FDA: Georgia pharmacy recalling all sterile drugs
- Article by: MATTHEW PERRONE
- Associated Press
- March 21, 2013 - 5:49 PM
WASHINGTON - The Food and Drug Administration notified doctors Thursday that a Georgia compounding pharmacy responsible for a drug linked to eye infections has recalled all of its injectable medicines following a federal inspection.
Augusta, Ga.-based Clinical Specialties Compounding Pharmacy issued a recall earlier this week on dozens of lots of the Roche drug Avastin after receiving reports of eye infections in five patients treated with the medication.
The infections, called endophthalmitis, occur inside the eyeball and can lead to permanent vision loss, the FDA said in a statement.
The FDA said Thursday that its inspectors found issues at the pharmacy that raise questions about the sterility of its drugs. The company voluntarily agreed to recall all of its sterile products.
The recall includes dozens of drugs, including the antibiotic, vancomycin, and the preterm labor drug, hydroxyprogesterone.
Clinical Specialties' lead pharmacist Austin Gore told the Associated Press on Wednesday that the company has processed about 100,000 doses of Avastin since 2005 without any prior incidents.
"We're always concerned for the patient, that's the most important thing," Gore said.
Avastin is approved for cancer, but many eye doctors prescribe it for macular degeneration, a common vision disorder among older people. Avastin is structurally similar to the eye drug Lucentis, also made by Roche, and costs much less. The pharmacy repackages the drug into smaller doses and them sells them to doctors' offices
Roche has long discouraged the practice, pointing out that Avastin was not designed for use in the eye.
The announcement is the second nationwide recall by a compounding pharmacy in less than a week. On Monday the New Jersey pharmacy Med Prep Consulting Inc. recalled all of its drugs after hospital staffers in Connecticut discovered mold in five infusion bags distributed by the company.
"A compromised sterile product puts patients at risk for serious infections," said Janet Woodcock, director of the FDA's drug center. "Health care professionals should ensure that any medicines they administer to patients are obtained from appropriate, reliable sources and are properly administered."
Compounding pharmacies are supposed to mix customized prescriptions based on doctors' instructions. However, some of the pharmacies have grown into larger businesses, supplying bulk quantities of intravenous and injectable drugs to hospitals across the country.
The FDA has been stepping up inspections of compounding pharmacies after a nationwide fungal meningitis outbreak last year tied to compounded drugs.
A tainted steroid distributed by a Massachusetts-based compounding pharmacy killed 50 people and has sickened more than 720 nationwide. Many of the cases involved a rare form of meningitis tied to fungus found in the New England Compounding Center's facilities. The company has been shut down since the outbreak was discovered in September.
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