Adbry and Weight increased - a phase IV clinical study of FDA data

Summary:

Weight increased is reported as a side effect among people who take Adbry (tralokinumab), especially for people who are female, 40-49 old, also take Hydroxyzine, and have Dermatitis atopic.

The phase IV clinical study analyzes which people have Weight increased when taking Adbry. It is created by eHealthMe based on reports of 1,898 people who have side effects when taking Adbry from the FDA, and is updated regularly.

What is Adbry?

Adbry has active ingredients of tralokinumab. eHealthMe is studying from 1,899 Adbry users. Check the latest studies of Adbry.

What is Weight increased?

Weight increased is found to be associated with 2,899 drugs and 3,932 conditions by eHealthMe. Check the latest studies of Weight increased.



On Feb, 04, 2026

1,898 people reported to have side effects when taking Adbry.
Among them, 16 people (0.84%) have Weight increased.

Could Adbry cause Weight increased?

Among these 16 people:

What is the gender of people who have Weight increased when taking Adbry? *

  • female: 93.75 %
  • male: 6.25 %

What is the age of people who have Weight increased when taking Adbry? *

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 14.29 %
  • 40-49: 42.86 %
  • 50-59: 28.57 %
  • 60+: 14.29 %

What are other drugs people take besides Adbry? *

  1. Zolmitriptan: 1 person, 6.25%
  2. Lorazepam: 1 person, 6.25%
  3. Albuterol Sulfate: 1 person, 6.25%
  4. Amlodipine Besylate: 1 person, 6.25%
  5. Ativan: 1 person, 6.25%
  6. Dupixent: 1 person, 6.25%
  7. Effexor Xr: 1 person, 6.25%
  8. Eplerenone: 1 person, 6.25%
  9. Flovent Hfa: 1 person, 6.25%
  10. Hydroxyzine: 1 person, 6.25%

What are other side effects people have besides Weight increased? *

  1. Drug Ineffective: 3 people, 18.75%
  2. Fatigue (feeling of tiredness): 2 people, 12.50%
  3. Oedema (fluid collection in tissue): 2 people, 12.50%
  4. Hair Loss: 2 people, 12.50%
  5. Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 1 person, 6.25%
  6. Back Pain: 1 person, 6.25%
  7. Conjunctivitis (pink eye): 1 person, 6.25%
  8. Dermatitis Atopic (inflammatory, chronically relapsing, non-contagious and pruritic skin disorder): 1 person, 6.25%
  9. Dry Eyes (lack of adequate tears): 1 person, 6.25%
  10. Stress And Anxiety: 1 person, 6.25%

What are the existing conditions these people have? *

  1. Dermatitis Atopic (inflammatory, chronically relapsing, non-contagious and pruritic skin disorder): 10 people, 62.50%
  2. Dermatitis Allergic (inflammation of the skin due allergic reaction): 2 people, 12.50%
  3. Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 1 person, 6.25%

* Approximation only. Some reports may have incomplete information.

Do you take Adbry and have Weight increased?

- Check whether Weight increased is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously



Related studies:

Effectiveness of, long term effects of, and alternative drugs to Adbry:

Weight increased treatments and more:

How severe was Weight increased and when was it recovered:

Expand to all the drugs that have ingredients of tralokinumab:

Sub-studies by gender and age:

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Browse all side effects of Adbry:

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

Browse all the drugs that are associated with Weight increased:

Browse all the conditions that are associated with Weight increased:


How the study uses the data?

The study uses data from the FDA. It is based on tralokinumab (the active ingredients of Adbry) and Adbry (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.

How to use the study?

DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.

Who is eHealthMe?

With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

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. Our phase IV clinical studies alone cannot establish cause-effect relationship. 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.

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



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