Hervycta 440Mg Inj Substitute
RXLupin Ltd
₹18885.5
(₹897.06/ 1ml)
RXCelon Laboratories Pvt Ltd
₹30000
(₹1230.0/ 1ml)
RXAlkem Laboratories Ltd
₹51246
(₹2101.09/ 1ml)
RXAbbott India Ltd
₹54264
(₹2224.82/ 1ml)
RXRPG Life Sciences Ltd
₹57500
(₹2357.5/ 1ml)
RXMankind Pharma Pvt Ltd
₹22982.5
(₹18845.7 per unit)
RXDelarc Pharmaceuticals Pvt Ltd
₹19874
(₹19874.0 per unit)
RX₹30000
(₹24600.0 per unit)
RXDr Reddy's Laboratories Ltd
₹40425
(₹33148.5 per unit)
RXHetero Drugs Ltd
₹51759.5
(₹42442.8 per unit)
RXHalsted Pharma Pvt Ltd
₹54663
(₹44823.66 per unit)
RXSayre Therapeutics Pvt Ltd
₹61132
(₹50128.24 per unit)
RXAxiommax Oncology Pvt Ltd
₹55687
(₹55687.0 per unit)
RXAmneal Healthcare Pvt Ltd
₹57457
(₹57457.0 per unit)
RXRoche Diagnostics India Pvt Ltd
₹110700
(₹90774.0 per unit)
Patients may explore substitutes in the following scenarios:
Before you switch from Hervycta 440Mg Inj to another medicine, here are some important points to keep in mind:
Same salt, different brands:
Most substitutes contain the same active ingredient - TRASTUZUMAB-440MG, but the fillers, coating, or manufacturing quality may vary slightly.
Consult your doctor first:
Even if the salt is the same, your doctor can confirm if the substitute is right for your condition, dosage, and health history.
Watch out for allergies or reactions:
Some people may react differently to certain brands due to inactive ingredients. If you notice any side effects, inform your doctor immediately.
Price ≠ effectiveness:
A lower-priced substitute doesn't mean it's less effective. Many generic medicines work just as well as branded ones.
Check the dosage form and strength:
Always match the substitute’s strength (e.g., 5mg, 10mg) and form (tablet, capsule, syrup) with what your doctor prescribed.
Hervycta 440Mg Inj is used in the treatment of Breast Cancer and Stomach Cancer. The detailed uses of Hervycta 440Mg Inj are as follows:
Hervycta 440Mg Inj contains Trastuzumab, which is used for treating patients with HER2-positive breast cancer and HER2-positive metastatic gastroesophageal adenocarcinoma. This medicine works by inhibiting the excess production of a human epidermal growth factor receptor 2 (HER2) protein in the mammalian cells. This causes inhibition of the cancer cell growth and, finally, initiation of programmed cell death.
The substitutes of Hervycta 440Mg Inj contain the same active salt(s) - TRASTUZUMAB-440MG. However, they may differ in price, manufacturing quality, and inactive ingredients. Speak to your doctor to find a suitable option.
Switching to a generic substitute medicine in the place of Hervycta 440Mg Inj is often possible if it has the same salt, strength, and dosage form. But always check with your doctor before making any changes to your medication.
Generics versions of Hervycta 440Mg Inj are typically more affordable because they don’t include the original brand's research, development, and marketing costs. They contain the same active ingredient and are approved for safety and effectiveness.
Most people don’t notice any difference. However, some may react to different fillers or coatings. If you notice any unusual symptoms after switching, consult your doctor.
Make sure the new medicine has the same active salt, strength, dosage form. Always confirm the change with your doctor or pharmacist.
Substitutes of Hervycta 440Mg Inj meet the same safety and efficacy standards as Hervycta 440Mg Inj, but small differences in absorption or formulation can exist. A doctor can help you choose the right one for your needs.
Yes. Substitutes of Hervycta 440Mg Inj may vary in color, size, or shape due to differences in manufacturing and branding, but this does not affect how they work.
