heparin sodium hospira

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PRODUCT MONOGRAPH HEPARIN SODIUM INJECTION

Heparin Sodium Injection is supplied syringes that contain a concentrated dose of 5000 units per syringe. Fatal hemorrhages have occurred in pediatric patients due to medication errors in which 1 mL Heparin Sodium Injection vials were confused with 1 mL "catheter lock flush" vials.

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HIGHLIGHTS OF PRESCRIBING INFORMATION

Intravenous solutions with heparin sodium (derived from porcine intestinal mucosa) are sterile, nonpyrogenic fluids for intravenous administration. Each 100 mL contains heparin sodium 200 USP Units; sodium chloride, 0.9 g; citric acid, monohydrate, 40 mg and dibasic sodium phosphate, heptahydrate, 434 mg added as buffers.

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Sterile Injectable Medication

Pfizer Alternate Site brings its customers the same diverse product portfolio as Pfizer Injectables with the added knowledge and local, personalized service that only 25+ years of dedication to alternate sites of care, and an extensive network of professionals, can provide.. For more information, email Pfizer Alternate Site at [email protected].

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Hospira Heparin Sodium, 1,000 USP Heparin Units/500 mL In

Sep 16, 2014Hospira Heparin Sodium, 1,000 USP Heparin Units/500 mL In 0.9% Sodium Chloride Injection, Recalled: AttorneyOne Monitors and Keeps Consumers Informed Share Article On September 12, Hospira, Inc. announced the recall of one lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL due to particulate matter.

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Heparin Sodium (by Hospira, Inc.)

Oral anticoagulants: Heparin sodium may prolong the one-stage prothrombin time. Therefore, when heparin sodium is given with dicumarol or warfarin sodium, a period of at least 5 hours after the last intravenous dose should elapse before blood is drawn if a valid PROTHROMBIN time is to be obtained.

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Heparin Sodium Injection USP 5,000 Units, 10mL # 00409

Heparin Sodium Injection USP 5,000 Units, 10mL. Multiple Dose Glass Fliptop Vial Non-DEHP Latex Free: Latex Information: Natural rubber latex has not been used in the manufacture of this device or drug container closure system Manufacturer: Hospira . View Link / View MSDS

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heparin sodium

Protamine, a strongly basic compound, forms complexes with heparin sodium or heparin calcium, which are acidic compounds. Formation of this complex can result in disruption of the heparin-antithrombin III complex responsible for the anticoagulant activity of heparin. Protamine is used therapeutically to reverse the activity of heparins.

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Heparina Sodica Hospira Price Comparison: Uses, Dosage

Heparina Sodica Hospira is an anticoagulant that prevents the formation of blood clots. Heparina Sodica Hospira flush is used to flush (clean out) an intravenous (IV) catheter, which helps prevent blockage in the tube after you have received an IV infusion. Heparina Sodica Hospira flush should not be used to treat or prevent blood clots in the body.

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Heparin (Heparin): Side Effects, Interactions, Warning

May 11, 2018Heparin Sodium Injection, USP is a sterile, nonpyrogenic solution of heparin sodium (derived from porcine intestinal mucosa) in water for injection. Each container contains 10000, 12500, 20000 or 25,000 USP Heparin Units; 40 or 80 mg sodium chloride added to render isotonic (see HOW SUPPLIED section for various sizes and strength).

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Sterile Injectable Medication

Pfizer Alternate Site brings its customers the same diverse product portfolio as Pfizer Injectables with the added knowledge and local, personalized service that only 25+ years of dedication to alternate sites of care, and an extensive network of professionals, can provide.. For more information, email Pfizer Alternate Site at [email protected].

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Heparin Sodium

Heparin Sodium - USP method Introduction Heparin is a highly sulfated glycosaminoglycan widely used as an injectable anticoagulant. Phar-maceutical grade heparin is derived from mucosal tissues of slaughtered meat animals such as porcine (pig) intestines or bovine (cattle) lungs.

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Heparin (Heparin): Side Effects, Interactions, Warning

May 11, 2018Heparin Sodium Injection, USP is a sterile, nonpyrogenic solution of heparin sodium (derived from porcine intestinal mucosa) in water for injection. Each container contains 10000, 12500, 20000 or 25,000 USP Heparin Units; 40 or 80 mg sodium chloride added to render isotonic (see HOW SUPPLIED section for various sizes and strength).

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URGENT: Important Safety Information

Hospira, a Pfizer company (Hospira) is issuing this Important Safety Information Letter to alert Health Care Providers to the potential of cracked needle hubs and particulate in multiple products manufactured in the Carpuject™ Luer Lock Glass Syringe Products ("Carpuject syringe ") currently in your control listed in Table 1. Table 1.

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Anticoagulant Heparin Sodium 1,000U / mL, 25X10mL NDC

Product Description. Anticoagulant Heparin Sodium 1,000U / mL Subcutaneous or IV Use Injection Vial 10mL HOSPIRA Anticoagulant Heparin Sodium STRENGTH 1000 U/ML, 10 ML/VIAL, 25 VIALS/PACK. THIS ITEM WOULD BE SOLD ONLY TO SPECIALISTS WITH VALID MEDICAL ( DEA ) LICENSE AND IS NOT RETURNABLE.

