| Term 
 
        | What are the four categories of antiemetics to know? |  | Definition 
 
        | Phenothiazines 5HT3 Inhibitors
 Benzamides
 H1 antihistamines
 |  | 
        |  | 
        
        | Term 
 
        | What is the phenothiazine to know? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What are the three 5-HT3 inhibitors to know? What do they all end in? |  | Definition 
 
        | Ondansetron* Granisetron
 Dolasetron
 -setron
 |  | 
        |  | 
        
        | Term 
 
        | What is the one benzamide to know? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What are the four H1 antihistamines to know? |  | Definition 
 
        | Diphenhydramine (Benadryl)* Meclizine
 Hyoscine
 |  | 
        |  | 
        
        | Term 
 
        | Most efficacious class of antiemetic? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What antiemetic is used in patients with unrelenting nausea and vomiting, traveler's diarrhea? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | MOA of Phenothiazines (Prochlorperazine)? |  | Definition 
 
        | Blockade of dopamine receptors |  | 
        |  | 
        
        | Term 
 
        | Adverse effects of Prochlorperazine? |  | Definition 
 
        | Increase in dose improves antiemetic effect, but limited by adverse effects: sedation
 extrapyramidal symptoms
 |  | 
        |  | 
        
        | Term 
 
        | What is the most important 5-HT3 inhibitor to know? |  | Definition 
 
        | Ondansetron (Zofran)* "At a party but feeling queasy? Keep ON DANCing with ONDANSetron!"
 |  | 
        |  | 
        
        | Term 
 
        | MOA of Ondansetron (and the other -setrons)? |  | Definition 
 
        | Central 5-HT3 receptor blockade in the vomiting center and chemoreceptor trigger zone |  | 
        |  | 
        
        | Term 
 
        | What are 5-HT3 inhibitors useful for? |  | Definition 
 
        | Highly efficacious for prevention of chemotherapy induced emesis (administered prior to chemotherapy) Also, post-operative nausea & vomiting and radiotherapy-induced nausea & vomiting.
 Long duration of action (8-10 hours)
 |  | 
        |  | 
        
        | Term 
 
        | When must dosage be adjusted for the 5-HT3 inhibitors? |  | Definition 
 
        | Dosage adjustment required in hepatic insufficiency |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | The antiemetic action of Metoclopramide* is due to its antagonist activity at D2 receptors in the chemoreceptor trigger zone (CTZ) in the central nervous system (CNS)—this action prevents nausea and vomiting triggered by most stimuli. Metoclopramide also has gastroprokinetic activity that is mediated by muscarinic activity, D2 receptor antagonist activity and 5-HT4 receptor agonist activity.
 |  | 
        |  | 
        
        | Term 
 
        | Adverse effects of Metoclopramide? |  | Definition 
 
        | Avoid high doses due to extrapyramidal side effects** Knocks out dopamine and induces Parkinsonian effects |  | 
        |  | 
        
        | Term 
 
        | What is Metoclopramide useful for? |  | Definition 
 
        | Prevention of chemotherapy induced emesis. Gastroperesis (acts on gastric smooth muscle to accelerate GI emptying).
 (Also increased lower esophageal sphincter tone to prevent gastric reflux)***KNOW THIS FOR KRISNA!
 |  | 
        |  | 
        
        | Term 
 
        | How are the H1 antihistamines used to prevent nausea & vomiting? |  | Definition 
 
        | H1 antihistamines are combined with other antiemetics for the prevention of motion sickness. |  | 
        |  | 
        
        | Term 
 
        | Adverse effects of H1 antihistamines? |  | Definition 
 
        | Use is limited by sedation, dizziness, confusion, dry mouth, and urinary retention (spillover to anti-muscarinic effects) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Bulk-forming laxatives Stool surfactant agents (softeners)
 Osmotic laxatives
 Stimulant laxatives
 |  | 
        |  | 
        
        | Term 
 
        | What two drugs have huge side effects of constipation and need laxatives for treatment?** What laxative is used to treat these conditions?
 |  | Definition 
 
        | Morphine Verapamil
 Use Docusate, a stool softener
 |  | 
        |  | 
        
        | Term 
 
        | Name a Bulk-forming laxative? |  | Definition 
 
        | Psyllium (nonabsorbably agents that increase water retention and stool bulk; this distends the bowel and stimulates peristalsis) |  | 
        |  | 
        
