Will you have Camptocormia with Cymbalta - from FDA reports


Camptocormia is reported only by a few people who take Cymbalta. We study 95,293 people who have side effects while taking Cymbalta from FDA. Among them, 2 have Camptocormia. Find out below who they are, when they have Camptocormia and more.

What's eHealthMe?

eHealthMe is a health data analysis company based in Mountain View, California. eHealthMe monitors and analyzes the outcomes of drugs and supplements that are currently on the market. The results are readily available to health care professionals and consumers.

eHealthMe has released original studies on market drugs and worked with leading universities and institutions such as IBM, London Health Science Centre, Mayo Clinic, Northwestern University and VA. eHealthMe studies have now been referenced in over 500 peer-reviewed medical publications.

How we gather our data?

Healthcare data is obtained from a number of sources including the Food and Drug Administration (FDA). This information is aggregated and used to produce personalized reports that patients can reference.

The information that eHealthMe collects includes:

  • Side effects (including severity and how people recover from them)
  • Associated conditions or symptoms
  • Drug effectiveness
  • Demographic data regarding drug use

How the study uses the data?

The study is based on duloxetine hydrochloride (the active ingredients of Cymbalta) and Cymbalta (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Synonyms of Camptocormia are also considered in the study.

What is Cymbalta?

Cymbalta has active ingredients of duloxetine hydrochloride. It is often used in depression. (latest outcomes from Cymbalta 103,222 users)

What is Camptocormia?

Camptocormia (abnormal posture of the trunk) has been reported by people with parkinson's disease, psychotic disorder, schizophrenia, delusional disorder, unspecified type, schizophrenia, paranoid type (latest reports from 91 Camptocormia patients).

How to use the study?

Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.

On Mar, 14, 2019

95,293 people reported to have side effects when taking Cymbalta.
Among them, 2 people (0.0%) have Camptocormia

Number of reports submitted per year:

Could Cymbalta cause Camptocormia?

Gender of people who have Camptocormia when taking Cymbalta *:

  • female: 100 %
  • male: 0.0 %

Age of people who have Camptocormia when taking Cymbalta *:

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

Top conditions involved for these people *:

  1. Constipation: 2 people, 100.00%

Top co-used drugs for these people *:

  1. Vesicare: 2 people, 100.00%
  2. Valium: 2 people, 100.00%
  3. Movicol: 2 people, 100.00%
  4. Lyrica: 2 people, 100.00%
  5. Lamictal: 2 people, 100.00%
  6. Abilify: 2 people, 100.00%
  7. Tramadol: 1 person, 50.00%

Top other side effects for these people *:

  1. Muscle Injury: 2 people, 100.00%

* Approximation only. Some reports may have incomplete information.

Do you have Camptocormia while taking Cymbalta?

You are not alone:

Related studies

Drugs that are associated with Camptocormia
Camptocormia (59 drugs)
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Camptocormia (60 conditions)
Cymbalta side effects

Browse side effects 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 Cymbalta
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 Cymbalta and have Camptocormia

FDA reports used in this study

Recent updates

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No recent updates.

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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