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MarketScreener Homepage  >  Equities  >  Xetra  >  Fresenius SE & Co. KGaA    FRE   DE0005785604


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Fresenius : Kabi Introduces Neostigmine Methylsulfate Injection, USP Simplist Prefilled Syringe in 3 mg per 3 mL Presentation

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06/11/2019 | 10:06am EDT

LAKE ZURICH - Fresenius Kabi announced today the immediate availability in the United States of Neostigmine Methylsulfate Injection, USP in 3 mg per 3 mL Simplist ready-to-administer prefilled syringes.

Fresenius Kabi is a global health company that specializes in medicines and technologies for infusion, transfusion and clinical nutrition.

The Fresenius Kabi Simplist Neostigmine Injection prefilled syringe is the first manufacturer-prepared, ready-to-administer prefilled syringe on the market. Fresenius Kabi has sold Neostigmine Injection, USP in 0.5 mg per 1 mL and 1 mg per 1 mL vial presentations since 2015.

'Fresenius Kabi is pleased to continue the expansion of our convenient Simplist prefilled syringe portfolio,' said John Ducker, president and CEO of Fresenius Kabi USA. 'This is the fourth Simplist product we've introduced this year and represents the strength of our pipeline of important therapies and delivery systems that can help physicians practice more efficiently.'

About Simplist Neostigmine Methylsulfate Injection, USP

Neostigmine Methylsulfate Injection, a cholinesterase inhibitor, is indicated for intravenous use for reversal of the effects of nondepolarizing neuromuscular blocking agents (NMBA) after surgery.

Important Safety Information

An anticholinergic agent, e.g., atropine sulfate or glycopyrrolate, should be administered prior to or concomitantly with neostigmine methylsulfate.

Neostigmine is contraindicated in patients with: Hypersensitivity to neostigmine.

Peritonitis or mechanical obstruction of the urinary or intestinal tracts.

Neostigmine has been associated with bradycardia: Atropine or glycopyrrolate should be administered prior to administration of neostigmine methylsulfate injection to lessen risk of bradycardia.

Coexisting Conditions: Patients with known cardiac disease, cardiac arrhythmias, or recent coronary artery occlusion may be particularly sensitive to the hemodynamic effects of neostigmine; their blood pressure and electrocardiogram should be continuously monitored with the initiation of neostigmine treatment and for a duration sufficient to assure hemodynamic stability.

Neuromuscular Dysfunction: Can occur if large doses of neostigmine methylsulfate are administered when there is minimal neuromuscular blockade; reduce the dose if recovery from neuromuscular blockade is nearly complete.

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.

This Important Safety Information does not include all the information needed to use Neostigmine Methylsulfate Injection, USP safely and effectively.

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.


Lake Zurich

Tel: (847) 550-2300

Email: communications.USA@fresenius-kabi.com

(C) 2019 Electronic News Publishing, source ENP Newswire

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Financials (EUR)
Sales 2019 35 389 M
EBIT 2019 4 676 M
Net income 2019 1 846 M
Debt 2019 20 659 M
Yield 2019 1,85%
P/E ratio 2019 13,1x
P/E ratio 2020 12,0x
EV / Sales2019 1,27x
EV / Sales2020 1,11x
Capitalization 24 163 M
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