Local Pharmacist Discusses FDA Recall


SPRINGFIELD — A local pharmacist sheds light on a potentially life-threatening label mix-up that has led to a nationwide recall of a high blood pressure medication, according to the U.S. Food and Drug Administration.

Accord Healthcare Inc. is voluntarily recalling one lot of 12.5 mg hydrochlorothiazide tablets after a 100-count bottle of the drug was found to contain 100 tablets of another drug, spironolactone.

Both medications are used to treat high blood pressure, but the FDA warns that taking spironolactone instead of hydrochlorothiazide could pose the risk of hyperkalemia, or an unsafe increase in potassium levels, in some people. This can result in “adverse events that range from limited health consequences to life-threatening situations in certain individuals,” the FDA said in a statement.

Rex Phipps with Midtown Pharmacy in Springfield explains the risks with those levels changing. 

“Milder things like an effect on your muscles, weakness, tiredness that sort of thing. The main thing to be worried about with getting your potassium levels really off whether it be high or low, is your heart. Being a muscle, is something going on involving your heartbeat and that sort of thing,” Phipps says. 

 While none of this recalled blood pressure medication was found on the shelves at Midtown Pharmacy, Phipps says when they do have a recall on their shelves they have to follow a strict procedure.

“We get a fax straight from the FDA. See if you have it on the shelf, then it is immediatley returned back to the warehouse. There are so many of these recalls,” Phipps says.  

So far, Accord has received no reports of anyone getting sick.

The company became aware of the mix-up through a complaint reported from a pharmacy.

Only a single lot of the drug, labeled PW05264, is being recalled.

“Based on findings of both preliminary and interim investigations carried out at the manufacturing site, Accord believes that no other lots of Hydrochlorothiazide Tablets are involved in this mix-up,” the FDA says.

Accord is reaching out to wholesalers, distributors and retailers by letter and is arranging for return of all recalled products.

 The hydrochlorothiazide tablets are light orange to peach colored, round, and debossed with an “H” on one side and a “1” on another side.

If the tablets in a bottle of Accord hydrochlorothiazide 12.5 mg do not match this description, or if consumers are unsure, they should return to their pharmacy or healthcare provider for confirmation, the FDA said.

Consumers or pharmacies with questions regarding this recall can contact Accord Healthcare, Inc. by phone at 1-855-869-1081 or e-mail at rxrecalls@inmar.com.

Copyright 2021 Nexstar Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

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