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Adverse event reporting can be found at the bottom of the page
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Information on how to access prescribing information and adverse event reporting can be found towards the bottom of the page.
In three studies, ATGAM® was administered over 8 or 10 days to a total of 115 patients with moderate-to-severe aplastic anaemia1-3
Dosing regimens consisted of 20 mg/kg for 8 days or 16 mg/kg for 10 daysa
Overall haematological responseb rates for ATGAM®-treated patients were 39–52% at either 3 or 6 months1-3
Survival rates ranged between 50–83% over 1–2 years1-3
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search
for MHRA Yellow Card in Google Play or Apple App Store
Adverse events should also be reported to Pfizer Medical Information on 01304 616161
To access further materials, resources and receive communication about medicines and vaccines promoted by Pfizer.
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These pages are not intended for patients or for members of the general public. The healthcare professional web pages contain promotional content.
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PP-UNP-GBR-7812. January 2024