Publication
Article
Pharmacy Practice in Focus: Health Systems
The pharmaceutical industry continually develops novel therapeutics, many of which require refrigeration and are associated with high costs. In the event of such temperature excursions as a breach in the cold chain protocol, pharmacists are looked upon as experts who can deter- mine whether medications are still viable.
The pharmaceutical industry continually develops novel therapeutics, many of which require refrigeration and are associated with high costs. In the event of such temperature excursions as a breach in the cold chain protocol, pharmacists are looked upon as experts who can deter- mine whether medications are still viable. Besides resulting in a quantifiable loss, temperature excursions can expose medications to temperature insults that lead to chemical (eg, potency, antigenic) and physical (eg, dissolution, particulates)1 changes in the properties of the drug product. The clinical implications of excursions include a subpotent product, packaging contamination, patient harm, and therapeutic failure.2,3
For medication stability inquiries during temperature excursions above 8oC, many resources are available, including medication package inserts that typically indicate recommended storage environments (Table5-24). Peer-reviewed articles, such as “Room-Temperature Storage of Medications Labeled for Refrigeration” by Cohen et al2 from 2007, are also an asset when determining the viability of high-cost refrigerated medications. An abundance of guidance for storage conditions above manufacturers’ recommendations was noted in our research. However, it was challenging to find published information on temperature excursions below recommended refrigeration temperatures.
In the event of a break in the cold chain process used to maintain high-cost medications, a privileged pool of data, beyond what is required for package labeling, typically exists for reference. Federal regulations mandate that manufacturers ensure product'quality, essentially until'patient treatment.4 Because'of the immense aggregate'cost of a medication passed'through full drug development and supply chain'processes, manufacturers'of high-cost medications'routinely conduct additional distribution stability studies to ascertain a'product’s temperature limitations with respect to product integrity and quality.1 This information is generally reserved for “in-house” use during distribution and transport to ensure drug products endure temperature excursions during shipping and handling, as well as meet meticulous distribution protocols. If used, this unpublished data could help your pharmacy recoup over $200,000 in pharmaceutical products, including medications for which there is a national shortage.
Recent breaches in the cold chain process of select high-cost medications led to their exposure to freezing temperatures for more than 4 hours, which prompted preemptive action to ensure patient safety and product quality. After taking inventory, a clinical specialist from each manufacturer of a product affected by the breach was contacted with an inquiry into “temperature excursions.” Specifics (ie, lot number, expiration date, exposure temperature, duration of exposure, return time to refrigerator temperature) were provided at the request of the manufacturer. With each conversation, the manufacturer was asked to send a letter stating its temperature excursion data for the medication in question. This written confirmation of stability should not be over- looked. Once all manufacturer conversations had been properly documented, the medications deemed unaffected by the breach were specially marked in case they might need to be re-pulled from hospital supply. This process is an example of how health systems can use resources just behind the curtain. All it takes is a few good ideas, a few good people, and a few good hours.
Generic Name
(Brand Name)
Stability at Temperature
Excursions Below 2°Ca
(For specific information,
contact the manufacturerb)
Manufacturer
Contact Information
Beractant (Survanta)
Based on information provided, product use supported by manufacturer
AbbVie, Inc
800-633-9110
Travoprost (Travatan Z)
Manufacturer gave verbal in-house temperature excursion data to support use of product after site-specific breach
Alcon
800-757-9785
Botulinum Toxin Type A (Botox)
Prior to 2012, Botox was approved for storage in the freezer; product use supported by manufacturer
Allergan
714-246-4500
Filgrastim (Neupogen)
Based on site-specific breach details, product use supported by manufacturer
Amgen
800-772-6436
Phenylephrine 2.5% and 10% Drops
Product found to be stable after a freeze-thaw cycle
Paragon Bio Teck, Inc
503-465-3802
Crotalidae Immune Fab (CroFab)
Unreconstituted vials remain stable if exposed to —10°C to +2°C during 1 continuous excursion of ≤12 hr
BTG International, Inc
877-377-3784
Digoxin Immune Fab (DigiFab)
Unreconstituted vials remain stable if exposed to —25°C to +25°C during 1 continuous excursion of ≤7 days
Rho(D) Immune Globulin
(Rhophylac)
Specific breach conditions will have NEGATIVE impact on product
CSL Behring
800-504-5434
Alteplase
(Activase)
NO DATA on stability of unreconstituted vials exposed to negative temperature excursions; controlled room temperature (8°C-30°C) is OK
Genentech, Inc
800-821-8590
Rabies Immune Globulin (HyperRAB S/D)
Data indicate freezing point of Hyperimmune products to be —19°C; at temperatures <2°C, container closure integrity due to product expansion is a potential risk
Grifols, Inc
800-520-2807
Risperidone Long-acting Injection
(Risperdal Consta)
Manufacturer gave verbal in-house temperature excursion data to support use of product after site-specific breach
Janssen Pharmaceuticals, Inc
800-526-7736
Daptomycin
(Cubicin)
Unreconstituted vials did not show any significant change following weekly freeze-thaw cycling over 4 wk
Merck & Co, Inc
800-672-6372
Eptifibatide
(Integrilin)
Based on site-specific breach details, the product would not be adversely affected; may be stored at room temperature (25°C) for up to 2 months
Interferon Alfa-2b recombinant (Intron A)
Based on site-specific breach details, the product would not be adversely affected
Tobramycin Inhalation Solution
(Tobi)
Data support no change in stability after 3 freeze cycles to —20°C;
may be stored at room temperature (25°C) for up to 28 days
Novartis Pharmaceuticals Corporation
855-275-4642
Penicillin G benzanthine + penicillin G procaine injectable suspension
(Bicillin C-R and Bicillin C-R 900/300)
Data indicate the product failed to meet quality specifications when freeze/thaw testing was conducted
Pfizer, Inc
800-438-1985
Penicillin G benzanthine injectable suspension
(Bicillin L-A)
Rabies Vaccine
(Imovax Rabies IM)
Based on site-specific breach details, the product would not be adversely affected
Sanofi Pasteur
800-822-2463
Bacitracin
(Baciim)
Manufacturer indicates nature of freez-dried product has no stability issues based on site-specific breach details
X-GEN Pharmaceuticals, Inc
866-390-4411
Neomycin/Polymyxin B GU Irr — Amp (Neosporin GU Irrigant)
Freezing study indicates no stability issues based on site-specific breach details
aRecommended storage conditions are refrigerate at 2°C to 8°C based upon package labeling, unless otherwise indicated.
bTemperature stability determined on a case-by-case basis. Contact manufacturer and provide lot number and expiration date, length of time exposed to room temperature, and maximum exposure temperature. The authors of this article do not recommend the use of any pharmaceutical product that is in any way inconsistent with its prescribing information. Clinical judgment should be used regarding the use of material that has been subject to temperatures outside of those recommended by the manufacturer.
References
Jillian J. Bishop is an intern pharmacy student at the Denver Health & Hospital Authority and a PharmD candidate, class of 2017, at the University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences.
Michelle Then, PharmD, MBA, is the acute care pharmacy operations manager at the Denver Health & Hospital Authority.