Who have Rls with Acyclovir sodium - from FDA reports


Rls is reported only by a few people who take Acyclovir Sodium. We study 1,079 people who have side effects while taking Acyclovir sodium from FDA. Among them, 4 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.

Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials). If you find eHealthMe useful, please help us to spread the words below or leave us a testimonial.



On Dec, 24, 2018

1,079 people reported to have side effects when taking Acyclovir sodium.
Among them, 4 people (0.37%) have Rls


Number of reports submitted per year:

Could Acyclovir sodium cause Rls?

Gender of people who have Rls when taking Acyclovir sodium *:

  • female: 75 %
  • male: 25 %

Age of people who have Rls when taking Acyclovir sodium *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 75 %
  • 50-59: 25 %
  • 60+: 0.0 %

Top conditions involved for these people *:

  1. Pain: 2 people, 50.00%
  2. Oedema (fluid collection in tissue): 2 people, 50.00%
  3. Hypomania (a mild form of mania, marked by elation and hyperactivity): 2 people, 50.00%

Top co-used drugs for these people *:

  1. Percocet: 4 people, 100.00%
  2. Xanax: 4 people, 100.00%
  3. Aredia: 4 people, 100.00%
  4. Coumadin: 3 people, 75.00%
  5. Lyrica: 3 people, 75.00%
  6. Neurontin: 3 people, 75.00%
  7. Flovent: 2 people, 50.00%
  8. Sertraline Hydrochloride: 2 people, 50.00%
  9. Clonidine: 2 people, 50.00%
  10. Cipro: 2 people, 50.00%

Top other side effects for these people *:

  1. Injury: 4 people, 100.00%
  2. Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 4 people, 100.00%
  3. Hypoaesthesia (reduced sense of touch or sensation): 4 people, 100.00%
  4. Joint Pain: 4 people, 100.00%
  5. Pain: 4 people, 100.00%
  6. Osteonecrosis Of Jaw (death of bone of jaw): 4 people, 100.00%
  7. Stress And Anxiety: 4 people, 100.00%
  8. Neuropathy Peripheral (surface nerve damage): 4 people, 100.00%
  9. Haemorrhoids (a swollen vein or group of veins in the region of the anus): 3 people, 75.00%
  10. Pain In Extremity: 3 people, 75.00%

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study



Do you have Rls while taking Acyclovir sodium?


You are not alone:




Related studies

Acyclovir sodium

Acyclovir sodium has active ingredients of acyclovir sodium. (latest outcomes from Acyclovir sodium 1,093 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 (1,901 drugs)
Could your condition cause Rls
Rls (1,409 conditions)
Acyclovir sodium 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 Acyclovir sodium
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 Acyclovir sodium and have Rls


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!