Review: could Lortab cause Rls?


Summary

Rls is found among people who take Lortab, especially for people who are female, 60+ old , have been taking the drug for 10+ years, also take medication Zometa, and have Pain . We study 20,376 people who have side effects while taking Lortab from FDA and social media. Among them, 176 have Rls. Find out below who they are, when they have Rls and more.

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Lortab

Lortab has active ingredients of acetaminophen; hydrocodone bitartrate. It is often used in pain. (latest outcomes from Lortab 22,327 users)

Rls

Rls (restless legs syndrome) has been reported by people with restless leg syndrome, pain, drug ineffective, pathological gambling, drowsiness (latest reports from 24,337 Rls patients).

On Sep, 16, 2016

20,376 people reported to have side effects when taking Lortab.
Among them, 176 people (0.86%) have Rls


Number of reports submitted per year:

Could Lortab cause Rls?

Time on Lortab when people have Rls *:

  • < 1 month: 0.0 %
  • 1 - 6 months: 33.33 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 66.67 %

Gender of people who have Rls when taking Lortab *:

  • female: 79.75 %
  • male: 20.25 %

Age of people who have Rls when taking Lortab *:

  • 0-1: 0.0 %
  • 2-9: 0.78 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 5.43 %
  • 40-49: 24.81 %
  • 50-59: 23.26 %
  • 60+: 45.74 %

Severity if Rls when taking Lortab **:

  • least: 33.33 %
  • moderate: 0.0 %
  • severe: 33.33 %
  • most severe: 33.33 %

How people recovered from Rls **:

  • while on drug: 0.0 %
  • after off the drug: 50 %
  • not yet: 50 %

Top conditions involved for these people *:

  • Pain (33 people, 18.75%)
  • Depression (31 people, 17.61%)
  • Neoplasm Malignant (29 people, 16.48%)
  • Metastases To Spine (29 people, 16.48%)
  • Lung Neoplasm (29 people, 16.48%)

Top co-used drugs for these people *:

  • Zometa (110 people, 62.50%)
  • Coumadin (89 people, 50.57%)
  • Ambien (87 people, 49.43%)
  • Nexium (57 people, 32.39%)
  • Lasix (56 people, 31.82%)

Top other side effects for these people *:

  • Pain (131 people, 74.43%)
  • Hypertension (105 people, 59.66%)
  • Dyspnoea (103 people, 58.52%)
  • Anxiety (99 people, 56.25%)
  • Fatigue (98 people, 55.68%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

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

Do you have Rls when taking Lortab?

Browse all side effects of Lortab

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

Drugs that are associated with Rls

Rls

Could your condition cause Rls

Rls

Related studies

Can you answer these questions?

More questions for: Lortab, Rls

You may be interested in these reviews

More reviews for: Lortab, Rls


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.