Fresenius Kabi Expands MicroVault® Packaging to include Simplist® Morphine Sulfate Injection, USP Ready-to-Administer Prefilled Syringes
Simplist MicroVault packaging supports diversion deterrence and secure dispensing of controlled substances
June 23, 2020
LAKE ZURICH, Ill., June 23, 2020 – Fresenius Kabi announced today the availability in the United States of Simplist® Morphine Sulfate Injection, USP 2 mg per 1 mL and 4 mg per 1 mL ready-to-administer prefilled syringes in MicroVault packaging.
MicroVault is next-generation packaging designed and manufactured in the U.S. to support secure dispensing and diversion deterrence with hard plastic packaging and a tamper evident seal. It is also designed to make narcotic inventory management easier with the use of 5-pack bundling and 10-pack cartons.
Fresenius Kabi is a leading producer of generic injectable medicines including a growing U.S. portfolio of prefilled syringes.
“We are focused on designing, developing and introducing products and labeling that support the safe dispensing of all products, but particularly controlled substances,” said John Ducker, president and CEO of Fresenius Kabi USA. “A MicroVault portfolio that now includes morphine is the latest example of our commitment to the secure dispensing of controlled substances.”
MicroVault packaging features include:
- Slim packaging that takes up less room than a blister pack in the locked compartments of automated dispensing cabinets (ADCs).
- A diversion-deterrent polypropylene shell that is rigid and transparent, allowing bar code scanning and visual inspection.
- A twist-to-open cap that facilitates access to the syringe.
Fresenius Kabi’s Simplist prefilled syringes were associated with a four times lower error rate when compared to traditional medication administration practice1, according to a study published in the Journal of Patient Safety in 2018. The Simplist Morphine Sulfate Injection, USP prefilled syringe is manufacturer prepared, with a 24-month shelf life, and is a single unit dose. Learn more about the Simplist® Ready-to-Administer Prefilled Syringe portfolio at www.simplist-us.com.
About Simplist® Morphine Sulfate Injection, USP MicroVault Prefilled Syringe
Produced at the company’s advanced manufacturing center in North Carolina, Simplist® Morphine MicroVault Prefilled Syringe joins Fresenius Kabi’s comprehensive portfolio of securely packaged narcotics.
INDICATIONS AND USAGE
Morphine Sulfate Injection is indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate.
Limitations of Use: Because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses, reserve Morphine Sulfate Injection for use in patients for whom alternative treatment options [e.g., non-opioid analgesics or opioid combination products]: have not been tolerated, are not expected to be tolerated, have not provided adequate analgesia, or are not expected to provide adequate analgesia.
IMPORTANT SAFETY INFORMATION
IMPORTANT SAFETY INFORMATION (cont.)
Morphine Sulfate Injection is contraindicated in patients with: significant respiratory depression, acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment, concurrent use of monoamine oxidase inhibitors (MAOIs) or use of MAOIs within the last 14 days, known or suspected gastrointestinal obstruction, including paralytic ileus, and hypersensitivity to morphine.
Cardiovascular Instability: High doses are excitatory. Have Naloxone Injection and resuscitative equipment immediately available.
Life-Threatening Respiratory Depression in Patients with Chronic Pulmonary Disease or in Elderly, Cachectic, or Debilitated Patients: Monitor closely, particularly during initiation and titration.
Adrenal Insufficiency: If diagnosed, treat with physiologic replacement of corticosteroids, and wean patient off of the opioid.
Severe Hypotension: Monitor during dosage initiation and titration. Avoid use of Morphine Sulfate Injection in patients with circulatory shock.
Risks of Use in Patients with Increased Intracranial Pressure, Brain Tumors, Head Injury, or Impaired Consciousness: Monitor for sedation and respiratory depression. Avoid use of Morphine Sulfate Injection in patients with impaired consciousness or coma.
The most serious adverse reactions encountered are respiratory depression, apnea, circulatory depression, respiratory arrest, shock and cardiac arrest. Common frequently observed adverse reactions include: sedation, lightheadedness, dizziness, nausea, vomiting, constipation and diaphoresis.
To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC, at 1-800-551-7176 option 5 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Overdosage: Acute overdose with Morphine Sulfate Injection can be manifested by respiratory depression, somnolence progressing to stupor or coma, skeletal muscle flaccidity, cold and clammy skin, constricted pupils, and, in some cases, pulmonary edema, bradycardia, hypotension, partial or complete airway obstruction, snoring, and death.
This important safety information does not include all the information needed to use MORPHINE SULFATE INJECTION safely and effectively. Please see prescribing information, including BOXED WARNING, for MORPHINE SULFATE INJECTION at https://tinyurl.com/ya2kz572.
About Fresenius Kabi
Fresenius Kabi (www.fresenius-kabi.com/us) is a global health care company that specializes in medicines and technologies for infusion, transfusion and clinical nutrition. The company’s products and services are used to help care for critically and chronically ill patients. The company’s U.S. headquarters is in Lake Zurich, Illinois. The company’s global headquarters is in Bad Homburg, Germany. To learn about U.S. career opportunities at Fresenius Kabi, visit us at https://www.fresenius-kabi.com/us/join-us.
1Hertig JB, Degnan DD, Scott CR, Lenz JR, Li X, Anderson CM. A comparison of error rates between intravenous push methods: a prospective, multisite, observational study [published online ahead of print September 8, 2017]. J Patient Saf. doi:10.1097/PTS.0000000000000419