A certain amount of blood pressure medication was recalled after a bottle of this lot was labeled as incorrect, according to a statement by the Food and Drug Administration (FDA).

The bottle should contain hydrochlorothiazide tablets USP 12.5 mg, a drug used to treat high blood pressure, instead contained USP 25 mg spironolactone tablets – used to treat congestive heart failure, cirrhosis, and other diseases.

The FDA says that the effects of mixing the drugs on the

Accord Healthcare Inc. voluntarily recalled a single batch of the drug PW05264 after research revealed that it was the only potentially affected batch.

Accord & # 39 ; s hydrochlorothiazide tablets USP 12.5 mg can be identified by a visual Leader . The tablets should be bright orange or peach-colored and round. They have an "H" and a "1" on opposite sides.

For individuals holding Accord Hydrochlorothiazide tablets that do not conform to this description, the FDA recommends that you check with a pharmacy or health care provider.

Accord says there have been no reports of adverse events related to this recall under FDA clearance.


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