Coping with chronic pain, depression, and high blood pressure
Can you prevent the hunched back of kyphosis?
What is ventricular bigeminy?
Emojis in electronic health records could be confusing
Doing different types of exercise linked to a longer life
CPR on TV may be misleading
How gum disease may raise heart disease risk
FDA approves nasal spray to treat rapid heart rhythm
Smart watch may improve detection of atrial fibrillation
4 keys to a heart-healthy diet
HHP Medication Safety Watch: September 2024
This list contains selected items from the full FDA list of recalls, withdrawals, and alerts for medicines and certain health products. We've provided links to FDA information for each product and its maker. Unless otherwise noted, these actions apply only to the specific brand name of the product listed. Talk to your healthcare provider before stopping or changing any medicines or treatments that they have recommended for you.
Over-the-counter products and medicines
Herbal capsules recalled due to contamination with two drugs
- Vail-Bon Jie Yang Wan Capsules (maker: 123Herbals)
Comment: All lots of this product have been recalled by the maker due to contamination with dexamethasone and chlorpheniramine. Dexamethasone is a steroid medicine that can have serious side effects, including increased blood sugar and blood pressure and reduced function of adrenal glands. Chlorpheniramine is an antihistamine that can cause drowsiness, loss of coordination, or seizures if too much is taken.
Vail-Bon Jie Yang Wan Capsules are sold as a treatment for itchy skin, including eczema.
Antibiotic recalled due to bacterial contamination
- Atovaquone Oral Suspension, 750mg/mL (distributor: Biopharma Inc.)
Comment: The distributor of this antibiotic has recalled one lot due to contamination with Cohnella bacteria. Taking this medicine could cause a serious or even life-threatening infection, especially among people with a weakened immune system.
Atovaquone is prescribed to prevent or treat a rare type of pneumonia caused by the fungus Pneumocystis jirovecii.
Prescription medicines
FDA warning about medicine for menopausal hot flashes
- Veozah (fezolinetant), 45 mg (maker: Amneal Pharmaceuticals, LLC)
Comment: The FDA released a warning about rare liver injury due to Veozah because a patient reportedly developed severe liver disease after taking Veozah for more than a month. Anyone taking Veozah who develops signs or symptoms of liver disease (such as fatigue, nausea, or yellowing of the skin or whites of the eyes) should stop taking the medicine and seek medical care. In addition, health care providers are urged to monitor liver tests before and during treatment.
Veozah was approved in May 2023 as a nonhormonal treatment for hot flashes due to menopause.
Read additional issues of HHP Medication Safety Watch
Disclaimer:
As a service to our readers, Harvard Health Publishing provides access to our library of archived content. Please note the date of last review or update on all articles.
No content on this site, regardless of date, should ever be used as a substitute for direct medical advice from your doctor or other qualified clinician.
Coping with chronic pain, depression, and high blood pressure
Can you prevent the hunched back of kyphosis?
What is ventricular bigeminy?
Emojis in electronic health records could be confusing
Doing different types of exercise linked to a longer life
CPR on TV may be misleading
How gum disease may raise heart disease risk
FDA approves nasal spray to treat rapid heart rhythm
Smart watch may improve detection of atrial fibrillation
4 keys to a heart-healthy diet
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