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.
Personalized health information
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA since 1977. Our original studies have been referenced on 400+ peer-reviewed medical publications, including: The Lancet, and Mayo Clinic Proceedings.
No report is found.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Subscribe to the study: get notified of updates to the study.
Do you take Tarceva and have Injection site joint effusion?
- Check whether a drug or a condition causes Injection site joint effusion
- Predict new side effects and undetected conditions
- Share you experience to help people like you
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 effusionInjection site joint effusion
Could your condition cause Injection site joint effusionInjection site joint effusion
Expand the study to include all drugs with the same ingredientsInjection site joint effusion and drugs with ingredients of erlotinib hydrochloride.
Expand the study to include reports from both FDA and eHealthMeInjection site joint effusion and Tarceva from FDA and eHealthMe reports
Tarceva side effects
- Tarceva side effects (19,883 reports)
Browse all side effects of Tarcevaa 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
Analysis tools (to study 684 million drug outcomes from FDA)
- Check symptoms - identify the cause of a symptom: from a drug or from a condition?
- Check drugs - find out common side effects or drug interactions of my drugs.
- Compare drugs - compare the side effects and efficacy of multiple drugs side by side.
What would happen?
You are not alone. Join our personalized support groups:
- Support group for people who take Tarceva and have Injection Site Joint Effusion
- Support group for people who have Injection Site Joint Effusion
- Support group for people who take Tarceva
- Will you have Hair Loss In Women with Repatha?
- Will you have Aspartate Aminotransferase Increased with Broccoli?
- Nitrofurazone and Aromasin drug interaction
- Will you have Enlarged Prostate with Tekturna?
- Will you have Bhp with Tekturna?
Active Support Groups
- Support group for people who take Repatha and have Hair Loss In Women?
- Support group for people who take Broccoli and have Aspartate Aminotransferase Increased?
- Support group for people who take Nitrofurazone and Aromasin
- Support group for people who take Tekturna and have Enlarged Prostate?
- Support group for people who take Tekturna and have Bhp?
- What to expect when you take Repatha and have Hair Loss In Women?
- What to expect when you take Broccoli and have Aspartate Aminotransferase Increased?
- What to expect when you take Nitrofurazone and Aromasin
- What to expect when you take Tekturna and have Enlarged Prostate?
- What to expect when you take Tekturna and have Bhp?
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.