Diphen and Post procedural cellulitis - a phase IV clinical study of FDA data

Summary:

Post procedural cellulitis is reported as a side effect among people who take Diphen (diphenhydramine hydrochloride), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Norco, and have Immunodeficiency common variable.

The phase IV clinical study analyzes which people have Post procedural cellulitis when taking Diphen. It is created by eHealthMe based on reports of 113,958 people who have side effects when taking Diphen from the FDA, and is updated regularly.

What is Diphen?

Diphen has active ingredients of diphenhydramine hydrochloride. It is often used in insomnia. eHealthMe is studying from 115,432 Diphen users. Check the latest studies of Diphen.

What is Post procedural cellulitis?

Post procedural cellulitis (post procedural bacterial infection of the skin and soft tissues) is found to be associated with 69 drugs and 133 conditions by eHealthMe. Check the latest studies of Post procedural cellulitis.

On Jul, 13, 2026

113,958 people reported to have side effects when taking Diphen.
Among them, 11 people (0.01%) have Post procedural cellulitis.

Could Diphen cause Post procedural cellulitis?

Among these 11 people:

How long have people been on Diphen when they have Post procedural cellulitis? *

What is the gender of people who have Post procedural cellulitis when taking Diphen? *

female: 100 %
male: 0.0 %

What is the age of people who have Post procedural cellulitis when taking Diphen? *

What are other drugs people take besides Diphen? *

What are other side effects people have besides Post procedural cellulitis? *

Sinusitis (inflammation of sinus): 6 people, 54.55%
Pneumonia: 5 people, 45.45%
Hip Fracture: 5 people, 45.45%
Oropharyngeal Pain: 5 people, 45.45%
Nasopharyngitis (inflammation of the nasopharynx): 4 people, 36.36%
Injection Site Pruritus (severe itching at injection site): 4 people, 36.36%
Neuralgia (pain in one or more nerves): 4 people, 36.36%
Urinary Tract Infection: 4 people, 36.36%
Rosacea (a skin condition that causes facial redness): 4 people, 36.36%
Fall: 4 people, 36.36%

What are the existing conditions these people have? *

Immunodeficiency Common Variable: 9 people, 81.82%
Thyroid Diseases: 1 person, 9.09%
Postmenopause: 1 person, 9.09%
Infusion Related Reaction: 1 person, 9.09%
Hypomagnesaemia (electrolyte disturbance in which there is an abnormally low level of magnesium in the blood): 1 person, 9.09%
Hypokalemia (low potassium): 1 person, 9.09%
Hypogammaglobulinaemia (an abnormally low concentration of gamma globulin in the blood and increased risk of infection): 1 person, 9.09%
High Blood Cholesterol: 1 person, 9.09%
Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 1 person, 9.09%
Depression: 1 person, 9.09%

* Approximation only. Some reports may have incomplete information.

Do you take Diphen and have Post procedural cellulitis?

- Check whether Post procedural cellulitis is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Diphen:

Diphen (115,432 reports)

Browse all side effects of Diphen:

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

Browse all the drugs that are associated with Post procedural cellulitis:

Post procedural cellulitis (69 drugs)

Browse all the conditions that are associated with Post procedural cellulitis:

Post procedural cellulitis (133 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on diphenhydramine hydrochloride (the active ingredients of Diphen) and Diphen (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.

How to use the study?

DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.

Who is eHealthMe?

With medical big data and proven AI/ML 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 800+ peer-reviewed 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.