Dymista and Lidoderm drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Dymista (azelastine hydrochloride; fluticasone propionate) and Lidoderm (lidocaine). Common drug interactions include nausea among females and complex regional pain syndrome among males.
The phase IV clinical study analyzes what interactions people have when they take Dymista and Lidoderm. It is created by eHealthMe based on reports of 41 people who take the same drugs from the FDA, and is updated regularly.
What is Dymista?
Dymista has active ingredients of azelastine hydrochloride; fluticasone propionate. It is often used in allergies. eHealthMe is studying from 4,407 Dymista users. Check the latest studies of Dymista.
What is Lidoderm?
Lidoderm has active ingredients of lidocaine. It is often used in pain. eHealthMe is studying from 10,524 Lidoderm users. Check the latest studies of Lidoderm.
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 >>>.
41 people who take Dymista and Lidoderm together, and have interactions are studied.

What are the common drug interactions of Dymista and Lidoderm, by gender? *:
female:
- Nausea (feeling of having an urge to vomit)
- Asthenia (weakness)
- Disturbance in attention
- Dysstasia (difficulty in standing)
- Insomnia (sleeplessness)
- Nervousness
- Pustular psoriasis (raised bumps on the skin that are filled with pus)
- Speech disorder
- Therapeutic response unexpected
- Chronic kidney disease
male:
- Complex regional pain syndrome (long lasting pain condition most often affecting one of the limbs (arms, legs, hands, or feet))
- Cough
- Osteoporosis (bones weak and more likely to break)
- Postural orthostatic tachycardia syndrome (abnormal increase in heart rate on becoming upright)
- Renal impairment (severely reduced kidney function)
- Therapeutic response unexpected
- Upper limb fracture
- Dyspepsia (indigestion)
- Abdominal discomfort
- Cardiac failure
What are the common drug interactions of Dymista and Lidoderm, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Seizure (abnormal excessive or synchronous neuronal activity in the brain)
- Anaemia (lack of blood)
- Ataxia (loss of full control of bodily movements)
- Cataplexy (loss of muscle tone accompanied by full conscious awareness)
- Dizziness
- Migraine (headache)
- Nausea (feeling of having an urge to vomit)
- Periodic limb movement disorder
- Restless legs syndrome (a powerful urge to move your legs)
- Scoliosis (a medical condition in which a person's spine is curved from side to side)
40-49:
- Chronic kidney disease
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Injection site haemorrhage (bleeding from injection site)
- Nausea (feeling of having an urge to vomit)
- Rash vesicular (rash with a small bubble)
- Swelling face
50-59:
- Nausea (feeling of having an urge to vomit)
- Asthenia (weakness)
- Disturbance in attention
- Dysstasia (difficulty in standing)
- Insomnia (sleeplessness)
- Nervousness
- Pustular psoriasis (raised bumps on the skin that are filled with pus)
- Speech disorder
- Therapeutic response unexpected
- Headache (pain in head)
60+:
- Abdominal discomfort
- Drug ineffective
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal failure (kidney dysfunction)
- Neuropathy peripheral (surface nerve damage)
- Respiratory tract infection
- Urticaria (rash of round, red welts on the skin that itch intensely)
- Cardiac failure
- Cardiac failure congestive
What are the existing conditions these people have? *
- Fibromyalgia (a long-term condition which causes pain all over the body): 12 people, 29.27%
- Neuralgia (pain in one or more nerves): 9 people, 21.95%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 9 people, 21.95%
- High Blood Pressure: 7 people, 17.07%
- Dyspnea (difficult or laboured breathing): 6 people, 14.63%
- Insomnia (sleeplessness): 5 people, 12.20%
- Complex Regional Pain Syndrome (long lasting pain condition most often affecting one of the limbs (arms, legs, hands, or feet)): 5 people, 12.20%
- Stress And Anxiety: 5 people, 12.20%
- High Blood Cholesterol: 5 people, 12.20%
- Nausea (feeling of having an urge to vomit): 5 people, 12.20%
* Approximation only. Some reports may have incomplete information.
Do you take Dymista and Lidoderm?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Dymista and Lidoderm:
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 zSub-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 Dymista:
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 zBrowse all side effects of Lidoderm:
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 zBrowse all interactions between Dymista 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 zBrowse all interactions between Lidoderm 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 zHow the study uses the data?
The study uses data from the FDA. It is based on azelastine hydrochloride; fluticasone propionate and lidocaine (the active ingredients of Dymista and Lidoderm, respectively), and Dymista and Lidoderm (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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