Friday, May 31, 2013

Arkansas investigating product from compounding pharmacy 1:54 PM, May 30, 2013

LITTLE ROCK, Ark. -- The Arkansas Department of Health along with federal health organizations and other states are investigating reports of infections among 20 patients in Illinois (5), North Carolina (2), and Florida (13) who received injections of a steroid, methylprednisolone acetate (MPA), after Dec. 6, 2012, produced by Main Street FamilyPharmacy, LLC, (MSFP) in Newbern, Tenn. Complications identified thus far appear to be limited to skin abscesses at the site of injection and joint infections. There are no reports of meningitis, stroke or death.
Ten clinics in Arkansas have received MPA from the MSFP. All ten have been contacted and are assembling information to assist in the investigation. Individuals who are experiencing any unexplained health problems following an injection of methylprednisolone acetate from one of these clinics are encouraged to contact the clinic or their regular health care provider.

Why does Nancy Loomis, RPh have an active license with ZERO discipline recorded, not even a public complaint, when the pharmacy she owned and operated as a supervising pharmacist plead GUILTY to a FELONY?)

I  have previously posted about Signature Pharmacy which was located in Orlando, Florida  See links below.  Guess who was an owner in Signature Pharmacy and guess who is an owner in Olympia Pharmacy, which just initiated a volunteer recall.  You will want to read Dr. Ken Woliner's post below the previous post on this blog about Signature.

NY judge tosses convictions in Fla. steroids case



Orlando pharmacy pleads guilty to drug charge Signature Compounding Pharmacy of Orlando sold steroids 


Signature Compounding case Lawsuit against Soares dropped Case facing Albany County prosecutor ends after pharmacy admits felony

Written by Dr. Ken Woliner, MD, ABFM
www.holisticfamilymed.com


Olympia Pharmacy is owned by Nancy and Stan Loomis (with Nancy Loomis, R.Ph. being the prescription department manager). These are the same owners of the defunct Signature Pharmacy that was the center of "Operation Which Doctor" that Albany County (NY) State Attorney prosecuted against this pharmacy and several "rejuvenation clinics"

Thursday, May 30, 2013

Lowlite Investments Inc, doing business as Olympia Pharmacy in Orlando, Florida, has initiated a voluntary recall of all unexpired sterile drug products compounded by the pharmacy because of a lack of sterility assurance.

Lowlite Investments Inc, doing business as Olympia Pharmacyin Orlando, Florida, has initiated a voluntary recall of all unexpired sterile drug products compounded by the pharmacy because of a lack of sterility assurance.
"The recall is being initiated due to concerns associated with prior quality control procedures that impacted sterility," the company says in a press release posted May 29 on the FDAWeb site.
The affected product was compounded between December 17, 2012, and March 27, 2013. The recall includes all sterile products that Lowlite supplied to patients and offices of licensed medical professionals with a use-by date of September 25, 2013, or earlier.
complete list of the recalled products, lot numbers and expiration dates can be found on the FDA Web site.
The recall is being conducted as a "precautionary measure," the company says. To date, they have not received any reports of injury or illness associated with the recalled product. However, "in the event a sterile product is compromised patients are at risk for serious and possible life threatening infections."
Lowlite is notifying customers by telephone, fax, or mail to return the products to the pharmacy.
Source found here

NABP Surveyors to Assist With New Jersey Compounding Pharmacy Inspections Under Contract With the State

