| Term 
 | Definition 
 
        | Inhibit P2Y12 ADP platelet receptor activation |  | 
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        | Term 
 | Definition 
 
        | Inhibit P2Y12 ADP platelet receptor activation |  | 
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        | Term 
 | Definition 
 
        | Inhibit platelet activator TxA2 synthesis and secretion |  | 
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        | Term 
 | Definition 
 
        | Inhibit platelet activator TxA2 synthesis and secretion |  | 
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        | Term 
 | Definition 
 
        | increase platelet cAMP levels by acting on PLA2 |  | 
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        | Term 
 | Definition 
 
        | Inhibit GP IIbIIIa receptors |  | 
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        | Term 
 | Definition 
 
        | Inhibit GP IIbIIIa receptors |  | 
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        | Term 
 | Definition 
 
        | Inhibit GP IIbIIIa receptors |  | 
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        | Term 
 | Definition 
 
        | TPO agonist; is a nonpeptide mimetic; given oral |  | 
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        | Term 
 | Definition 
 
        | TPO agonist; is a peptide mimetic; given subcutaneous |  | 
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        | Term 
 | Definition 
 
        | inhibits Vitamin K Epoxide Reductase = VKOR |  | 
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        | Term 
 | Definition 
 
        | positively charged molecule that helps remove free heparin |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | pentasaccharide binds to antithrombin |  | 
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        | Term 
 | Definition 
 
        | Not used analog of fondaparinux - a pentasaccharide that binds to antithrombin |  | 
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        | Term 
 | Definition 
 
        | biotinlated idraparinux (which is a pentasaccharide that binds to antithrombin) |  | 
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        | Term 
 | Definition 
 
        | Direct thrombin inhibitor |  | 
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        | Term 
 | Definition 
 
        | direct thrombin inhibitor with smaller connecting chain than hirudin |  | 
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        | Term 
 | Definition 
 
        | Direct thromin inhibitor, binds only to catalytic site |  | 
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        | Term 
 | Definition 
 
        | oral direct thrombin inhibitor that only binds to catalytic site |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | antibody against C5, preventing terminal compliment activation |  | 
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        | Term 
 | Definition 
 
        | first line Fe chelator, subcu injection |  | 
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        | Term 
 | Definition 
 
        | orally active chelating agent, but not in US b/c of potential safety problems |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | increase amount of HbF for sickle cell disease |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | structral analog of thalidomide, anti angiogenic and immunomodulatory |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | anti-CD52 (lymphocyte marker) |  | 
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        | Term 
 | Definition 
 
        | alkylating agent, main toxicity is hemorrhagic cystitis |  | 
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        | Term 
 | Definition 
 
        | alkylating agent; main toxicity is CNS effects |  | 
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        | Term 
 | Definition 
 
        | platinum; toxicities = nephrotoxicity, nausea/vomitting, neurotoxicity, ototoxicity |  | 
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        | Term 
 | Definition 
 
        | platnium; toxicity = myelosuppression |  | 
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        | Term 
 | Definition 
 
        | platinum; toxicity = neurotoxicity, cold intolerance |  | 
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        | Term 
 | Definition 
 
        | anthracycline; toxicity = cardiac, myelosuppression, nausea/vomitting |  | 
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        | Term 
 | Definition 
 
        | antibiotic; toxicity = pulmonary, NOT bone marrow, oral mucositis |  | 
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        | Term 
 
        | Etoposide (epipodophyllotoxins) |  | Definition 
 
        | Topoisomerase II inhibitor (stabilizes double stranded breaks |  | 
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        | Term 
 
        | Irinotecan (camptothecins) |  | Definition 
 
        | Topoisomerase I inhibitor - stabilizes single strand breaks |  | 
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        | Term 
 | Definition 
 
        | folate analog; inhibits dihydrofolate reductase |  | 
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        | Term 
 | Definition 
 
