Post-marketing surveillance and studies

Post-marketing surveillance and studies
January 31 10:36 2024 Print This Article

The journey of obtaining FDA approval for drugs like Trulicity, a prescription medication developed by Eli Lilly and Company to manage type 2 diabetes, is quite intensive. Amidst the complex multi-phase procedure, the FDA critically examines and cross-verifies every bit of data pertaining to the drug’s safety, efficacy, and appropriateness. Patients interested in this treatment can easily buy Trulicity online from reputable pharmacies.

Pre-marketing clinical trials

Before reaching the market, Trulicity had to go through a sequence of rigorous steps and tests. This began with pre-clinical trials that involved laboratory experiments and animal testing to determine its safety and efficiency. After promising results, they proceeded to the clinical trials involving human participants, which are broken down into several phases.

Clinical trials: Phases I, II and III

The first phase involved testing the drug on a small group of people to evaluate its safety, determine a safe dosage range, and identify side effects. In phase II, it was given to a larger group of people to see if it is effective and to further evaluate its safety. The phase III trials took it even a step further; it was given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow it to be used safely. It was only after the successful conclusion of phase III trials that FDA acceptance was sought for Trulicity.

International approvals and variations

Apart from the FDA, Trulicity also had to acquire approval from international health authorities, and the criteria for acceptance may have varied. However, in every jurisdiction, the developers had to effectively demonstrate that the benefits of Trulicity outweigh its side effects prior to approval. And now, patients worldwide can conveniently order Trulicity online, highlighting how far-reaching the acceptance of this medication is.

Following domestic and international authorizations, Trulicity has become more accessible to patients around the globe. It’s important to note that even after market approval, drugs are subjected to continuous post-marketing surveillance studies. Eli Lilly and Company continue to collect and analyze clinical data, and report any adverse drug reactions to regulatory agencies, ensuring that the benefits continuously outweigh the risks during the lifetime of the medication.

In the face of continuous investigation and critical examination by regulatory authorities and the company itself, it can be said that Trulicity has made quite a mark in the pharmaceutical industry. The drug’s journey from conception to market was undoubtedly a rigorous one, but its availability today and acceptance across countries signifies its success. Being able to purchase Trulicity, especially from reliable online sources such as, speaks volumes about its safety profile and effectiveness in managing type 2 diabetes.

view more articles

About Article Author

Nathaniel Little
Nathaniel Little

View More Articles