Under a contract with the New Jersey Division of Consumer Affairs (Division) and the state’s Attorney General Jeffrey S. Chiesa, NABP will assist the Division with inspections of New Jersey pharmacies engaged in the practice of compounding. The planned pharmacysurveys will expand the Division’s already robust inspections of compounding pharmacies. As noted in a Division press release, New Jersey State Board of Pharmacy regulations hold compounding pharmacies to “stringent compounding standards, mirroring those of the U.S. Pharmacopeial Convention” and the Division’s inspectors have routinely inspected the state’s pharmacies to ensure compliance with regulations. The contract with NABP will enable New Jersey “inspectors to draw upon a greater body of expertise and experience to address this growing industry,” indicates Chiesa. Chiesa stated further that the Division “will act immediately on any violations that appear to threaten the public’s health and safety.” The expanded compounding pharmacy inspections have been initiated as a result of contamination issues discovered at Med Prep Consulting, Inc, in Tinton, NJ, and similar reports of contamination at compounding facilities in other states, as well as the fungalmeningitis outbreak linked to contaminated products compounded by the New England Compounding Center in Framingham, MA. New Jersey’s contract with NABP enables the Division to temporarily employ NABP inspectors on an as-needed basis. 
Similar inspection programs are under consideration in a number of other states, and NABP is in discussion with these states regarding how the Association can assist with these efforts to ensure the safety of compounded medications. In addition, NABP plans to establish an e-Profile for each pharmacy in the US, which will include verifications of licensure, disciplinary checks, and verification that a timely and robust inspection has occurred for each pharmacy, including those performing sterile and nonsterile compounding. The information in the e-Profiles for pharmacies will be sent proactively to boards of pharmacy for use in making licensure and registration determinations for nonresident pharmacies. 
A compounding inspection program conducted by NABP on behalf of the Iowa Board of Pharmacy was initiated in mid-December and is ongoing. More information about the Iowa compounding pharmacy inspection program and the information sharing network under development by NABP is included in the April 2013 NABP Newsletter article “Compounding Pharmacy Information Sharing Network Available to Boards Soon” (PDF).
quoted from here




May 30, 2013: Rep. Markey Introduces Bill to Support Compounding of Drug Products





Rep. Markey Introduces Bill to Support Compounding of Drug Products
Bill Introductions-House
Copyright © Targeted News Service, 2013
2013-05-30

by KAREN NARAG

WASHINGTON, May 30 -- Rep. Edward Markey, D-Mass., has introduced legislation (H.R. 2186) to amend the Federal Food, Drug, and Cosmetic Act to "provide for the compounding of drug products."

----
Contact: Eben Burnham-Snyder, Rep. Ed Markey, 202-225-2836
Follows Investigation Showing Lax Oversight of Compounding
WASHINGTON (May 23, 2013) – After his recent report showed that some states across the country are turning a blind eye to the risks of compounding pharmacies, Rep. Ed Markey (D-Mass.) today introduced new legislation to make compounding pharmacies safer for patients. The legislation will strengthen federal regulations for compounding pharmacies, especially high-risk sterile compounding and compounding pharmacies that ship drugs across state lines.
An investigation led by Rep. Markey and his Energy and Commerce Committee colleagues found last month that compounding pharmacies are going largely untracked, unregulated, and under-inspected by states across America, demonstrating the need for more federal oversight of the industry. Many of the risks from compounders were revealed following the 55 deaths and 741 illnesses in 20 states that originated from drugs created at the New England Compounding Center located in Rep. Markey’s Congressional District.
“We know some compounders are acting more like large drug manufacturers. We know that patients continue to be at risk for injury or death. And we know that some states are not doing their jobs to protect patients,” said Rep. Markey. “That’s why we need legislation that gives FDA more authority, while still allowing smaller mom-and-pop compounders to do their work for their patients.”
Massachusetts Governor Deval Patrick today praised Rep. Markey for his leadership on compounding pharmacy oversight. Governor Patrick has instituted a top-to-bottom review and proposed actions to increase the health and safety of compounding pharmacies in Massachusetts following the NECC tragedy.
“Congressman Markey’s legislation, coupled with the important steps we took at the state level, is critical to closing a regulatory gap created over the past several years for a variety of reasons,” said Governor Deval Patrick. “I commend Congressman Markey for his leadership. No one should live in fear that their medicine is unsafe.”
The legislation, the VALID Compounding Act, updates previous legislation introduced in 2012 by Rep. Markey. Original co-sponsors of the bill are Louise Slaughter (D-N.Y.), WM. Lacy Clay (D-Mo.), and Charles Rangel (D-N.Y.).
A one-pager on the VALID Act is available HERE, and the legislation includes the following main elements:
--Provides the FDA with sole regulatory authority over compounding pharmacies that engage in interstate commerce and high-risk sterile compounding without or in advance of a prescription. 
--Preserves State regulatory authority for traditional small compounding pharmacies. 
--Allows compounding pharmacies to compound drugs before receiving prescriptions for the drug provided that they register with the FDA and meet specified safety standards, and allows capable State regulators to oversee these pharmacies.  
--Increases communication between the States and federal government.
--Increases transparency to patients and consumers.
A full copy of the legislation can be found HERE and a section-by-section document HERE.
“This bill will save lives because it improves safeguards for all types of important medications made by the largest compounding pharmacies,” said Diana Zuckerman, PhD, president of the Cancer Prevention and Treatment Fund and National Research Center for Women & Families. “At the same time, it protects the thousands of small 'Mom & Pop' traditional compounders that some patients need.”
The legislation has been endorsed by the National Consumers League, National Research Center for Women and Families, Cancer Prevention and Treatment Fund, National Women’s Health Network, Our Bodies Ourselves, Union of Concerned Scientists, U.S. PIRG, Community Catalyst, The TMJ Association, and WoodyMatters. A copy of the endorsement letter can be found HERE

