<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brownlee S</submitter><funding>Octapharma</funding><pagination>342-348</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9680362</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(4)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Subcutaneous immunoglobulin (SCIG) treatment is generally tolerable, but some patients may experience adverse events to one or more SCIG products. We investigated whether 16.5% Cutaquig&lt;sup>®&lt;/sup> treatment offered a tolerable and safe alternative treatment for immunodeficient patients.&lt;h4>Methods&lt;/h4>A one-year prospective cohort study was conducted at a single center in Ottawa, Canada. Adult immunodeficient patients who reported previous intolerability, adverse events, or other difficulty to other 20% SCIG product(s) were recruited to start on 16.5% Cutaquig&lt;sup>®&lt;/sup>. Treatment tolerability, safety, and quality of life were observed and described.&lt;h4>Results&lt;/h4>Seven out of ten patients tolerated Cutaquig&lt;sup>®&lt;/sup>. There were no serious or severe adverse events </pubmed_abstract><journal>Hematology reports</journal><pubmed_title>Cutaquig&lt;sup>®&lt;/sup> Is Well Tolerated in Immunodeficient Patients Who Did Not Tolerate Other Subcutaneous Immunoglobulin Products.</pubmed_title><pmcid>PMC9680362</pmcid><funding_grant_id>NA</funding_grant_id><pubmed_authors>Cowan J</pubmed_authors><pubmed_authors>Kana'an MF</pubmed_authors><pubmed_authors>Cameron DW</pubmed_authors><pubmed_authors>Allen C</pubmed_authors><pubmed_authors>Brownlee S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cutaquig&lt;sup>®&lt;/sup> Is Well Tolerated in Immunodeficient Patients Who Did Not Tolerate Other Subcutaneous Immunoglobulin Products.</name><description>&lt;h4>Objective&lt;/h4>Subcutaneous immunoglobulin (SCIG) treatment is generally tolerable, but some patients may experience adverse events to one or more SCIG products. We investigated whether 16.5% Cutaquig&lt;sup>®&lt;/sup> treatment offered a tolerable and safe alternative treatment for immunodeficient patients.&lt;h4>Methods&lt;/h4>A one-year prospective cohort study was conducted at a single center in Ottawa, Canada. Adult immunodeficient patients who reported previous intolerability, adverse events, or other difficulty to other 20% SCIG product(s) were recruited to start on 16.5% Cutaquig&lt;sup>®&lt;/sup>. Treatment tolerability, safety, and quality of life were observed and described.&lt;h4>Results&lt;/h4>Seven out of ten patients tolerated Cutaquig&lt;sup>®&lt;/sup>. There were no serious or severe adverse events </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T00:35:08.899Z</modification><creation>2025-02-19T04:37:30.316Z</creation></dates><accession>S-EPMC9680362</accession><cross_references><pubmed>36412628</pubmed><doi>10.3390/hematolrep14040048</doi></cross_references></HashMap>