        | Term 
 
        | Name a Stimulant laxative? |  | Definition 
 
        | Senna (acts directly on intestinal smooth muscle to increase peristalsis) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Docusate (emulsifies stool, softening it and making its passage easier) |  | 
        |  | 
        
        | Term 
 
        | Name two Osmotic laxatives? (In FA, but not covered in class much) |  | Definition 
 
        | Magnesium citrate* Lactulose*
 |  | 
        |  | 
        
        | Term 
 
        | What class of drugs are the most effective antidiarrheal agents? |  | Definition 
 
        | Opioids (and their derivatives) |  | 
        |  | 
        
        | Term 
 
        | What are the two opioids to know for treating diarrhea? |  | Definition 
 
        | Diphenoxylate* Loperamide*
 |  | 
        |  | 
        
        | Term 
 
        | General MOA of opioid antidiarrheal agents? |  | Definition 
 
        | These are derivatives of an opioid that slow GI peristaltic activity through actions of peripheral opioid receptors. This prolongs the transit time of intestinal contents. |  | 
        |  | 
        
        | Term 
 
        | What opioid antidiarrheal has sedative effects? |  | Definition 
 
        | Diphenoxylate* - it has peripheral and CNS opiate effects It is formulated with an antimuscarinic alkaloid (atropine) to reduce abuse - results in patient with anti-muscarinic side effects (blurriness, dry mouth) if abused.
 |  | 
        |  | 
        
        | Term 
 
        | What opioid antidiarrheal has peripheral opiate effects ONLY? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What opiod would be given to a patient with unrelenting diarrhea for the last 72 hours (traveler's diarrhea) who has had little or no sleep?** |  | Definition 
 
        | Give Diphenoxylate because it has peripheral & CNS opiate effects** It has sedative effects so that the patient can sleep.
 |  | 
        |  | 
        
        | Term 
 
        | What antisecretory agent helps in treatment of diarrhea? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What are the four classes of drugs used to treat IBD? |  | Definition 
 
        | Aminosalicylates Corticosteroids
 Immunosuppressive antimetabolites
 Monoclonal antibodies
 |  | 
        |  | 
        
        | Term 
 
        | Into what two major subtypes is IBD usually divided? |  | Definition 
 
        | Ulcerative colitis Crohn's disease
 |  | 
        |  | 
        
        | Term 
 
        | What is the aminosalicylate used to treat IBD? |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Acts as an anti-inflammatory drug (5-aminosalicylic acid) and antibacterial (sulfapyridine). |  | 
        |  | 
        
        | Term 
 
        | Where does Sulfasalazine* work better? |  | Definition 
 
        | It works much better against the symptoms of ulcerative colitis thatn Crohn's disease, since Crohn's often involves the small bowel, where the drug is not active. |  | 
        |  | 
        
        | Term 
 
        | What are the Mesalamine compounds to know? |  | Definition 
 
        | Pentasa (time release) Asacol
 Rowasa
 |  | 
        |  | 
        
        | Term 
 
        | MOA of Mesalamine compounds? |  | Definition 
 
        | These release 5-aminosalicyclic acid to have an anti-inflammatory effect. Also a free radical scavenger or inhibitor of TNF. |  | 
        |  | 
        
        | Term 
 
        | What corticosteroids could you use to treat IBD? |  | Definition 
 
        | Prednisone/Prednisolone Methylprednisolone
 Hydrocortisone
 |  | 
        |  | 
        
        | Term 
 
        | What are the five immunosuppressants to know for treating IBD? |  | Definition 
 
        | Azathioprine* 6-Mercaptopurine*
 Methotrexate*
 Cyclosporine
 Infliximab*
 |  | 
        |  | 
        
        | Term 
 
        | What BRM is used to treat IBD? |  | Definition 
 
        | Infliximab* This is a LAST RESORT for treating IBD (noted for treating Crohn's specifically)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Monoclonal antibody to TNF-alpha. Inhibition of induction of pro-inflammatory cytokines (IL-1, IL-6) |  | 
        |  | 
        
        | Term 
 
        | Algorithm for treatment of IBD? |  | Definition 
 
        | (Drugs should be used in this order) Aminosalicylates (Sulfasalazine*)
 Antibiotics
 Non-systemic steroids
 Systemic corticosteroids
 Immunosuppressive antimetabolites (Azathioprine*, Methotrexate*, Cyclosporine*)
 Monoclonal antibodies (Infliximab*)
 Surgery
 |  | 
        |  | 
        
