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Zolazepam

It is around four times the potency of diazepam but it is both water-soluble and un-ionized at physiological pH meaning that its onset is very fast.

Eszopiclone

Eszopiclone was initially approved by the FDA in 2004.[L6769] … One major benefit of eszopiclone is that it is approved by the FDA for the long-term treatment of insomnia.

Ulipristal

The exact mechanism of action for ulipristal is still currently debated, though there is evidence that it functions by inhibiting ovulation.

Soy isoflavones

Desirudin

Common side effects include: Bleeding gums, collection of blood under the skin, coughing up blood, deep, dark purple bruise and difficulty with breathing or swallowing.

Torasemide

[A319] Torasemide was first approved for clinical use by the FDA in 1993.[L5257]

MK-7145

MK-7145 has been used in trials studying the treatment of Hypertension and Renal Insufficiency.

WU-NK-101

WU-NK-101 is an allogeneic CD3-depleted, CD56-enriched activated natural killer-cell product

Melatonin

In mammals, melatonin is produced by the pineal gland. … pineal gland is small endocrine gland, about the size of a rice grain and shaped like a pine cone (hence the name), that is located in the center of the brain (rostro-dorsal to the superior colliculus) but

Tetradecyl hydrogen sulfate (ester)

Sodium tetradecyl sulfate is an anionic surface-active agent which is used for its wetting properties in the industry and is also used in medicine as a blood vessel irritant and sclerosing agent for hemorrhoids and varicose veins . Sodiu...