Forteo 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 Forteo (teriparatide recombinant human), especially for people who are female, 60+ old, have been taking the drug for 6 - 12 months also take Aspirin, and have Pain.
The phase IV clinical study analyzes which people have Post procedural complication when taking Forteo. It is created by eHealthMe based on reports of 126,656 people who have side effects when taking Forteo from the FDA, and is updated regularly.
What is Forteo?
Forteo has active ingredients of teriparatide recombinant human. It is often used in osteoporosis. eHealthMe is studying from 127,076 Forteo users. Check the latest studies of Forteo.
What is Post procedural complication?
Post procedural complication is found to be associated with 1,091 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 >>>.
126,656 people reported to have side effects when taking Forteo.
Among them, 319 people (0.25%) have Post procedural complication.
Among these 319 people:
How long have people been on Forteo when they have Post procedural complication? *
What is the gender of people who have Post procedural complication when taking Forteo? *
What is the age of people who have Post procedural complication when taking Forteo? *
What are other drugs people take besides Forteo? *
What are other side effects people have besides Post procedural complication? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Forteo 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 Forteo:
- Forteo (127,076 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 teriparatide recombinant human:
- Post procedural complication and drugs with ingredients of teriparatide recombinant human (282 reports)
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 Forteo:
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 (1,091 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 teriparatide recombinant human (the active ingredients of Forteo) and Forteo (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.
Recent studies on eHealthMe:
- Could Benazepril Hydrochloride cause Deep Venous Thrombosis? - 2 seconds ago
- Could Famotidine cause Fibrin Degradation Products Increased? - 3 seconds ago
- Could Phenergan cause Cardiac Arrest? - 8 seconds ago
- Could Digoxin cause Enterococcal Sepsis? - 11 seconds ago
- Zide and Metformin drug interactions for girls aged 10-19 - 11 seconds ago
- Femara and Xerophthalmia for Women aged 50-59 - 13 seconds ago
- Femara and Keratoconjunctivitis Sicca for Women aged 50-59 - 13 seconds ago
- Femara and Keratitis Sicca for Women aged 50-59 - 14 seconds ago
- Femara and Dry Eye Syndrome for Women aged 50-59 - 14 seconds ago
- Could Fiorinal W/Codeine cause Atrial Fibrillation/Flutter? - 14 seconds ago