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FDA Alerts

Alopecia Areata, blad head
FDA Alerts
07/30/2024
The FDA has approved deuruxolitinib (LEQSELVI) 8 mg tablets for the treatment of adults with severe alopecia areata, a condition affecting approximately 300,000 individuals in the United States.
The FDA has approved deuruxolitinib (LEQSELVI) 8 mg tablets for the treatment of adults with severe alopecia areata, a condition affecting approximately 300,000 individuals in the United States.
The FDA has approved...
07/30/2024
The Dermatologist
Atopic dermatitis
FDA Alerts
07/09/2024
The US Food and Drug Administration has approved roflumilast cream 0.15% for the treatment of mild to moderate atopic dermatitis in adults and children aged 6 and older.
The US Food and Drug Administration has approved roflumilast cream 0.15% for the treatment of mild to moderate atopic dermatitis in adults and children aged 6 and older.
The US Food and Drug...
07/09/2024
The Dermatologist
AD
FDA Alerts
06/15/2024
Riya Gandhi, MA, Associate Editor
The US Food and Drug Administration has approved a new Adbry (tralokinumab-ldrm) 300 mg single-dose autoinjector, offering a new administration option for adult patients with moderate-to-severe atopic dermatitis.
The US Food and Drug Administration has approved a new Adbry (tralokinumab-ldrm) 300 mg single-dose autoinjector, offering a new administration option for adult patients with moderate-to-severe atopic dermatitis.
The US Food and Drug...
06/15/2024
The Dermatologist
Actinic Keratosis
FDA Alerts
06/11/2024
Riya Gandhi, MA, Associate Editor
The US Food and Drug Administration (FDA) has recently approved an expansion for the use of Klisyri (tirbanibulin) to treat actinic keratosis (AK) on larger areas of the face or scalp, up to 100 cm².
The US Food and Drug Administration (FDA) has recently approved an expansion for the use of Klisyri (tirbanibulin) to treat actinic keratosis (AK) on larger areas of the face or scalp, up to 100 cm².
The US Food and Drug...
06/11/2024
The Dermatologist
Atopic Derm
FDA Alerts
01/19/2024
Riya Gandhi, MA, Associate Editor
The US FDA has approved an update to the label for Dupixent (dupilumab) for atopic dermatitis for patients ages 12 years and older with AD and uncontrolled moderate to severe involvement of the hands and/or feet.
The US FDA has approved an update to the label for Dupixent (dupilumab) for atopic dermatitis for patients ages 12 years and older with AD and uncontrolled moderate to severe involvement of the hands and/or feet.
The US FDA has approved an...
01/19/2024
The Dermatologist
atopic dermatitis
FDA Alerts
12/18/2023
Jessica Garlewicz, Digital Managing Editor
The US Food and Drug Administration recently announced approval of tralokinumab-ldrm (Adbry) to include pediatric patients aged 12 to 17 years with moderate to severe atopic dermatitis.
The US Food and Drug Administration recently announced approval of tralokinumab-ldrm (Adbry) to include pediatric patients aged 12 to 17 years with moderate to severe atopic dermatitis.
The US Food and Drug...
12/18/2023
The Dermatologist
 Roflumilast Topical Foam
FDA Alerts
12/18/2023
Jessica Garlewicz, Digital Managing Editor
As the first drug approved for seborrheic dermatitis with a new mechanism of action in over 2 decades, roflumilast foam, 0.3% is indicated for treatment of seborrheic dermatitis in adult and pediatric patients.
As the first drug approved for seborrheic dermatitis with a new mechanism of action in over 2 decades, roflumilast foam, 0.3% is indicated for treatment of seborrheic dermatitis in adult and pediatric patients.
As the first drug approved for...
12/18/2023
The Dermatologist
FDA Alerts
11/01/2023
Jessica Garlewicz, Digital Managing Editor
The US Food and Drug Administration recently announced approval of Cosentyx (secukinumab) for the treatment of hidradenitis suppurativa.
The US Food and Drug Administration recently announced approval of Cosentyx (secukinumab) for the treatment of hidradenitis suppurativa.
The US Food and Drug...
11/01/2023
The Dermatologist
psoriasis
FDA Alerts
10/19/2023
Jessica Garlewicz, Digital Managing Editor
The US Food and Drug Administration recently announced approval of bimekizumab-bkzx for the treatment of adults with moderate to severe plaque psoriasis.
The US Food and Drug Administration recently announced approval of bimekizumab-bkzx for the treatment of adults with moderate to severe plaque psoriasis.
The US Food and Drug...
10/19/2023
The Dermatologist
FDA Alerts
10/19/2023
Jessica Garlewicz, Digital Managing Editor
The US Food and Drug Administration recently announced approval of nivolumab as an adjuvant treatment for eligible patients with stage IIB or IIC completely resected melanoma.
The US Food and Drug Administration recently announced approval of nivolumab as an adjuvant treatment for eligible patients with stage IIB or IIC completely resected melanoma.
The US Food and Drug...
10/19/2023
The Dermatologist

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