If you take this medicine, call your doctor now, FDA warns

This tablet could lead to serious unfavorable health events, officials warn.


Tablets or capsules of your drug cabinet are intended to mitigate health problems. But sometimes, the pills you appear can unfortunately have the opposite effect - and this is the case with a thyroid medicine that the Food & Drug Administration (FDA) has announced a reminder of.

More than 20 million people in the United States have athyroid disorder, the American Thyroid Association (ATA) declares. And in many cases, these thyroid diseases are treated with drugs. Your thyroid, the butterfly gland located at the base of the neck, helps to regulate many functions of your body. The management of irregularities with drugs is therefore essential for your general well-being. But if you take a particular prescription medication for your thyroid, you can really compromise your health, according to a new national reminder. Keep reading to learn what medicine FDA says to contact your doctor and more pills that can put you at risk, seeIf you take this popular vitamin, stop immediately, the FDA warns.

Acella Pharmaceuticals, LLC, recalled NP Thyroid® Nationwide.

acella, thyroid medicine recall, pills
FDA

On April 30, the FDA announced that Acella Pharmaceuticals, LLC, had voluntarily recalled a thyroid medicine called NP Thyroid®, made of levothyroxin and liothyronine and is used for people with hypothyroidism. Company tablets of 15 mg, 30 mg, 60 mg, 90 mg and 120 mg thyroid® thyroid® were all recalled.

The drug was distributed nationally on wholesalers, pharmacies and health offices.

"Products submitted to reminders are packed in 100 accounts and 7 accounts," says the notice. The announcement of the FDA lists 35 100 counting bottles and three cylinders at 7 accounts among those recalled. You can check theFull list on the FDA website.

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The problem with NP Thyroid® tablets is that they are not good power.

pill box on table with glass of water
Refuge

The routine tests revealed that the NP thyroid® tablets contained less than 90% of the marked amount of lothyronin (T3) and / or levothyroxine (T4) - which makes it less powerful and therefore less efficient.

"Patients treated for hypothyroidism (under-active thyroid), which receive signs and symptoms of hypothyroidism (under-money thyroid)," the notice posted on the FDA website warns. CI include "fatigue,increased cold sensitivity, constipation, dry skin, inflated face, hair loss, slow heart rate, depression, swelling of the thyroid gland and / or unexplained weight gain or difficulty to lose weight. "

And for another sign that your thyroid can be out of whack,If you notice that with your eyes, have your thyroid check, say doctors.

Nearly 50 serious adverse events potentially related to the thyroid medicine have been reported.

Man looking at bottles from medicine cabinet
Tom Merton / iStock

As of April 30, 43 serious adverse events with a possible link with NP thyroid® had been reported to Acella.

"There is a reasonable risk of serious injury in newborns or pregnant women with hypothyroidism, including an early miscarriage, fetal hyperthyroidism and / or deficiencies for the development of neural and skeletal fetal", explains the opinion of The FDA.

In addition, seniors and patients with underlying heart disease have an increased risk of "toxic heart events of hyperthyroidism" when taking recalled medications, including cardiac arrhythmias, palpitations and cardiac pain .

And for more things to get out of your drug cabinet,If you have these supplements at home, the FDA says "destroy them".

Patients taking NP Thyroid® should not stop taking it without contacting their doctor.

woman talking to young female doctor in glasses
exit

Acella is working to inform anyone that they have shipped the drug to stop the distribution of thyroid® NP tablets in question. According to the notice, "Patients who currently take NP Thyroid® from the recalled batches should not interrupt the use without contacting their health care provider for new guidelines and / or a replacement order".

Anyone with questions about the reminder should send an email to Acella Pharmaceuticals to [email protected] or call the representatives of the Company at 1-888-424-4341. The FDA MedWatch Adverse Event Declaration Program collects additional reports on adverse effects or other recalled drug issues.

And for another reason to see your doctor, If you can not stop doing this at night, have your thyroid check .


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