Infliximab with Yellow Fever Vaccine Interaction Details
Brand Names Associated with Infliximab
- Anti-TNF-alpha
- Anti-tumor Necrosis Factor-alpha
- Avsola® (Infliximab-axxq)
- cA2
- Inflectra® (Infliximab-dyyb)
- Infliximab Injection
- Remicade® (Infliximab)
- Renflexis® (Infliximab-abda)
Brand Names Associated with Yellow Fever Vaccine
- Yellow Fever Vaccine
- YF-VAX®
Medical Content Editor Dr. Brian Staiger, PharmD
Last updated
Dec 03, 2023
Interaction Effect
An increased risk of infection by the live vaccine
Interaction Summary
Vaccination with a live vaccine or therapeutic infectious agents such as live attenuated bacteria (eg Bacillus Calmette-Guerin [BCG]) is not recommended in patients receiving infliximab or infliximab biosimilar products as clinical infections, including disseminated infection may occur. In a case report, a 4.5-month infant died of disseminated BCG infection following in-utero exposure to infliximab .
Severity
Major
Onset
Delayed
Evidence
Theoretical
How To Manage Interaction
Vaccination with a live vaccine, or use of a therapeutic infectious agent (eg, Bacillus Calmette-Guerin [BCG]), while receiving infliximab or infliximab biosimilar products are not recommended as clinical infections, including disseminated infections, may occur.
Mechanism Of Interaction
Decreased immune response allows live vaccine to produce infection
Literature Reports
A) A 4.5-month infant died of disseminated Bacillus Calmette Guerin (BCG) infection following in-utero exposure to infliximab. The 28-year-old mother received infliximab 10 mg/kg every 8 weeks for refractory Crohn disease, which was continued throughout her pregnancy. The baby was healthy at birth but soon after receiving BCG vaccine at 3 months experienced irritability, a lack of weight gain, head lag, and eczema. The baby was found floppy and unresponsive and later died despite in hospital resuscitative efforts. Post-mortem evaluation revealed hemorrhages in the lungs, thymus, and heart, and disseminated granulomatous inflammation with multiple non-caseating tuberculoid granulomas in the lungs, liver, and dura were noted indicative of disseminated mycobacterial infection. The mother discontinued infliximab during a second pregnancy resulting in the birth of an infant who remained in the neonatal unit for 5 weeks, but has been well thereafter .
Infliximab Overview
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Infliximab injection products are used to relieve the symptoms of certain autoimmune disorders (conditions in which the immune system attacks healthy parts of the body and causes pain, swelling, and damage) including:
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rheumatoid arthritis (a condition in which the body attacks its own joints, causing pain, swelling, and loss of function) that is also being treated with methotrexate (Rheumatrex, Trexall),
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Crohn's disease (a condition in which the body attacks the lining of the digestive tract, causing pain, diarrhea, weight loss, and fever) in adults and children 6 years of age or older that has not improved when treated with other medications,
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ulcerative colitis (condition that causes swelling and sores in the lining of the large intestine) in adults and children 6 years of age or older that has not improved when treated with other medications,
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ankylosing spondylitis (a condition in which the body attacks the joints of the spine and other areas causing pain and joint damage),
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plaque psoriasis (a skin disease in which red, scaly patches form on some areas of the body) in adults when other treatments are less appropriate,
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and psoriatic arthritis (a condition that causes joint pain and swelling and scales on the skin).
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Infliximab injection products are in a class of medications called tumor necrosis factor-alpha (TNF-alpha) inhibitors. They work by blocking the action of TNF-alpha, a substance in the body that causes inflammation.
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Definitions
Severity Categories
Contraindicated
These drugs, generally, should not be used together simultaneously due to the high risk of severe adverse effects. Combining these medications can lead to dangerous health outcomes and should be strictly avoided unless otherwise instructed by your provider.
Major
This interaction could result in very serious and potentially life-threatening consequences. If you are taking this drug combination, it is very important to be under close medical supervision to minimize severe side effects and ensure your safety. It may be necessary to change a medication or dosage to prevent harm.
Moderate
This interaction has the potential to worsen your medical condition or alter the effectiveness of your treatment. It's important that you are monitored closely and you potentially may need to make adjustments in your treatment plan or drug dosage to maintain optimal health.
Minor
While this interaction is unlikely to cause significant problems, it could intensify side effects or reduce the effectiveness of one or both medications. Monitoring for changes in symptoms and your condition is recommended, and adjustments may be made if needed to manage any increased or more pronounced side effects.
Onset
Rapid: Onset of drug interaction typically occurs within 24 hours of co-administration.
Delayed: Onset of drug interaction typically occurs more than 24 hours after co-administration.
Evidence
Level of documentation of the interaction.
Established: The interaction is documented and substantiated in peer-reviewed medical literature.
Theoretical: This interaction is not fully supported by current medical evidence or well-documented sources, but it is based on known drug mechanisms, drug effects, and other relevant information.
How To Manage The Interaction
Provides a detailed discussion on how patients and clinicians can approach the identified drug interaction as well as offers guidance on what to expect and strategies to potentially mitigate the effects of the interaction. This may include recommendations on adjusting medication dosages, altering the timing of drug administration, or closely monitoring for specific symptoms.
It's important to note that all medical situations are unique, and management approaches should be tailored to individual circumstances. Patients should always consult their healthcare provider for personalized advice and guidance on managing drug interactions effectively.
Mechanism Of Interaction
The theorized or clinically determined reason (i.e., mechanism) why the drug-drug interaction occurs.
Disclaimer: The information provided on this page is for informational purposes only and should not be considered medical advice. Always consult with a qualified healthcare professional regarding your specific circumstances and medical conditions.
Where Does Our Information Come From?
Information for our drug interactions is compiled from several drug compendia, including:
The prescribing information for each drug, as published on DailyMED, is also used.
Individual drug-drug interaction detail pages contain references specific to that interaction. You can click on the reference number within brackets '[]' to see what reference was utilized.
The information posted is fact-checked by HelloPharmacist clinicians and reviewed quarterly.