Lamisil and Solu-medrol drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Lamisil (terbinafine hydrochloride) and Solu-medrol (methylprednisolone sodium succinate). Common drug interactions include acute respiratory distress syndrome among females and cardiac failure congestive among males.

The phase IV clinical study analyzes what interactions people have when they take Lamisil and Solu-medrol. It is created by eHealthMe based on reports of 45 people who take the same drugs from the FDA, and is updated regularly.

What is Lamisil?

Lamisil has active ingredients of terbinafine hydrochloride. It is often used in pulmonary aspergilloma (mycetoma). eHealthMe is studying from 14,080 Lamisil users. Check the latest studies of Lamisil.

What is Solu-medrol?

Solu-medrol has active ingredients of methylprednisolone sodium succinate. It is often used in multiple sclerosis. eHealthMe is studying from 39,410 Solu-medrol users. Check the latest studies of Solu-medrol.



On Jul, 20, 2026

45 people who take Lamisil and Solu-medrol together, and have interactions are studied.

Lamisil and Solu-medrol drug interactions.

What are the common drug interactions of Lamisil and Solu-Medrol, by gender? *:

female:

  1. Acute respiratory distress syndrome
  2. Anhedonia (inability to experience pleasure from activities usually found enjoyable)
  3. Anisocytosis (patient's red blood cells are of unequal size)
  4. Anxiety
  5. Asthenia (weakness)
  6. Beta 2 microglobulin increased
  7. Blood calcium decreased
  8. Blood glucose increased
  9. Blood lactate dehydrogenase increased
  10. Blood triglycerides increased

male:

  1. Cardiac failure congestive
  2. Dyspnoea (difficult or laboured respiration)
  3. Oxygen saturation decreased
  4. Respiratory failure (inadequate gas exchange by the respiratory system)
  5. Anaphylactic reaction (serious allergic reaction)
  6. Antasthmatic drug level above therapeutic
  7. Arteriosclerosis (thickening and hardening of arteries)
  8. Arthralgia (joint pain)
  9. Asthenia (weakness)
  10. Blood immunoglobulin e increased

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

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

  1. Abdominal pain upper
  2. Acute respiratory distress syndrome
  3. Anhedonia (inability to experience pleasure from activities usually found enjoyable)
  4. Anisocytosis (patient's red blood cells are of unequal size)
  5. Anxiety
  6. Asthenia (weakness)
  7. Back pain
  8. Beta 2 microglobulin increased
  9. Blood calcium decreased
  10. Blood glucose increased

40-49:

  1. Renal failure (kidney dysfunction)
  2. Abdominal discomfort
  3. Abdominal distension
  4. Abdominal hernia
  5. Abdominal pain upper
  6. Acute respiratory distress syndrome
  7. Acute respiratory failure
  8. Adrenal disorder
  9. Agitation (state of anxiety or nervous excitement)
  10. Alopecia (absence of hair from areas of the body)

50-59:

  1. Headache (pain in head)
  2. Musculoskeletal chest pain (pain in chest muscle or nerve or bones)
  3. Heart rate increased
  4. Palpitations (feelings or sensations that your heart is pounding or racing)
  5. Abdominal discomfort
  6. Actinomyces test positive
  7. Anaphylactic reaction (serious allergic reaction)
  8. Anxiety
  9. Arteriosclerosis (thickening and hardening of arteries)
  10. Ataxia (loss of full control of bodily movements)

60+:

  1. Dyspnoea (difficult or laboured respiration)
  2. Interstitial lung disease
  3. Respiratory failure (inadequate gas exchange by the respiratory system)
  4. Antasthmatic drug level above therapeutic
  5. Asthenia (weakness)
  6. Blood immunoglobulin e increased
  7. Death
  8. Dyspnoea exertional (breathlessness or shortness of breath)
  9. Fall
  10. Fatigue (feeling of tiredness)

What are the existing conditions these people have? *

  1. High Blood Pressure: 7 people, 15.56%
  2. Tinea Infection (fungal skin infection): 6 people, 13.33%
  3. Diabetes: 6 people, 13.33%
  4. Polychondritis (progressive inflammation of cartilage and other connective tissue): 5 people, 11.11%
  5. Ocular Pemphigoid (inflammatory autoimmune disorder characterized by blistering lesions that affect mucous membrane covering of eye): 4 people, 8.89%
  6. High Blood Cholesterol: 4 people, 8.89%
  7. Urosepsis (secondary infection that occurs when a urinary tract infection spreads to the bloodstream): 3 people, 6.67%
  8. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 6.67%
  9. Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat): 3 people, 6.67%
  10. Arrhythmias (irregular heartbeat): 3 people, 6.67%

* Approximation only. Some reports may have incomplete information.

Do you take Lamisil and Solu-medrol?

- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously



Related studies:

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

Browse all drug interactions of Lamisil and Solu-medrol:

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 Lamisil:

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 Solu-medrol:

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 Lamisil 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 Solu-medrol 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 terbinafine hydrochloride and methylprednisolone sodium succinate (the active ingredients of Lamisil and Solu-medrol, respectively), and Lamisil and Solu-medrol (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.



Recent studies on eHealthMe: