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Case study provided by: Arvind Madan, MD - Nephrology Associates of Central Florida, Orlando, Florida
This case study is provided for general medical education purposes only and is not a substitute for independent clinical medical judgment. The intent of this case study is to present the experience of an individual patient, which may not represent outcomes in the overall patient population. Response to treatment may vary from patient to patient.
A 36-year-old woman presenting with edema and fatigue for the last 6 weeks
Treatment history
Results after a 6-month treatment regimen that included Acthar Gel*:
UPCR=urine protein/creatinine ratio.
*Overall treatment included Acthar Gel, torsemide, and lisinopril.
Clinical outcomes may not be solely attributable to
Acthar Gel.
Commonly reported postmarketing
adverse reactions for Acthar include injection site
reaction, asthenic conditions (including fatigue,
malaise, asthenia, and lethargy), fluid retention
(including peripheral swelling), insomnia, headache,
and blood glucose increased.
Dosage should be
individualized according to the medical condition of
each patient. Frequency and dose of the drug should be
determined by considering the severity of the disease
and the initial response of the patient.
Sudden
withdrawal of Acthar Gel after prolonged use may lead
to adrenal insufficiency or recurrent symptoms. It may
be necessary to taper the dose and increase the
injection interval to gradually discontinue the
medication.
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