to treat 

· Decrease the chance of infection caused by low levels of white blood cells in patients with certain types of cancer (non-myeloid) receiving bonemarrow suppressing anti-cancer drugs.

·  To increase the survival rate in patients receiving radiation therapy that suppresses bone marrow activity.

Safety Advices For Pegex 6mg Injection  

Pregnancy

Pegex 6mg Injection is unsafe when administered during pregnancy because it may cause birth defects in your baby. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.   

Breast Feeding

It is unsafe to breastfeed during the treatment with this Pegex 6mg Injection because it may cause harm to the baby. Please consult your doctor before breastfeeding.   

Lungs

It is unknown whether Pegex 6mg Injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver

It is unknown whether Pegex 6mg Injection can be administered in patients with liver disorders. Inform your physician if you have any liver problems before starting treatment with this Injection.   

Alcohol

It is unsafe to consume alcohol with Pegex 6mg Injection. Please consult your doctor for more advice.  

Driving

It is unsafe to travel, drive vehicles or operate heavy machinery after taking (1 hour)  Pegex 6mg Injection. Please consult your doctor.

Side Effects Of Pegex 6mg Injection

 Common
· Pain in the bones, joints and muscles
· Pain at the site of Injection
· Itchiness and skin rash
· Nausea
· Headaches
· Dizziness and tiredness

 Serious
· Inflammation of Aorta
· Capillary leak syndrome (plasma leaks out of tiny blood vessels)
· Hypersensitivity reactions
· Changes in urine color
· Swelling in hands, feet, face, and abdomen
· Difficulty in breathing
· Sickle cell anemia

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Actilyse 50mg Injection

Actilyse 50mg injection contains an active component as Alteplase. It is also known as recombinant tissue plasminogen activator (rt-PA), used to treat certain medical conditions involving blood clots. It is a thrombolytic agent, meaning it helps to break down blood clots. This medication is commonly used to manage acute ischemic strokes, where a blood clot blocks blood flow to the brain, leading to potential brain damage. By administering atelpase within a specific time frame after the onset of stroke symptoms, doctors aim to restore blood flow to the affected brain tissue and reduce the risk of long-term disability.

Patients who have a known allergy or hypersensitivity to Actilyse 50mg injection or any of its components should not receive this medication. Patients with significant trauma within the past three months due to an increased risk of bleeding should avoid this medication.

Uses Of Actilyse 50mg Injection

·         Actilyse 50mg injection is used to treat the following:
·         Heart attack
·         Acute ischemic stroke
·         Acute massive pulmonary embolism (blood clots in the lung)

Safety Advices For Actilyse 50mg Injection  

Pregnancy

If a pregnant woman requires treatment with Actilyse 50mg injection, then they should consult a healthcare provider. They will weigh the potential benefits of resolving the critical situation against the potential risks to the developing fetus.  

Breast Feeding

If you are breastfeeding, it is essential to consult with a healthcare professional for personalized advice and guidance before starting treatment with ateplase.  

Lungs

Using Actilyse 50mg injection for lung-related conditions requires expert medical care and a multidisciplinary approach. It should only be administered in a hospital setting by healthcare professionals experienced in managing such cases.  

Liver

Using Actilyse 50mg injection in patients with liver impairment requires consultation with a qualified healthcare professional, who will consider the patient's medical history, liver function, and overall risk profile.   

Alcohol

Regarding the safety of Actilyse 50mg injection and alcohol consumption, it is generally recommended to avoid consuming alcohol while taking it. Alcohol can have various effects on the body, potentially affecting the cardiovascular system and increasing the risk of adverse reactions.  

Driving

Actilyse 50mg injection can cause certain side effects that may impair your driving ability. These side effects can include dizziness, lightheadedness, blurred vision, and transient changes in heart rhythm. These effects can interfere with your concentration, alertness, and coordination, making driving potentially unsafe.

Side Effects Of Actilyse 50mg Injection

Serious:
· Bleeding
· Allergic reactions
· Hypotension (low blood pressure)
· Cardiac arrhythmias
· Hypersensitivity reactions

Common:
· Low blood pressure
· Chest pain
· Fluid on the lungs
· Bleeding of the damaged blood vessel
· Bleeding at the injection site

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction to Geftinat 250mg Tablet

Geftinat 250mg Tablet is an antineoplastic drug belonging to the tyrosine kinase inhibitors, containing the active ingredient Gefitinib. It is used to treat non-small cell lung cancer. Non-small cell lung cancer is a disorder in which cells multiply in an uncontrolled and abnormal manner in the tissues of the lung. It is used in patients where the NSCLC cancer has spread to other parts of the body, who have certain types of abnormal epidermal growth factor (EGFR) genes, and patients who have not received any cancer treatment.

