Diphtheria Toxoid / Haemophilus B Conjugate (prp-t) Vaccine / Pertussis, Acellular / Poliovirus Vaccine, Inactivated / Tetanus Toxoid Side Effects
Medically reviewed by Drugs.com. Last updated on Sep 13, 2024.
Applies to diphtheria toxoid / haemophilus b conjugate (prp-t) vaccine / pertussis, acellular / poliovirus vaccine, inactivated / tetanus toxoid: intramuscular powder for suspension, intramuscular suspension.
Precautions
It is very important that you call the doctor right away if you or your child have any unwanted effects after receiving the vaccine. This may include fainting, seizures, a high fever, crying that will not stop, or severe redness or swelling where the shot was given.
This vaccine may cause a serious type of allergic reaction called anaphylaxis, which can be life-threatening and requires immediate medical attention. Tell your doctor right away if you have a rash, itching, swelling of the tongue and throat, or trouble breathing after you get the injection.
Tell your child’s doctor about all other vaccines your child has had, especially if those vaccines were part of a series. This vaccine might be used to finish a series of vaccines.
This vaccine will not treat an active infection. If your child has an infection due to diphtheria, tetanus, pertussis, polio, or Haemophilus influenzae type b, your child will need medicines to treat these infections. .
Fainting may occur after you receive this vaccine. You may also have vision changes, numbness or tingling in your arms, hands, or feet, or jerky movements of the arms and legs. Call the doctor right away if you or your child have any of these symptoms.
Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.
Serious side effects
Along with its needed effects, diphtheria toxoid/haemophilus b conjugate (prp-t) vaccine/pertussis, acellular/poliovirus vaccine, inactivated/tetanus toxoid may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur while taking diphtheria toxoid / haemophilus b conjugate (prp-t) vaccine / pertussis, acellular / poliovirus vaccine, inactivated / tetanus toxoid:
More common side effects
- chest pain or tightness
- confusion
- coughing
- crying, persistent and inconsolable, occurring within 48 hours and lasting 3 or more hours
- decreased urination
- diarrhea
- dizziness
- dry mouth
- fainting
- fever
- increase in heart rate
- lightheadedness
- loss of appetite
- nausea
- noisy, rapid, or trouble breathing
- sneezing
- sore throat
- stomach pain
- sunken eyes
- thirst
- unusual tiredness or weakness
- wrinkled skin
Incidence not known
- bluish color of the fingernails, lips, skin, palms, or nail beds
- chills
- cold or flu-like symptoms
- drowsiness
- fainting
- fast heartbeat
- general feeling of illness
- hives
- hoarseness
- irritation
- itching
- joint pain, stiffness, or swelling
- rash
- redness of the skin
- runny nose
- severe headache
- slow breathing
- sneezing
- stiff neck or back
- stuffy nose
- swelling of the eyelids, face, lips, hands, or feet
Other side effects
Some side effects of diphtheria toxoid / haemophilus b conjugate (prp-t) vaccine / pertussis, acellular / poliovirus vaccine, inactivated / tetanus toxoid may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
More common side effects
- irritability
- tenderness at the injection site
- unusual drowsiness, dullness, tiredness, weakness, or feeling of sluggishness
Incidence not known
- bleeding, blistering, burning, coldness, discoloration of the skin, feeling of pressure, hives, infection, inflammation, itching, lumps, numbness, pain, rash, redness, scarring, soreness, stinging, swelling, tenderness, tingling, ulceration, or warmth at the injection site
- change in skin color at the injection site
- paleness of the skin
- sleepiness or unusual drowsiness
- vomiting
For healthcare professionals
Applies to diphtheria toxoid / haemophilus b conjugate (prp-t) vaccine / pertussis, acellular / poliovirus vaccine, inactivated / tetanus toxoid: intramuscular kit.
Psychiatric adverse events
- Very common (10% or more): Fussiness/irritability (76.9%)
- Postmarketing reports: Screaming
Other
- Very common (10% or more): Inconsolable crying (59.3%), fever (16.3%)
- Rare (less than 0.1%): Death
- Postmarketing reports: Vaccination failure/therapeutic response decreased[Ref]
Four deaths occurred in the clinical trials. Causes of death were asphyxia due to suffocation, head trauma, Sudden Infant Death Syndrome, and neuroblastoma which occurred at 8, 23, 52, and 256 days post-vaccination respectively.[Ref]
Nervous system
- Very common (10% or more): Decreased activity/lethargy (45.8%)
- Rare (less than 0.1%): Seizures, encephalopathy
- Frequency not reported: Hypotonia[Ref]
Four patients experienced a seizure within 7 days of vaccination. One case of encephalopathy occurred 30 days post-vaccination and was secondary to cardiac arrest after cardiac surgery.[Ref]
Local
- Very common (10% or more): Injection site tenderness (56.1%), increase in arm circumference (33.6%), injection site redness (17.3%)
- Common (1% to 10%): Injection site swelling
- Postmarketing reports: Injection site reactions (including inflammation, mass, abscess, sterile abscess), extensive swelling of the injected limb (including swelling involving adjacent joints)[Ref]
Hypersensitivity
- Postmarketing reports: Anaphylaxis/anaphylactic reaction, hypersensitivity (such as rash and urticaria)[Ref]
Respiratory
- Frequency not reported: Asthma
- Postmarketing reports: Apnea, cough[Ref]
Asthma was a serious adverse event that occurred within 30 days following the 4th dose of vaccine.[Ref]
Immunologic
- Frequency not reported: Bronchiolitis, gastroenteritis, pneumonia
- Postmarketing reports: Meningitis, rhinitis, viral infection[Ref]
Bronchiolitis, gastroenteritis, and pneumonia were serious adverse events that occurred within 30 days following the 4th dose of vaccine.[Ref]
Cardiovascular
- Postmarketing reports: Cyanosis, pallor[Ref]
Dermatologic
- Postmarketing reports: Erythema, skin discoloration[Ref]
Metabolic
- Postmarketing reports: Decreased appetite[Ref]
Gastrointestinal
- Postmarketing reports: Vomiting, diarrhea[Ref]
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References
1. (2008) "Product Information. Pentacel (DTaP-IPV/Hib) (diphtheria/haemophilus/pertussis/tetanus/polio vaccine)." sanofi pasteur
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Diphtheria toxoid/haemophilus b conjugate (prp-t) vaccine/pertussis, acellular/poliovirus vaccine, inactivated/tetanus toxoid side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.