Tolbutamide and Language impairment - from FDA reports


Language impairment is reported only by a few people who take Tolbutamide. We study 615 people who have side effects while taking Tolbutamide from FDA. Among them, 5 have Language impairment. Find out below who they are, when they have Language impairment 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).



On Oct, 16, 2018

615 people reported to have side effects when taking Tolbutamide.
Among them, 5 people (0.81%) have Language impairment


Number of reports submitted per year:

Could Tolbutamide cause Language impairment?

Gender of people who have Language impairment when taking Tolbutamide *:

  • female: 20 %
  • male: 80 %

Age of people who have Language impairment when taking Tolbutamide *:

Top conditions involved for these people *:

  1. Metastatic Renal Cell Carcinoma (spreadable kidney cell tumour): 1 person, 20.00%
  2. Hypoaesthesia (reduced sense of touch or sensation): 1 person, 20.00%
  3. High Blood Pressure: 1 person, 20.00%
  4. Ankylosing Spondylitis (type of arthritis affecting the spine): 1 person, 20.00%

Top co-used drugs for these people *:

  1. Symbicort: 1 person, 20.00%
  2. Sunitinib Malate: 1 person, 20.00%
  3. Simvastatin: 1 person, 20.00%
  4. Omeprazole: 1 person, 20.00%
  5. Norvasc: 1 person, 20.00%

Click here to view more results or personalize the results to your gender and age

Top other side effects for these people *:

  1. Cognitive Disorder (mental health disorders affects learning, memory, perception, and problem solving): 2 people, 40.00%
  2. Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 1 person, 20.00%
  3. Stress And Anxiety: 1 person, 20.00%
  4. Blood Pressure Systolic Increased: 1 person, 20.00%
  5. Cerebral Haemorrhage (bleeding within the brain): 1 person, 20.00%

Click here to view more results or personalize the results to your gender and age

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study



Do you have Language impairment while taking Tolbutamide?


You are not alone:




Related studies

Tolbutamide

Tolbutamide has active ingredients of tolbutamide. It is often used in diabetes. (latest outcomes from Tolbutamide 618 users)

Language impairment

Language impairment (language does not develop normally in child) has been reported by people with multiple sclerosis, high blood pressure, depression, pain, rheumatoid arthritis (latest reports from 53,364 Language impairment patients).


Drugs that are associated with Language impairment
Language impairment (2,599 drugs)
Could your condition cause Language impairment
Language impairment (2,680 conditions)
Tolbutamide side effects
Browse all side effects of Tolbutamide
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 Tolbutamide and have Language impairment


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.