Some formulations of this drug may contain lactose as an inactive ingredient in which the body is unable to digest lactose, a sugar found in milk and dairy products. It can cause symptoms such as bloating, and abdominal pain. If you have lactose intolerance, inform your doctor before starting this therapy. Talk with your healthcare provider if you have kidney or liver disease, vision problems, lung problems, or taking any blood thinner like warfarin. Your healthcare provider will check regular blood tests to prevent complications. Avoid consuming alcohol as it may cause dizziness.

Your healthcare practitioner will conduct a pregnancy test before you start treatment with this tablet. Discuss with your doctor effective birth control methods and utilize them for at least two weeks following the last dose. Avoid breastfeeding your baby while on the treatment as it is unknown if this drug passes into the breast milk.

Uses of Geftinat 250mg Tablet

Geftinat 250mg Tablet is used to treat

Non-small cell lung cancer.

Safety Advices for Geftinat 250mg Tablet  

Pregnancy

It is unsafe to use during pregnancy whether Geftinat 250mg Tablet can be taken during pregnancy. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding

It is unsafe to breastfeed during the treatment with this Geftinat 250mg Tablet because it may cause harm to the baby. Please consult your doctor before breastfeeding.  

Lungs

It is unknown whether Geftinat 250mg Tablet can be used for patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver

It is unknown whether Geftinat 250mg Tablet can be used for patients with liver disorders. Inform your physician if you have any liver problems before starting treatment.  

Alcohol

It is unknown whether consuming alcohol interacts with the Geftinat 250mg Tablet. Please consult your doctor for more advice.  

Driving

It is unsafe to drive vehicles or operate heavy machinery after taking the Geftinat 250mg Tablet because it contains a small amount of alcohol which may cause dizziness and impair your concentration.

Side Effects of Geftinat 250mg Tablet

Side effects are unwanted symptoms caused by medicines. Even though all drugs cause side effects, not everyone gets them.

 Common
·      diarrhea
·      nausea
·      vomiting
·      loss of appetite
·      weakness
·      red or sore mouth
·      increased liver enzymes
·      itchy or cracked skin
·      dry mouth
·      red or itchy eyes
·      nail problems
·      hair loss
·      fever
·      blood in the urine and burning sensation while urinating

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Product Introduction

Intacept 25 Solution for Injection is a medicine used to treat a variety of conditions such as ankylosing spondylitis, rheumatoid arthritis, psoriasis, ulcerative colitis, and Crohn’s disease. It provides relief from swelling, pain, and redness associated with various disorders and improves physical function.

Intacept 25 Solution for Injection is given by a healthcare professional and should not be self-administered. You should use it regularly and at the same time each day to get the maximum benefit from it. Continue using it as recommended by your doctor and complete the dose even if you feel better.

To make sure the medicine is safe for you, before taking it, let your doctor know of all the other medicines you are taking. Your doctor may also monitor your blood counts by taking regular blood tests to make sure the medicine is not affecting your blood counts. It is important for pregnant and breastfeeding women to ask the advice of their doctors before taking this medicine.

Uses Of Intacept Solution For Injection
·         Ankylosing spondylitis
·         Rheumatoid arthritis
·         Psoriasis
·         Ulcerative colitis
·         Crohn’s disease

Side Effects Of Intacept Solution For Injection

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 Intacept
·         Allergic reaction
·         Upper respiratory tract infection
·         Itching
·         Rash
·         Injection site reaction

How To Use Intacept Solution For Injection

Your doctor or nurse will guide you how to use this medicine.

Safety Advice

Alcohol

Consuming alcohol with Intacept 25 Solution for Injection does not cause any harmful side effects.

Pregnancy

Intacept 25 Solution for Injection is generally considered safe to use during pregnancy. Animal studies have shown low or no adverse effects to the developing baby; however, there are limited human studies.

Breast Feeding

Intacept 25 Solution for Injection is probably safe to use during breastfeeding. Limited human data suggests that the drug does not represent any significant risk to the baby.

Driving

It is not known whether Intacept 25 Solution for Injection alters the ability to drive. Do not drive if you experience any symptoms that affect your ability to concentrate and react.

Kidney

Intacept 25 Solution for Injection is probably safe to use in patients with kidney disease. Limited data available suggests that dose adjustment of Intacept 25 Solution for Injection may not be needed in these patients.

Liver

Intacept 25 Solution for Injection is probably safe to use in patients with liver disease. Limited data available suggests that dose adjustment of Intacept 25 Solution for Injection may not be needed in these patients.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Product Description

Opdivo 240mg/ml  is a cancer medicine that is used alone or in combination with other medicines that works with your immune system to interfere with the growth and spread of cancer cells in the body.

The Brand name of this medicine is Opdivo 240mg/ml . Opdivo 240mg/ml medicine contains generic Nivolumab (240mg). Opdivo 240mg/ml are available in form of solution for infusion. One Pack of Opdivo 240mg/ml contains 1 injection in 1 vial. Manufactured company name of Opdivo 240mg/ml is BMS India Pvt Ltd.

