Who have Rls with Lutein - from FDA reports

Rls is found among people who take Lutein, especially for people who are female, 60+ old also take medication Vitamin D, and have Depression. This study is created by eHealthMe based on reports of 3,856 people who have side effects when taking Lutein from FDA, and is updated regularly.

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On Feb, 04, 2019

3,856 people reported to have side effects when taking Lutein.
Among them, 8 people (0.21%) have Rls

Number of reports submitted per year:

Could Lutein cause Rls?

Gender of people who have Rls when taking Lutein *:

  • female: 100 %
  • male: 0.0 %

Age of people who have Rls when taking Lutein *:

  • 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: 40 %
  • 60+: 60 %

Top conditions involved for these people *:

  1. Osteoporosis (bones weak and more likely to break): 2 people, 25.00%
  2. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 25.00%
  3. Depression: 2 people, 25.00%
  4. Crohn's Disease (condition that causes inflammation of the gastrointestinal tract): 1 person, 12.50%
  5. Haemorrhagic Anaemia (anaemia due to excessive bleeding): 1 person, 12.50%
  6. Gastric Disorder (disease of stomach): 1 person, 12.50%
  7. Fluid Retention (an abnormal accumulation of fluid in the blood): 1 person, 12.50%
  8. Facial Pain: 1 person, 12.50%
  9. Dizziness: 1 person, 12.50%
  10. Vitreous Floaters (spots before the eyes): 1 person, 12.50%

Top co-used drugs for these people *:

  1. Coq10: 2 people, 25.00%
  2. Tramadol: 2 people, 25.00%
  3. Multivitamin: 2 people, 25.00%
  4. Fosamax: 2 people, 25.00%
  5. Omega-3 Marine Triglycerides: 2 people, 25.00%
  6. Magnesium: 2 people, 25.00%
  7. Vitamin D: 2 people, 25.00%
  8. Betaseron: 1 person, 12.50%
  9. Diovan: 1 person, 12.50%
  10. Leflunomide: 1 person, 12.50%

Top other side effects for these people *:

  1. Back Pain: 4 people, 50.00%
  2. Impaired Healing: 3 people, 37.50%
  3. Joint Pain: 3 people, 37.50%
  4. Fatigue (feeling of tiredness): 3 people, 37.50%
  5. Fall: 3 people, 37.50%
  6. Pain: 3 people, 37.50%
  7. Breathing Difficulty: 2 people, 25.00%
  8. Femur Fracture: 2 people, 25.00%
  9. Joint Dislocation (a joint position is changed from normal position): 2 people, 25.00%
  10. Osteoarthritis (a joint disease caused by cartilage loss in a joint): 2 people, 25.00%

* Approximation only. Some reports may have incomplete information.

Do you have Rls while taking Lutein?

You are not alone:

Related studies


Lutein has active ingredients of lutein. It is often used in macular degeneration. (latest outcomes from Lutein 3,993 users)


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
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Could your condition cause Rls
Rls (1,410 conditions)
Lutein 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 Lutein
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Compare Lutein to similar drugs:

What would happen?

Predict new side effects and undetected conditions when you take Lutein and have Rls

FDA reports used in this study

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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.

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