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2. Vibegron - Wikipedia

   en.wikipedia.org/wiki/Vibegron

   Here vibegron differs from the previous overactive bladder drug mirabegron, which was known to be associated in various drug–drug interactions by inhibiting CYP2D6 or inducing CYP3A4, CYP2D6 and CYP2C9 in the liver. [13] [4] [14] [15] [16] [17]

3. Palopegteriparatide - Wikipedia

   en.wikipedia.org/wiki/Palopegteriparatide

   The US Food and Drug Administration (FDA) prescription label for palopegteriparatide includes warnings for a potential risk of risk of unintended changes in serum calcium levels related to number of daily injections and total delivered dose, serious hypocalcemia and hypercalcemia (blood calcium levels that are too high), osteosarcoma (a rare bone cancer) based on findings in rats, orthostatic ...

4. Empagliflozin/linagliptin - Wikipedia

   en.wikipedia.org/wiki/Empagliflozin/linagliptin

   The most common side effects include urinary infections, nasopharyngitis, and upper respiratory tract infections . [5] [6] The most serious side effects include ketoacidosis (high blood levels of acids called ‘ketoacids’), pancreatitis (inflammation of the pancreas), hypersensitivity (allergic reactions) and hypoglycaemia (low blood sugar levels).

5. Glatiramer acetate - Wikipedia

   en.wikipedia.org/wiki/Glatiramer_acetate

   Glatiramer acetate (also known as Copolymer 1, Cop-1), sold under the brand name Copaxone among others, is an immunomodulator medication used to treat multiple sclerosis. [1] [2] Glatiramer acetate is approved in the United States to reduce the frequency of relapses, but not for reducing the progression of disability.

6. Teriflunomide - Wikipedia

   en.wikipedia.org/wiki/Teriflunomide

   Teriflunomide is an immunomodulatory drug inhibiting pyrimidine de novo synthesis by blocking the enzyme dihydroorotate dehydrogenase. It is uncertain whether this explains its effect on MS lesions. It is uncertain whether this explains its effect on MS lesions.

7. Mirtazapine - Wikipedia

   en.wikipedia.org/wiki/Mirtazapine

   A single 15 mg dose of mirtazapine to healthy volunteers has been found to result in over 80% occupancy of the H 1 receptor and to induce intense sleepiness. [92] After a short period of chronic treatment, however, the H 1 receptor tends to sensitize and the antihistamine effects become more tolerable. Many patients may also dose at night to ...