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INTEL REMS Cardiovascular Adverse Event Reporting Former Prescribers patients most recent echocardiogram observed signs of valvular heart disease (VHD), pulmonary arterial hypertension (PAH), or other

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How to fill out fintepla rems cardiovascular adverse

01

Obtain the Fintepla REMS (Risk Evaluation and Mitigation Strategy) program materials, including the Prescriber Brochure and the Patient-Prescriber Agreement Form.

02

Review the Prescriber Brochure to understand the potential cardiovascular adverse effects associated with Fintepla.

03

Ensure that the patient meets the criteria for receiving Fintepla according to the updated prescribing information.

04

Discuss the risks and benefits of Fintepla with the patient and obtain informed consent.

05

Complete the Patient-Prescriber Agreement Form with the patient, documenting the discussion of risks and benefits.

06

Submit the completed Patient-Prescriber Agreement Form to the Fintepla REMS program as directed.

07

Monitor the patient for cardiovascular adverse effects while taking Fintepla and report any adverse events to the appropriate authorities.

Who needs fintepla rems cardiovascular adverse?

01

Patients who have been prescribed Fintepla for the treatment of seizures.

02

Healthcare providers who are prescribing Fintepla to patients.

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What is fintepla rems cardiovascular adverse?

Fintepla rems cardiovascular adverse refers to the potential cardiovascular side effects of the medication Fintepla.

Who is required to file fintepla rems cardiovascular adverse?

Healthcare providers who prescribe Fintepla are required to file reports on any cardiovascular adverse events.

How to fill out fintepla rems cardiovascular adverse?

Healthcare providers can fill out the Fintepla REMS cardiovascular adverse event form online or by contacting the manufacturer directly.

What is the purpose of fintepla rems cardiovascular adverse?

The purpose of monitoring Fintepla REMS cardiovascular adverse events is to ensure patient safety and assess any potential risks.

What information must be reported on fintepla rems cardiovascular adverse?

Any cardiovascular adverse events experienced by patients taking Fintepla must be reported, including symptoms, severity, and outcome.

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