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Tag: fda approval

You Searched For "FDA Approval"
FDA approves ENTADFI, a New Treatment for Benign Prostatic Hyperplasia

FDA approves ENTADFI, a New Treatment for Benign Prostatic Hyperplasia

Hina Zahid16 Dec 2021 9:00 AM IST
MIAMI- Veru Inc. (NASDAQ: VERU) The U.S. Food and Drug Administration (FDA) has approved ENTADFITM for the treatment of urinary tract symptoms caused...
FDA Approves ruxolitinib cream for treatment of Atopic Dermatitis

FDA Approves ruxolitinib cream for treatment of Atopic Dermatitis

Dr Kartikeya Kohli22 Sept 2021 9:30 PM IST
The US food and drug administration has approved a topical selective Janus kinase (JAK)1/JAK2 inhibitor ruxolitinib (Opzelura) for the treatment of...
In a first, Pfizer-BioNTech COVID-19 vaccine receives full FDA approval

In a first, Pfizer-BioNTech COVID-19 vaccine receives full FDA approval

Hina Zahid25 Aug 2021 8:30 AM IST
The vaccine was found to be 91% effective in preventing COVID-19 disease.USA: The U.S. Food and Drug Administration has approved the Pfizer-BioNTech...
FDA expands approval to DALVANCE for Treatment of Acute Bacterial Skin Infections in kids

FDA expands approval to DALVANCE for Treatment of Acute Bacterial Skin Infections in kids

Hina Zahid28 July 2021 3:15 PM IST
The U.S. Food and Drug Administration (FDA) has approved DALVANCE (dalbavancin) for the treatment of acute bacterial skin and skin structure...
FDA approves spinal cord stimulation device for patients with painful diabetic neuropathy

FDA approves spinal cord stimulation device for patients with painful diabetic neuropathy

Dr. Kamal Kant Kohli21 July 2021 6:00 PM IST
USA: The Food and drugs administration has approved first spinal cord stimulation device (HFX) for painful diabetic neuropathy (PDN). The device is...
Enfortumab vedotin-ejfv receives FDA approval and expanded indication for urothelial cancer

Enfortumab vedotin-ejfv receives FDA approval and expanded indication for urothelial cancer

Medha Baranwal14 July 2021 12:00 AM IST
USA: Padcev (enfortumab vedotin-ejfv) has received the FDA's (Food and Drug Administration) regular approval for the treatment of adults with locally...
FDA approves secnidazole for  treatment of trichomoniasis in adults

FDA approves secnidazole for treatment of trichomoniasis in adults

Dr. Kamal Kant Kohli2 July 2021 9:02 AM IST
The U.S Food and drug administration (FDA) has approved an expanded indication for SOLOSEC (secnidazole) to include the treatment of trichomoniasis in...
First treatment for hypoplasminogenemia receives FDA approval

First treatment for hypoplasminogenemia receives FDA approval

Hina Zahid8 Jun 2021 10:40 AM IST
USA: The U.S. Food and Drug Administration approved Ryplazim (plasminogen, human-tmvh) for the treatment of patients with plasminogen deficiency type...
Alzheimers drug Aduhelm receives FDAs accelerated approval

Alzheimer's drug Aduhelm receives FDA's accelerated approval

Hina Zahid8 Jun 2021 10:32 AM IST
USA: Aduhelm (aducanumab) has received the US FDA's accelerated approval for the treatment of Alzheimer's disease. Aduhelm was approved using...
Myfembree receives FDA approval for uterine fibroids associated heavy menstrual bleeding

Myfembree receives FDA approval for uterine fibroids associated heavy menstrual bleeding

Hina Zahid29 May 2021 7:15 AM IST
USA: The Food and Drug Administration (FDA) has approved Myfembree, a once-a-day therapy for managing heavy menstrual bleeding associated with...
FDA approves first immunotherapy for treatment of gastric cancer

FDA approves first immunotherapy for treatment of gastric cancer

Dr. Kamal Kant Kohli17 April 2021 7:45 AM IST
The U.S. Food and Drug Administration has approved first immunotherapy for the first-line treatment of gastric cancer. Opdivo (nivolumab), in...
FDA approves cellular gene therapy for refractory multiple myeloma

FDA approves cellular gene therapy for refractory multiple myeloma

Dr Satabdi Saha5 April 2021 10:53 AM IST
In a recent development,FDA has given a nod to the first gene therapy for patients of relapsed or refractory multiple myeloma who have received at...
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