Warning: Keep out of the reach and sight of children and away from pets, never share your medicines with others, and use this medication only for the indication prescribed. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects.

Warnings

Opdivo 240mg/ml can cause side effects in many different parts of your body. Some side effects may need to be treated with other medicine, and your cancer treatments may be delayed.

Call your doctor at once if you have: a cough, shortness of breath, vision changes, muscle pain or weakness, stomach pain, diarrhea, blood in your stools, little or no urinating, bruising or bleeding, dark urine, yellowing of your skin or eyes, frequent headaches, dizziness, confusion, increased thirst or urination, skin problems, numbness or tingling, feeling cold, or weight gain or loss.

 Opdivo 240mg/ml  Side Effects

Get emergency medical help if you have signs of an allergic reaction to Opdivo 240mg/ml  (hives, difficult breathing, swelling in your face or throat) or a severe skin reaction.

Some side effects may occur during the injection. 

Call your doctor at once if you have:

·       severe or ongoing diarrhea, severe stomach pain, bloody or tarry stools;
· eye pain, vision changes, sensitivity to light;

· severe muscle pain or weakness;
· confusion, memory problems, neck stiffness, drowsiness, balance problems;
· numbness or tingling in your arms or legs;
· kidney problems - little or no urination, swelling in your feet or ankles, blood in your urine;
· liver problems - severe nausea or vomiting, right-sided upper stomach pain, easy bruising or bleeding, dark urine, jaundice (yellowing of the skin or eyes);
· lung problems - new or worsening cough, chest pain, feeling short of breath;
· skin problems - rash, itching, redness, swelling, pain, sores, blisters, sores in your mouth or nose or on your genitals;
· signs of a hormonal disorder - frequent or unusual headaches, vision problems, fast heartbeats, dizziness, fainting, tiredness, mood or behavior changes, hunger, increased thirst or urination, constipation, hair loss, hoarse or deepened voice, sweating, feeling cold, weight gain or loss

Common Opdivo side effects may include:

· nausea, vomiting, stomach pain, loss of appetite, diarrhea, constipation;
· mouth sores, altered sense of taste;
· itching, rash, redness or blisters on your hands or feet;
· hormonal problems;
· liver problems;
· numbness, tingling, or burning pain in your hands or feet;
· fever, body aches;
· feeling weak, tired, or short of breath;
· cold symptoms such as runny or stuffy nose, cough, sore throat;
· headache, dizziness, increased blood pressure
· weight loss.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Product Description

Opdivo 40mg/ml is a cancer medicine that is used alone or in combination with other medicines that works with your immune system to interfere with the growth and spread of cancer cells in the body.

The Brand name of this medicine is Opdivo 40mg/ml. Opdivo 40mg/ml medicine contains generic Nivolumab (40mg). Opdivo 40mg/ml are available in form of solution for infusion. One Pack of Opdivo 40mg/ml contains 1 injection in 1 vial. Manufactured company name of Opdivo 40mg/ml is BMS India Pvt Ltd.

Warning: Keep out of the reach and sight of children and away from pets, never share your medicines with others, and use this medication only for the indication prescribed. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects.

Warnings

Opdivo can cause side effects in many different parts of your body. Some side effects may need to be treated with other medicine, and your cancer treatments may be delayed.

Call your doctor at once if you have: a cough, shortness of breath, vision changes, muscle pain or weakness, stomach pain, diarrhea, blood in your stools, little or no urinating, bruising or bleeding, dark urine, yellowing of your skin or eyes, frequent headaches, dizziness, confusion, increased thirst or urination, skin problems, numbness or tingling, feeling cold, or weight gain or loss.

 Opdivo Side Effects

Get emergency medical help if you have signs of an allergic reaction to Opdivo (hives, difficult breathing, swelling in your face or throat) or a severe skin reaction (fever, sore throat, burning eyes, skin pain, red or purple skin rash with blistering and peeling).

Some side effects may occur during the injection. 

Call your doctor at once if you have:
· severe or ongoing diarrhea, severe stomach pain, bloody or tarry stools;
· eye pain, vision changes, sensitivity to light;
· severe muscle pain or weakness;
· confusion, memory problems, neck stiffness, drowsiness, balance problems;
· numbness or tingling in your arms or legs;
· kidney problems - little or no urination, swelling in your feet or ankles, blood in your urine;
· liver problems - severe nausea or vomiting, right-sided upper stomach pain, easy bruising or bleeding, dark urine, jaundice (yellowing of the skin or eyes);
· lung problems - new or worsening cough, chest pain, feeling short of breath;
· skin problems - rash, itching, redness, swelling, pain, sores, blisters, sores in your mouth or nose or on your genitals;
· signs of a hormonal disorder - frequent or unusual headaches, vision problems, fast heartbeats, dizziness, fainting, tiredness, mood or behavior changes, hunger, increased thirst or urination, constipation, hair loss, hoarse or deepened voice, sweating, feeling cold, weight gain or loss

