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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 />

177. Mifepristone: A small-molecule progesterone and glucocorticoid antagonist has now been approved to control<br />

hyperglycemia secondary to hypercortisolism in adults with endogenous Cushing’s syndrome who have type II<br />

diabetes mellitus or glucose intolerance and have failed surgery or are not candidates for surgery.<br />

178. Milnacipran: Serotonin and norepinephrine reuptake inhibitor indicated for the management <strong>of</strong> fibromyalgia.<br />

179. Miltefosine and Sitamaquine: New drugs for the treatment <strong>of</strong> kala azar.<br />

180. Miltefosine: It possess in vitro activity against the promastigote and amastigote stages <strong>of</strong> Leishmania species. It is<br />

specifically indicated for adults and adolescents >12 years <strong>of</strong> age for oral treatment <strong>of</strong>: visceral leishmaniasis due to<br />

Leishmania donovani, cutaneous leishmaniasis due to Leishmania braziliensis, Leishmania guyanensis, and Leishmania<br />

panamensis and mucosal leishmaniasis due to Leishmania braziliensis<br />

181. Mipomersen: An anti-sense oligonucleotide inhibitor <strong>of</strong> mRNA <strong>of</strong> apolipoprotein B-100 synthesis indicated for the<br />

treatment <strong>of</strong> patients with homozygous familial hypercholesterolemia. It is administered as a weekly injection.<br />

182. Mirabegron: It is a selective beta-3 adrenoceptor (Beta3-AR) agonist. The drug activates Beta3-ARs on the detrusor muscle<br />

<strong>of</strong> the bladder to facilitate filling <strong>of</strong> the bladder and storage <strong>of</strong> urine. It is specifically indicated for the oral treatment <strong>of</strong><br />

overactive bladder (OAB) with symptoms <strong>of</strong> urge urinary incontinence, urgency, and urinary frequency.<br />

183. Mirtazapine: Newer antidepressant drug also known as nor-adrenergic and specific serotonergic antidepressant (NSSA)<br />

It acts by inhibiting presynaptic auto- and hetero-a2 receptors.<br />

184. Mizolastine, Ebastine and Acrivastine: Newer second generation antihistaminics.<br />

185. Moxonidine and Rilmenidine: Longer acting imidazoline receptor agonists (that modulate a2 activity) useful in the<br />

treatment <strong>of</strong> hypertension (similiar to clonidine).<br />

186. Natalizumab: Monoclonal antibody used for the managment <strong>of</strong> multiple sclerosis.<br />

187. Nesiritide: Recombinant BNP useful in CHF.<br />

188. Nikkomycin: Antifungal drug acting via the inhibition <strong>of</strong> chitin synthesis.<br />

189. Obinutuzumab: It is a humanized anti-CD20 monoclonal antibody <strong>of</strong> the IgG1 subclass. It is specifically indicated for use<br />

in combination with chlorambucil for the treatment <strong>of</strong> patients with previously untreated chronic lymphocytic leukemia.<br />

190. Ocriplasmin: It is an alpha-2 antiplasmin reducer. It is a truncated form <strong>of</strong> the natural human protein plasmin. Ocriplasmin<br />

has proteolytic activity against protein components <strong>of</strong> the vitreous body and the vitreoretinal interface, thereby dissolving<br />

the protein matrix responsible for the vitreomacular adhesion. It is specifically indicated for the treatment <strong>of</strong> symptomatic<br />

vitreomacular adhesion by intravitreal injection.<br />

191. Octreotide, Vapreotide, Seglitide and Lanreotide: Long acting somatostatin analogs useful for acromegaly, secretory<br />

diarrhoea and esophageal varices.<br />

192. Ofatumumab: A CD-directed cytolytic monoclonal antibody indicated for the treatment <strong>of</strong> patients with chronic<br />

lymphocytic leukemia.<br />

193. Olopatadine: An antihistamine nasal spray for the treatment <strong>of</strong> symptoms <strong>of</strong> seasonal allergic rhinitis in adults and<br />

adolescents twelve years <strong>of</strong> age and older.<br />

194. Omacetaxine: It is a first-in-class small molecule drug for the treatment <strong>of</strong> adult patients with chronic or accelerated<br />

phase CML. It inhibits protein translation by preventing the initial elongation step <strong>of</strong> protein synthesis. It interacts with<br />

the ribosomal A-site and prevents the correct positioning <strong>of</strong> amino acid side chains <strong>of</strong> incoming aminoacyl-tRNAs.<br />

195. Omapatrilat and Sampatrilat: Vasopeptidase inhibitors (inhibit two enzymes; ACE and NEP) useful in CHF.<br />

196. OnabotulinumtoxinA: Botulinum toxin indicated to prevent headaches in adult patients with chronic migraine To treat<br />

chronic migraines, it is given approximately every 12 weeks as multiple injections around the head and neck to try to dull<br />

future headache symptoms It has not been shown to work for the treatment <strong>of</strong> migraine headaches that occur 14 days or<br />

less per month, or for other forms <strong>of</strong> headache.<br />

197. Oprelvekin: Recombinant IL-11 useful for the treatment and prevention <strong>of</strong> chemotherapy induced thrombocytopenia.<br />

198. Ospemifene: It is a SERM indicated for the treatment <strong>of</strong> moderate to severe dyspareunia (pain during sexual intercourse),<br />

a symptom <strong>of</strong> vulvar and vaginal atrophy due to menopause. It acts similar to estrogen the vaginal epithelium building<br />

vaginal wall thickness which in turn reduces the pain associated with dyspareunia. The boxed warning <strong>of</strong> the medication<br />

indicates that the drug may thicken the endometrium which could lead to unusual bleeding and endometrial cancer.<br />

199. Palifermin: Keratinocyte growth factor for oral mucositis.<br />

200. Paliperidone: Metabolite <strong>of</strong> risperidone developed as a seperate drug for schizophrenia.<br />

201. Palivizumab: Monoclonal antibody used for RSV infections.<br />

202. Pasireotide: An orphan drug approved for the treatment <strong>of</strong> Cushing’s disease in patients who fail or are ineligible<br />

for surgical therapy. It is a somatostatin analog (like octreotide) which has a 40-fold increased affinity to somatostatin<br />

receptor 5 than other somatostatin analogs.<br />

203. Pazopanib: A multitargeted tyrosine kinase inhibitor against VEGF receptor -1, -2, and-3, PDGF receptor-α, β, and c-kit<br />

indicated for the treatment <strong>of</strong> patients with advanced renal cell carcinoma and advanced s<strong>of</strong>t tissue sarcoma.<br />

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