Who have Rls with Actigall - from FDA reports


Rls is reported only by a few people who take Actigall. We study 1,502 people who have side effects while taking Actigall from FDA. Among them, 2 have Rls. Find out below who they are, when they have Rls 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.



On Jan, 15, 2019

1,502 people reported to have side effects when taking Actigall.
Among them, 2 people (0.13%) have Rls


Number of reports submitted per year:

Could Actigall cause Rls?

Gender of people who have Rls when taking Actigall *:

  • female: 100 %
  • male: 0.0 %

Age of people who have Rls when taking Actigall *:

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

Top conditions involved for these people *:

  1. Pain: 2 people, 100.00%

Top co-used drugs for these people *:

  1. Zosyn: 2 people, 100.00%
  2. Melatonin: 2 people, 100.00%
  3. Aspirin: 2 people, 100.00%
  4. Baclofen: 2 people, 100.00%
  5. Cefazolin: 2 people, 100.00%
  6. Celebrex: 2 people, 100.00%
  7. Clonazepam: 2 people, 100.00%
  8. Cymbalta: 2 people, 100.00%
  9. Diazepam: 2 people, 100.00%
  10. Dilaudid: 2 people, 100.00%

Top other side effects for these people *:

  1. High Blood Pressure: 2 people, 100.00%
  2. Muscle Function Loss: 2 people, 100.00%
  3. Memory Loss: 2 people, 100.00%
  4. Dizziness: 2 people, 100.00%
  5. Malabsorption (a state arising from abnormality in absorption of food nutrients across the gastrointestinal (gi) tract): 2 people, 100.00%
  6. Joint Pain: 2 people, 100.00%
  7. Breast Infection: 2 people, 100.00%
  8. Intervertebral Disc Degeneration (spinal disc degeneration): 2 people, 100.00%
  9. Internal Hernia (protrusion of an intraperitoneal viscous into a compartment or under a constricting band within the abdominal cavity): 2 people, 100.00%
  10. Hypoaesthesia (reduced sense of touch or sensation): 2 people, 100.00%

* Approximation only. Some reports may have incomplete information.

Do you have Rls while taking Actigall?


You are not alone:




Related studies

Actigall

Actigall has active ingredients of ursodiol. It is often used in gallstones. (latest outcomes from Actigall 1,511 users)

Rls

Rls (restless legs syndrome) has been reported by people with restless leg syndrome, depression, osteoporosis, multiple sclerosis, pain (latest reports from 31,750 Rls patients).


Drugs that are associated with Rls
Rls (1,902 drugs)
Could your condition cause Rls
Rls (1,410 conditions)
Actigall 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 Actigall
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 Actigall and have Rls


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!