Common Opdivo side effects may include:
· nausea, vomiting, stomach pain, loss of appetite, diarrhea, constipation;
· mouth sores, altered sense of taste;
· itching, rash, redness or blisters on your hands or feet;
· hormonal problems;
· liver problems;
· numbness, tingling, or burning pain in your hands or feet;
· fever, body aches;
· feeling weak, tired, or short of breath;
· cold symptoms such as runny or stuffy nose, cough, sore throat;
· headache, dizziness, increased blood pressure; or
· weight loss.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction

120 Mg (Sotorasib) is used to treat a certain type of lung cancer (non-small cell lung cancer; NSCLC) that has spread to other parts of the body or cannot be removed by surgery in adults who have received at least one other treatment. Sotorasib is in a class of medications called KRAS inhibitors. It works by blocking the action of the abnormal protein that signals cancer cells to multiply. This helps stop or slow the spread of cancer cells. Some forms of lung cancer can be treated with this medication. Adults who have already undergone at least one other systemic therapy are the typical recipients.

Sotoxen 120 Mg Precautions

Tell your doctor and pharmacist if you are allergic to any other medications, or any of the ingredients in sotorasib tablets. Ask your pharmacist for a list of the ingredients.

Tell your doctor and pharmacist what other prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention any of the following: carbamazepine (Carbatrol, Epitol, Equetro, Tegretol, others); digoxin (Lanoxin); H2 blockers such as cimetidine, famotidine (Pepcid, in Duexis), nizatidine (Axid), or ranitidine (Zantac); midazolam (Versed); phenobarbital; phenytoin (Dilantin, Phenytek); proton-pump inhibitors such as esomeprazole (Nexium, in Vimovo), lansoprazole (Prevacid), omeprazole (Prilosec, in Zegerid), pantoprazole (Protonix), or rabeprazole (Aciphex); and rifampin (Rifadin, Rimactane, in Rifamate, in Rifater). Your doctor may need to change the doses of your medications or monitor you carefully for side effects. Many other medications may also interact with sotorasib, so be sure to tell your doctor about all the medications you are taking, even those that do not appear on this list.

If you are taking sotorasib and an antacid, take sotorasib either 4 hours before or 10 hours after the antacid.

Tell your doctor if you have or have ever had liver disease, or lung or breathing problems other than lung cancer.

Tell your doctor if you are pregnant, or plan to become pregnant. If you become pregnant while taking sotorasib, call your doctor immediately.

Tell your doctor if you are breastfeeding or plan to breastfeed. You should not breastfeed while receiving sotorasib and for 1 week after your final dose.

Side Effect

Sotorasib may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

• diarrhea
• vomiting
• nausea
• constipation
• loss of appetite
• stomach pain
• muscle or bone pain
• joint pain
• rash 

Some Side Effects Can Be Serious. If You Experience Any Of These Symptoms, Call Your Doctor Immediately Or Get Emergency Medical Treatment:

Yellowing of skin or eyes, dark-colored urine, bleeding or bruising more easily than normal, loss of appetite, decreased energy, or pain on the right side of stomach area

Shortness of breath, cough, or fever

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

About Ponaxen 45mg (Ponatinib)

This medication is prescribed to patients suffering from specific forms of chronic myeloid leukemia in order to treat their condition. It belongs to the category of tyrosine-kinase inhibitors that can block multiple targets at once. The half-life of its elimination ranges somewhere between 12 and 66 hours. As a treatment for chronic myeloid leukemia, it is very effective against the T315I mutation. This medication is more commonly known by its generic name, ponatinib. Everest Pharma is the company that produces and distributes this particular medication. Ponaxen is a targeted chemotherapy drug which is used for the treatment of chronic myelogenous leukemia (CML) and Philadelphia chromosome positive acute lymphoblastic leukemia. Ponaxen (Ponatinib), is an oral drug under the generic of Ponatinib, for the first-line therapy of the people affected with chronic myelogenous leukemia.

It is a highly potential and multi-targeted third generation Bcr-Abl tyrosine-kinase inhibitors (TKI) which is indicated for the adult patients with chronic phase, accelerated phase or blast phase chronic myeloid leukemia (CML) or Ph+ALL for those who have no other TKI therapy.

It is also indicated for the adult patients with T315I-positive CML (chronic phase, accelerated phase of blast phase) or T315I-positive Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL).

Dosages 

When beginning treatment with Ponaxen 45mg, the recommended starting dosage is 45 mg taken orally once daily. You can take it either with the food or on an empty stomach. You must ensure that the entire pill goes down.

