Who have Ultrasound scan abnormal with Soriatane - from FDA reports


Ultrasound scan abnormal is reported only by a few people who take Soriatane. We study 2,751 people who have side effects while taking Soriatane from FDA. Among them, 1 have Ultrasound scan abnormal. Find out below who they are, when they have Ultrasound scan abnormal and more.

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


Peer to Peer mobile support

Peer support for this study is available on our Ginger Health app. It's free, anonymous and secure. The app is ideal for people taking multiple medications or having multiple conditions.



On Feb, 10, 2019

2,751 people reported to have side effects when taking Soriatane.
Among them, 1 person (0.04%) has Ultrasound scan abnormal


Number of reports submitted per year:

Could Soriatane cause Ultrasound scan abnormal?

Time on Soriatane when people have Ultrasound scan abnormal *:

  • < 1 month: 100 %
  • 1 - 6 months: 0.0 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Ultrasound scan abnormal when taking Soriatane *:

  • female: 0.0 %
  • male: 100 %

Age of people who have Ultrasound scan abnormal when taking Soriatane *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 0.0 %
  • 50-59: 0.0 %
  • 60+: 100 %

Top co-used drugs for these people *:

  1. Synthroid: 1 person, 100.00%
  2. Potassium: 1 person, 100.00%
  3. Humira: 1 person, 100.00%
  4. Coumadin: 1 person, 100.00%

Top other side effects for these people *:

  1. Skin Irritation: 1 person, 100.00%
  2. Non-Hodgkin's Lymphoma (malignant (cancer) cells form in the lymph system): 1 person, 100.00%
  3. Infection: 1 person, 100.00%
  4. Deep Venous Thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis): 1 person, 100.00%
  5. Cellulitis (infection under the skin): 1 person, 100.00%

* Approximation only. Some reports may have incomplete information.

Do you have Ultrasound scan abnormal while taking Soriatane?


You are not alone:




Related studies

Soriatane

Soriatane has active ingredients of acitretin. It is often used in psoriasis. (latest outcomes from Soriatane 2,816 users)

Ultrasound scan abnormal

Ultrasound scan abnormal has been reported by people with hiv infection, high blood pressure, multiple sclerosis, rheumatoid arthritis, osteoporosis (latest reports from 473 Ultrasound scan abnormal patients).


Drugs that are associated with Ultrasound scan abnormal
Ultrasound scan abnormal (559 drugs)
Could your condition cause Ultrasound scan abnormal
Ultrasound scan abnormal (303 conditions)
Soriatane side effects

Browse 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 Soriatane
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

What would happen?

Predict new side effects and undetected conditions when you take Soriatane and have Ultrasound scan abnormal


FDA reports used in this study



Recent updates

Recent general studies
Recent personal studies

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.

Submit your testimonial

  • Please fill in your Testimonial.
  • Please enter a minimum of 10 characters for your Testimonial.
  • Please fill in your Name.

Please wait...

{progressItem}

Thank you!