Effexor and Keratosis follicular - from FDA reports


Keratosis follicular is reported only by a few people who take Effexor. We study 74,228 people who have side effects while taking Effexor from FDA. Among them, 1 have Keratosis follicular. Find out below who they are, when they have Keratosis follicular and more.

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On Nov, 14, 2018

74,228 people reported to have side effects when taking Effexor.
Among them, 1 person (0.0%) has Keratosis follicular


Number of reports submitted per year:

Could Effexor cause Keratosis follicular?

Time on Effexor when people have Keratosis follicular *:

  • < 1 month: 0.0 %
  • 1 - 6 months: 100 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Keratosis follicular when taking Effexor *:

  • female: 0.0 %
  • male: 100 %

Age of people who have Keratosis follicular when taking Effexor *:

  • 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: 100 %
  • 60+: 0.0 %

Top co-used drugs for these people *:

  1. Atenolol: 1 person, 100.00%

Top other side effects for these people *:

  1. Acanthosis (thickening of the skin): 1 person, 100.00%

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study



Do you have Keratosis follicular while taking Effexor?


You are not alone:




Related studies

Effexor

Effexor has active ingredients of venlafaxine hydrochloride. It is often used in depression. (latest outcomes from Effexor 80,229 users)

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Keratosis follicular (condition in which there are numerous rough follicular spots, which may be skin coloured, red or brown) has been reported by people with multiple sclerosis, herpes simplex, keratosis follicular, chronic myeloid leukaemia, itching (latest reports from 162 Keratosis follicular patients).


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What would happen?

Predict new side effects and undetected conditions when you take Effexor and have Keratosis follicular


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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).

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