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Seizures have been reported during treatment with doripenem (see section 6.2). In clinical trials, doripenem-treated patients with pre-existing central nervous system (CNS) disorders (e.g. stroke or history of seizures), patients with compromised renal function and patients given doses greater than 500 mg every 8 hours appear to be at greater risk for developing seizures </small> | Seizures have been reported during treatment with doripenem (see section 6.2). In clinical trials, doripenem-treated patients with pre-existing central nervous system (CNS) disorders (e.g. stroke or history of seizures), patients with compromised renal function and patients given doses greater than 500 mg every 8 hours appear to be at greater risk for developing seizures </small> | ||
<ref>https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/022106s012lbl.pdf</ref> | <ref>https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/022106s012lbl.pdf</ref> | ||
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==ATC== | ==ATC== | ||
<ref>[https://karmel.miraheze.org/m/6Sy | {| style="background:Ivory; color:black" border=1 cellspacing=1 cellpadding=5 | ||
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[[File:Doripenem_vert1.jpg|292px]] | |||
: [[wikipedia:doripenem|doripenem]] | |||
<ref>[https://www.whocc.no/atc_ddd_index/?code=J01DH04 J01DH04]</ref></center> | |||
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<ref>[https://karmel.miraheze.org/m/6Sy karmel(miraheze) es:Doripenem]</ref> | |||
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Latest revision as of 21:28, 2 September 2021
Doripenem is a beta-lactam antibiotic agent belonging to the carbapenem group
Seizures have been reported during treatment with doripenem (see section 6.2). In clinical trials, doripenem-treated patients with pre-existing central nervous system (CNS) disorders (e.g. stroke or history of seizures), patients with compromised renal function and patients given doses greater than 500 mg every 8 hours appear to be at greater risk for developing seizures [1] |
ATC
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