        | Folate supplement used to prevent toxicity from methotrexate |  | 
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        | Term 
 | Definition 
 
        | antimetabolite; inhibits thymidylate synthetase, which converts dUMP to dTMP |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | cytosine analog anti-metabolite |  | 
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        | Term 
 | Definition 
 
        | adenosine analog anti-metabolite |  | 
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        | Term 
 | Definition 
 
        | adenosine analog anti-metabolite |  | 
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        | Term 
 | Definition 
 
        | adenosine analog anti-metabolite |  | 
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        | Term 
 | Definition 
 
        | guanine analog anti-metabolite |  | 
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        | Term 
 | Definition 
 
        | bind to tubulin to stabilize the spindle |  | 
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        | Term 
 | Definition 
 
        | vinca alkaloid; toxicity = neuropathy |  | 
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        | Term 
 | Definition 
 
        | vinca alkaloid; toxicity = myelosuppression |  | 
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        | Term 
 | Definition 
 
        | radioimmunotherapy that is anti-CD |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | all trans retinoic acid for APL |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | inhibitor of protein elongation (CML) |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | synthetic androgen w/ anabolic properties |  | 
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        | Term 
 | Definition 
 
        | androgen recptor antagonist |  | 
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        | Term 
 | Definition 
 
        | androgen receptor antagonists |  | 
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        | Term 
 | Definition 
 
        | 5alpha reductase inhibitor |  | 
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        | Term 
 | Definition 
 
        | 5alpha reductase inhibitor |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | estrogen causing vaginal cancer |  | 
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        | Term 
 | Definition 
 
        | androgens that bind to progestin receptors |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | oral synthetic progestin receptor agonist |  | 
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        | Term 
 | Definition 
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 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | SERM blocking feedback of estrogen |  | 
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        | Term 
 | Definition 
 
        | progestin antagonist;   glucocorticoid receptor antagonist |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | integrate into bone, inhibit osteoclasts |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | inhibit thyroid peroxidase |  | 
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        | Term 
 | Definition 
 
        | inhibits thyroid peroxidase, inhibits T4-->T3 |  | 
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        | Term 
 | Definition 
 
        | beta adrenergic receptor blocker |  | 
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        | Term 
 | Definition 
 
        | inhibit thyroid hormone release; antagonize TSH, inhibit thyroid peroxidase |  | 
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        | Term 
 | Definition 
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        | Term 
 | Definition 
 
        | inhibit steroid synthesis |  | 
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        | Term 
 | Definition 
 
        | insulin given with protamine, medium duration |  | 
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        | Term 
 | Definition 
 
        | modifications of insulin to prevent dimerization --> quick acting |  | 
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        | Term 
 | Definition 
 
        | modification in insulin --> less dimerization --> fast acting |  | 
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        | Term 
 | Definition 
 
        | form microprecipitates of insulin, so longer acting |  | 
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        | Term 
 | Definition 
 
        | form precipitates of insulin, so longer lasting |  | 
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        | Term 
 | Definition 
 
        | closes Katp channels, leading to insulin release |  | 
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        | Term 
 | Definition 
 
        | closes Katp channels, leading to insulin release |  | 
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        | Term 
 | Definition 
 
        | increases glucose-dependent release of insulin, increased weight loss / satiety |  | 
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        | Term 
 
        | dipeptidylpeptidase inhibitors |  | Definition 
 
        | inhibits enzyme that breaks down GLP-1 |  | 
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        | Term 
 | Definition 
 
        | increases insulin sensitivity in muscle and adipose by binding to PPARgamma |  | 
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        | Term 
 
        | alpha-glucosidase inhibitor |  | Definition 
 
        | prevents breakdown of sugars, so prevents absorption |  | 
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        | Term 
 | Definition 
 
        | affects satiety, post prandial glucose concentrations |  | 
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        | Term 
 | Definition 
 
        | decrease glucose production by liver, increase utilization |  | 
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