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Drug Information on Heparin Sodium

Intravenous solutions with heparin sodium (derived from porcine intestinal mucosa) are sterile, nonpyrogenic fluids for intravenous administration. Each 100 mL contains heparin sodium 200 USP Units; sodium chloride, 0.9 g; citric acid, monohydrate, 40 mg and dibasic sodium phosphate, heptahydrate, 434 mg added as buffers.

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Heparin products

Heparin products. The TGA has completed its testing of heparin sodium products currently distributed in Australia by Astra Zeneca, Hospira, Pfizer and Baxter. Only Astra Zeneca's heparinised saline product has been found to contain this contaminant. Astra Zeneca has recalled affected batches.

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MATERIAL SAFETY DATA SHEET Product Name: Heparin Lock

Active Ingredient Name Heparin Sodium Chemical Formula Heparin is an acidic, polymeric mucopolysaccharide composed of units of glucuronic acid and sulfated glucosamine Preparation Non-hazardous ingredients include Water for Injection. Hazardous ingredients present at less than 1% include sodium chloride, edetate disodium and benzyl alcohol; sodium hydroxide is used to adjust the pH.

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HEPARIN SODIUM INJECTION (heparin sodium)

HEPARIN SODIUM INJECTION (heparin sodium) This product information is intended only for residents of the United States. for Health Care Professionals: HEPARIN SODIUM INJECTION U.S. Physician Prescribing Information. Heparin Sodium Injection – Vials U.S. Physician Prescribing Information.

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Hospira

Sodium thiopental production. Sodium thiopental is an anesthetic discovered by Abbott Laboratories in the 1930s. Hospira manufactured the drug after splitting off from Abbott under the brand name Pentothal. The WHO considers it an essential drug. However, it is also used as part of

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Heparin Sodium (by Hospira, Inc.)

Oral anticoagulants: Heparin sodium may prolong the one-stage prothrombin time. Therefore, when heparin sodium is given with dicumarol or warfarin sodium, a period of at least 5 hours after the last intravenous dose should elapse before blood is drawn if a valid PROTHROMBIN time is to be obtained.

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DailyMed

HEPARIN SODIUM IN 0.45% SODIUM CHLORIDE INJECTION is a sterile preparation of heparin sodium (derived from porcine intestinal mucosa) for intravenous administration. It contains no bacteriostatic or antimicrobial agent or added buffer. The solution may contain sodium hydroxide and/or hydrochloric acid for pH adjustment.

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Recall: Hospira Heparin Sodium

Recall: Hospira Heparin Sodium On 2014-09-11, the FDA announced that Hospira is conducting a recall on Heparin Sodium due to possible contamination with foreign matter . The recalled products were sold under the brand name(s) Hospira from June 2014 to August

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Hospira, Inc.

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Heparin Sodium Monograph for Professionals

Oct 23, 2017Hospira, Inc. Intravenous solutions with heparin sodium injection (12,500 USP heparin units/250 mL, 25,000 USP heparin units/500 mL, or 25,000 USP heparin units/250 mL of heparin sodium in 0.45% sodium chloride injection) prescribing information.

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Heparin Hospira Price Comparison: Uses, Dosage, Form

Heparin Hospira is an anticoagulant that prevents the formation of blood clots. Heparin Hospira flush is used to flush (clean out) an intravenous (IV) catheter, which helps prevent blockage in the tube after you have received an IV infusion. Heparin Hospira flush should not be

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Heparin SODIUM Vial

How to use Heparin SODIUM Vial. This medication is given by injection into a vein or under the skin as directed by your doctor. Do not inject this medication into a muscle. The dosage and how often you use it are based on your medical condition, weight, and response to

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HEPARINA HOSPIRA Sol. iny. 1%

HEPARIN SODIUM HOSPIRA CONCENTRATE solution for injection 10 000 IU/5 ml HEPARIN SODIUM HOSPIRA PRESERVATIVE FREE solution for injection 5 000 IU/0.5 ml HEPARIN SODIUM HOSPIRA solution for injection 1 000 IU/1 ml HEPARIN SODIUM HOSPIRA solution for injection 10 000 IU/1 ml

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FDA update on heparin recall

Hospira and B. Braun also supply some heparin sodium for injection: Hospira in single-use syringes, vials and bags and B. Braun in pre-mixed bags for infusion. There are other FDA approved anticoagulants, including low molecular weight heparins and direct thrombin inhibitors; however, these products are not approved for use in all the same clinical settings as heparin.

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Hospira recalls heparin vials due to contamination with

Sep 14, 2014Hospira, Inc., is recalling one lot of its blood thinner Heparin after confirming that a piece of human hair was found floating in a sealed vial. The nationwide user-level recall involves one lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL) in 0.9 percent Sodium Chloride Injection, 500 mL, NDC 0409-7620-03 Lot 41-046-JT with expiration date of 01NOV 2015.

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Anticoagulant Heparin Sodium 1,000U / mL, 25X10mL NDC

Anticoagulant Heparin Sodium 1,000U / mL Subcutaneous or IV Use Injection Vial 10mL HOSPIRA Anticoagulant Heparin Sodium STRENGTH 1000 U/ML, 10 ML/VIAL, 25 VIALS/PACK. THIS ITEM WOULD BE SOLD ONLY TO SPECIALISTS WITH VALID MEDICAL ( DEA )

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