Who have Haemodialysis-induced symptom with Ultravist 240 - from FDA reports
There is no Haemodialysis-induced symptom reported by people who take Ultravist 240 yet. This review analyzes which people have Haemodialysis-induced symptom with Ultravist 240. It is created by eHealthMe based on reports from FDA, and is updated regularly.
How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.
Peer to Peer mobile support
Peer support for this study is available on our Ginger Health app. It's free, anonymous and secure. The app is ideal for people taking multiple medications or having multiple conditions.
No report is found.
Do you have Haemodialysis-induced symptom while taking Ultravist 240?
- Check whether a drug or a condition causes Haemodialysis-induced symptom
- Subscribe to monitor Haemodialysis-induced symptom in Ultravist 240
You are not alone:
- Connect with people like you who take Ultravist 240 and have Haemodialysis-induced symptom
- Use your healthcare experience to help people like you, and be rewarded
Ultravist 240 has active ingredients of iopromide. (latest outcomes from Ultravist 240 55 users)
Haemodialysis-induced symptom has been reported by people with rheumatoid arthritis, chronic kidney disease, fabry's disease, diabetes, allergic rhinitis (latest reports from 30 Haemodialysis-induced symptom patients).
Drugs that are associated with Haemodialysis-induced symptomHaemodialysis-induced symptom
Could your condition cause Haemodialysis-induced symptomHaemodialysis-induced symptom
Ultravist 240 side effects
- Ultravist 240 side effects (54 reports)
Browse by gender and age
Browse all side effects of Ultravist 240a 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?
Recent general studies
- Will you have Fatty Liver with Lamisil? - now
- Will you have Liver Fatty with Lamisil? - now
- Trihexyphenidyl Hydrochloride and Chlorpromazine Hydrochloride drug interaction - now
- Will you have Ear Tag with Iron Edta? - a second ago
- Boys aged 2-9 who have Tongue Infection with Akineton - 2 seconds ago
- Rabeprazole and Nexium drug interaction - 2 seconds ago
- Will you have Sepsis with Potassium Gluconate? - 2 seconds ago
- Will you have Postpartum Vaginal Laceration with L-Glutamine? - 3 seconds ago
- Hydralazine Hydrochloride and Yarrow drug interaction - 3 seconds ago
- Evening Primrose Oil and Jambolan Plum drug interaction - 4 seconds ago
Recent personal studies
- A study for a 45 year old man who takes Losartan Potassium - 23 minutes ago
- A study for a 62 year old woman who takes Dextroamphetamine Sulfate, Naltrexone Hydrochloride, Cortef - 29 minutes ago
- A study for a 12 year old boy who takes Clindamycin Hydrochloride - 3 hours ago
- A study for a 59 year old man who takes Metoprolol Tartrate, Abacavir - 3 hours ago
- A study for a 65 year old woman who takes Trintellix, Ativan - 7 hours ago
- A study for a 41 year old woman who takes Prevacid, Progesterone - 8 hours ago
- A study for a 34 year old woman who takes Zoloft, Nexplanon - 10 hours ago
- A study for a 30 year old woman who takes Toprol-xl, Lexapro, Abilify - 10 hours ago
- Prediction of Edarbi, Omeprazole for a 57 year old man - 18 hours ago
- A study for a 24 year old woman who takes Vyvanse, Lamictal Xr - 19 hours ago
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.