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Review of Pharmacology - 9E (2015)

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<strong>Review</strong> <strong>of</strong> <strong>Pharmacology</strong><br />

New Drugs<br />

722<br />

28. Avasimibe: Hypolipidemic drug acting as ACAT- 1 inhibitor.<br />

29. Aviptadil: VIP analog useful for erectile dysfunction.<br />

30. Axitinib: It inhibits receptor tyrosine kinases including vascular endothelial growth factor receptors (VEGFR)-1,<br />

VEGFR-2, and VEGFR-3. It is specifically approved for the oral treatment <strong>of</strong> advanced renal cell carcinoma after failure<br />

<strong>of</strong> one prior systemic therapy.<br />

31. Azilsartan medoxomil: An angiotensin II receptor blocker (ARB) for the treatment <strong>of</strong> hypertension.<br />

32. Basiliximab and Daclizumab: Monoclonal antibodies used as immunosuppressants.<br />

33. Bazedoxifene: It is a selective estrogen receptor modulator (SERM) indicated for the treatment <strong>of</strong> moderate to severe<br />

vasomotor symptoms associated with menopause and the prevention <strong>of</strong> postmenopausal osteoporosis in combination<br />

with estrogen.<br />

34. Bedaquiline: An inhibitor <strong>of</strong> mycobacterial ATP synthase indicated as a part <strong>of</strong> combination therapy in adults with<br />

pulmonary MDR and XDR tuberculosis. It ncreases QT interval and thus should not be combined with any other drug<br />

causing QT prolongation.<br />

35. Belatacept: It is a a selective T-cell (lymphocyte) costimulation blocker It binds to CD 80 and CD 86 on antigen-presenting<br />

cells, thereby blocking CD 28 mediated costimulation <strong>of</strong> T lymphocytes. It is specifically indicated for the prophylaxis <strong>of</strong><br />

organ rejection in adult patients receiving a kidney transplant. It is approved for use in combination with basiliximab<br />

induction, mycophenolate m<strong>of</strong>etil, and corticosteroids.<br />

36. Belimumab: It is a B-lymphocyte stimulator (BLyS)-specific inhibitor indicated for the treatment <strong>of</strong> adult patients with<br />

active, autoantibody-positive, systemic lupus erythematosus.<br />

37. Bendamustine: A purine alkylator hybrid chemotherapy agent indicated for the treatment <strong>of</strong> patients with chronic<br />

lymphocytic leukemia (CLL) and relapsed indolent non-Hodgkin’s lymphoma.<br />

38. Beractant and Poractant: Surfactants for neonatal RDS.<br />

39. Besifloxacin ophthalmic suspension: A topical quinolone antimicrobial for the treatment <strong>of</strong> bacterial conjunctivitis,<br />

commonly referred to as “pink eye”.<br />

40. Bevacizumab: A monoclonal antibody against vascular endothelial growth factor (VEGF) used as angiogenesis inhibitor<br />

recently approved for glioblastomas and metastatic renal cell carcinoma. It is also indicated for treatment <strong>of</strong> metastatic<br />

colorectal cancer.<br />

41. Bicalutamide and Nilutamide: Androgen receptor blockers similiar to flutamide for prostate cancer.<br />

42. Bimatoprost: Indicated for the treatment <strong>of</strong> hypotrichosis (or reduced amount <strong>of</strong> hair) <strong>of</strong> the eyelashes Growth <strong>of</strong> the<br />

eyelashes is a well documented side effect <strong>of</strong> bimatoprost which is currently approved for the treatment <strong>of</strong> glaucoma.<br />

43. Bortezomib: Proteosome inhibitor useful in refractory and relapsing multiple myeloma. Protoesome normally inhibits<br />

the apoptosis and inhibition <strong>of</strong> this protein by bortezmib results in accelerated apoptosis.<br />

44. Bosentan and sitaxentan: Endothelin receptor antagonists useful for primary pulmonary hypertension.<br />

45. Bosutinib: It is specifically indicated for the treatment <strong>of</strong> adults with chronic, accelerated, or blast phase Philadelphia<br />

chromosome-positive (Ph+) chronic myelogenous leukemia with resistance or intolerance to prior therapy. It inhibits<br />

the Bcr-Abl kinase that promotes CML amd also inhibits the Src-family kinases.<br />

46. Brentuximab vedotin: It is a CD 30-directed antibody-drug conjugate (ADC) consisting <strong>of</strong> three components: 1) the<br />

chimeric IgG 1 antibody cAC10, specific for human CD 30, 2) the microtubule disrupting agent monomethyl auristatin E<br />

(MMAE) and 3) a protease-cleavable linker that covalently attaches MMAE to cAC 10. Brentuximab vedotin is designed<br />

to be stable in the bloodstream, but to release MMAE upon internalization into CD-30 expressing tumor cells, resulting<br />

in a targeted cell-killing effect It is specifically approved for 1) Hodgkin lymphoma after failure <strong>of</strong> autologous stem cell<br />

transplant (ASCT) or after failure <strong>of</strong> at least two prior multi-agent chemotherapy regimens in patients who are not ASCT<br />

candidates and 2) systemic anaplastic large cell lymphoma after failure <strong>of</strong> at least one prior multi-agent chemotherapy<br />

regimen It is administered intravenously.<br />

47. Brimonidine: An alpha-2 adrenergic agonist with potent vasoconstrictive activity. Its once daily topical gel formulation<br />

is specifically indicated for the topical treatment <strong>of</strong> persistent (nontransient) erythema <strong>of</strong> rosacea in adults 18 years <strong>of</strong><br />

age or older.<br />

48. Cabazitaxel: A microtubule inhibitor indicated in combination with prednisone for treatment <strong>of</strong> patients with hormonerefractory<br />

metastatic prostate cancer.<br />

49. Cabozantinib: It is a tyrosine kinase inhibitor approved for treatment <strong>of</strong> patients with progressive, metastatic medullary<br />

thyroid cancer. It acts as a small molecule inhibitor <strong>of</strong> the tyrosine kinases activated by c-Met and VEGFR2, and has been<br />

shown to reduce tumor growth, metastasis, and angiogenesis.<br />

50. Calcitriol Ointment: Vitamin D analog indicated for the topical treatment <strong>of</strong> mild to moderate plaque psoriasis in adults<br />

18 years and older.<br />

51. Canagliflozin: A sodium-glucose co-transporter 2 (SGLT2) inhibitor. Inhibiting SGLT2 is believed to reduce blood<br />

glucose levels by increasing the amount <strong>of</strong> glucose excreted in the urine. It is specifically indicated as an adjunct to diet<br />

and exercise to improve glycemic control in adults with type 2 diabetes mellitus.<br />

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