---
title: PDR Update Newsletters
description: "The PDR Update Insert shows recent FDA changes to the PI, prescribing information, including: FDA recalls, warnings, boxed warnings changes and other updates to the label content."
---

# PDR Update

Type Drug Name Here

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- Labeling Updates as of September 1, 2024 - Issue 9
- Drug Updates

Labeling Updates as of September 1, 2024 - Issue 9

- Key
- ![](https://www.pdr.net/hubfs/lynton/homepage/BlackBox_opt.jpeg) Boxed Warning
- ![](https://www.pdr.net/hubfs/lynton/homepage/Triangle_opt.jpeg) Other Warnings*
  
  *Warnings and Precautions; Adverse Reactions; Drug Interactions; and Contraindications
- ![](https://www.pdr.net/hubfs/lynton/homepage/Circle_opt.jpeg) Updates to Indications/Dosage
- ![](https://www.pdr.net/hubfs/lynton/homepage/Diamond_opt.jpeg) Other Updates†
  
  †Other labeling changes; added to PDR database

| ![Labeling Updates has Boxed Warning](https://www.pdr.net/hubfs/lynton/homepage/BlackBox_opt.jpeg "Boxed Warning") | ![Labeling Updates has Other Warnings](https://www.pdr.net/hubfs/lynton/homepage/Triangle_opt.jpeg "Other Warnings") | ![Labeling Updates has Indications/Dosage Updates](https://www.pdr.net/hubfs/lynton/homepage/Circle_opt.jpeg "Indications/Dosage") | ![Labeling Updates has Other Updates](https://www.pdr.net/hubfs/lynton/homepage/Diamond_opt.jpeg "Other Updates") | **Labeling Updates**No updates this month |
| --- | --- | --- | --- | --- |

Drug Updates

Get more information on PDR's monthly Drug Updates, including the latest in FDA news.

[View the latest drug updates](https://www.pdr.net/edrug-updates?hsLang=en)

To have full prescribing information faxed or mailed to you, call 1-800-261-2313.

| The FDA encourages healthcare professionals to recognize and report misleading prescription drug advertising. To report: call 855-RX-BADAD (855-792-2323) or email [BadAd@fda.gov](mailto:BadAd@fda.gov). For more information, visit [www.fda.gov](http://www.fda.gov/). |
| --- |
| Report adverse events to [MedWatch](https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program). |

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