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Crystalline zinc insulin
Glyburide
Insulin glargine
NPH insulin
Tolbutamide
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Dilutional hyponatremia
Hypoglycemia
Increased bleeding tendency
Pancreatitis
Severe hypertension
Morning injections of mixed insulin lispro and insulin aspart
Evening injections of mixed regular insulin and insulin glargine
Morning and evening injections of regular insulin, supplemented by small amounts ofNPH insulin at mealtimes
Morning injections of insulin glargine, supplemented by small amounts of insulinlispro at mealtimes
Morning injection of NPH insulin and evening injection of regular insulin
Acarbose
Glipizide
Metformin
Miglitol
Pioglitazone
Increased conversion of amino acids into glucose
Increased gluconeogenesis
Increased glucose transport into cells
Inhibition of lipoprotein lipase
Stimulation of glycogenolysis
A disulfiram-like reaction
Excessive weight gain
Hypoglycemia
Lactic acidosis
Serious hepatotoxicity
Acarbose
Exenatide
Glipizide
Pioglitazone
Repaglinide
Activating adenylyl cyclase and increasing the intracellular concentration of cAMP
Inactivating a cellular inhibitor of the GLUT2 glucose transporter
Inhibiting acid glucosidase, a key enzyme in glycogen breakdown pathways
Regulating transcription of genes involved in glucose utilization
Stimulating the activity of a tyrosine kinase that phosphorylates the insulin receptor
Acarbose
Glyburide
Metformin
Miglitol
Rosiglitazone
An 18-year-old woman who took an overdose of cocaine and now has a blood pressureof 190/110 mm Hg
A 27-year-old woman with severe diarrhea caused by a flare in her inflammatory boweldisease
A 57-year-old woman with type 2 diabetes who has not taken her glyburide for the last3 d
A 62-year-old man with severe bradycardia and hypoten- sion resulting fromingestion of an overdose of atenolol
A 74-year-old man with lactic acidosis as a complication of severe infection and shock
Cholecalciferol
Calcitriol
Gallium nitrate
Sevelamer
Plicamycin
Fluoride
Hydrochlorothiazide
Pamidronate
Raloxifene
Teriparatide
Decrease the absorption of calcium from bone
Increase PTH formation
Increase renal production of erythropoietin
Increase the absorption of calcium from the gastrointes- tinal tract
Lower the serum phosphate concentration
Chronic kidney failure
Hypoparathyroidism
Intestinal osteodystrophy
Postmenopausal osteoporosis
Rickets
Lovastatin
Metformin
Prednisone
Propranolol
Thiazide diuretic
Cholelithiasis
Diarrhea
Constipation
Erosive esophagitis
Pernicious anemia
Calcitonin
Calcitriol
Cinacalcet
Cortisol
Teriparatide
Calcitriol
Cholecalciferol
Furosemide
Gallium nitrate
Risedronate
Calcitriol
Cholecalciferol
Furosemide
Paricalcitol
Risedronate
Activating a steroid receptor that inhibits expression of the PTH gene
Activating the calcium-sensing receptor in parathyroid cells
Activating transporters in the GI tract that are involved in calcium absorption
Inducing the liver enzyme that converts vitamin D3 to 25-hydroxyvitamin D3
Option 5
Increased muscle mass
Hypoglycemia
Inhibition of leukotriene synthesis
Improved wound healing
Increased excretion of salt and water
A “lupus-like” syndrome
Adrenal gland neoplasm
Hepatotoxicity
Osteoporosis
Precocious puberty in children
Betamethasone
Cortisol
Fludrocortisone
Ketoconazole
Triamcinolone
Increased adrenal estrogen synthesis
Inhibition of adrenal aldosterone synthesis
Prevention of hypoglycemia
Recovery of normal immune function
Suppression of ACTH secretion
A protein regulator that controls the interaction between an activated steroid receptor and DNA
A short DNA sequence that binds tightly to RNA polymerase
A small protein that binds to an unoccupied steroid receptor protein
A specific nucleotide sequence that is recognized by a steroid hormone receptor-hormone complex
The portion of the steroid receptor that binds to DNA
Chemotherapy-induced vomiting
Essential hypertension
Hyperprolactinemia
Parkinson’s disease
Type II diabetes
Depressed release of insulin from pancreatic B cells
Hematopoiesis in the bone marrow
Normal osteoblast function
The control by vasopressin of water excretion
Option 5
A moon face
Dehydration
Hyperglycemia
Hypertension
Hyperthermia
Aldosterone and fludrocortisone
Cortisol and fludrocortisone
Dexamethasone and metyrapone
Fludrocortisone and metyrapone
Triamcinolone and dexamethasone
Aminoglutethimide
Beclomethasone
Ketoconazole
Mifepristone
Spironolactone
