Will you have Angioneurotic oedema with Lorazepam - from FDA reports


Angioneurotic oedema is found among people who take Lorazepam, especially for people who are female, 60+ old , have been taking the drug for < 1 month, also take medication Famotidine, and have Convulsion. This study is created by eHealthMe based on reports of 91,829 people who have side effects when taking Lorazepam from FDA, and is updated regularly.

What's eHealthMe?

eHealthMe is a health data analysis company based in Mountain View, California. eHealthMe monitors and analyzes the outcomes of drugs and supplements that are currently on the market. The results are readily available to health care professionals and consumers.

eHealthMe has released original studies on market drugs and worked with leading universities and institutions such as IBM, London Health Science Centre, Mayo Clinic, Northwestern University and VA. eHealthMe studies have now been referenced in over 500 peer-reviewed medical publications.

How we gather our data?

Healthcare data is obtained from a number of sources including the Food and Drug Administration (FDA). This information is aggregated and used to produce personalized reports that patients can reference.

The information that eHealthMe collects includes:

  • Side effects (including severity and how people recover from them)
  • Associated conditions or symptoms
  • Drug effectiveness
  • Demographic data regarding drug use

How the study uses the data?

The study is based on lorazepam (the active ingredients of Lorazepam) and Lorazepam (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Synonyms of Angioneurotic oedema are also considered in the study.

What is Lorazepam?

Lorazepam has active ingredients of lorazepam. It is often used in stress and anxiety. (latest outcomes from Lorazepam 95,213 users)

What is Angioneurotic oedema?

Angioneurotic oedema (swelling that occurs just beneath the surface of the skin or mucous membranes) has been reported by people with high blood pressure, pain, ill-defined disorder, rheumatoid arthritis, high blood cholesterol (latest reports from 7,931 Angioneurotic oedema patients).

How to use the study?

Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.

On Feb, 25, 2019

91,829 people reported to have side effects when taking Lorazepam.
Among them, 71 people (0.08%) have Angioneurotic oedema

Number of reports submitted per year:

Could Lorazepam cause Angioneurotic oedema?

Time on Lorazepam when people have Angioneurotic oedema *:

  • < 1 month: 100 %
  • 1 - 6 months: 0.0 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Angioneurotic oedema when taking Lorazepam *:

  • female: 62.86 %
  • male: 37.14 %

Age of people who have Angioneurotic oedema when taking Lorazepam *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 4.35 %
  • 20-29: 4.35 %
  • 30-39: 15.94 %
  • 40-49: 17.39 %
  • 50-59: 20.29 %
  • 60+: 37.68 %

Top conditions involved for these people *:

  1. High Blood Pressure: 6 people, 8.45%
  2. Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body): 6 people, 8.45%
  3. Abnormal Behavior: 3 people, 4.23%
  4. Depression: 2 people, 2.82%
  5. Colon Cancer: 2 people, 2.82%
  6. Ovarian Cancer (cancer of ovary): 1 person, 1.41%
  7. Bipolar Disorder (mood disorder): 1 person, 1.41%
  8. Breast Cancer Metastatic: 1 person, 1.41%
  9. Parkinson's Disease: 1 person, 1.41%
  10. Deep Venous Thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis): 1 person, 1.41%

Top co-used drugs for these people *:

  1. Ibuprofen: 9 people, 12.68%
  2. Famotidine: 9 people, 12.68%
  3. Nifedipine: 8 people, 11.27%
  4. Haloperidol: 7 people, 9.86%
  5. Lisinopril: 7 people, 9.86%
  6. Gabapentin: 7 people, 9.86%
  7. Metoprolol Tartrate: 7 people, 9.86%
  8. Nystatin: 6 people, 8.45%
  9. Prednisone: 6 people, 8.45%
  10. Clonidine: 6 people, 8.45%

Top other side effects for these people *:

  1. Rashes (redness): 10 people, 14.08%
  2. Cardiac Arrest: 9 people, 12.68%
  3. Face Oedema (swelling of face): 9 people, 12.68%
  4. Hypotension (abnormally low blood pressure): 8 people, 11.27%
  5. Itching: 8 people, 11.27%
  6. Tongue Oedema (swelling of tongue): 7 people, 9.86%
  7. Speech Impairment (Adult) (inability to speak (adult)): 7 people, 9.86%
  8. Urticaria (rash of round, red welts on the skin that itch intensely): 7 people, 9.86%
  9. Urosepsis (secondary infection that occurs when a urinary tract infection spreads to the bloodstream): 6 people, 8.45%
  10. Respiratory Acidosis (respiratory failure or ventilatory failure, causes the ph of blood and other bodily fluids to decrease): 6 people, 8.45%

* Approximation only. Some reports may have incomplete information.

Do you have Angioneurotic oedema while taking Lorazepam?

You are not alone:

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Lorazepam side effects

Browse side effects by gender and age

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+

Browse all side effects of Lorazepam
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 Lorazepam and have Angioneurotic oedema

FDA reports used in this study

Recent updates

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Recent personal studies

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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