FDA Warns Florida Compounder for Lacking Prescriptions, Contamination
The FDA has warned a specialty pharmacy in Florida for compounding drugs without prescriptions, a key point in the agency’s push for more compounding oversight powers.
Axium Healthcare Pharmacy was inspected by the FDA back in March as part
of an enforcement blitz prompted by an outbreak of meningitis linked to
a compounder in Massachusetts. Outbreaks of infections tied to
compounding concerns have since occurred in Tennessee and Texas.
Agency investigators said many of the products that Axium “manufactures
and distributes” are unapproved and misbranded drugs because they aren’t
backed by a valid prescription for individually identified patients.
Many of those same products, intended for conditions that are not
amenable to self-diagnosis and treatments by individuals who are not
health practitioners, also lack adequate directions for use, the warning
letter states.
The letter, posted Aug. 27, also notes FDA concern with Axium’s sterile
drug production processes, which the agency said took place under
unsanitary conditions. The letter chides Axium for poor gowning
practices, namely that employees wore non-sterile gowns that exposed
bare skin and allowed for extending arms over sterile, uncovered vials.
Employees also failed to move in a “slow, deliberative manner in the aseptic processing area,” the agency said.
A Form 483 issued after the March inspection stated that one lot of
triamcinolone acetonide injectable solution, 60 mg/ml contained black
particles. “One of the vials appeared to contain more than one of these
particles,” the form reads. The agency also found a vial in one lot of
chromium chloride injectable solution, 4 mcg/ml contained a cloth-like
filament.
Axium recalled two lots of contaminated products due to the observations, the FDA said.
The Florida pharmacy now says it plans to leave the compounding
business, which it says makes up less than one percent of its total
revenue.
“Compounding is not part of Axium’s core strategy to grow in the
specialty pharmacy business, so we made a business decision to close
that operation,” the company said, adding that all of its sterile
compounding practices were brought to a halt back in April.
Pharmacies that compound products without a prescription have drawn
particular scrutiny from the FDA, especially after a meningitis outbreak
last year was tied to drugs mixed at the New England Compounding
Center. The agency believes that regulating traditional compounders,
which make products based on valid prescriptions, should be left to the
states. However, it has asked Congress for additional authority to go
after the larger compounders that make products without a prescription
and ship them to other states.
The Government Accountability Office agreed with the agency in a recent report outlining the need for clearer authority.
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