US House Shows Little Support for Senate Version of Compounding Bill

read this article here

The Sterility Risks in Pharmacy Compounding Can Be Limited, Not Eliminated, Experts Stress at USP Forum May 29th, 2013

to read this article click here

Louisiana Proposed Rule Changes: Some pharmacists concerned about proposed rule changes By Bill Lodge Advocate staff writer

Proposed changes in regulations could push some pharmacists out of the specialty medicine business in Louisiana, according to a Baton Rouge pharmacist with 37 years of experience.
Patricea Angelle, a compounding pharmacist in Baton Rouge, said the rule changes would impose an enormous cost burden on some compounding pharmacies and create serious problems for patients who depend on the medicines they provide.
Compounding pharmacies prepare medicines prescribed for patients with allergies or other negative reactions to some medications they need in order to recover from illness or injury.
Some of those special medicines may be needed by patients for whom other medications simply don’t work. Compounding pharmacists also prepare medicines that some physicians want to keep stocked at their offices.
Malcolm J. Broussard, executive director of the Louisiana Board of Pharmacy, said he hasn’t “heard from any pharmacies telling us the proposed rule would force them to close.”
If so, others will fill those gaps, Broussard said.
A public hearing on the pharmacy board’s proposals is scheduled for 1 p.m. Thursday at the board office, 3388 Brentwood Drive.
The proposed rule changes in Louisiana follow an incident late last year in which dozens of recipients of medicines from a compounding pharmacy in Massachusetts contracted fungal meningitis and died.
The Louisiana Board of Pharmacy declared an emergency in January, and members announced they planned to adopt a rule that would bar the state’s compounding pharmacists from deriving more than 10 percent of their business from the sale of medicines by purchase order to physicians for use at their offices.
“The quality and safety standards for products made pursuant to a purchase order are ordinarily more stringent than the quality and safety standards for preparations made pursuant to a patient-specific prescription,” Broussard, said in an email exchange this week.
“When pharmacies make products pursuant to purchase orders in compliance with the less stringent standards applicable to patient-specific prescriptions, there is a potential risk,” Broussard added. “The proposed rule is an attempt to mitigate that risk by limiting such activity to no more than 10 percent of a pharmacy’s activity.”
In Washington, D.C., Sarah Dodge, the International Association of Compounding Pharmacists’ vice president for government affairs, said such rules seem arbitrary.“That concerns us,” Dodge added.
Dodge explained that one proposed federal law calls for greater controls on compounding pharmacies that send sterile compounds across state lines to recipients who are not patients.
Inside one state’s boundaries, Dodge said, “What we prefer is that the state allow what has been usual for (physicians’) office use.” She said her organization does not support an arbitrary cap.
“The federal proposal is far more palatable than the Louisiana proposal,” Dodge said.
Broussard said, “In the event a pharmacy is currently preparing more than 10 percent of itsactivity pursuant to (physicians’) purchase orders, that pharmacy will need to make a business decision.”
continue reading here

FDA to Once Again Allow Import of Unapproved Drugs to Solve Shortages

29 May 2013


By Alexander Gaffney, RF News Editor

Responding quickly to congressional pressure and the needs of critically ill neonates, the US Food and Drug Administration (FDA) today announced that it would allow the import of several types of [Read More...

Edwards, Hospira Warn Investors of Receipt of FDA Warning Letters

30 May 2013


By Alexander Gaffney, RF News Editor

Two major life sciences companies, Hospira and Edwards Lifesciences, have separately warned their respective investors about their receipt of Warning Letters from the US Food and Drug Administration [Read More...