Slow the Flow – Managing Diarrhea in the Outpatient Setting
A Case of IBS-D
This podcast is a case-based discussion around diagnosis and management of chronic diarrhea in the outpatient setting. The conversation between a PCP and an expert will address clinical presentation, differential diagnosis, workup, and treatment of IBS-D.
Advisory Boards for Allergan; Ironwood Pharmaceuticals; Salix Pharmaceuticals, Inc.; Shire; Synergy Pharmaceuticals Inc.; and Takeda Pharmaceutical Company. Speaker’s Bureau for Allergan; GI Health Foundation; Ironwood Pharmaceuticals; Salix Pharmaceuticals, Inc.; Synergy Pharmaceuticals Inc.; and Medscape.
Non-faculty contributors and others involved in the planning, development, and editing/review of the content have no relevant financial relationships to disclose.
pmiCME is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
pmiCME designates this enduring material for a maximum of 0.50 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
pmiCME is accredited by the American Association of Nurse Practitioners as an approved provider of nurse practitioner continuing education. Provider Number 040308.
This program has been approved for 0.50 contact hour of continuing education, which includes 0.26 hour of pharmacology.
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Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.50 Medical Knowledge MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM
Salix Pharmaceuticals, Inc.
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Clinical judgment must guide each clinician in weighing the possible risks, benefits, or contraindications of any diagnostics, interventions or treatments discussed. Clinicians should review manufacturers’ product information and consider these with the recommendations of other authorities when applying the assessment and/or clinical management strategies discussed in this activity to the care of their patients.
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Discussion of Off-Label Uses and Investigational Products
During the course of their presentations, the faculty may mention uses of products that have not been approved in the United States for the indication(s) being discussed. All presenters are instructed to notify participants when they are discussing unapproved uses or investigational agents. In addition, specific slides will include notation of the off-label use or investigational agent being discussed. Views presented related to unapproved uses of products are solely those of the presenter(s) and are not endorsed by pmiCME or DBC Pri-Med, LLC.
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