Yes, it’s generally safe to switch between multiple substitutes of Hervycta 440Mg Inj if they have the same salt and strength. However, always inform your doctor so they can monitor how your body responds.
Yes, many people safely use substitutes of Hervycta 440Mg Inj for long-term treatment. Just ensure it’s done under medical supervision.
If your symptoms stay under control or lab results remain stable, the substitute for Hervycta 440Mg Inj is likely working well. Regular follow-ups with your doctor are important.
Absolutely. Even with the same salt, small differences can affect how your body responds when switching from Hervycta 440Mg Inj to its substitute. Always consult your doctor before switching.
Hervycta 440Mg Inj is used to treat Breast Cancer and Stomach Cancer.
Hervycta 440Mg Inj contains Trastuzumab, which works by inhibiting the excess production of a protein called human epidermal growth factor receptor 2 (HER2) in mammalian cells. This causes inhibition of the cancer cell growth.
Inform your doctor whether you have received any other cancer treatment. Hervycta 440Mg Inj may cause a decrease in left ventricular ejection fraction, cardiomyopathy, hypersensitivity reactions, pulmonary toxicity, and embryo-fetal toxicity during the treatment. Hence, inform your oncologist if you have any cardiovascular conditions, liver/kidney disease, lung problems, are pregnant, are planning to become pregnant, or are breastfeeding before receiving Hervycta 440Mg Inj.
Consult the doctor immediately, if you experience symptoms of an infection, such as a high temperature, chills, or feeling unwell despite a normal temperature. It could be due to a reduced white blood cell count caused by Hervycta 440Mg Inj, increasing your risk of severe infections. Additionally, swollen feet or ankles, stomach pain, or lower back pain may indicate heart problems.
It is recommended to wait at least 6 months after completing Hervycta 440Mg Inj therapy before trying to get pregnant. This is because the medication can remain in the body for some time and may potentially affect pregnancy. However, it is essential to consult the doctor for personalized advice and to ensure that it is safe for you to become pregnant after this treatment.
The duration of treatment with Hervycta 440Mg Inj will depend on an individual treatment plan, which your doctor will determine based on your specific condition. It may vary based on personal medical conditions and how you respond to the therapy. In some cases, the treatment duration may be shorter or longer. Always attend follow-up appointments as instructed by the doctor for effective treatment.
Fasting is not typically required before administering Hervycta 440Mg Inj. However, it is always best to follow the doctor's specific instructions regarding preparations before treatment. If fasting is necessary, your doctor will provide detailed guidance.
Hervycta 440Mg Inj should be administered through subcutaneous (SC) or intravenous (IV) routes by the doctor or nurse. Do not self-administer.
Hervycta 440Mg Inj should not be administered to patients with HER2-negative cancer cells as it is a monoclonal antibody that specifically targets a protein called human epidermal growth factor receptor 2 (HER2), which is present in high amounts on the surface of specific cancer cells.
The doctor may recommend heart investigations while you are taking Hervycta 440Mg Inj as it may potentially affect heart function. It has been associated with heart-related side effects, including a decrease in left ventricular ejection fraction, which could lead to heart failure in some patients. Monitoring heart health helps detect any issues early, ensuring prompt action to manage the risk. Always follow the doctor's recommendations for regular check-ups during treatment.
During treatment with Hervycta 440Mg Inj for advanced-stage disease, cardiac monitoring was conducted every 3 to 8 months for up to 2 years. However, the doctor will adjust the frequency of heart investigations based on your specific condition and response to treatment. It's essential to follow their advice for optimal monitoring and early detection of any heart-related issues.
The side effects of Hervycta 440Mg Inj include abdominal pain, chills, headache, diarrhoea, fatigue, nausea, back pain, bone pain, oedema, insomnia, fever, dizziness, vomiting, cough, rash, and injection site reactions. Consult the doctor if any of these side effects persist or worsen.
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