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Prescribing Information
Prescribing Information

... Clinical studies of Methergine did not include sufficient number of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in response between the elderly and younger patients. In general dose s ...
The Development of New Therapeutics for Alzheimerʼns Disease
The Development of New Therapeutics for Alzheimerʼns Disease

... commencing with protein misfolding and ultimately culminating in behavioral symptoms. If a therapeutic target is “high” in this cascade (e.g., protein misfolding), the resulting agent may be disease-modifying or even curative; if a therapeutic target is “low” is this cascade (e.g., neurotransmitter ...
Fungal Infections
Fungal Infections

... molds or filamentous fungi ...
Quarter 1 Mnemonics
Quarter 1 Mnemonics

... Pregnancy contraindication/ Pancreatitis/ Pressure drop (first dose hypertension) Renal failure (and renal artery stenosis contraindication)/ Rash Indomethacin inhibition Leukopenia/ Liver toxicity ...
ADVANCE IN TREATMENT OF TYPE 2 D.M.
ADVANCE IN TREATMENT OF TYPE 2 D.M.

... doses, with most patients progressing to the higher dose) than does insulin. • Although the original product requires twice-daily injections, a long-acting exenatide formulation that is given once weekly (Bydureon) has been developed and has been found to provide significantly greater improvement in ...
Selective mutation in ATP-binding site reduces affinity of drug to the
Selective mutation in ATP-binding site reduces affinity of drug to the

... Mutation in protein kinases is very common in cancer and causes constitutive activation of protein kinases resulting in hyper activation of survival pathways. Recent studies suggest that mutation in ATP binding site of kinases confers resistance to the chemotherapy [1]. Thus, understanding how muta ...
Diuretics and Synthetic Hypoglycemic Drugs
Diuretics and Synthetic Hypoglycemic Drugs

... Sulfonylureas(磺酰脲类)  The hypoglycemic(降血糖)effect of salicylates(水杨酸 盐)has been known for 100 years. Clinical use of salicylates was not feasible, since the very large doses required produced intolerable side effects.  The hypoglycemic effects of the thiadiazole sulfonamide known as IPTD, used to ...
Version 1
Version 1

... should be used with caution in patients with mild to moderate renal dysfunction (creatinine clearance between 10 and 80 ml/min) (see section 4.2 “Posology and method of administration”). The combination of a calcium antagonist with a drug that exerts a negative inotropic effect may lead ...
ACE inhibitors vs. angiotensin II receptor blockers in acute
ACE inhibitors vs. angiotensin II receptor blockers in acute

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Psychopharmacs - antidepressants
Psychopharmacs - antidepressants

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1315_Ansell_EB4E2
1315_Ansell_EB4E2

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Lopinavir/Ritonavir solution (Kaletra)
Lopinavir/Ritonavir solution (Kaletra)

... physician or pharmacist if any side effects occur and remain persistent. Redistribution or accumulation of body fat, blood fat changes and/or diabetes may occur in patients receiving antiretroviral therapy. Your doctor or pharmacist can provide you with further information on this topic. ...
Major Depression PPT
Major Depression PPT

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Is there a difference between an angiotensin

... agent compared to placebo. There was a difference of -2 to -4 mmHg between the ACE inhibitor and placebo, and a difference of -2 to -3.7 mmHg between the ARB and placebo. Many other drugs were used as well by the patients in both arms of the trials. Despite the small reduction in BP, strokes were re ...
Pharmacological Management of Congestive Heart Failure
Pharmacological Management of Congestive Heart Failure

... Treatment of toxicity • Stop digitalis • Oral or parenteral potassium supplements • For ventricular arrhythmias: – Lidocaine IV drug of choice ...
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Antiviral for respiratory viral infection

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Chapter 16 Cholinesterase Inhibitors
Chapter 16 Cholinesterase Inhibitors

... against MI, stroke, and death from cardiovascular (CV) causes in high-risk patients Migraine headache May prevent development of diabetic retinopathy New data show that ACE inhibitors and angiotensin II receptor blockers (ARBs) are not effective for primary prevention of nephropathy in normotensive ...
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Drugs Used in Coagulation Disorders
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Glucocorticoids
Glucocorticoids

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acetylcholinesterase inhibitors: information for
acetylcholinesterase inhibitors: information for

... antidepressants affecting serotonin) and those with a previous history of peptic ulceration Although not very common, vagotonic effects including bradycardia have been noted with use of acetylcholinesterase inhibitors in particular galantamine. This should be considered in patients receiving drugs t ...
click here to the doc
click here to the doc

... (rate of absorption) and AUC (extent of absorption) by 30% each. However, time of administration does not affect the plasma LDL-C lowering efficacy of Atosta. Atosta is highly protein bound (≥98%). The primary proposed mechanism of Atosta metabolism is through cytochrome P450 3A4 hydroxylation to fo ...
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pharm 22 A [4-20

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Document
Document

... Norepinephrine reuptake inhibitors (NRIs), also known as noradrenaline reuptake inhibitors (NARIs), are compounds that elevate the extracellular level of the neurotransmitter norepinephrine in the central nervous system by inhibiting its reuptake from the synaptic cleft into the presynaptic neuronal ...
NOVEL FAK-SELECTIVE INHIBITORS
NOVEL FAK-SELECTIVE INHIBITORS

... FAK is a non-receptor tyrosine kinase which is overexpressed (through either gene amplification or increased levels of protein expression), or over-activated in many human cancers (including solid tumours and acute myelogenous leukaemia (AML)). Increased levels of FAK and/or phosphorylated FAK are o ...
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Metalloprotease inhibitor

Metalloprotease inhibitors are cellular inhibitors of the matrix metalloprotease (or metalloproteinase) family of proteins (MMP).Several other proteins have similar inhibitory effects, however none as effective (netrins, procollagen C-terminal proteinase enhancer (PCPE), reversion-inducing cysteine-rich protein with Kazal motifs (RECK) and tissue factor pathway inhibitor (TFPI-2)). They might have other biological activities which have yet been fully characterised.There are three classes of commonly used inhibitors for metalloproteinases. In vitro, EDTA, 1,10-phenanthroline and other chelating compounds lower the concentration of metal to the point where the metal is removed from the enzyme active site. Classical lock and key inhibitors such as phosphoramidon and bestatin bind tightly by approximating the transition state of the hydrolysis of the peptide, preventing it from acting on other substrates. Protein inhibitors such as α2-macroglobulin are known to work with metalloproteinases.↑
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