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Embremma Injection

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Prescription Required

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Emcure Pharmaceuticals Ltd

Salt Composition

Eribulin Mesylate (0.5mg/ml)

Overview Embremma Injection

Oncaspar Injection treats advanced breast cancer in adults. It's indicated for patients whose cancer has metastasized and who have undergone prior anticancer therapies. Oncaspar may be administered alone or in combination with other medications as part of a chemotherapy regimen. Administered intravenously under medical supervision, the dosage and frequency are determined by your physician based on your individual needs and may vary. Strict adherence to the prescribed regimen is crucial; incorrect usage or overdose can lead to severe adverse reactions. Therapeutic benefits might not be immediately apparent, potentially taking weeks or months; discontinue only under your doctor's instruction. Common side effects include fatigue, alopecia, nausea, and bowel irregularity. A reduction in blood cell counts, increasing infection risk, is possible; regular blood tests monitoring blood cell levels, cardiac function, liver health, uric acid, and electrolytes are essential. Peripheral neuropathy, manifested as numbness, tingling, or paresthesia in the extremities, may occur; report persistent or bothersome symptoms to your doctor. Prior to commencing treatment, disclose any pre-existing heart, liver, or kidney conditions, and all medications, particularly those for infections, as drug interactions are possible. This medication is contraindicated during pregnancy and lactation; effective contraception for both partners is mandatory throughout treatment.

Uses of Embremma Injection

Advanced breast cancer with distant spread

Major Benefits of Embremma Injection:

This medication will be administered by your healthcare provider; self-medication is strictly prohibited.

Common Side effects of Embremma Injection:

  • Anemia (low number of red blood cells)
  • Weakness
  • Hair loss
  • Nausea
  • Constipation
  • Decreased white blood cell count
  • Fatigue
  • Peripheral neuropathy (tingling and numbness of feet and hand)

How to use Embremma Injection:

This medication will be administered by your healthcare provider; self-medication is strictly prohibited.

How Embremma Injection works:

Embremma Injection is a cancer treatment that disrupts the microtubules crucial for cancer cell division and proliferation. This disruption halts the cancer cells' growth cycle, leading to their demise.

SAFETY ADVICE

AlcoholAlcoholCONSULT YOUR DOCTOR

Alcohol consumption alongside Embremma Injection may pose unknown risks. Seek medical advice before combining them.

PregnancyPregnancyCONSULT YOUR DOCTOR

Administering Embremma Injection during pregnancy is contraindicated due to established risk to the fetus. In exceptional, life-threatening circumstances, a physician might prescribe it if the potential benefits outweigh the known hazards. Physician consultation is advised.

Breast feedingBreast feedingUNSAFE

Administering Embremma Injection while breastfeeding is contraindicated. Evidence indicates potential infant toxicity from this medication.

DrivingDrivingUNSAFE

Administration of Embremma Injection can induce drowsiness, blurred vision, and dizziness, potentially impairing alertness. Driving should be avoided if these effects are experienced.

KidneyKidneyCAUTION

Careful consideration should be given to administering Embremma Injection to individuals with impaired renal function. Dosage modification for Embremma Injection might be necessary. Physician consultation is advised.

LiverLiverCAUTION

For individuals with hepatic impairment, Embremma Injection requires careful administration. Dosage modification of Embremma Injection might be necessary. Physician consultation is advised.

What if you forget to take Embremma Injection :

NA

Facts to Know About Embremma Injection

LabelValue
Chemical Type Halichondrin B analog
Developing Habits No.
Type of Therapy Cancer Medications
Action Class Non-Taxane Microtubule Inhibitors

FAQs on Embremma Injection

Embremma Injection may cause hair loss, a side effect that can be reversible but varies in severity. Discuss any hair loss concerns with your doctor.
Embremma Injection is typically administered on days 1 and 8 of each 21-day treatment cycle. Treatment length is individualized, with the number of cycles determined by your physician. Blood test results may necessitate a delay or dose adjustment as directed by your doctor.
A doctor or healthcare professional will administer Embremma Injection intravenously over 2 to 5 minutes. Dosage is determined by your body surface area (m²), calculated from your height and weight, and may be adjusted based on blood test results or other factors. Following administration, a saline flush is recommended to ensure complete delivery of the Embremma Injection.
Embremma Injection carries serious risks, including a dangerously low white blood cell count (neutropenia), potentially causing fatal infections. Numbness, tingling, or pain in the hands and feet (peripheral neuropathy) is also common, sometimes severe. Furthermore, it may harm a developing fetus if administered during pregnancy.
Women of childbearing age must use effective contraception for three months following Embremma Injection treatment. This medication may cause serious birth defects and should not be used during pregnancy unless absolutely essential after thorough consideration of risks to both mother and baby.
Handle Embremma Injection with care, avoiding contact with skin, eyes, mouth, or nasal passages. Wear gloves, goggles, and protective clothing. In case of skin contact, wash thoroughly with soap and water. If contact occurs with eyes, mouth, or nose, flush the area thoroughly with water. Pregnant personnel should not handle this medication.
Embremma Injection must be diluted with no more than 100 ml of 0.9% sodium chloride solution; dilution with 5% dextrose is prohibited. Administration requires the oversight of an oncologist and must be performed by a qualified healthcare professional.
Embremma Injection
17,590
MRP 21,430
17% off