Cefdinir and Emla drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Cefdinir (cefdinir) and Emla (lidocaine; prilocaine). Common drug interactions include alopecia among females and nausea among males.

The phase IV clinical study analyzes what interactions people have when they take Cefdinir and Emla. It is created by eHealthMe based on reports of 17 people who take the same drugs from the FDA, and is updated regularly.

What is Cefdinir?

Cefdinir has active ingredients of cefdinir. It is often used in sinusitis. eHealthMe is studying from 9,210 Cefdinir users. Check the latest studies of Cefdinir.

What is Emla?

Emla has active ingredients of lidocaine; prilocaine. eHealthMe is studying from 5,276 Emla users. Check the latest studies of Emla.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.



On Aug, 31, 2026

17 people who take Cefdinir and Emla together, and have interactions are studied.

Cefdinir and Emla drug interactions.

What are the common drug interactions of Cefdinir and Emla, by gender? *:

female:

  1. Alopecia (absence of hair from areas of the body)
  2. Aspartate aminotransferase increased
  3. Cardiac murmur (an heart sound in valve abnormality)
  4. Constipation
  5. Failure to thrive (inadequate weight gain and physical growth in children)
  6. Fall
  7. Herpes zoster
  8. Hypotension (abnormally low blood pressure)
  9. Ileus (a painful obstruction of the ileum or other part of the intestine)
  10. Influenza like illness

male:

  1. Nausea (feeling of having an urge to vomit)
  2. Beta haemolytic streptococcal infection (infection with streptococcus pyogenes, a beta-haemolytic bacterium cause mild to moderately severe respiratory tract, skin, and soft tissue)
  3. Death
  4. Gastrointestinal disorder (functional problems of gastrointestinal tract)
  5. Pyrexia (fever)
  6. Terminal state (the transitional states between life and biological death)
  7. Waist circumference increased

What are the common drug interactions of Cefdinir and Emla, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

  1. Crohn's disease (a condition that causes inflammation of the gastrointestinal tract)

10-19:

n/a

20-29:

  1. Beta haemolytic streptococcal infection (infection with streptococcus pyogenes, a beta-haemolytic bacterium cause mild to moderately severe respiratory tract, skin, and soft tissue)
  2. Gastrointestinal disorder (functional problems of gastrointestinal tract)
  3. Infusion related reaction
  4. Pyrexia (fever)
  5. Rash erythematous (redness of the skin)
  6. Waist circumference increased

30-39:

n/a

40-49:

n/a

50-59:

  1. Cardiac murmur (an heart sound in valve abnormality)
  2. Constipation
  3. Fatigue (feeling of tiredness)
  4. Herpes zoster
  5. Ileus (a painful obstruction of the ileum or other part of the intestine)
  6. Influenza like illness
  7. Muscular weakness (muscle weakness)
  8. Musculoskeletal pain (pain affects the bones, muscles, ligaments, tendons, and nerves)
  9. Nasopharyngitis (inflammation of the nasopharynx)
  10. Pericardial effusion (fluid around the heart)

60+:

  1. Failure to thrive (inadequate weight gain and physical growth in children)
  2. Fall
  3. Pruritus (severe itching of the skin)
  4. Pyrexia (fever)
  5. Bone marrow disorder
  6. Death
  7. Hypotension (abnormally low blood pressure)

What are the existing conditions these people have? *

  1. Pain: 8 people, 47.06%
  2. Nausea (feeling of having an urge to vomit): 5 people, 29.41%
  3. Constipation: 4 people, 23.53%
  4. Metastases To Central Nervous System (cancer spreads to central nervous system): 4 people, 23.53%
  5. Acute Myeloid Leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts): 3 people, 17.65%
  6. Malignant Melanoma (skin cancer rises from melancytes): 3 people, 17.65%
  7. Stress And Anxiety: 2 people, 11.76%
  8. Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 2 people, 11.76%
  9. Blood Magnesium Decreased: 2 people, 11.76%
  10. Brain Neoplasm Malignant (brain cancer tumour): 2 people, 11.76%

* Approximation only. Some reports may have incomplete information.

Do you take Cefdinir and Emla?

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Cefdinir and Emla:

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

Sub-studies 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 Cefdinir:

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 side effects of Emla:

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 interactions between Cefdinir 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

Browse all interactions between Emla 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 cefdinir and lidocaine; prilocaine (the active ingredients of Cefdinir and Emla, respectively), and Cefdinir and Emla (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.

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.



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