FDA - HealthQuill

Research uncovers significant discrepancies in ingredient labels and presence of banned compounds

US combats new high of animal sedative Tranq, fentanyl, heroin mix

HQ Team July 12, 2023: Xylazine hydrochloride, a sedative used in animals to provide relief from pain, is increasingly being found in the.

by HealthQuill
July 12, 2023
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The FDA has told e-cigarette maker Fontem US, LLC, not to market or distribute its product myblu menthol in the US as it did not provide any “added benefits.”

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FDA bans Fontem US from selling e-cigarette myblu menthol

HQ Team July 11, 2023: The FDA has told e-cigarette maker Fontem US, LLC, not to market or distribute its product myblu menthol.

by HealthQuill
July 11, 2023
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The USFDA has granted a standard approval for Eisai and Biogen's Alzheimer injection, Leqembi —the first treatment to secure the traditional approval, paving the way for wider insurance coverage of the drug.

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USFDA grants green light to Eisai, Biogen’s Alzheimer’s drug Leqembi

HQ Team July 7, 2023: The USFDA has granted a standard approval for Eisai and Biogen’s Alzheimer injection, Leqembi —the first treatment to secure the.

by HealthQuill
July 7, 2023
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Two United States companies have announced that the FDA and the Department of Agriculture have approved their plan to produce and sell lab-grown or cell-cultivated chicken in the US.

Climate Health Medical Pharma

FDA allows two food tech companies to sell laboratory-grown chicken in US

HQ Team June 22, 2023: Two United States companies have announced that the FDA and the Department of Agriculture have approved their plan.

by HealthQuill
June 22, 2023
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British pharmaceutical company, GSK Plc’s vaccine against the respiratory syncytial virus has shown positive data on its efficacy to treat older adults during a phase III stage trial.

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GSK’s RSV vaccine shows positive data on efficacy in older adults

HQ Team June 21, 2023: British pharmaceutical company, GSK Plc’s vaccine against the respiratory syncytial virus has shown positive data on its efficacy.

by HealthQuill
June 21, 2023
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The USFDA has approved Pfizer Inc’s oral Talzenna drug in combination with Xtandi to treat advanced prostate cancer in adult patients, according to a statement.

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Pfizer gets FDA nod for combination drug to treat advanced prostate cancer

HQ Team June 21, 2023: The USFDA has approved Pfizer Inc’s oral Talzenna drug in combination with Xtandi to treat advanced prostate cancer.

by HealthQuill
June 20, 2023
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Indian pharmaceutical company, Lupin Limited, has introduced its thiamine injection in the US market and has got FDA’s ‘no action required’ classification for its domestic facility in the country’s south.

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India’s Lupin unveils thiamine injection in US, receives FDA’s NAR for Vizag unit

HQ Team June 20, 2023: Indian pharmaceutical company, Lupin Limited, has introduced its thiamine injection in the US market and has got FDA’s.

by HealthQuill
June 20, 2023
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Valneva SE, a French vaccine maker, announced that its last-stage trials for its single-shot chikungunya registered a 98.9% vaccination success rate.

Drugs Medical Pharma

France’s Valneva says trial vaccine for chikungunya post 98.9% rate

HQ Team June 13, 2023: Valneva SE, a French vaccine maker, announced that its last-stage trials for its single-shot chikungunya registered a 98.9%.

by HealthQuill
June 13, 2023
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FDA’s advisory panel backs Sanofi, AstraZeneca’s investigational drug for newborns

HQ Team June 9, 2023: An advisory committee of the USFDA has given a “favourable benefit-risk profile” for Sanofi and AstraZeneca’s experimental drug.