Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A study to determine frequencies of known serious side effects among DPP-4 inhibitors in patients with diabetes using FDA adverse event reporting system

Next Previous
Trial Profile

A study to determine frequencies of known serious side effects among DPP-4 inhibitors in patients with diabetes using FDA adverse event reporting system

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 20 Jan 2023

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Alogliptin (Primary) ; Anagliptin (Primary) ; Linagliptin (Primary) ; Omarigliptin (Primary) ; Saxagliptin (Primary) ; Sitagliptin (Primary) ; Teneligliptin (Primary) ; Trelagliptin (Primary) ; Vildagliptin (Primary)
  • Indications Diabetes mellitus
  • Focus Adverse reactions

Most Recent Events

  • 20 Jan 2023 New trial record
  • 13 Jan 2023 Results published in the Clinical Drug Investigation

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top