Pentacel – Diphtheria Toxoid Tetanus Toxoid Acellular Pertussis Vaccine DTaP Haemophilus influenzae type b Conjugate Vaccine Inactivated Poliovirus Vaccine IPV

Diphtheria Toxoid Tetanus Toxoid Acellular Pertussis Vaccine DTaP Haemophilus influenzae type b Conjugate Vaccine Inactivated Poliovirus Vaccine IPV Brand Name – Pentacel

What is Diphtheria Toxoid Tetanus Toxoid Acellular Pertussis Vaccine DTaP Haemophilus influenzae type b Conjugate Vaccine Inactivated Poliovirus Vaccine IPV

Diphtheria Toxoid Tetanus Toxoid Acellular Pertussis Vaccine DTaP Haemophilus influenzae type b Conjugate Vaccine Inactivated Poliovirus Vaccine IPV (Pentacel) is the first FDA-approved pentavalent vaccine for immunization against diphtheria, tetanus, pertussis, polio, and Haemophilus influenzae type b.

The pentavalent vaccine will reduce the number of required injections for protection against diphtheria, tetanus, pertussis, haemophilus influenza type b, and polio.

Pentacel is administered intramuscularly in infants at least 6 weeks of age and children less than 5 years of age.

Four doses constitute a primary immunization course against pertussis, and three doses constitute a primary immunization course against diphtheria, tetanus, H. influenzae type b invasive disease, and poliomyelitis; the fourth dose constitutes a booster vaccination against diphtheria, tetanus, H. influenzae type b invasive disease, and poliomyelitis.

Of note, the 2008 recommended immunization schedule from the Centers for Disease Control calls for an inactivated poliovirus vaccine at 2 months of age, 4 months of age, between 6 and 18 months of age, and at 4—6 years of age.

Consult the current CDC immunization schedule. The FDA approved Pentacel® in June 2008.

Indications

  1. diphtheria prophylaxis
  2. Haemophilus influenzae type b prophylaxis
  3. pertussis prophylaxis
  4. poliovirus prophylaxis
  5. tetanus prophylaxis

Side Effects

  1. aluminum toxicity
  2. anaphylactic shock
  3. anaphylactoid reactions
  4. angioedema
  5. anorexia
  6. apnea
  7. arthralgia
  8. bronchospasm
  9. chills
  10. cyanosis
  11. diarrhea
  12. drowsiness
  13. dyspnea
  14. encephalopathy
  15. erythema
  16. fever
  17. Guillain-Barre syndrome
  18. headache
  19. hemolytic anemia
  20. hypoesthesia
  21. hypotension
  22. hypotonia
  23. inconsolable crying
  24. increased intracranial pressure
  25. injection site reaction
  26. irritability
  27. lethargy
  28. lymphadenopathy
  29. maculopapular rash
  30. muscle paralysis
  31. myelitis
  32. nausea
  33. neuritis
  34. paresthesias
  35. peripheral neuropathy
  36. pruritus
  37. purpura
  38. rash
  39. seizures
  40. syncope
  41. thrombotic thrombocytopenic purpura (TTP)
  42. urticaria
  43. vomiting
  44. weakness

Monitoring Parameters

  • laboratory monitoring not necessary

Contraindications

  • albumin hypersensitivity
  • anticoagulant therapy
  • breast-feeding
  • children
  • coagulopathy
  • encephalopathy
  • fever
  • geriatric
  • Guillain-Barre syndrome
  • hemophilia
  • immunosuppression
  • infants
  • infection
  • intraarterial administration
  • intravenous administration
  • neomycin hypersensitivity
  • neonates
  • neurological disease
  • polymyxin hypersensitivity
  • polysorbate 80 hypersensitivity
  • pregnancy
  • premature neonates
  • seizure disorder
  • seizures
  • shock
  • subcutaneous administration
  • thrombocytopenia
  • vitamin K deficiency

Interactions

  • Ocrelizumab
  • Siponimod
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