ATGAM® Other

(lymphocyte immune globulin, anti-thymocyte globulin [equine])

Healthcare providers should refer to labels.fda.gov or DailyMed for the most updated version of the labeling.

This product's labeling may have been updated. For the most current prescribing information, please visit www.pfizer.com. For medical information about ATGAM, please visit www.pfizermedinfo.com or call 1-800-438-1985.

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U.S. Govt. License No. 1216

LAB-0019-12.0

Find ATGAM® medical information:

Find ATGAM® medical information:

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ATGAM® Quick Finder

Medication Guide

Health Professional Information

Other

Healthcare providers should refer to labels.fda.gov or DailyMed for the most updated version of the labeling.

This product's labeling may have been updated. For the most current prescribing information, please visit www.pfizer.com. For medical information about ATGAM, please visit www.pfizermedinfo.com or call 1-800-438-1985.

Logo

U.S. Govt. License No. 1216

LAB-0019-12.0

Prescribing Information
Download Prescribing Information

Health Professional Information

Other

Healthcare providers should refer to labels.fda.gov or DailyMed for the most updated version of the labeling.

This product's labeling may have been updated. For the most current prescribing information, please visit www.pfizer.com. For medical information about ATGAM, please visit www.pfizermedinfo.com or call 1-800-438-1985.

Logo

U.S. Govt. License No. 1216

LAB-0019-12.0

Resources

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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.