Clarithromycin and Cefoxitin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Clarithromycin (clarithromycin) and Cefoxitin (cefoxitin sodium). Common drug interactions include leukocytoclastic vasculitis among females and thrombocytopenia among males.
The phase IV clinical study analyzes what interactions people have when they take Clarithromycin and Cefoxitin. 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 Clarithromycin?
Clarithromycin has active ingredients of clarithromycin. It is often used in sinusitis. eHealthMe is studying from 45,044 Clarithromycin users. Check the latest studies of Clarithromycin.
What is Cefoxitin?
Cefoxitin has active ingredients of cefoxitin sodium. eHealthMe is studying from 611 Cefoxitin users. Check the latest studies of Cefoxitin.
45 people who take Clarithromycin and Cefoxitin together, and have interactions are studied.

What are the common drug interactions of Clarithromycin and Cefoxitin, by gender? *:
female:
- Leukocytoclastic vasculitis (inflammation of small blood vessels (usually post-capillary venules in the dermis), characterized by palpable purpura)
- Drug ineffective
- Lip swelling
- Nausea (feeling of having an urge to vomit)
- Rash
- General physical health deterioration (weak health status)
- Abdominal pain
- Drug level increased
- Erythema (redness of the skin)
- Lipase increased
male:
- Thrombocytopenia (decrease of platelets in blood)
- Neutropenia (an abnormally low number of neutrophils)
- Dyspnoea (difficult or laboured respiration)
- Haematuria (presence of blood in urine)
- Lactic acidosis (low ph in body tissues)
- Nausea (feeling of having an urge to vomit)
- Pancreatitis acute (sudden inflammation of pancreas)
- Pulmonary haemorrhage (acute bleeding from the lung)
- Acute respiratory failure
- Ankle fracture
What are the common drug interactions of Clarithromycin and Cefoxitin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Death
10-19:
- Abdominal pain
- Chest pain
- Drug ineffective
- Pancreatitis acute (sudden inflammation of pancreas)
- Pulmonary haemorrhage (acute bleeding from the lung)
- Deafness neurosensory
- Pleural effusion (water on the lungs)
- Cough
- Dyspnoea (difficult or laboured respiration)
- Neutropenia (an abnormally low number of neutrophils)
20-29:
- Abdominal pain
- Drug level increased
- Haematuria (presence of blood in urine)
- Lipase increased
- Nausea (feeling of having an urge to vomit)
- Neuropathy peripheral (surface nerve damage)
- Thrombocytopenia (decrease of platelets in blood)
- Vomiting
- Anaphylactic reaction (serious allergic reaction)
- Chronic sinusitis (long lasting inflammation of the paranasal sinuses)
30-39:
- Nephropathy toxic (damage to kidney due to toxins)
- Neuropathy peripheral (surface nerve damage)
- Neutropenia (an abnormally low number of neutrophils)
- Renal injury (kidney injury)
- Erythema (redness of the skin)
- Lip swelling
- Pallor
- Swelling face
- Swollen tongue (swelling of tongue)
- Urticaria (rash of round, red welts on the skin that itch intensely)
40-49:
- Rash maculo-papular (red area on the skin that is covered with small confluent bumps)
- Drug intolerance (drug sensitivity)
- Thrombocytopenia (decrease of platelets in blood)
- Paradoxical drug reaction
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Pancytopenia (medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets)
- Pulmonary tuberculosis (lungs tuberculosis)
50-59:
- Leukocytoclastic vasculitis (inflammation of small blood vessels (usually post-capillary venules in the dermis), characterized by palpable purpura)
- Rash
60+:
- Drug ineffective
- General physical health deterioration (weak health status)
- Hepatotoxicity (chemical-driven liver damage)
- Hypotension (abnormally low blood pressure)
- Nausea (feeling of having an urge to vomit)
- Pleuritic pain
- Thrombocytopenia (decrease of platelets in blood)
- Tinnitus (a ringing in the ears)
- Renal failure acute (rapid kidney dysfunction)
- Tubulointerstitial nephritis (a form of nephritis affecting the interstitium of the kidneys surrounding the tubules)
What are the existing conditions these people have? *
- Mycobacterium Abscessus Infection (rapid growing bacterial infection): 18 people, 40.00%
- Mycobacterial Infection: 9 people, 20.00%
- Mycobacterium Chelonae Infection (bacterial infection): 5 people, 11.11%
- Lung Infection: 3 people, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Clarithromycin and Cefoxitin?
- 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:
- Clarithromycin (45,044 reports)
- Cefoxitin (611 reports)
Browse all drug interactions of Clarithromycin and Cefoxitin:
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 Clarithromycin:
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 Cefoxitin:
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 Clarithromycin 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 Cefoxitin 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 clarithromycin and cefoxitin sodium (the active ingredients of Clarithromycin and Cefoxitin, respectively), and Clarithromycin and Cefoxitin (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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