Effexor and Salmonellosis - from FDA reports

Salmonellosis is found among people who take Effexor, especially for people who are female, 60+ old also take medication Tamoxifen Citrate, and have Breast cancer. This study is created by eHealthMe based on reports of 69,058 people who have side effects when taking Effexor from FDA, and is updated regularly.

Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our independent and original studies have been referenced on 400+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO.

On Aug, 12, 2018

69,058 people reported to have side effects when taking Effexor.
Among them, 7 people (0.01%) have Salmonellosis

Number of reports submitted per year:

Could Effexor cause Salmonellosis?

Gender of people who have Salmonellosis when taking Effexor *:

  • female: 100 %
  • male: 0.0 %

Age of people who have Salmonellosis when taking Effexor *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 0.0 %
  • 50-59: 20 %
  • 60+: 80 %

Top conditions involved for these people *:

  1. Osteoporosis (bones weak and more likely to break): 4 people, 57.14%
  2. Breast Cancer: 4 people, 57.14%
  3. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 28.57%
  4. Psoriasis (immune-mediated disease that affects the skin): 1 person, 14.29%
  5. Abdominal Discomfort: 1 person, 14.29%
Check whether a drug or a condition causes Salmonellosis

Top co-used drugs for these people *:

  1. Femara: 4 people, 57.14%
  2. Fosamax: 4 people, 57.14%
  3. Tamoxifen Citrate: 4 people, 57.14%
  4. Alendronate Sodium: 2 people, 28.57%
  5. Celebrex: 1 person, 14.29%
  6. Ditropan Xl: 1 person, 14.29%
  7. Cozaar: 1 person, 14.29%
  8. Cogentin: 1 person, 14.29%
  9. Clozaril: 1 person, 14.29%
  10. Clozapine: 1 person, 14.29%
Subscribe to monitor Salmonellosis in Effexor

Top other side effects for these people *:

  1. Fall: 5 people, 71.43%
  2. Poor Quality Sleep: 5 people, 71.43%
  3. Foot Fracture: 5 people, 71.43%
  4. Osteoarthritis (a joint disease caused by cartilage loss in a joint): 5 people, 71.43%
  5. Drug Administration Error: 4 people, 57.14%
  6. Post Procedural Haematoma (post procedural clotting of blood): 4 people, 57.14%
  7. Haematocrit Decreased: 4 people, 57.14%
  8. Osteoporosis Post-Menopausal (weak bone with possibility to break after stopped menstrual cycles): 4 people, 57.14%
  9. Muscle Aches (muscle pain): 4 people, 57.14%
  10. Femur Fracture: 4 people, 57.14%
Click here to get more results

* Approximation only. Some reports may have incomplete information.

Are you new to Effexor or have questions?

Volunteer or get paid to help people with your care experience

Related studies


Effexor has active ingredients of venlafaxine hydrochloride. It is often used in depression. (latest outcomes from Effexor 75,059 users)


Salmonellosis (an infection with salmonella bacteria) has been reported by people with rheumatoid arthritis, crohn's disease, multiple sclerosis, osteoporosis, multiple myeloma (latest reports from 818 Salmonellosis patients).

Drugs that are associated with Salmonellosis
Salmonellosis (416 drugs)
Could your condition cause Salmonellosis
Salmonellosis (369 conditions)
Effexor side effects
Browse all side effects of Effexor
a 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?

Predict new side effects and undetected conditions when you take Effexor and have Salmonellosis

You are not alone. Join our personalized support groups:

You may be interested in these posts

More posts for: Effexor, Salmonellosis

Recent updates

General studies

You could also:

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.