Who have Weakness with Abstral - from FDA reports


Weakness is found among people who take Abstral, especially for people who are female, 60+ old also take medication Flaxseed, and have Lung cancer - non-small cell. This study is created by eHealthMe based on reports of 673 people who have side effects when taking Abstral from FDA, and is updated regularly.

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


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On Jan, 22, 2019

673 people reported to have side effects when taking Abstral.
Among them, 16 people (2.38%) have Weakness


Number of reports submitted per year:

Could Abstral cause Weakness?

Gender of people who have Weakness when taking Abstral *:

  • female: 62.5 %
  • male: 37.5 %

Age of people who have Weakness when taking Abstral *:

  • 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: 20 %
  • 60+: 80 %

Top conditions involved for these people *:

  1. Pain: 4 people, 25.00%
  2. Nausea (feeling of having an urge to vomit): 4 people, 25.00%
  3. Lung Cancer - Non-Small Cell (lung cancer): 4 people, 25.00%
  4. Constipation: 3 people, 18.75%
  5. B-Cell Type Acute Leukaemia (cancer of the white blood cells): 3 people, 18.75%
  6. Neuralgia (pain in one or more nerves): 3 people, 18.75%
  7. Breakthrough Pain: 3 people, 18.75%
  8. Sleep Disorder: 3 people, 18.75%
  9. Tumor Pain: 2 people, 12.50%
  10. Prostate Cancer Metastatic: 2 people, 12.50%

Top co-used drugs for these people *:

  1. Zovirax: 3 people, 18.75%
  2. Neurontin: 3 people, 18.75%
  3. Oxycodone: 3 people, 18.75%
  4. Oxycontin: 3 people, 18.75%
  5. Keppra: 3 people, 18.75%
  6. Folvite: 3 people, 18.75%
  7. Prilosec: 3 people, 18.75%
  8. Septra: 3 people, 18.75%
  9. Temovate: 3 people, 18.75%
  10. Flaxseed: 3 people, 18.75%

Top other side effects for these people *:

  1. Arrhythmias (irregular heartbeat): 4 people, 25.00%
  2. Nausea (feeling of having an urge to vomit): 4 people, 25.00%
  3. Musculoskeletal Stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves): 3 people, 18.75%
  4. Oedema Peripheral (superficial swelling): 3 people, 18.75%
  5. Graft Versus Host Disease In Skin (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the skin): 3 people, 18.75%
  6. Death: 3 people, 18.75%
  7. Joint Pain: 3 people, 18.75%
  8. Joint Range Of Motion Decreased (disease of joint movement): 3 people, 18.75%
  9. Mucosal Dryness (dryness of mucous membrane): 3 people, 18.75%
  10. Swelling Face: 3 people, 18.75%

* Approximation only. Some reports may have incomplete information.

Do you have Weakness while taking Abstral?


You are not alone:




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Could your condition cause Weakness
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Abstral 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 Abstral
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 Abstral and have Weakness


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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