Abdominal cramps is found among people who take Megace, especially for people who are female, 60+ old , have been taking the drug for 1 - 6 months, also take medication Zometa, and have Breast cancer metastatic . We study 5,643 people who have side effects while taking Megace from FDA and social media. Among them, 282 have Abdominal cramps. Find out below who they are, when they have Abdominal cramps 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 free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>
Megace has active ingredients of megestrol acetate. It is often used in appetite - decreased. (latest outcomes from Megace 5,973 users)
Abdominal cramps has been reported by people with breathing difficulty, pain, abdominal pain upper, cholecystitis chronic, abdominal pain (latest reports from 75,746 Abdominal cramps patients).
On Jul, 28, 2016
5,643 people reported to have side effects when taking Megace.
Among them, 282 people (5.0%) have Abdominal Cramps
* 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 microprolactinoma as well endometrial hyperlasia with athypia, hence on both cabergoline and megace. Ttc as well after the hyperlasia subsides. Want to know everyones experience with these meds
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.