ISPE

MARCH 8, 2023

Identification and Analysis of Contamination Trends Three major recall databases—those of the US FDA, the United Kingdom’s Medicine and Healthcare Products Regulatory Agency (UK MHRA), and Australia’s Therapeutic Goods Administration (TGA)—were searched to assess contamination trends in the past five years.

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The Checkup by Singlecare

JUNE 14, 2024

A 2015 study found that DHA was much better than EPA on the liver health scale, particularly for preventing tissue scarring caused by NAFLD. Milk thistle: This flowering herb contains an active compound called silymarin that has been linked in some studies to protecting liver cells, preventing liver damage, and reducing liver-related deaths.

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Pharmaceutical Technology

OCTOBER 25, 2022

Pharmaceutical companies – and the FDA – are embracing FDCs. From 1990 through 2013, the FDA approved 131 FDC products, on average 5.7 From 1990 through 2013, the FDA approved 131 FDC products, on average 5.7 Between 2010 and the end of 2015, of the 655 New Drug Applications (NDAs) approved by the FDA, 63 were for FDCs.

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pharmaphorum

AUGUST 25, 2021

It’s now globally accessible due to Gilead’s work with a network of generic manufacturers and their ability to sign licensing agreements just days after the US FDA registered its authorisation. When the news was getting out from China, our virologists in San Francisco were already scanning compounds, seeing which ones were the most effective.

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European Pharmaceutical Review

FEBRUARY 14, 2024

The first drug products to achieve biological licence approval (BLA) from the US Food and Drug Administration (FDA) are whole community products derived from human faecal matter and are indicted for Clostridium difficile infection. 2015; 69(1):381–403 5. Leveraging Quorum Sensing to Manipulate Microbial Dynamics. 2021; 19:100306 4.

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The Thyroid Pharmacist

FEBRUARY 17, 2023

After a warning letter from the FDA was issued in July 2020, there was a subsequent debate on whether or not NAC should be sold as a supplement, because it had previously been approved for use as a drug in 1963. NAC’s sulfurous compounds can often cause a “rotten-egg” smell — but that is normal! Nutrition & Metabolism (London).

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The Checkup by Singlecare

JANUARY 11, 2024

Key takeaways | Drug interactions | Food interactions | Other interactions | Avoiding interactions | When to see a doctor Sumatriptan , marketed under the brand name Imitrex, is a triptan approved by the Food and Drug Administration (FDA) for treating migraines , with or without aura. It works by attaching to serotonin receptors in the brain.

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The Checkup by Singlecare

APRIL 4, 2024

According to the United States Food and Drug Administration (FDA), taking Zyrtec with food won’t alter its effectiveness, but it may delay its peak concentration by 1.7 The FDA says Zyrtec’s effects typically last around 24 hours, and according to studies , its elimination half-life is around 8.3 How long does Zyrtec last?

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The Spirit Pharmacist

FEBRUARY 21, 2023

The only FDA approved treatment for post-partum depression is a progesterone analogue that must be delivered over a 60-hour IV infusion and appears mildly efficacious. Hum Psychopharmacol, 2015. How Do Psychedelics Compare to Current Treatment Options? There are a couple notable advantages [1]. Pediatrics, 2012. 130 (3): p.

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The Checkup by Singlecare

FEBRUARY 10, 2024

Studies suggest that certain bioactive compounds in ashwagandha, such as withanolides, may support cognitive function. Regulates blood sugar levels The active compounds in ashwagandha may also influence sugar metabolism and overall blood sugar levels. These functions are key for overall mental health and daily life.

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The Thyroid Pharmacist

SEPTEMBER 20, 2024

Plecanatide : This is one of the newest medications for IBS-C that has been approved by the FDA. Tenapanor : Tenapanor was approved by the FDA in September of 2019 for IBS-C. According to a 2015 research review, 100 milligrams of ginger extract may increase bowel movements. [63] Integr Med (Encinitas). 2020;19(1):32-36. [90]

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European Pharmaceutical Review

SEPTEMBER 25, 2023

NMR relaxation methods distinguish between components (phases or compounds) that have different molecular mobilities For monoclonal antibodies, identification methodologies can employ chromatography, spectroscopy, isoelectric focusing, capillary electrophoresis and peptide mapping techniques. 2015; 35(3): 77-79. Cited 2023Feb].

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The Thyroid Pharmacist

JULY 29, 2022

I’ve seen a number of airborne toxins showing up as frequent triggers/exacerbating factors for my clients’ autoimmune conditions — mold, volatile organic compounds (VOCs), and artificial/synthetic fragrances, in particular. For cleaning products, only compounds need to be identified. Volatile Organic Compounds (VOCs) .

