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Liquid PedvaxHIB Side Effects

Generic name: haemophilus b conjugate (prp-omp) vaccine

Note: This document provides detailed information about Liquid PedvaxHIB Side Effects associated with haemophilus b conjugate (prp-omp) vaccine. Some dosage forms listed on this page may not apply specifically to the brand name Liquid PedvaxHIB.

Applies to haemophilus b conjugate (prp-omp) vaccine: intramuscular suspension.

Important warnings This medicine can cause some serious health issues

Tell your doctor if your child uses other medicines or have other medical conditions or allergies.

Get emergency medical help if your child has signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Keep track of any and all side effects your child has after receiving this vaccine. When the child receives a booster dose, you will need to tell the doctor if the previous shot caused any side effects.

Call your doctor at once if your child has:

Common side effects may include:

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

For healthcare professionals

Applies to haemophilus b conjugate (prp-omp) vaccine: intramuscular suspension.

General

The most common adverse events were irritability, sleepiness, injections site pain/soreness, injection site swelling, unusual high-pitched crying, prolonged crying (over 4 hours), diarrhea, vomiting, crying, pain, otitis media, rash, and upper respiratory infection.[Ref]

Other

Gastrointestinal

Local

Psychiatric

Dermatologic

Immunologic

Nervous system

Hematologic

Respiratory

References

1. (2022) "Product Information. Liquid PedvaxHIB (haemophilus b conjugate (PRP-OMP) vaccine)." Merck & Co., Inc

Further information

Liquid PedvaxHIB 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.

Some side effects may not be reported. You may report them to the FDA.