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Anvisa suspends 10 lots of medicines for hypertension

Anvisa suspends 10 lots of medicines for hypertension

The National Agency of Sanitary Vigilance (Anvisa) suspended on Monday (03) ten batches the drug Captopril 25 mg, indicated for patients with arterial hypertension.

The product is manufactured by the Pharmaceutical Laboratory of Pernambuco (Lafepe), which identified problems during the quality control of the products. In stability tests evaluating the quality of the drug upon ready, it was shown that the amount of the active substance disulfide of captopril in the tablets was different from the standard. The active principle is the substance that gives the identity of the drug and makes it work in the patient's body.

The decision prohibits the distribution, trade and use of the drug. Therefore, patients who are using any of the suspended lots should make the exchange of the drug.

According to the agency, patients can contact the company to find out how to exchange the product or, if necessary, if you prefer, consult your doctor to evaluate the change in treatment. The other lots of the product produced by Lafepe are still released. Check the bans that have been forbidden:

15081401 (validity: August 2017), 15081402 (validity: August 2017), 15081403 (validity: August 2017), 15090230 (validity: September 2017) 2017), 15090232 (validity: September 2017), 15121446 (validity: December 2017), 16030251 (validity: March 2018), 16030254 (validity: March 2018) and 16030255 (validity: March 2018). >


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