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Sudafed and Flax seed drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Sudafed and Flax seed. Common interactions include application site reaction among females and abdominal pain upper among males.

The phase IV clinical study analyzes what interactions people who take Sudafed and Flax seed have. It is created by eHealthMe based on reports of 6 people who take Sudafed and Flax seed from the FDA, and is updated regularly. You can use the study as a second opinion to make health care decisions.

Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 600+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.

On Jan, 19, 2023

6 people who take Sudafed and Flax seed together, and have interactions are studied.

What is Sudafed?

Sudafed has active ingredients of pseudoephedrine hydrochloride. It is often used in nasal congestion. eHealthMe is studying from 11,941 Sudafed users for its effectiveness, alternative drugs and more.

What is Flax seed?

Flax seed has active ingredients of flaxseed. eHealthMe is studying from 642 Flax seed users for its effectiveness, alternative drugs and more.

Number of Sudafed and Flax seed reports submitted per year:

Sudafed and Flax seed drug interactions.

Common Sudafed and Flax Seed drug interactions by gender *:

female:

  1. Application site reaction
  2. Diplopia
  3. Local swelling
  4. Peripheral swelling
  5. Therapeutic response decreased
  6. Hypoaesthesia
  7. Application site erythema
  8. Application site pruritus
  9. Application site rash

male:

  1. Abdominal pain upper
  2. Back pain
  3. Diarrhoea
  4. Dizziness
  5. Tongue ulceration
  6. Visual impairment

Common Sudafed and Flax Seed drug interactions by age *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

  1. Therapeutic response decreased
  2. Application site erythema
  3. Application site pruritus
  4. Application site rash
  5. Application site reaction

40-49:

n/a

50-59:

  1. Hypoaesthesia
  2. Peripheral swelling

60+:

  1. Diplopia
  2. Dizziness
  3. Tongue ulceration
  4. Visual impairment

* Approximation only. Some reports may have incomplete information.

Do you take Sudafed and Flax seed?

Personalize this study to your gender and age

How to use the study?

You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.

Related studies

Alternative drugs to, pros and cons of the 2 drugs:

Browse all drug interactions of Sudafed and Flax seed:

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

Common Sudafed side effects:

Browse all side effects of Sudafed:

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

Common Sudafed interactions:

Browse all interactions between Sudafed and drugs from A to Z:

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

Common Flax seed interactions:

Browse all interactions between Flax seed and drugs from A to Z:

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

How the study uses the data?

The study uses data from the FDA. It is based on pseudoephedrine hydrochloride and flaxseed (the active ingredients of Sudafed and Flax seed, respectively), and Sudafed and Flax seed (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study. Patients in the study may take other drugs besides Sudafed and Flax seed.

Who is eHealthMe?

With medical big data and proven AI algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 600+ medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

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. Our phase IV clinical studies alone cannot establish cause-effect relationship. 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.

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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