My WebLink
|
Help
|
About
|
Sign Out
Home
Browse
Search
2022-100 Resolution
Document-Host
>
City North Olmsted
>
Legislation
>
2022
>
2022-100 Resolution
Metadata
Thumbnails
Annotations
Entry Properties
Last modified
11/2/2022 3:24:14 PM
Creation date
11/2/2022 3:22:27 PM
Metadata
Fields
Template:
North Olmsted Legislation
Legislation Number
2022-100
Legislation Date
11/1/2022
Year
2022
Legislation Title
Permit Moratorium Kava, Kratum
There are no annotations on this page.
Document management portal powered by Laserfiche WebLink 9 © 1998-2015
Laserfiche.
All rights reserved.
/
19
PDF
Print
Pages to print
Enter page numbers and/or page ranges separated by commas. For example, 1,3,5-12.
After downloading, print the document using a PDF reader (e.g. Adobe Reader).
Show annotations
View images
View plain text
15 76,22 12 04 DM p Ings . drove avoet Dee & emairrrannab,)-1 cera -a r -1C I FDA <br />containing products. Additionally, animal poison control centers have indicated a sharp overall <br />increase in accidental exposure of pets to these products. Keep these products out of reach of <br />children and pets. <br />Why is the FDA notifying the public about delta -8 THC? <br />A combination of factors has led the FDA to provide consumers with this information. 'These <br />factors include: <br />An uptick in adverse event reports to the FDA and the nation's poison control centers. <br />Marketing, including online marketing of products, that is appealing to children. <br />Concerns regarding contamination duc to methods of manufacturing that may in some <br />cases be used to produce marketed delta -R MC products <br />- <br />The FDA is actively working with federal and state partners to eirther address the concerns <br />related to these products and monitnling the market for product complaints, adverse events, <br />and other emerging cannabis -derived products of potential concern. The FDA will warn <br />consumers about public health and safety issues and take action, when necessary, when FDA - <br />regulated products violate the law. <br />How to report complaints and cases of accidental exposure or <br />adverse events: <br />If you think you are raving a serious side eftect Inat is an immediate danger to your health, call <br />9-1-1 or go to yourlocal emergency r,0111 Health care professionals and patients are encouraged <br />to repott complaints and cases of accidental exposure aid adverse events to the FDA's <br />McTtVatch Safety lefonnation and Adverse Event Reporting Program: <br />• Call an FDA Consumer Compca!nt Coordinator (-safety,, repor, problem-idaiconsumer <br />complaint coordinators) it you wish to speak directly to a person about your problem. <br />• Complete an electronic V-olurtare lled titch form <br />(htt�s 1 www zecessdata fdn-gov, scripts; Fncdwatch!) Online or call i-800-332-1088 to <br />request a reporting form, then complete and return to the address on the foram, or submit <br />J), fax to 1 Boo FDA 0178. <br />• Completea paper V_o>? untary Vl,�dW_elch_ Ito in <br />( ttps ,'(www fda-boa media, r>r1R download) and mail it to the FDA. <br />• To report adverse events in animals to the FDA's Center for Veterinary Medicine, please <br />download and submit Form FDA n332a found at: www.fda.go_�,'ReportArimalAH <br />(!animal veterinarys mpicuLproblern how -report -animal dreg and device-side-effeet8_ <br />and-product_problems 7. <br />ID,, _ 1,1 ,_n. le, S1h,9,, ., F., icy., -vi it rm. e. elle-e=or 4_ <br />
The URL can be used to link to this page
Your browser does not support the video tag.