        | Term 
 
        | What four treatments are used to relieve Irritable Bowel Syndrome? |  | Definition 
 
        | Make dietary modifications Antispasmodic agents
 Antidiarrheal agents
 Antidepressants - TCAs & SSRIs
 |  | 
        |  | 
        
        | Term 
 
        | What two antispasmodic agents are used in IBS? |  | Definition 
 
        | Dicyclomine Scopolomine* (motion sickness drug)
 |  | 
        |  | 
        
        | Term 
 
        | What treatments are used to relieve Gastroesophageal Reflux Disease (GERD)? |  | Definition 
 
        | Lifestyle changes Antacids
 H2 antagonists
 Proton pump inhibitors (PPIs)
 |  | 
        |  | 
        
        | Term 
 
        | What treatment is most effective in treating GERD? What treatment is least effective? |  | Definition 
 
        | PPIs are most efficacious because it knocks out the hydrogen-potassium pump. Antacids are the least efficacious because they provide symptomatic relief only. |  | 
        |  | 
        
        | Term 
 
        | What condition can GERD progress into? |  | Definition 
 
        | Peptic ulcer disease They are lesions in the stomach or duodenum occurring as a result of excessive pepsin and acid activity.
 |  | 
        |  | 
        
        | Term 
 
        | What is Zollinger-Ellison syndrome? |  | Definition 
 
        | Hypersecretion due to a gastrin-secreting tumor |  | 
        |  | 
        
        | Term 
 
        | Causative factors in peptic ulcer disease? |  | Definition 
 
        | NSAID use (NSAIDS remove the cytoprotective prostaglandins) Alcohol
 Smoking
 Stress
 H. pylori infection (90% of patients)
 |  | 
        |  | 
        
        | Term 
 
        | What is the most efficacious way to diagnose an H. pylori infection? |  | Definition 
 
        | Urea breath test (UBT) Stool antigen test (second best test)
 |  | 
        |  | 
        
        | Term 
 
        | What are the therapeutic objective to treating peptic ulcers? |  | Definition 
 
        | 1. Elimination of H. pylori 2. Reduction of gastric acid secretion or acid neutralization
 3. Protection of gastric mucosa from further damage
 |  | 
        |  | 
        
        | Term 
 
        | What five categories of drugs are used to treat peptic ulcer disease? |  | Definition 
 
        | Antacids H2 antagonists
 Cytoprotective agents
 PPIs
 Antimicrobial agents
 |  | 
        |  | 
        
        | Term 
 
        | What is the triple therapy to treat peptic ulcer disease? |  | Definition 
 
        | PPI plus two antimicrobial agents |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Gastric antacids are weak bases that react with gastric HCl to form a salt and water -> increased gastric pH. Effective SYMPTOMATIC treatment for pain of peptic ulceration. ONLY neutralizes gastric acid that has ALREADY been released; will not prevent gastric acid release and has no cytoprotective effect.
 |  | 
        |  | 
        
        | Term 
 
        | Name the active ingredients of antacids? |  | Definition 
 
        | Aluminum hydroxide* Magnesium hydroxide*
 Calcium carbonate* (Rolaids, Tums)
 Magnesium carbonate
 Sodium bicarbonate
 |  | 
        |  | 
        
        | Term 
 
        | What are the antacids to know? |  | Definition 
 
        | Aluminum hydroxide + Magnesium hydroxide (Maalox) Aluminum hydroxide + Magnesium hydroxide  + Simethicone (Mylanta)
 Aluminum hydroxide + Magnesium carbonate (Gaviscon)
 Calcium carbonate* (Rolaids, Tums)
 |  | 
        |  | 
        
        | Term 
 
        | Adverse effects of antacids? |  | Definition 
 
        | Prolonged use -> systemic alkalosis Diarrhea
 May interfere with drug absorption (by making environment alkaline) -> some drugs require acid environment (Digosin, Ketoconazole, Isoniazid)
 Increased gastric pH may cause premature dissolution of enteric-coated drugs
 Certain drugs may form complexes with aluminum, magnesium, and calcium
 Significant reduction in drug bioavailability (Tetracycline, Ciprofloxacillin)
 |  | 
        |  | 
        
        | Term 
 
        | What drug does antacids increase the acidity and toxicity of? |  | Definition 
 
        | Quinidine (a basic drug) -> absorption is INCREASED in an alkaline environment |  | 
        |  | 
        
