lidocaine hydrochloride injection, USP ANSYR, ABBOJECT Other

()

AQUEOUS SOLUTIONS FOR

ACUTE MANAGEMENT OF

VENTRICULAR ARRHYTHMIAS


Ansyr Plastic Syringe

LifeShield Abboject Syringe

Rx only

LIFESHIELD® is the trademark of ICU Medical, Inc. and is used under license.

LAB-1021-3.0

Revised: 04/2018

Find lidocaine hydrochloride injection, USP ANSYR, ABBOJECT medical information:

Find lidocaine hydrochloride injection, USP ANSYR, ABBOJECT medical information:

Our scientific content is evidence-based, scientifically balanced and non-promotional. It undergoes rigorous internal medical review and is updated regularly to reflect new information.

lidocaine hydrochloride injection, USP ANSYR, ABBOJECT Quick Finder

Prescribing Information
Download Prescribing Information

Health Professional Information

Other

AQUEOUS SOLUTIONS FOR

ACUTE MANAGEMENT OF

VENTRICULAR ARRHYTHMIAS


Ansyr Plastic Syringe

LifeShield Abboject Syringe

Rx only

LIFESHIELD® is the trademark of ICU Medical, Inc. and is used under license.

LAB-1021-3.0

Revised: 04/2018

Resources

Didn’t find what you were looking for? Contact us.

MI Digital Assistant

Chat online with Pfizer Medical Information regarding your inquiry on a Pfizer medicine.

Call 800-438-1985*

*Contact Medical Information. 8AM-9PM ET Monday to Friday; excluding holidays.

Medical Inquiry

Submit a medical question for Pfizer prescription products.

Report Adverse Event

Pfizer Safety

To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for this product, adverse events should be reported to your coordinating study site.

If you cannot use the above website, or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at (800) 438-1985.

FDA Medwatch

You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or call (800) 822-7967.