Review: could Orencia cause Infusion Related Reaction?


Summary

Infusion related reaction is found among people who take Orencia, especially for people who are female, 60+ old , have been taking the drug for < 1 month, also take medication Methotrexate, and have Rheumatoid arthritis . We study 9,659 people who have side effects while taking Orencia from FDA and social media. Among them, 64 have Infusion related reaction. Find out below who they are, when they have Infusion related reaction and more.

You are not alone

Join a support group for people who take Orencia and have Infusion related reaction >>>

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Orencia

Orencia has active ingredients of abatacept. It is often used in rheumatoid arthritis. (latest outcomes from Orencia 9,078 users)

Infusion Related Reaction

Infusion related reaction has been reported by people with swallowing difficulty, weakness, medical device complication, blood albumin decreased, serum sickness (latest reports from 14,607 Infusion related reaction patients).

On Aug, 23, 2016

9,659 people reported to have side effects when taking Orencia.
Among them, 64 people (0.66%) have Infusion Related Reaction


Number of reports submitted per year:

Could Orencia cause Infusion related reaction?

Time on Orencia when people have Infusion Related Reaction *:

  • < 1 month: 36.36 %
  • 1 - 6 months: 27.27 %
  • 6 - 12 months: 18.18 %
  • 1 - 2 years: 9.09 %
  • 2 - 5 years: 9.09 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Infusion Related Reaction when taking Orencia *:

  • female: 85.19 %
  • male: 14.81 %

Age of people who have Infusion Related Reaction when taking Orencia *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 5.13 %
  • 30-39: 7.69 %
  • 40-49: 23.08 %
  • 50-59: 20.51 %
  • 60+: 43.59 %

Top conditions involved for these people *:

  • Rheumatoid Arthritis (39 people)
  • Vasculitis (2 people)
  • Cardiac Disorder (2 people)
  • Drug Dependence (1 person)
  • Arthralgia (1 person)

Top co-used drugs for these people *:

  • Methotrexate (15 people)
  • Rituximab (6 people)
  • Remicade (6 people)
  • Prednisone (6 people)
  • Aspirin (6 people)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Infusion related reaction when taking Orencia?

Browse all side effects of Orencia

a b c d e f g h i j k l m n o p q r s t u v w x y z

Drugs that are associated with Infusion related reaction

Infusion related reaction

Could your condition cause Infusion related reaction

Infusion related reaction

Can you answer these questions?

More questions for: Orencia, Infusion related reaction

You may be interested in these reviews

More reviews for: Orencia, Infusion related reaction


NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.