Common Side effects

Some of the side effects associated with taking Ponatinb are as below, these side effects can be common or less common as well
·  High blood pressure
·  Neutropenia
·  Leukopenia
·  Blood sugar increased
·  Low platelets
·  Diarrhea
·  lood sugar decreased
·  Increased bleeding
·  Vomiting
·  Mouth sores
·  Phosphorous decreased
·   Anemia
·  Rash
·  Muscle aches
·  Swelling
·  Infection
·  Shortness of breat
·  Bilirubin increased
·  Pleural effusion
·   Cough
·  Abdominal pain
·  Constipation
·  Fatigue or weakness
·  Headache
·  Dry skin
·  Fever
·  Nausea
·   Appetite decreased
·  Joint pain

Storage 

This must be stored between 20 and 25 °C (68 and 77 °F), with a maximum excursion temperature of 15 to 30 °C (59 to 86 °F). Do not expose this to moisture or direct sunlight.

How it Works

Ponaxen is a tyrosine kinase inhibitor, Ponaxen works to block tyrosine kinases on the surface and within cancer cells, these targets are involved in angiogenesis and by blocking these targets the cancer will shrink.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

T-3 Liothyronine sodium 20 mcg
Product Description
Liothyronine is used to treat hypothyroidism (a condition where the thyroid gland does not produce enough thyroid hormone). Liothyronine is also used to treat a goiter (an enlarged thyroid gland) and to test for hyperthyroidism (a condition where the thyroid gland produces too much thyroid hormone).
Liothyronine is used to treat hypothyroidism, a condition wherein the thyroid gland does not produce enough thyroid hormone. It is also used to help decrease the size of enlarged thyroid glands (goiter) and treat thyroid cancer.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 to 13 Days

Product Details:

Introduction To Nuparp 200mg Tablet

Nuparp 200mg tablet contains the active ingredient rucaparib. It is an anti-cancer medicine that belongs to the class of medications called PARP (poly ADP-ribose polymerase) inhibitors. It is used to help maintain the response to other treatments for certain types of ovarian cancer, fallopian tube (a tube that transports eggs released by the ovaries to the uterus), and primary peritoneal (layer of tissue that lines the abdomen) cancer that has reoccurred in adults who have previously completely responded or partially responded to other chemotherapy treatments. 

It is also used to treat certain types of cancer in people with specific gene (BRCA) changes who have received treatment with at least two other chemotherapy treatments. It is also indicated as maintenance therapy immediately after chemotherapy which has caused the tumor to shrink. Do not take Nuparp 200mg tablet if you are allergic to Nuparp or any of the ingredients. This medication can cause low blood counts; hence your healthcare professional will advise you to take certain blood tests before and every month during the treatment.  

Uses of Nuparp 200mg Tablet
·         Ovarian cancer
·         Fallopian tube cancer
·         Primary peritoneal cancer
·         Prostate cancer

Safety Advices for Nuparp 200mg Tablet  

Pregnancy

Do not take Nuparp 200mg tablet if you are pregnant because this may harm the unborn baby. Inform your physician if you are pregnant, suspecting, or planning to get pregnant during the treatment. Use effective contraception during the treatment and for 6 months after the last dose.   

Breast Feeding

Breastfeeding is not recommended in patients taking Nuparp 200mg tablet because the medicine passes into the breast milk in small amounts and may harm your baby. Do not breastfeed during the treatment.   

Lungs

It is unknown whether Nuparp 200mg tablet is safe to be administer in patients with lung diseases. Inform your physician if you have any lung diseases before initiating the therapy.   

Liver

Nuparp 200mg tablet is safe when administered in patients with liver disease. No dose adjustments are necessary.   

Alcohol

It is not known whether it is safe to consume alcohol with Nuparp 200mg tablet.

Driving

Nuparp 200mg tablet may cause dizziness and drowsiness. Driving or operating heavy machinery is unsafe if you experience any symptoms that affect your ability to concentrate and react.

Side Effects of Nuparp 200mg Tablet

Side effects are unwanted symptoms caused by medicines. Even though all drugs cause side effects, not everyone gets them. 

 Common 
·      Rash
·     Constipation
·     Decrease in appetite
·     Diarrhea, indigestion
·      Nausea, vomiting
·     Changes in the blood count
·     Shortness of breath
·     Tiredness

Serious  
·     Severe anemia
·     Hypersensitivity reactions
·     Sepsis (blood infection)
·     Pneumonia

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Zoldonat 4mg Injection

Zoldonat 4mg Injection contains the active substance Zoledronic Acid. It belongs to the group of substances called bisphosphonates. It is used to reduce the amount of calcium in the blood in adult patients where it is too high due to the presence of a tumor. Tumors can accelerate normal bone change in such a way that the release of calcium from bone is increased. This condition is known as tumor-induced hypercalcemia (TIH). It is also used to prevent bone complications in adult patients with multiple myeloma and bone metastases from solid tumors (spread of cancer from the primary site to the bone), in addition to standard cancer therapy.   

