Injection site haemorrhage is found among people who take Vicoprofen, especially for people who are female, 60+ old also take medication Forteo, and have Osteoporosis . We study 1,375 people who have side effects while taking Vicoprofen from FDA and social media. Among them, 6 have Injection site haemorrhage. Find out below who they are, when they have Injection site haemorrhage and more.
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are simple to use, anonymous and free. Start now >>>
Vicoprofen has active ingredients of hydrocodone bitartrate; ibuprofen. It is often used in pain. (latest outcomes from Vicoprofen 1,495 users)
Injection site haemorrhage (bleeding from injection site) has been reported by people with rheumatoid arthritis, osteoporosis, multiple sclerosis, type 2 diabetes, crohn's disease (latest reports from 34,904 Injection site haemorrhage patients).
On Dec, 03, 2016
1,375 people reported to have side effects when taking Vicoprofen.
Among them, 6 people (0.44%) have Injection Site Haemorrhage
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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.
I have been taking Vicoprofen 7.5mg for aprox 10 years every day for aprox 4 years. I've been off it completely for 23 days but about 4 days ago i started itching at night, so bad it keeps me awake. How long does this last?
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.