The Checkup by Singlecare

AUGUST 6, 2024

Remicade: Key differences Remicade, made by the pharmaceutical company Janssen Biotech, was approved by the Food and Drug Administration (FDA) in 1998. According to the FDA , most biologics are complex mixtures that cannot be easily characterized or identified. They are also FDA approved for the same indications.

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The Checkup by Singlecare

APRIL 16, 2024

Avoid live vaccines while taking Stelara. Some examples of live vaccines include the measles, mumps, and rubella (MMR) vaccine, varicella, rotavirus, and nasal flu vaccine. You also should not receive a BCG vaccine (a type of tuberculosis vaccine) while taking Stelara or one year before and after taking Stelara.

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The Checkup by Singlecare

APRIL 3, 2024

BCPS, Lead Clinical Pharmacy Specialist at KSP Specialty Pharmacy. Keep up-to-date on vaccines as recommended by your provider. Herbal supplements are not regulated by the FDA, so the full extent of interactions with drugs like prednisone is unknown. These medications may interfere with prednisone.

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The Checkup by Singlecare

SEPTEMBER 10, 2024

It is approved by the Food and Drug Administration (FDA) to treat plaque psoriasis , psoriatic arthritis , Crohn’s disease , and ulcerative colitis. According to the FDA , biological products are complex medicines made from living cells, like those from plants or animals. Wezlana (ustekinumab-auub) was FDA approved on Oct.

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The Checkup by Singlecare

JUNE 7, 2024

Humira: Conditions treated Cyltezo and Humira are both approved by the Food and Drug Administration (FDA) for the same uses, although the ages for use vary for some indications. Cyltezo has the same FDA-approved uses as Humira, except Cyltezo is only FDA-approved for use in adults for ulcerative colitis, hidradenitis suppurativa, and uveitis.

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Vaccines Insurance FDA Insurance Coverage 52

PQA

DECEMBER 15, 2022

PQA is developing a set of standard pharmacy performance measures suitable for assessing pharmacy performance and for use in value-based arrangements (VBAs). State-specific and practice-specific variabilities hinder pharmacists’ ability to move the needle on outcomes of care related to immunizations.

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The Checkup by Singlecare

SEPTEMBER 13, 2024

The Food and Drug Administration (FDA) has approved Fasenra for maintenance treatment of severe asthma. Nucala has a more robust array of indications and has been FDA approved to treat severe eosinophilic asthma, eosinophilic granulomatosis with polyangiitis (EGPA), hypereosinophilic conditions, and rhinosinusitis with nasal polyps.

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