Review: could Lisinopril cause Sperm count decreased?
Summary: Sperm count decreased is reported only by a few people who take Lisinopril.
We study 93,797 people who have side effects while taking Lisinopril from FDA and social media. Among them, 4 have Sperm count decreased. Find out below who they are, when they have Sperm count decreased and more.
You are not alone: join a support group for people who take Lisinopril and have Sperm count decreased >>>
Lisinopril has active ingredients of lisinopril. It is often used in high blood pressure. (latest outcomes from 99,275 Lisinopril users)
Sperm count decreased
Sperm count decreased has been reported by people with depression, psoriasis, enlarged prostate, attention deficit hyperactivity disorder, epilepsy. (latest reports from 238 Sperm count decreased patients)
On Mar, 16, 2015: 93,797 people reported to have side effects when taking Lisinopril. Among them, 4 people (0.00%) have Sperm Count Decreased.
Time on Lisinopril when people have Sperm count decreased * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Sperm count decreased||0.00%||0.00%||0.00%||0.00%||0.00%||100.00%||0.00% |
Gender of people who have Sperm count decreased when taking Lisinopril * :
|Sperm count decreased||0.00%||100.00% |
Age of people who have Sperm count decreased when taking Lisinopril * :
|Sperm count decreased||0.00%||0.00%||0.00%||0.00%||33.33%||0.00%||33.33%||33.33% |
Top conditions involved for these people * :
- Hypertension (3 people, 75.00%)
- Pain (2 people, 50.00%)
- Bronchitis chronic (2 people, 50.00%)
- Hormone replacement therapy (2 people, 50.00%)
- Diabetes mellitus (2 people, 50.00%)
Top co-used drugs for these people * :
- Viagra (2 people, 50.00%)
- Doxycycline (2 people, 50.00%)
- Hydromorphone (2 people, 50.00%)
- Depo-testosterone (2 people, 50.00%)
- Insulin (2 people, 50.00%)
* 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.
Get connected: join our support group of lisinopril and sperm count decreased on
Do you have Sperm Count Decreased while taking Lisinopril?
You are not alone! Join a mobile support group on :
- support group for people who take Lisinopril and have Sperm Count Decreased
- support group for people who take Lisinopril
- support group for people who have Sperm Count Decreased
Drugs in real world that are associated with:
Could your condition cause:
- A study of drug interactions between Prednisone, Lisinopril, Prednisone, Myfortic, Prograf for a 59-year old woman with Transplant - Kidney, High Blood Pressure. The patient has Weight Gain, Blood Creatinine Increased
- A study of side effects of Lisinopril for a 41-year old man with High Blood Pressure. The patient has Hernia (hernia happens when part of an internal organ or tissue bulges through a weak area of muscle)
- A study of drug interactions between Bupropion Hydrochloride, Lantus, Lisinopril for a 72-year old man with Depression, Diabetes Mellitus Insulin-dependent, High Blood Pressure. The patient has Erectile Dysfunction
- A study of side effects of Lisinopril for a 47-year old man with Hypertension. The patient has Erection Problems
- A study of drug interactions between Lisinopril, Hydrochlorothiazide, Synthroid for a 52-year old woman with High Blood Pressure, Hypothyroidism. The patient has Night Sweats, Hot Flashes, Cough
Recent Lisinopril 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.