Diclofenac sodium and Post procedural complication - a phase IV clinical study of FDA data
Summary:
Post procedural complication is reported as a side effect among people who take Diclofenac sodium (diclofenac sodium), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Acetaminophen, and have Rheumatoid arthritis.
The phase IV clinical study analyzes which people have Post procedural complication when taking Diclofenac sodium. It is created by eHealthMe based on reports of 41,731 people who have side effects when taking Diclofenac sodium from the FDA, and is updated regularly.
What is Diclofenac sodium?
Diclofenac sodium has active ingredients of diclofenac sodium. It is often used in arthritis. eHealthMe is studying from 43,018 Diclofenac sodium users. Check the latest studies of Diclofenac sodium.
What is Post procedural complication?
Post procedural complication is found to be associated with 1,092 drugs and 1,363 conditions by eHealthMe. Check the latest studies of Post procedural complication.
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 >>>.
41,731 people reported to have side effects when taking Diclofenac sodium.
Among them, 74 people (0.18%) have Post procedural complication.

Among these 74 people:
How long have people been on Diclofenac sodium when they have Post procedural complication? *
- < 1 month: 50.0 %
- 1 - 6 months: 16.67 %
- 6 - 12 months: 11.11 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 22.22 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Post procedural complication when taking Diclofenac sodium? *
- female: 66.22 %
- male: 33.78 %
What is the age of people who have Post procedural complication when taking Diclofenac sodium? *
- 0-1: 0.0 %
- 2-9: 4.69 %
- 10-19: 4.69 %
- 20-29: 3.12 %
- 30-39: 7.81 %
- 40-49: 12.5 %
- 50-59: 17.19 %
- 60+: 50.0 %
What are other drugs people take besides Diclofenac sodium? *
- Acetaminophen: 14 people, 18.92%
- Morphine: 10 people, 13.51%
- Propofol: 10 people, 13.51%
- Furosemide: 9 people, 12.16%
- Methotrexate: 9 people, 12.16%
- Humira: 8 people, 10.81%
- Vitamin D3: 8 people, 10.81%
- Fentanyl: 7 people, 9.46%
- Gabapentin: 7 people, 9.46%
- Folic Acid: 7 people, 9.46%
What are other side effects people have besides Post procedural complication? *
- Haemoglobin Decreased: 14 people, 18.92%
- Joint Pain: 11 people, 14.86%
- Nausea (feeling of having an urge to vomit): 9 people, 12.16%
- Intervertebral Disc Protrusion (spinal disc protrusion): 8 people, 10.81%
- Hypotension (abnormally low blood pressure): 7 people, 9.46%
- Nausea And Vomiting: 7 people, 9.46%
- Infection: 7 people, 9.46%
- Weight Decreased: 7 people, 9.46%
- Staphylococcal Infection (an infection with staphylococcus bacteria): 7 people, 9.46%
- Fall: 7 people, 9.46%
What are the existing conditions these people have? *
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 5 people, 6.76%
- Femur Fracture: 4 people, 5.41%
- Spinal Cord Herniation (extra growth of spinal cord): 4 people, 5.41%
- Psoriatic Arthropathy (inflammation of the skin and joints with kin condition which typically causes patches (plaques) of red, scaly skin to develop): 4 people, 5.41%
- Immunodeficiency Common Variable: 4 people, 5.41%
- Anaesthesia: 3 people, 4.05%
- General Anaesthesia: 2 people, 2.70%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 2 people, 2.70%
- Haemorrhage (bleeding): 2 people, 2.70%
- High Blood Pressure: 2 people, 2.70%
* Approximation only. Some reports may have incomplete information.
Do you take Diclofenac sodium and have Post procedural complication?
- Check whether Post procedural complication 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 Diclofenac sodium:
- Diclofenac sodium (43,018 reports)
Post procedural complication treatments and more:
- Post procedural complication (25,253 reports)
How severe was Post procedural complication and when was it recovered:
Expand to all the drugs that have ingredients of diclofenac sodium:
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 Diclofenac sodium:
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 Post procedural complication:
- Post procedural complication (1,092 drugs)
Browse all the conditions that are associated with Post procedural complication:
- Post procedural complication (1,363 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on diclofenac sodium (the active ingredients of Diclofenac sodium) and Diclofenac sodium (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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