Albuterol
Atenolol
Metoprolol
Prazosin
Timolol
It is preferable that she does not take the drug in the evening
Muscle cramps and twitches can sometimes occur
She should tell you if she anticipates using other prescription drugs
The antidepressant effects of paroxetine may take 2 weeks or more to become effective
All of the above
Bupropion inhibits 5-HT reuptake into nerve endings in the CNS
Chronic treatment with tricyclic antidepressants leads to upregulation of adrenoceptors in the CNS
Decreased levels of NE and 5-HT in cerebrospinal fluid are characteristic of depressed patients before drug therapy
Nefazodone blocks 5-HT receptors in the CNS
Selegiline selectively decreases the metabolism of serotonin
Bupropion
Fluoxetine
Imipramine
Paroxetine
Venlafaxine
Chronic use of antidepressants increases the activity of hepatic drug metabolizing enzymes
In the treatment of major depressive disorders, sertraline is usually more effective than fluoxetine
Tricyclics are highly effective in depressions with attendant anxiety, phobic features, and hypochondriasis
Weight gain often occurs during the first few months in patients taking SSRIs
When selecting an appropriate drug for treatment of depression, the history of patient response to specific drugs is a valuable guide
Administer bicarbonate and potassium chloride (to correct acidosis and hypokalemia)
Administer lidocaine (to control cardiac arrhythmias)
Initiate hemodialysis (to hasten drug elimination)
Maintain heart rhythm by electrical pacing
Use intravenous diazepam to control seizures
Citalopram
Doxepin
Trazodone
Triazolam
Zolpidem
Amitriptyline
Mirtazapine
Phenelzine
Sertraline
Trazodone
Bulimia
Chronic pain of neuropathic origin
Generalized anxiety disorder
Obsessive-compulsive disorder
Premenstrual dysphoric disorder
Amitriptyline
Clomipramine
Doxepin
Nefazodone
Venlafaxine
Clonazepam
Ethosuximide
Gabapentin
Felbamate
Phenobarbital
Diazepam facilitates GABA-mediated inhibitory actions
Ethosuximide selectively blocks potassium ion (K+) channels in thalamic neurons
Phenobarbital has multiple actions, including enhancement of the effects of GABA antagonism of glutamate receptors, and blockade of sodium ion (Na+) channels
Phenytoin prolongs the inactivated state of the Na+ channel
Zonisamide blocks voltage-gated Na+ channels
Carbamazepine
Clonazepam
Gabapentin
Valproic acid
Vigabatrin
Ethosuximide and valproic acid are preferred drugs
Gastrointestinal side effects are common with ethosuximide
She should be examined every 2 or 3 month for deep tendon reflex activity
The use of valproic acid in pregnancy may cause congenital malformations
Weight gain is common in patients on valproic acid
Block of sodium ion channels
Block of calcium ion channels
Facilitation of GABA actions on chloride ion channels
Glutamate receptor antagonism
Inhibition of GABA transaminase
Buspirone
Eszopiclone
Flurazepam
Secobarbital
None of the above
Abstinence syndromes are more severe during withdrawal from phenobarbital than from secobarbital
Alkalinization of the urine accelerates the elimination of phenobarbital
Barbiturates may increase the half-lives of drugs metabolized by the liver
Compared with barbiturates, the benzodiazepines exhibit a steeper dose-response relationship
Respiratory depression caused by barbiturate over dosage can be reversed by flumazenil
A need to continually increase drug dosage because of tolerance
A significant effect of the drug on memory
Additive CNS depression with alcoholic beverages
That the drug is likely to take a week or more to begin working
That if he stops taking the drug abruptly, he will experience withdrawal signs
Activate GABAB receptors in the spinal cord
Block glutamate receptors in hierarchical neuronal pathways in the brain
Increase frequency of opening of chloride ion channels coupled to GABAA receptors
Inhibit GABA transaminase to increase brain levels of GABA
Stimulate release of GABA from nerve endings in the brain
Ambulatory dysfunction does not occur in elderly patients taking one half of the conventional adult dose
Hypertension is a common adverse effect of benzodiazepines in elderly patients
Over-the-counter cold medications may antagonize the hypnotic effects of the drug
The patient may experience amnesia, especially if she also consumes alcoholic beverages
Triazolam is distinctive in that it does not cause rebound insomnia on abruptdiscontinuance
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