Kaletra and Dyspnea paroxysmal nocturnal - a phase IV clinical study of FDA data

Summary:

Dyspnea paroxysmal nocturnal is reported only by a few people who take Kaletra.

The phase IV clinical study analyzes which people take Kaletra and have Dyspnea paroxysmal nocturnal. It is created by eHealthMe based on reports of 21,685 people who have side effects while taking Kaletra from the FDA, and is updated regularly.

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 600+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.



On Oct, 01, 2022

21,685 people reported to have side effects when taking Kaletra.
Among them, 2 people (0.01%) have Dyspnea paroxysmal nocturnal.


What is Kaletra?

Kaletra has active ingredients of lopinavir; ritonavir. It is often used in hiv infection. eHealthMe is studying from 21,876 Kaletra users for its effectiveness, alternative drugs and more.

What is Dyspnea paroxysmal nocturnal?

Dyspnea paroxysmal nocturnal is found to be associated with 655 drugs and 210 conditions by eHealthMe.

Number of Kaletra and Dyspnea paroxysmal nocturnal reports submitted per year:

Could Kaletra cause Dyspnea paroxysmal nocturnal?

Time on Kaletra when people have Dyspnea paroxysmal nocturnal *:

  • < 1 month: 0.0 %
  • 1 - 6 months: 100 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Dyspnea paroxysmal nocturnal when taking Kaletra *:

  • female: 0.0 %
  • male: 100 %

Age of people who have Dyspnea paroxysmal nocturnal when taking Kaletra *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 100 %
  • 50-59: 0.0 %
  • 60+: 0.0 %

Common drugs people take besides Kaletra *:

  1. Combivir: 2 people, 100.00%
  2. Truvada: 1 person, 50.00%
  3. Retrovir: 1 person, 50.00%
  4. Lamivudine: 1 person, 50.00%
  5. Bactrim: 1 person, 50.00%

Common side effects people have besides Dyspnea paroxysmal nocturnal *:

  1. Oedema Peripheral (superficial swelling): 2 people, 100.00%
  2. Cardiac Failure: 2 people, 100.00%
  3. Congestive Cardiomyopathy (weakening of heart muscle): 2 people, 100.00%
  4. Weight Increased: 1 person, 50.00%
  5. Cough: 1 person, 50.00%
  6. Fatigue (feeling of tiredness): 1 person, 50.00%
  7. Electrocardiogram T Wave Inversion: 1 person, 50.00%
  8. Electrocardiogram St Segment Abnormal: 1 person, 50.00%
  9. Electrocardiogram Qt Prolonged: 1 person, 50.00%
  10. Ejection Fraction Decreased (systolic heart failure): 1 person, 50.00%

* Approximation only. Some reports may have incomplete information.

Do you take Kaletra and have Dyspnea paroxysmal nocturnal?

Check whether Dyspnea paroxysmal nocturnal is associated with a drug or a condition

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 studies

How severe was Dyspnea paroxysmal nocturnal and when was it recovered:

Expand to all the drugs that have ingredients of lopinavir; ritonavir:

Alternative drugs to, pros and cons of Kaletra:

Common Kaletra side effects:

Browse all side effects of Kaletra:

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

Dyspnea paroxysmal nocturnal treatments and more:

COVID vaccines that are related to Dyspnea paroxysmal nocturnal:

Common drugs associated with Dyspnea paroxysmal nocturnal:

All the drugs that are associated with Dyspnea paroxysmal nocturnal:

All the conditions that are associated with Dyspnea paroxysmal nocturnal:

How the study uses the data?

The study uses data from the FDA. It is based on lopinavir; ritonavir (the active ingredients of Kaletra) and Kaletra (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.

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 600+ 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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