Baclofen and Missed period - from FDA reports


There is no Missed period reported by people who take Baclofen yet. This review analyzes which people have Missed period with Baclofen. It is created by eHealthMe based on reports from FDA, and is updated regularly.



On Jul, 21, 2018

No report is found.

What's next:

You could also:



Related studies

Baclofen

Baclofen has active ingredients of baclofen. It is often used in muscle spasms. (latest outcomes from Baclofen 50,608 users)

Missed Period

Missed period has been reported by people with birth control, depression, schizophrenia, heavy or prolong menstrual bleeding, endometriosis (latest reports from 371 Missed period patients).


Drugs that are associated with Missed period
Missed period
Could your condition cause Missed period
Missed period
Baclofen side effects
Browse all side effects of Baclofen
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 Baclofen and have Missed period


You are not alone. Join our personalized support groups:


Recent updates

General studies
Active Support Groups
Latest posts

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.