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Erbitux 5mg

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Erbitux 5mg

International Name : Erbitux

Contains : Cetuximab

Manufacturer : Merck

Form : Injection

Packing : 1 Vial

Strength : 5 mg

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Erbitux 5mg

Erbitux is an epidermal development factor receptor (EGFR) foe demonstrated for treatment of Head and Neck Cancer and Colorectal Cancer. ERBITUX (Cetuximab) ought to be directed under the supervision of a certified doctor experienced in the employments of malignancy chemotherapeutic specialists.Erbitux (cetuximab) is a recombinant, human/mouse illusory monoclonal counter acting agent that ties explicitly to the extracellular area of the human epidermal development factor receptor (EGFR). Cetuximab is made out of the Fv districts of a murine enemy of EGFR immune response with human IgG1 substantial and kappa light chain consistent locales and has an inexact atomic load of 152 kDa. Cetuximab is delivered in mammalian (murine myeloma) cell culture.

Uses :

Erbitux Infusion is utilized for the treatment, control, avoidance, and enhancement of the accompanying ailments, conditions and side effects:

  • Squamous cell carcinoma of the head and neck
  • Colon disease
  • Disease of rectum .

Precautions/warnings :

  • Measurement depends on your condition. Imperative guiding focuses are recorded underneath.
  • Try not to nurture inside 2 months of having gotten this prescription
  • Heart issues
  • Lung issues
  • Ras-freak mCRC patients
  • Tell your specialist promptly on the off chance that you encounter fever, chills, or trouble relaxing
  • Utilize powerful contraception while taking this prescription
  • Use sunscreen or keep away from the sun amid and for 2 months after treatment

Side Effects :

  • Shortcoming
  • Fever
  • Cerebral pain
  • Disease
  • Chills
  • Queasiness
  • Spewing
  • Looseness of the bowels
  • Acid reflux
  • Weight reduction
  • Erbitux Infusion may likewise cause reactions not recorded here.

If you notice other side-effects not listed above, contact your doctor for medical advice. You may also report side-effects to your local food and drug administration authority.

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