        | Term 
 
        | Four H2 antagonists to know? |  | Definition 
 
        | Cimetidine* (Tagamet) Ranitidine* (Zantac)
 Nazatidine* (Axid)
 Famotidine* (Pepcid)
 |  | 
        |  | 
        
        | Term 
 
        | Most potent H2 antagonist? Lest potent H2 antagonist?
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | MOA of H2 antagonists in reducing gastric acid? |  | Definition 
 
        | Competitively and reversibly bind H2 receptors on parietal cells Diminish cytosolic cAMP production and secretion of histamine-stimulated gastric acid
 Complete inhibition of gastric acid secretion induced by histamine or gastrin.
 Partial inhibition of gastric acid secretion induced by ACh.
 |  | 
        |  | 
        
        | Term 
 
        | Adverse effects of Cimetidine*? |  | Definition 
 
        | Cimetidine is a strong inhibitor of the cytochrome P-450 system and therefore can slow the metabolism of drugs normally broken down through this system. Decreases metabolism of Warfarin, Phonobarbital, Phenytoin, Diazepam, Propranolol |  | 
        |  | 
        
        | Term 
 
        | What other adverse effect may Cimetidine* cause? |  | Definition 
 
        | Gynecomastia** and decreased libido (due to its antiandrogenic effects) |  | 
        |  | 
        
        | Term 
 
        | What H2 antagonist can be used at a lower dose and doesn't mess with cytochrome P-450 much? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What drug is the most efficacious in treating Peptic ulcer disease? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Three PPIs to know for treating Peptic ulcer disease? |  | Definition 
 
        | Omeprazole* (Prilosec) Lansoprazole* (Prevacid)
 Esomeprazole* (Nexium)
 -prazole
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Irreversible inhibitors of H+/K+ ATPase. Marked suppression of acid secretion by stomach parietal cells.
 |  | 
        |  | 
        
        | Term 
 
        | When should PPIs be taken? |  | Definition 
 
        | Most effective when taken 30 minutes before meals |  | 
        |  | 
        
        | Term 
 
        | What two PPIs have dangerous adverse effects? What are the adverse effects? |  | Definition 
 
        | Omeprazole* and Esomeprazole* selectively inhibit cytochrome P-450. can slow the metabolism of drugs normally broken down through this system. Decreases metabolism of Warfarin, Phenytoin, Diazepam. Rabeprazole* and Pantoprazole* have almost no interaction with the cytochrome P-450 system. |  | 
        |  | 
        
        | Term 
 
        | What drug acts as a cytoprotective agent? |  | Definition 
 
        | Bismuth* Subsalicylate (Pepto-Bismol) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Bismuct compounds appear to work by selectively binding to an ulcer, coating it and protecting it from acid and pepsin. |  | 
        |  | 
        
        | Term 
 
        | What other therapeutic actions are possible? |  | Definition 
 
        | Bismuch compounds may have some antimicrobial activity against H. pylori. |  | 
        |  | 
        
        | Term 
 
        | What is the drug regimen for eradication of H. pylori? |  | Definition 
 
        | Combination therapy ("triple therapy") PPI + Metronidazole or Amoxicillin + Clarithromycin
 |  | 
        |  | 
        
        | Term 
 
        | What PPI is used in the combination therapy regimen? |  | Definition 
 
        | Omeprazole* 
 Regimen:
 Omeprazole*
 Metronidazole or Amoxicillin
 Clarithromycin
 |  | 
        |  | 
        
        | Term 
 
        | Why is Clarithromycin used in the combination therapy to eliminate H. pylori? |  | Definition 
 
        | Clarithromycin doesn't interact with the cytochrome P450 system |  | 
        |  | 
        
        | Term 
 
        | When would a Bismuth*-based regimen be used to eliminate H. pylori? |  | Definition 
 
        | If there is an open ulcer bed |  | 
        |  | 
        
        | Term 
 
        | What is the Bismuth*-based four drug regimen for eliminating H. pylori? |  | Definition 
 
        | Omeprazole* Bismuth* subsalicylate
 Metronidazole
 Tetracycline
 |  | 
        |  | 
        
        | Term 
 
        | If a patient gets an ulcer from taking NSAIDs, what do you do? |  | Definition 
 
        | If the patient needs to continue taking NSAIDS, put them on a COX-2 inhibitor. If cardiac issues, give a single dose of PPI. |  | 
        |  | 
        
        | Term 
 
        | What is the DOC to treat Zollinger-Ellison (ZE) syndrome? |  | Definition 
 | 
        |  |