Flurbiprofen and Haemoglobin decreased - a phase IV clinical study of FDA data
Summary:
Haemoglobin decreased is reported as a side effect among people who take Flurbiprofen (flurbiprofen), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Amlodipine, and have High blood pressure.
The phase IV clinical study analyzes which people have Haemoglobin decreased when taking Flurbiprofen. It is created by eHealthMe based on reports of 2,660 people who have side effects when taking Flurbiprofen from the FDA, and is updated regularly.
What is Flurbiprofen?
Flurbiprofen has active ingredients of flurbiprofen. It is often used in rheumatoid arthritis. eHealthMe is studying from 2,677 Flurbiprofen users. Check the latest studies of Flurbiprofen.
What is Haemoglobin decreased?
Haemoglobin decreased is found to be associated with 2,408 drugs and 3,129 conditions by eHealthMe. Check the latest studies of Haemoglobin decreased.
2,660 people reported to have side effects when taking Flurbiprofen.
Among them, 41 people (1.54%) have Haemoglobin decreased.

Among these 41 people:
How long have people been on Flurbiprofen when they have Haemoglobin decreased? *
- < 1 month: 94.44 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 5.56 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Haemoglobin decreased when taking Flurbiprofen? *
- female: 46.15 %
- male: 53.85 %
What is the age of people who have Haemoglobin decreased when taking Flurbiprofen? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 5.26 %
- 20-29: 5.26 %
- 30-39: 2.63 %
- 40-49: 23.68 %
- 50-59: 7.89 %
- 60+: 55.26 %
What are other drugs people take besides Flurbiprofen? *
- Amlodipine: 6 people, 14.63%
- Methotrexate: 5 people, 12.20%
- Furosemide: 5 people, 12.20%
- Vancomycin: 4 people, 9.76%
- Hydrocortisone Sodium Succinate: 4 people, 9.76%
- Minocycline: 4 people, 9.76%
- Sulfamethoprim: 4 people, 9.76%
- Zosyn: 4 people, 9.76%
- Vancomycin Hydrochloride: 3 people, 7.32%
- Prednisolone Acetate: 3 people, 7.32%
What are other side effects people have besides Haemoglobin decreased? *
- Haematocrit Decreased: 13 people, 31.71%
- Thrombocytopenia (decrease of platelets in blood): 12 people, 29.27%
- Red Blood Cell Count Decreased: 10 people, 24.39%
- White Blood Cell Count Decreased: 9 people, 21.95%
- Fever: 8 people, 19.51%
- Blood Albumin Decreased: 7 people, 17.07%
- Blood Lactate Dehydrogenase Increased: 7 people, 17.07%
- Gastrointestinal Haemorrhage (bleeding gastrointestinal tract): 6 people, 14.63%
- Lymphocyte Count Decreased: 5 people, 12.20%
- White Blood Cell Count Increased: 5 people, 12.20%
What are the existing conditions these people have? *
- Pain: 7 people, 17.07%
- High Blood Pressure: 7 people, 17.07%
- Constipation: 5 people, 12.20%
- Aplastic Anemia: 4 people, 9.76%
- Back Pain: 4 people, 9.76%
- Transient Ischaemic Attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow)): 4 people, 9.76%
- Stress And Anxiety: 4 people, 9.76%
- Drug Ineffective: 4 people, 9.76%
- Generalized Anxiety Disorder (excessive, uncontrollable, unexplained and often irrational worry): 4 people, 9.76%
- Haemorrhoids (a swollen vein or group of veins in the region of the anus): 4 people, 9.76%
* Approximation only. Some reports may have incomplete information.
Do you take Flurbiprofen and have Haemoglobin decreased?
- Check whether Haemoglobin decreased is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, long term effects of, and alternative drugs to Flurbiprofen:
- Flurbiprofen (2,677 reports)
Haemoglobin decreased treatments and more:
- Haemoglobin decreased (141,785 reports)
How severe was Haemoglobin decreased and when was it recovered:
Expand to all the drugs that have ingredients of flurbiprofen:
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 Flurbiprofen:
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 the drugs that are associated with Haemoglobin decreased:
- Haemoglobin decreased (2,408 drugs)
Browse all the conditions that are associated with Haemoglobin decreased:
- Haemoglobin decreased (3,129 conditions)
Related publications that referenced our studies
- Yaylaci S, Kocayigit I, Genc A, Tamer A, Gunduz H, "Sinus bradycardia caused by flurbiprofen intoxication", Nigerian Journal of Cardiology, 2015 Jan .
- Yaylaci S, Kocayigit I, Genc A, Tamer A, Gunduz H, "Sinus bradycardia caused by flurbiprofen intoxication", Nigerian Journal of Cardiology, 2015 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on flurbiprofen (the active ingredients of Flurbiprofen) and Flurbiprofen (the brand name). 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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