Oprelvekin rh IL 11

Oprelvekin rh IL 11 Brand Name– Neumega

What is Oprelvekin rh IL 11

Oprelvekin rh IL 11 is a recombinant version of human interleukin-11 (IL-11) derived from genetically altered Escherichia coli. Unlike endogenous IL-11, oprelvekin lacks the amino-terminal proline residue.

The biological activity of oprelvekin and endogenous IL-11 is essentially the same. Endogenous IL-11 is produced by a variety of stromal cells including fibroblasts, epithelial cells and osteoblasts and has a wide spectrum of biological activity involving the hematopoietic, lymphopoietic, hepatic, adipose, neuronal and osteoclast systems.

IL-11 belongs to a family of human growth factors, which includes granulocyte colony-stimulating factor (G-CSF), human growth hormone, and other growth factors.

Oprelvekin is used clinically to prevent severe chemotherapy-induced thrombocytopenia and to reduce the need for platelet transfusions following myelosuppressive chemotherapy for nonmyeloid malignancies.

Oprelvekin is undergoing investigation in children for the same indication.

Oprelvekin is not effective for patients undergoing bone marrow transplantation and should not be used after myeloablative chemotherapy.

Oprelvekin was approved on November 25, 1997 for patients who are at high risk for developing severe chemotherapy-induced thrombocytopenia; however, it was denied approval for use as primary prophylaxis.

Indications

  • chemotherapy-induced thrombocytopenia

For the prevention of severe chemotherapy-induced thrombocytopenia and to reduce the need for platelet transfusions following myelosuppressive chemotherapy in patients with non-myeloid malignancies who are at high risk of severe thrombocytopenia

NOTE: Oprelvekin has been designated an orphan drug by the FDA for this indication.

Side Effects

  1. abdominal pain
  2. alopecia
  3. anemia
  4. angioedema
  5. anorexia
  6. antibody formation
  7. asthenia
  8. atrial fibrillation
  9. atrial flutter
  10. blurred vision
  11. bone pain
  12. candidiasis
  13. capillary leak syndrome
  14. cardiac arrest
  15. chest pain (unspecified)
  16. chills
  17. constipation
  18. cough
  19. dehydration
  20. diarrhea
  21. dizziness
  22. dysarthria
  23. dyspepsia
  24. dyspnea
  25. ecchymosis
  26. edema
  27. exfoliative dermatitis
  28. fever
  29. fluid retention
  30. flushing
  31. headache
  32. heart failure
  33. hypoalbuminemia
  34. hypocalcemia
  35. hypokalemia
  36. hypotension
  37. infection
  38. injection site reaction
  39. insomnia
  40. laryngeal edema
  41. myalgia
  42. nausea
  43. ocular hemorrhage
  44. ocular infection
  45. palpitations
  46. papilledema
  47. paresthesias
  48. pericardial effusion
  49. peripheral edema
  50. pharyngitis
  51. pleural effusion
  52. pulmonary edema
  53. rash
  54. renal failure (unspecified)
  55. rhinitis
  56. serious hypersensitivity reactions or anaphylaxis
  57. sinus tachycardia
  58. skin discoloration
  59. stroke
  60. syncope
  61. urticaria
  62. visual impairment
  63. vomiting
  64. wheezing

Monitoring Parameters

  • CBC
  • platelet count
  • serum electrolytes

Contraindications

  • acute bronchospasm
  • anemia
  • angioedema
  • ascites
  • atrial fibrillation
  • atrial flutter
  • brain tumor
  • breast-feeding
  • cardiac arrhythmias
  • cardiac disease
  • cerebrovascular disease
  • chemotherapy
  • children
  • driving or operating machinery
  • electrolyte imbalance
  • geriatric
  • heart failure
  • hypokalemia
  • increased intracranial pressure
  • infants
  • intracranial mass
  • leukemia
  • multiple myeloma
  • oprelvekin hypersensitivity
  • papilledema
  • pericardial effusion
  • pleural effusion
  • pregnancy
  • pulmonary edema
  • renal disease
  • renal failure
  • renal impairment
  • serious hypersensitivity reactions or anaphylaxis
  • stroke
  • urticaria
  • ventricular dysfunction
  • visual disturbance

Interactions

  • Bumetanide
  • Ethacrynic Acid
  • Furosemide
  • Loop diuretics
  • Thiazide diuretics
  • Torsemide
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