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M O S News

'Drug Take Back Day' is Saturday: Check for Leftover Opioids in Your Home

FRIDAY, April 26, 2024 – Each year, thousands of Americans head home after a surgery clutching prescription opioids to help ease post-surgical pain. Trouble is, most won't use all those pills, and...

Prescription Opioids Linked to Increased Risk for Serious Fall Events

TUESDAY, Feb. 20, 2024 – For adults of all ages, especially those aged 85 years or older, prescription opioids are associated with an increased risk for serious fall events, according to a study...

Mom's Opioid Use in Pregnancy Raises Child's Asthma, Eczema Risk

THURSDAY, Jan. 18, 2024 – Fetal exposure to opioids may change a baby's immune system, triggering a rise in risks for eczema and asthma through early childhood, new research shows. Children born to...

Personalized Protocol Cuts Opioid Prescribing After C-Section

TUESDAY, Jan. 2, 2024 – A personalized protocol for opioid prescriptions after cesarean delivery reduces the median morphine milligram equivalents prescribed at discharge, according to a study...

Teen Surgery-Linked Opioid Prescription Rates Stable From 2015 to 2020

TUESDAY, Oct. 10, 2023 – For U.S. adolescents, there was a decrease in opioid prescription rates from 2015 to 2020 for nonsurgical indications, but opioid prescription rates associated with surgery...

Most Patients Seen in Emergency Department for Pain Consume Few Opioids After Discharge

THURSDAY, Sept. 21, 2023 – Opioid prescriptions following emergency department discharge should be adapted to specific acute pain conditions, according to a study presented at the annual European...

FDA Medwatch Alert: Drug Safety Communication: All Opioid Pain Medicines - FDA Updates Prescribing Information to Provide Additional Guidance for Safe Use

ISSUE: The FDA is requiring several updates to the prescribing information for both immediate-release (IR) and extended release/long acting (ER/LA) opioid pain medicines. This includes stating for a...

FDA Medwatch Alert: Bryant Ranch Prepack Inc. Issues Voluntary Nationwide Recall of Morphine Sulfate 30 mg Extended Release and Morphine Sulfate 60 mg Extended-Release Due to Label-Mix Up

June 28, 2022 – Burbank, California, Bryant Ranch Prepack Inc. is voluntarily recalling one lot of Morphine Sulfate 30 mg Extended-Release tablets (Comprised of 10 bottles), and one lot of Morphine S...

FDA Medwatch Alert: Injectable Products by SCA Pharmaceuticals: Recall - Potential Contamination

ISSUE: SCA Pharmaceuticals LLC (“SCA Pharmaceuticals”) is voluntarily recalling various lots of injectable products to the hospital level. There is a potential for the products to contain microbial co...

FDA Medwatch Alert: Opioid Pain or Cough Medicines Combined With Benzodiazepines: Drug Safety Communication - FDA Requiring New Boxed Warnings About Serious Risks and Death

ISSUE: FDA review has found that the growing combined use of opioid medicines with benzodiazepines or other drugs that depress the central nervous system (CNS) has resulted in serious side effects,...

FDA Medwatch Alert: Opioid Pain Medicines: Drug Safety Communication - New Safety Warnings Added to Prescription Opioid Medications

ISSUE: FDA is warning about several safety issues with the entire class of opioid pain medicines. See the FDA Drug Safety Communication for a complete listing. These safety risks are potentially h...

FDA Medwatch Alert: Morphine Sulfate 0.5 mg/mL Preservative Free in 0.9 percent Sodium Chloride by by Pharmakon Pharmaceuticals: Recall - Super-potent Product

ISSUE: FDA is alerting health care professionals of a voluntary recall of morphine sulfate 0.5 mg/mL preservative free in 0.9% sodium chloride, 1 mL syringe, CII, for intravenous use made and...

FDA Medwatch Alert: Compounded Drugs Stored in Becton-Dickinson (BD) 3 ml and 5 ml Syringes: FDA Warning - Do Not Use

ISSUE: FDA is alerting health care professionals not to administer to patients compounded or repackaged drugs that have been stored in 3 milliliter (ml) and 5ml syringes manufactured by...

FDA Medwatch Alert: Meridian Medical Technologies Auto-Injectors: Extension of Expiration Dates

including Auto-Injectors for Atropen (atropine) DuoDote (atropine/pralidoxime chloride) morphine sulfate pralidoxime chloride diazepam   [Posted 11/22/2013] ISSUE: FDA is aware of a disruption in ...

FDA Medwatch Alert: Morphine Sulfate Injection USP, 4 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject by Hospira, Inc: Recall - May Contain More Than Intended Fill Volume

ISSUE: Customer report of two Carpujects syringes containing more than the 1 mL labeled fill volume. Opioid pain medications such as morphine have life-threatening consequences if overdosed. Those...

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