Who have Cluster headaches with Pravastatin sodium - from FDA reports


There is no Cluster headaches reported by people who take Pravastatin sodium yet. This review analyzes which people have Cluster headaches with Pravastatin sodium. 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, 17, 2019

No report is found.

Do you have Cluster headaches while taking Pravastatin sodium?


You are not alone:




Related studies

Pravastatin Sodium

Pravastatin sodium has active ingredients of pravastatin sodium. It is often used in high blood cholesterol. (latest outcomes from Pravastatin sodium 16,024 users)

Cluster Headaches

Cluster headaches (one-sided head pain with tearing) has been reported by people with generalized anxiety disorder, attention deficit hyperactivity disorder, stress and anxiety, dysthymia, high blood pressure (latest reports from 390 Cluster headaches patients).


Drugs that are associated with Cluster headaches
Cluster headaches
Could your condition cause Cluster headaches
Cluster headaches
Pravastatin sodium 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 Pravastatin sodium and have Cluster headaches




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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.

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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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