Tarceva and Injection site joint effusion - from FDA reports


There is no Injection site joint effusion reported by people who take Tarceva yet. This review analyzes which people have Injection site joint effusion with Tarceva. It is created by eHealthMe based on reports from FDA, and is updated regularly.



On Jul, 23, 2018

No report is found.

What's next:

You could also:



Related studies

Tarceva

Tarceva has active ingredients of erlotinib hydrochloride. It is often used in lung cancer. (latest outcomes from Tarceva 20,088 users)

Injection Site Joint Effusion

Injection site joint effusion (presence of increased intra-articular fluid at injection site) has been reported by people with atrial fibrillation/flutter (latest reports from 2 Injection site joint effusion patients).


Drugs that are associated with Injection site joint effusion
Injection site joint effusion
Could your condition cause Injection site joint effusion
Injection site joint effusion
Tarceva side effects
Browse all side effects of Tarceva
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 Tarceva and have Injection site joint effusion


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.