Zoldonat 4mg Injection is also indicated to prevent or treat osteoporosis (a condition in which the bones become thin and weak and break easily) in women who have undergone menopause. It is also used to treat osteoporosis in men. It is used to treat Paget’s disease of bone (a condition in which the bones are soft and weak and may be deformed, painful, or easily broken). Other uses include treating or preventing osteoporosis in men and women taking glucocorticoids (a corticosteroid medication that may cause osteoporosis). 

Uses Of Zoldonat 4mg Injection
·         Treat hypercalcemia of malignancy
·         Multiple myeloma
·         Bone metastases from solid tumors
·         Osteoporosis in postmenopausal women
·         Osteoporosis in men
·         Paget’s disease of bone

Safety Advices For Zoldonat 4mg Injection  

Pregnancy

Zoldonat 4mg Injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant.   

Breast Feeding

Breastfeeding is not recommended in patients taking Zoldonat 4mg Injection because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs

It is unknown whether Zoldonat 4mg Injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.   

Liver

It is unknown whether Zoldonat 4mg Injection can be used in patients with liver disorders. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol

Caution is advised when consuming alcohol with Zoldonat 4mg Injection.

Driving

It is unsafe to drive or operate heavy machinery after using Zoldonat 4mg Injection as this medicine causes drowsiness and sleepiness. 

Side Effects Of Zoldonat 4mg Injection

 Common
·     Nausea, vomiting
·     Fatigue
·   Anemia
·   Bone pain
·   Constipation, diarrhea
·   dyspnea, and fever
·   Swelling in the legs and feet
·   Decreased weight
·   Abdominal pain
·   Muscle pain
·   Tiredness

Serious
·   Changes in heart rhythm
·   Severe hypersensitivity skin reactions
·   Decreased calcium levels
·   Severe bone pain
·   Severe kidney problems
·   Unusual fractures of the bone

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Nuparp 300mg Tablet

Nuparp 300mg tablet contains the active ingredient rucaparib. It is an anti-cancer medicine that belongs to the class of medications called PARP (poly ADP-ribose polymerase) inhibitors. It is used to help maintain the response to other treatments for certain types of ovarian cancer, fallopian tube (a tube that transports eggs released by the ovaries to the uterus), and primary peritoneal (layer of tissue that lines the abdomen) cancer that has reoccurred in adults who have previously completely responded or partially responded to other chemotherapy treatments. 

It is also used to treat certain types of cancer in people with specific gene (BRCA) changes who have received treatment with at least two other chemotherapy treatments. It is also indicated as maintenance therapy immediately after chemotherapy which has caused the tumor to shrink. Do not take Nuparp 300mg tablet if you are allergic to Nuparp or any of the ingredients. This medication can cause low blood counts; hence your healthcare professional will advise you to take certain blood tests before and every month during the treatment.  

Uses of Nuparp 300mg Tablet
·         Ovarian cancer
·         Fallopian tube cancer
·         Primary peritoneal cancer
·         Prostate cancer

Safety Advices for Nuparp 300mg Tablet  

Pregnancy

Do not take Nuparp 300mg tablet if you are pregnant because this may harm the unborn baby. Inform your physician if you are pregnant, suspecting, or planning to get pregnant during the treatment. Use effective contraception during the treatment and for 6 months after the last dose.   

Breast Feeding

Breastfeeding is not recommended in patients taking Nuparp 300mg tablet because the medicine passes into the breast milk in small amounts and may harm your baby. Do not breastfeed during the treatment.   

Lungs

It is unknown whether Nuparp 300mg tablet is safe to be administer in patients with lung diseases. Inform your physician if you have any lung diseases before initiating the therapy.   

Liver

Nuparp 300mg tablet is safe when administered in patients with liver disease. No dose adjustments are necessary.   

Alcohol

It is not known whether it is safe to consume alcohol with Nuparp 300mg tablet.

Driving

Nuparp 300mg tablet may cause dizziness and drowsiness. Driving or operating heavy machinery is unsafe if you experience any symptoms that affect your ability to concentrate and react.

Side Effects of Nuparp 300mg Tablet

Side effects are unwanted symptoms caused by medicines. Even though all drugs cause side effects, not everyone gets them. 

 Common 
· Rash
· Constipation
· Decrease in appetite
· Diarrhea, indigestion
· Nausea, vomiting
· Changes in the blood count
· Shortness of breath
· Tiredness

Serious  
· Severe anemia
· Hypersensitivity reactions
· Sepsis (blood infection)
· Pneumonia

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Immunocin Alpha Plus 1.6mg Injection

Immunocin alpha plus 1.6mg injection is an anti-cancer drug belonging to the class of synthetic thymic peptides containing the active ingredient Thymosin Alpha 1. This medication is an adjuvant therapy in treating chronic hepatitis B and C. It is also used to treat acquired immunodeficiency syndrome(AIDS). This drug can also be used in the treatment of various types of cancer, as it can enhance the function of immune cells and promote tumor cell death.

