Maxitrol and Neulasta drug interactions - a phase IV clinical study of FDA data
Drug interactions are reported among 7 people who take Maxitrol and Neulasta. Common interactions include sinus tachycardia among females, and gait disturbance among males.
The phase IV clinical study analyzes what interactions people who take Maxitrol and Neulasta have. It is created by eHealthMe based on reports from the FDA, and is updated regularly. You may use the study as a second opinion to make health care decisions.
Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 700+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
7 people who take Maxitrol and Neulasta together, and have interactions are studied.
What is Maxitrol?
Maxitrol has active ingredients of dexamethasone; neomycin sulfate; polymyxin b sulfate. Currently, eHealthMe is studying from 909 Maxitrol users.
What is Neulasta?
Neulasta has active ingredients of pegfilgrastim. It is used in agranulocytosis. Currently, eHealthMe is studying from 87,460 Neulasta users.
Number of Maxitrol and Neulasta reports submitted per year:
Common Maxitrol and Neulasta drug interactions by gender *:
- Sinus tachycardia
- Superior vena cava syndrome
- Tobacco abuse
- Tricuspid valve incompetence
- Weight increased
- Exposed bone in jaw
- Metastases to liver
- Neoplasm malignant
- Gait disturbance
- On and off phenomenon
- Dry skin
- Fluid intake reduced
- Freezing phenomenon
- Musculoskeletal disorder
- Stoma site reaction
Common Maxitrol and Neulasta drug interactions by age *:
- Osteonecrosis of jaw
- Pathological fracture
- Spinal osteoarthritis
* Approximation only. Some reports may have incomplete information.
Do you take Maxitrol and Neulasta?Personalize this study to your gender and age
How to use the study?
You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.
Related publications that referenced our studies
- Khan A, Yasin Z, "Hyperleukocytosis Caused By Neulasta Complicated By Leukostasis Versus Asymptomatic Uncomplicated Hyperleukocytosis In AML. Two Cases and When To Leukapherese.", Am Soc Hematology, 2017 Jan .
Drug side effects by duration, gender and age:
Common Maxitrol drug interactions:
- Maxitrol and Aspirin: 108 reports
Browse interactions between Maxitrol 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
Common Neulasta drug interactions:
Browse interactions between Neulasta 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 dexamethasone; neomycin sulfate; polymyxin b sulfate and pegfilgrastim (the active ingredients of Maxitrol and Neulasta, respectively), and Maxitrol and Neulasta (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. Patients in the study may take other drugs besides Maxitrol and Neulasta.
Who is eHealthMe?
With medical big data and proven AI 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 700+ 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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