-  This bill is not active in this session.
 

A04781 Summary:

BILL NOA04781B
 
SAME ASSAME AS S05091-B
 
SPONSORRosenthal D
 
COSPNSR
 
MLTSPNSR
 
Add §6811-c, Ed L
 
Requires pharmacies to make reasonable attempts to notify patients within seven days by phone or mail of class I drug recalls where such patients are currently taking such recalled drugs.
Go to top    

A04781 Actions:

BILL NOA04781B
 
02/05/2019referred to higher education
04/12/2019amend (t) and recommit to higher education
04/12/2019print number 4781a
05/08/2019amend and recommit to higher education
05/08/2019print number 4781b
05/21/2019reported
05/23/2019advanced to third reading cal.413
05/30/2019passed assembly
05/30/2019delivered to senate
05/30/2019REFERRED TO HIGHER EDUCATION
06/11/2019SUBSTITUTED FOR S5091B
06/11/20193RD READING CAL.1252
06/11/2019PASSED SENATE
06/11/2019RETURNED TO ASSEMBLY
10/11/2019delivered to governor
10/18/2019signed chap.379
Go to top

A04781 Memo:

NEW YORK STATE ASSEMBLY
MEMORANDUM IN SUPPORT OF LEGISLATION
submitted in accordance with Assembly Rule III, Sec 1(f)
 
BILL NUMBER: A4781B
 
SPONSOR: Rosenthal D
  TITLE OF BILL: An act to amend the education law, in relation to requiring pharmacies to make reasonable attempts to notify patients of certain drug recalls   PURPOSE: To require patient notification of recalled prescription medication   SUMMARY OF PROVISIONS: Section 1 adds a new section to education law; defines 'class I recall' and requires pharmacists to notify patients who have been issued class I recalled medication. Section 2 sets the effective date.   SUMMARY OF AMENDMENTS: -Provides that the pharmacy shall make reasonable attempts to contact the patient by phone or mail -Provides that the 3 day window of notification begins once the pharmacy is notified of the recall from the manufacturer, wholesaler, FDA or other means of notice - Provides that chain pharmacies may satisfy the requirements of this section by outreach from a central office   JUSTIFICATION: The FDA classifies drug recalls into 3 numerical categories. Class 1 recalls indicate the most serious adverse health implications. Drugs that are issued a Class 1 recall have a high probability of exposing patients to products that may cause serious adverse health consequences or death. Currently, there is no requirement for pharmacies to notify patients who have been dispensed recalled drugs of their status. Given the severity of the risk associated with such products, especially to elderly patients and those taking long-term maintenance medications, patient notification becomes paramount. As pharmacies often act as the most direct point of contact for many patients, this legislation helps to protect at risk consumers from potentially harmful medication.   LEGISLATIVE HISTORY: This is a new bill   FISCAL IMPLICATIONS: None to the state   EFFECTIVE DATE: This act shall take effect immediately
Go to top

A04781 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                         4781--B
 
                               2019-2020 Regular Sessions
 
                   IN ASSEMBLY
 
                                    February 5, 2019
                                       ___________
 
        Introduced  by  M.  of  A. D. ROSENTHAL -- read once and referred to the
          Committee on Higher Education -- committee discharged,  bill  amended,
          ordered  reprinted  as  amended  and  recommitted to said committee --
          again reported from said committee with amendments, ordered  reprinted
          as amended and recommitted to said committee

        AN  ACT  to amend the education law, in relation to requiring pharmacies
          to make reasonable attempts to notify patients of certain drug recalls
 
          The People of the State of New York, represented in Senate and  Assem-
        bly, do enact as follows:
 
     1    Section 1. The education law is amended by adding a new section 6811-c
     2  to read as follows:
     3    §  6811-c.  Patient notification of recalled drugs. 1. For purposes of
     4  this section the term "class I recall" shall mean a situation  in  which
     5  the United States food and drug administration deems there is reasonable
     6  probability  that  the  use  of  or exposure to a violative product will
     7  cause serious adverse health consequences or death.
     8    2. Where there has been a class I recall of a prescription drug, phar-
     9  macies shall make a reasonable attempt to notify all patients that  have
    10  been  prescribed  and  who  are  currently  taking  such  recalled  drug
    11  dispensed from such pharmacy by phone or by mail within  three  days  of
    12  the  pharmacy being notified by the United States food and drug adminis-
    13  tration, a manufacturer, a wholesaler or by other notice of such recall.
    14    3. The notification required by this section may  be  provided  by  an
    15  individual  pharmacy  or  by  a central office in the case of a pharmacy
    16  that is part of a chain.
    17    § 2. This act shall take effect immediately.
 
 
         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD06542-06-9
Go to top

A04781 LFIN:

 NO LFIN
Go to top