Review: could Citalopram hydrobromide cause Cholelithiasis (Gallstones)?
Summary: Cholelithiasis is found among people who take Citalopram hydrobromide, especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months, also take medication Celexa, and have Depression.
We study 23,307 people who have side effects while taking Citalopram hydrobromide from FDA and social media. Among them, 153 have Cholelithiasis. Find out below who they are, when they have Cholelithiasis and more.
You are not alone: join a support group for people who take Citalopram hydrobromide and have Cholelithiasis >>>
Citalopram hydrobromide has active ingredients of citalopram hydrobromide. It is often used in depression. (latest outcomes from 24,937 Citalopram hydrobromide users)
Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts) has been reported by people with birth control, multiple sclerosis, acne, premenstrual syndrome, high blood pressure. (latest reports from 25,143 Cholelithiasis patients)
On Apr, 9, 2015: 23,307 people reported to have side effects when taking Citalopram hydrobromide. Among them, 153 people (0.66%) have Cholelithiasis.
Time on Citalopram hydrobromide when people have Cholelithiasis * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Age of people who have Cholelithiasis when taking Citalopram hydrobromide * :
Severity of Cholelithiasis when taking Citalopram hydrobromide ** :
How people recovered from Cholelithiasis ** :
Top conditions involved for these people * :
- Depression (44 people, 28.76%)
- Contraception (28 people, 18.30%)
- Anxiety (21 people, 13.73%)
- Multiple myeloma (19 people, 12.42%)
- Premenstrual syndrome (18 people, 11.76%)
Top co-used drugs for these people * :
- Celexa (45 people, 29.41%)
- Yasmin (45 people, 29.41%)
- Furosemide (40 people, 26.14%)
- Yaz (37 people, 24.18%)
- Aredia (31 people, 20.26%)
* 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.
Do you have Cholelithiasis while taking Citalopram Hydrobromide?
You are not alone! Join a support group on :
- support group for people who take Citalopram hydrobromide and have Cholelithiasis
- support group for people who take Citalopram hydrobromide
- support group for people who have Cholelithiasis
Drugs in real world that are associated with:
Could your condition cause:
- A study of drug interactions between Levonorgestrel And Ethinyl Estradiol, Citalopram Hydrobromide for a 37-year old woman with Contraception, Depression. The patient has Asthma, Gerd, Cough
- A study of drug interactions between Flonase, Lamictal, Latuda, Celexa, Methadone Hydrochloride, Klonopin, Wellbutrin Sr for a 35-year old woman with Nasal Allergies, Bipolar 2, Drug Addiction, Anxiety. The patient has Anorgasmia
- A study of side effects of Celexa for a 69-year old woman with Depression. The patient has Low Blood Pressure
- A study of drug interactions between Ortho Tri-cyclen, Celexa, Zolpidem for a 34-year old woman with Birth Control, Depression, Insomnia. The patient has Migraine, Fatigue - Chronic, Binge Eating
- A study of side effects of Celexa for a 45-year old man with Depression. The patient has Motion Sickness
Recent Citalopram hydrobromide related drug comparison:
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.