Zemplar and Sinus tachycardia - a phase IV clinical study of FDA data

Summary:

Sinus tachycardia is reported as a side effect among people who take Zemplar (paricalcitol), especially for people who are male, 40-49 old, have been taking the drug for 1 - 2 years also take Lipitor, and have High blood cholesterol.

The phase IV clinical study analyzes which people have Sinus tachycardia when taking Zemplar. It is created by eHealthMe based on reports of 15,456 people who have side effects when taking Zemplar from the FDA, and is updated regularly.

What is Zemplar?

Zemplar has active ingredients of paricalcitol. It is often used in kidney disease. eHealthMe is studying from 15,494 Zemplar users. Check the latest studies of Zemplar.

What is Sinus tachycardia?

Sinus tachycardia (a heart rhythm with elevated rate of impulses originating from the sinoatrial node) is found to be associated with 1,267 drugs and 1,412 conditions by eHealthMe. Check the latest studies of Sinus tachycardia.

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 >>>.

On Aug, 26, 2026

15,456 people reported to have side effects when taking Zemplar.
Among them, 20 people (0.13%) have Sinus tachycardia.

Among these 20 people:

How long have people been on Zemplar when they have Sinus tachycardia? *

What is the gender of people who have Sinus tachycardia when taking Zemplar? *

female: 10 %
male: 90 %

What is the age of people who have Sinus tachycardia when taking Zemplar? *

What are other drugs people take besides Zemplar? *

What are other side effects people have besides Sinus tachycardia? *

Weight Decreased: 9 people, 45.00%
Cardiac Failure Congestive: 9 people, 45.00%
Joint Pain: 9 people, 45.00%
Kidney Transplant Rejection: 9 people, 45.00%
Muscle Aches (muscle pain): 9 people, 45.00%
Pericardial Effusion (fluid around the heart): 9 people, 45.00%
Hyperkalemia (damage to or disease of the kidney): 8 people, 40.00%
Erythema Multiforme (a type of hypersensitivity reaction): 8 people, 40.00%
Tricuspid Valve Incompetence (inefficient heart valve): 8 people, 40.00%
Atherosclerosis (disorder of the arteries): 7 people, 35.00%

What are the existing conditions these people have? *

Hyperparathyroidism Secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary): 7 people, 35.00%
High Blood Cholesterol: 7 people, 35.00%
High Blood Pressure: 6 people, 30.00%
Gastritis (inflammation of stomach): 2 people, 10.00%
Nephrogenic Anaemia (anaemia due to kidney disease): 1 person, 5.00%
Iron Deficiency Anaemia: 1 person, 5.00%
Insomnia (sleeplessness): 1 person, 5.00%
Hyperuricaemia (level of uric acid in the blood that is abnormally high): 1 person, 5.00%
Chronic Renal Failure (kidney failure): 1 person, 5.00%

* Approximation only. Some reports may have incomplete information.

Do you take Zemplar and have Sinus tachycardia?

- Check whether Sinus tachycardia 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 Zemplar:

Zemplar (15,494 reports)

Browse all side effects of Zemplar:

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

Browse all the drugs that are associated with Sinus tachycardia:

Sinus tachycardia (1,267 drugs)

Browse all the conditions that are associated with Sinus tachycardia:

Sinus tachycardia (1,412 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on paricalcitol (the active ingredients of Zemplar) and Zemplar (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.