Levora 0.15/30-21 and Pharyngeal oedema - from FDA reports


Pharyngeal oedema is reported only by a few people who take Levora 0.15/30-21. We study 97 people who have side effects while taking Levora 0.15/30-21 from FDA. Among them, 4 have Pharyngeal oedema. Find out below who they are, when they have Pharyngeal oedema and more.

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

Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials).



On Oct, 18, 2018

97 people reported to have side effects when taking Levora 0.15/30-21.
Among them, 4 people (4.12%) have Pharyngeal oedema


Number of reports submitted per year:

Could Levora 0.15/30-21 cause Pharyngeal oedema?

Gender of people who have Pharyngeal oedema when taking Levora 0.15/30-21 *:

  • female: 100 %
  • male: 0.0 %

Age of people who have Pharyngeal oedema when taking Levora 0.15/30-21 *:

Top conditions involved for these people *:

  1. Iron Overload: 3 people, 75.00%
  2. Oral Contraception: 1 person, 25.00%
  3. Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 1 person, 25.00%
  4. Hypersensitivity: 1 person, 25.00%
  5. Asthma: 1 person, 25.00%

Top co-used drugs for these people *:

  1. Exjade: 3 people, 75.00%
  2. Zyrtec: 1 person, 25.00%
  3. Singulair: 1 person, 25.00%
  4. Rebif: 1 person, 25.00%
  5. Allegra: 1 person, 25.00%

Click here to view more results or personalize the results to your gender and age

Top other side effects for these people *:

  1. Urticaria (rash of round, red welts on the skin that itch intensely): 4 people, 100.00%
  2. Drug Hypersensitivity: 3 people, 75.00%
  3. Throat Tightness: 1 person, 25.00%
  4. Swallowing Difficulty: 1 person, 25.00%
  5. Prothrombin Level Abnormal: 1 person, 25.00%

Click here to view more results or personalize the results to your gender and age

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study



Do you have Pharyngeal oedema while taking Levora 0.15/30-21?


You are not alone:




Related studies

Levora 0.15/30-21

Levora 0.15/30-21 has active ingredients of ethinyl estradiol; levonorgestrel. It is often used in birth control. (latest outcomes from Levora 0.15/30-21 144 users)

Pharyngeal oedema

Pharyngeal oedema (abnormal accumulation of fluid in the cavities and intercellular spaces of the pharyngeal) has been reported by people with high blood pressure, rheumatoid arthritis, asthma, pain, multiple sclerosis (latest reports from 16,517 Pharyngeal oedema patients).


Drugs that are associated with Pharyngeal oedema
Pharyngeal oedema (1,479 drugs)
Could your condition cause Pharyngeal oedema
Pharyngeal oedema (976 conditions)
Levora 0.15/30-21 side effects
Browse all side effects of Levora 0.15/30-21
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 Levora 0.15/30-21 and have Pharyngeal oedema


Recent updates

Recent general studies
Recent personal studies

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.