The safety of this drug during pregnancy and breastfeeding is unknown, and it is not recommended for use, so before planning for your pregnancy, please consult your doctor for more advice.This injection should not be used in individuals with allergies or known hypersensitivity to the medication or its components.

This drug is not recommended to individuals at increased risk of infections, such as those with a weakened immune system or those who have had recent surgery or invasive procedures, and they should be closely monitored for signs of infection while taking Immunocin alpha plus 1.6mg injection. It is also important to note that this drug should not be used in immunocompromised patients or those with suppressed immunity, such as organ transplant patients, as it may increase the risk of infections.

Uses Of Immunocin Alpha Plus 1.6mg Injection

Immunocin alpha plus 1.6mg injection has been indicated for the treatment of,

Hepatitis B & C

HIV/AIDS

Cancer (non-small cell lung cancer, liver cancer, melanoma)

How To Consume Immunocin Alpha Plus 1.6mg Injection

It should only be administered by a trained doctor or nurse experienced in chemotherapy. Immunocin alpha plus 1.6mg injection is usually administered as a subcutaneous injection (under the skin). Do not self-administer the injection. Your doctor will decide the dose and duration of the treatment based on your disease severity and other factors.

Safety Advices For Immunocin Alpha Plus 1.6mg Injection  

Pregnancy

Immunocin alpha plus 1.6mg injection is not recommended for pregnant women because there is no limited data on whether the medicine may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding

Breastfeeding is not recommended in patients taking Immunocin alpha plus 1.6mg injection because there is no limited data on whether the medicine passes into the breast milk in small amounts and may harm your baby.  

Lungs

It is unknown whether Immunocin alpha plus 1.6mg injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver

Inform your physician if you have liver problems before initiating the treatment with Immunocin alpha plus 1.6mg injection.  

Alcohol

Consuming alcohol may affect the effectiveness of the Immunocin alpha plus 1.6mg injection. Stop consuming alcohol if you are taking this medicine.   

Driving

Driving vehicles or operating heavy machinery is unsafe after taking Immunocin alpha plus 1.6mg injection it may cause dizziness and impair concentration.

Side Effects Of Immunocin Alpha Plus 1.6mg Injection

Serious
· Severe allergic reactions (difficulty in breathing or swallowing, swelling of hands, feet, lips, mouth, or throat, itchy rash)
· Pain at the site of injection (during or immediately after the injection)

Common
· Fever
· Muscle ache
· Tiredness
· Nausea
· Vomiting

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Introduction To Pomalid 2mg Capsule

Pomalid 2mg Capsule Is A Chemotherapy Medicine Containing The Active Constituent Pomalidomide. It Belongs To The Group Of Medications Known As Immuno Modulatory Agents. It Is Used To Treat Multiple Myeloma In Adults. Multiple Myeloma Is A Type Of Cancer Mainly Affecting Certain White Blood Cells Called The Plasma Cell. These Cells Grow Uncontrolled And Accumulate In The Bone Marrow, Damaging The Bones And Kidneys.  

Inform Your Medical Professional If You Are Allergic To Pomalid 2mg Capsule And Its Ingredients. Inform Your Doctor If You Have High Cholesterol Levels, Heart Disorders, Breathing Problems, Blood Clot Disorders, Hepatitis B Infection, Neuropathy (Pain In Hands Or Feet Caused By Nerve Damage), Or If You Smoke Before Taking This Chemotherapy Medicine. It Is Not Recommended For Adolescents And Children Under 18 Years Of Age. 

Uses Of Pomalid 2mg Capsule

Treatment Of Multiple Myeloma.

How To Consume Pomalid 2mg Capsule

Always Take Pomalid 2mg Capsule Exactly As Prescribed By Your Doctor. Take This Medicine With Or Without Food. Swallow The Capsule As A Whole With Water. Do Not Crush Or Chew The Capsule.

Safety Advices For Pomalid 2mg Capsule  

Pregnancy

Pomalid 2mg Capsule Is Unsafe To Use During Pregnancy As It May Cause Harmful Effects On The Unborn Baby. Inform Your Doctor If You Are Pregnant Or Planning To Get Pregnant Before Taking This Medicine.  

BreastFeeding

It Is Not Recommended To Use During Breastfeeding As It Is Unknown If Pomalid 2mg Capsule Passes Into Breast Milk And Harms The Baby.  

Lungs

It Is Unknown Whether Pomalid 2mg Capsule Can Be Given To Patients With Lung Disorders. Consult Your Doctor If You Have Any Lung Problems Before Starting The Treatment.   

