Who have Pulmonary vein occlusion with Lisinopril - from FDA reports

There is no Pulmonary vein occlusion reported by people who take Lisinopril yet. This review analyzes which people have Pulmonary vein occlusion with Lisinopril. It is created by eHealthMe based on reports from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.

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On Feb, 21, 2019

No report is found.

Do you have Pulmonary vein occlusion while taking Lisinopril?

You are not alone:

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Lisinopril has active ingredients of lisinopril. It is often used in high blood pressure. (latest outcomes from Lisinopril 228,281 users)

Pulmonary Vein Occlusion

Pulmonary vein occlusion (blockage in pulmonary vein) has been reported by people with primary pulmonary hypertension, stress and anxiety, depression, sinobronchitis, breathing difficulty (latest reports from 61 Pulmonary vein occlusion patients).

Drugs that are associated with Pulmonary vein occlusion
Pulmonary vein occlusion
Could your condition cause Pulmonary vein occlusion
Pulmonary vein occlusion
Lisinopril side effects

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Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

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What would happen?

Predict new side effects and undetected conditions when you take Lisinopril and have Pulmonary vein occlusion

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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.

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