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pharmaphorum

FEBRUARY 26, 2021

Moreover, after the passage of the Orphan Drug Act 1983, the FDA has approved nearly 500 orphan drugs, with 233 of them being approved between the year 2005 and 2015 alone. Nearly 44% of the drug approvals by the CDER in 2019 were related to orphan drugs.

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European Pharmaceutical Review

JANUARY 16, 2023

This also occupies a large resource, given the US Food and Drug Administration (FDA) requirement for double plate checking using a second ‘independent’ person. The FDA is doing this through the publications of Guidance for Industry. This places a continued reliance upon plate reading and the limitations of human vision.

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Pharmaceutical Technology

MAY 18, 2023

These obstacles have prompted the letter from concerned parliamentarians , which urges a return to “commitments to invest in the prevention and control of NTDs”, originally made during the 2015 Elmau Summit. Previous investment in this area has proved fruitful. However, progress has been hindered by financial challenges.

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The Thyroid Pharmacist

SEPTEMBER 8, 2023

In fact, in 2006, the Centers for Disease Control reported that the average American has 116 out of 148 synthetic compounds in their body! A 2015 British study found that medical practices in areas with fluoridated water were twice as likely to have patients with hypothyroidism. [22] Published 2015 Jan 10. 2015;13(1):39-51.

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The Thyroid Pharmacist

OCTOBER 7, 2022

Stevia is a natural sweetener derived from the plant Stevia rebaudiana , or “honey leaf,” which contains the sweet-tasting compounds known as steviol glycosides. Steviol glycosides, which are refined extracts of stevia, are recognized as safe by the Food and Drug Administration (FDA). May 21, 2015. Published 2015 Apr 2.

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The Thyroid Pharmacist

MAY 19, 2023

Many facts that you are going to read below, are based on the insights shared by over 2000 of my clients and readers, whom I surveyed back in 2015. A 2015 study out of England reported that people in an area with fluoridated drinking water were twice as likely as those in a non-fluoridated area to report hypothyroidism. [16]

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The Thyroid Pharmacist

JULY 20, 2023

In 2015, some 80 percent of my clients who took the gut tests that I recommended, tested positive for at least one gut infection!) In fact, a 2015 Polish study found the Epstein-Barr virus in the thyroid cells of 80 percent of people with Hashimoto’s, while controls did not have EBV present in their thyroid gland. [46] In: StatPearls.

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The Thyroid Pharmacist

JULY 14, 2022

Scientists in Bosnia first published this connection in 2015, though I’ve seen it clinically since 2013. (1). In 2015, 35 percent of my clients reported testing positive for Blasto. Berberine contains compounds called alkaloids that have broad-spectrum antimicrobial and antiparasitic properties. (33). Published 2015 Jul 30.

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ISPE

SEPTEMBER 11, 2023

Examples include platforms as small as autonomous units placed within a facility and mobile production trailers for compounding to platforms as large as a prefabricated, self-contained GMP facility. 1 May 2015. Journal of Biotechnology 213 (2015):120–30. Rockville, MD: US Pharmacopeial Convention, 2015. 12 April 2016.

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The Thyroid Pharmacist

JANUARY 6, 2023

This medication is also FDA-approved for smoking cessation. Beyond antidepressants, I’ve seen other mood-altering drugs being used for refractory depression (depression that doesn’t respond to medication treatment), some “off-label,” others with FDA approval. Published 2015 Jul 23. 2015;7(8):6055-6072. doi:10.3390/nu7085270.

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The Thyroid Pharmacist

JUNE 14, 2023

A 2015 case report documented the thyroid labs of a man who had recurrent hyperthyroid episodes after three of his wife’s pregnancies! In fact, in 2006, the Centers for Disease Control reported that the average American has 116 out of the 148 commonly tested synthetic compounds in their body. January 8, 2015. 2015;2015:940241.

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Pharmaceutical Technology

OCTOBER 10, 2022

The company plans to submit a request for advice from the FDA at the end of this year or the start of 2023, he adds. In 2015, the FDA approved Sprout Pharmaceuticals’s Addyi, also known under the generic name flibanserin, for use by pre-menopausal women with hypoactive sexual desire disorder (HSDD).

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The Thyroid Pharmacist

JANUARY 20, 2023

In 1998, the Food and Drug Administration (FDA) defined an adaptogen as a new kind of metabolic regulator that has been proven to help in environmental adaptation and to prevent external harms. A 2015 study published in Endokrynologia Polska found the Epstein-Barr virus in the thyroid cells of 80 percent of people with Hashimoto’s and 62.5

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