Liver

Pomalid 2mg Capsule Is Used With Caution In Severe Liver Disease Patients. A Dose Adjustment Is Required. Your Physician Will Perform Blood Tests To Monitor Your Liver Function During Treatment With This Medication.  

Alcohol

It Is Not Known Whether It Is Safe To Consume Alcohol With Pomalid 2mg Capsule.

Driving

Do Not Drive Or Operate Heavy Machines While Taking Pomalid 2mg Capsule, As It Can Cause Tiredness, Dizziness, And Confusion. 

Side Effects Of Pomalid 2mg Capsule

Side Effects Are Unwanted Symptoms Caused By Medicines. Even Though All Medicines Cause Side Effects, Not Everyone Gets Them. 

Serious:
·  Low White Blood Cells
·  Bleeding Or Bruising
·  Severe Or Bloody Diarrhea
·  Blood Clots (Chest Or Leg Pain, Swelling)
·  Severe Liver Problems (Yellowing Of Skin Or Eyes, Dark-Brow Color Urine, Abdominal Pain)
·  Severe Allergic Reactions (Swelling Of Face, Lips, Tongue, Or Throat, Difficulty Breathing)

Common:
·  Shortness Of Breath
·  Tiredness, Weakness
·  Nausea, Vomiting
·  Dizziness, Tremor
·  Low Potassium Level In The Blood (Hypokalaemia)
·  Back Pain, Bone Pain
·  Diarrhea, Constipation
·  Upper Respiratory Tract Infection
·  High Blood Sugar Levels
·  Loss Of Appetite, Lack Of Energy
·  Trouble Sleeping
·  Muscle Spasms, Muscle Weakness
·  Numbness, Tingling, Or Burning Sensation In The Skin, Pain In Hands Or Feet
·  Anemia

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days

Product Details:

Information Of Radizide Temozolomide 20mg Capsules

Radizide Temozolomide 20mg Capsules is used to treat a specific kind of brain cancer. It is used to treat brain tumours that have returned or worsened following normal therapy. It may also be used to treat other diseases that the doctor determines.

Radizide Temozolomide 20mg Capsules should be taken on an empty stomach at the same time every day to get the optimum impact. Your doctor will determine the appropriate dose and frequency of administration. This can vary depending on what you are being treated for and may alter over time. You should take it precisely as prescribed by your doctor. Taking it incorrectly or in excess might result in significant negative effects. It may take a few weeks or months for you to notice or feel the advantages, but do not stop taking it until your doctor instructs you to.

How To Use Radizide Temozolomide 20mg Capsules

Before you begin taking Radizide Temozolomide 20mg Capsules, and each time you obtain a refill, read the Patient Information Leaflet provided by your chemist. If you have any concerns.Take this medication by mouth as prescribed by your doctor, generally once a day on a daily basis. With a full glass of water, swallow the pills whole. 

Side Effects Of Radizide Temozolomide 20mg Capsules
· Red spots under the skin
· Signs of diabetes insipidus
· Piles
· Dry mouth
· Blisters on body or in mouth
· Skin peeling, skin eruption, painful reddening of the skin, severe rash with skin swelling
· Increased sensitivity to sunlight
· Urticaria (red, itchy skin)
· Increased sweating
· Change in skin color
· Vaginal bleeding or irritation
· Absent or heavy menstrual periods
· Breast pain
· Sexual impotence
· Shivering

Common Side Effects
· Nausea
· Vomiting
· Constipation
· Headache
· Fatigue
· Convulsion
· Coordination disorder
· Diarrhea
· Dizziness
· Fever
· Hair loss
· Hemiparesis (weakness on one side of the body)
· Insomnia (difficulty in sleeping)
· Loss of appetite
· Memory loss
· Rash
· Viral infection
· Weakness

Safety Advice Radizide Temozolomide 20mg Capsules

Alcohol

It is unknown whether drinking alcohol while taking Radizide Temozolomide 20mg Capsules is safe.

Pregnancy

Radizide Temozolomide 20mg Capsules should not be used during pregnancy because there is clear evidence that it causes a harm to the unborn child. However, in some life-threatening instances where the advantages outweigh the risks, the doctor may prescribe it..

Breast Feeding

It is not recommended to take Radizide Temozolomide 20mg Capsules while nursing. The medicine may induce toxicity in the newborn, according to the studies.

Driving

Radizide Temozolomide 20mg Capsules can make you drowsy and dizzy by lowering your alertness, affecting your vision, or making you sleepy and dizzy. If you have any of these symptoms, you should not drive.

Kidney

 In individuals with kidney difficulties, such as severe renal impairment,Radizide Temozolomide 20mg Capsules should be taken with caution. 

Liver

In patients with liver problems, Radizide Temozolomide 20mg Capsules should be used with caution. It is possible that the dosage does not need to be altered.

Additional Information:

• Production Capacity: 10000
• Delivery Time: 8 To 13 Days