A GI medication list is a clinical reference that groups gastrointestinal drugs by class, with brand names, typical doses, and indications for each. Gastroenterology practices and nursing teams use it when treating GERD, IBD, dysmotility, and other digestive disorders.
This one covers seven classes, from proton pump inhibitors (PPIs) and H2 blockers to laxatives, immunosuppressants, and pancreatic enzymes. It closes with the GI side effects of GLP-1 drugs, which gastroenterologists now meet in patients presenting with nausea.
Keeping the list current cuts prescribing and documentation errors, and it supports digital forms and clinical audits. Download the free PDF below and customize it for your formulary.
Download your free GI medication list
A printable fill-in list with the patient’s name, date of birth, and MRN at the top, plus tick-box rows for each item, quantity, and confirmation. Use the blank rows to record the GI drugs and doses from this guide that apply to your patient.
Download templateKey takeaways
A GI medication list organizes gastrointestinal drugs by class, with doses and indications, so the whole team prescribes from one reference.
Proton pump inhibitors (omeprazole, pantoprazole, esomeprazole) are first-line for GERD and peptic ulcer disease. H2 blockers such as famotidine suit selected patients.
Antiemetics span several classes: 5-HT3 antagonists (ondansetron), dopamine blockers (metoclopramide), and anticholinergics (hyoscine), each with its own indications and safety profile.
Pabau’s AI medical scribe and clinical record management help practices document medication lists and treatment notes for compliance.
What a GI medication list covers and who uses it
The list is a curated reference for the drugs most often prescribed or given in gastroenterology and digestive health settings. It documents generic names, brand names, typical dosing ranges, and clinical indications, creating a single source of truth for practice teams.
Gastroenterologists, nurse practitioners, physician assistants, registered nurses, and practice managers rely on medication lists to:
- Verify drug dosing during patient consultations and prescribing workflows
- Support compliance audits and quality assurance reviews
- Reduce prescribing errors and adverse drug interactions
- Onboard new clinical staff with approved practice protocols
- Integrate with prescription management and EHR documentation
A shared list also means a new hire or covering clinician doses from the same reference as the lead gastroenterologist.
How to put the template to work
Five steps take the PDF from download to a reference your team relies on.
- Download and fill in: Save the PDF and add the patient details at the top. Then list each GI drug using the classes and doses in this guide.
- Customize for your practice: Add or remove medications based on your prescribers’ formulary, local guidelines, and patient population. Flag any off-label uses or contraindications specific to your setting.
- Print and post: Place the list in clinical areas (consult rooms, treatment bays, nursing stations) for quick reference during patient care.
- Link to digital records: Store a copy in your practice software. In Pabau, the EHR and practice platform we build, you can link it from consultation forms and treatment templates.
- Review quarterly: Hold a brief team review each quarter. Check for new drugs, withdrawn agents (such as ranitidine, withdrawn in 2020), and updated dosing guidance.
Train new staff on the list during onboarding, and keep a version log that records each change and its approval date.
Proton pump inhibitors (PPIs) for GERD and ulcer disease
Proton pump inhibitors suppress gastric acid production and are the first-line treatment for gastroesophageal reflux disease (GERD), peptic ulcer disease, and acid-related gastrointestinal disorders.
Long-term PPI therapy requires monitoring for potential adverse effects, including bone loss and vitamin B12 deficiency. According to American College of Gastroenterology guidance, reassess the need for continued PPI therapy periodically.
H2 receptor antagonists and comparison to PPIs
H2 blockers (H2 receptor antagonists) reduce gastric acid by a different mechanism than PPIs and may be preferred for certain patients or conditions. Famotidine is now the primary H2 blocker following ranitidine’s 2020 FDA withdrawal.
PPIs are more potent and provide more sustained acid suppression than H2 blockers, making them the preferred first-line for erosive GERD and peptic ulcer disease. H2 blockers remain useful for patients who cannot tolerate PPIs or require less aggressive acid suppression.
Antiemetics and anti-nausea medications
Nausea and vomiting are frequent complaints in gastroenterology practice. Anti-nausea medication selection depends on the underlying mechanism (chemoreceptor trigger zone, vestibular, GI motility) and patient factors.
Ondansetron is widely used in GI practice for post-procedure nausea and chemotherapy-induced emesis. Metoclopramide offers both antiemetic and prokinetic effects but carries a black-box warning for tardive dyskinesia with long-term use.
Antispasmodics and anticholinergic drugs
Anticholinergic drugs reduce GI smooth muscle spasm and are commonly prescribed for irritable bowel syndrome, functional dyspepsia, and painful bowel conditions. These medications block acetylcholine receptors to decrease motility and spasm.
- Dicyclomine: 10-20 mg three to four times daily for IBS cramping and spasm
- Hyoscyamine: 0.125-0.25 mg as needed for acute abdominal cramping
- Propantheline: 15 mg three times daily before meals for GI motility reduction (less commonly used)
Anticholinergic medications carry anticholinergic side effects (dry mouth, blurred vision, urinary retention), so baseline patient assessment and symptom monitoring are essential.
Laxatives, stool softeners, and bowel regulators
Constipation management in GI practice requires categorizing laxatives by mechanism. Each class has distinct onset times, patient acceptability, and long-term safety profiles.
Osmotic laxatives (PEG solutions) are preferred for acute constipation and bowel prep. Stimulant laxatives carry a risk of dependence and should be reserved for short-term use. Bulk agents require adequate hydration and are contraindicated in bowel obstruction.
Onset is often what decides the choice. Stimulants work overnight, while bulk agents and stool softeners can take up to three days.

Immunosuppressants in IBD and GI disorders
Inflammatory bowel disease (Crohn’s disease and ulcerative colitis) frequently requires immunosuppressive therapy when conventional treatments fail. Immunosuppressant selection depends on disease severity, prior responses, and patient comorbidities.
- Azathioprine (Imuran): 1-2.5 mg/kg daily for Crohn’s and UC maintenance. Requires TPMT testing before initiation
- 6-mercaptopurine (6-MP): 0.5-1.5 mg/kg daily, useful for azathioprine-intolerant patients
- Infliximab (Remicade): TNF-alpha inhibitor given as IV infusion every 8 weeks for moderate-severe IBD
- Vedolizumab (Entyvio): Anti-integrin biologic for selective GI immune suppression. IV infusion at weeks 0, 2 and 6, then every 8 weeks
All immunosuppressants require baseline TB screening, hepatitis serology, and regular CBC monitoring. Counsel patients on infection risk and malignancy screening per your institution’s protocols.
For a condition-specific breakdown of these agents, our Crohn’s disease medication list covers each IBD drug class in more depth.
Pancreatic enzyme replacement therapy
Pancreatic enzyme replacement is essential for managing exocrine pancreatic insufficiency (EPI) caused by chronic pancreatitis, cystic fibrosis, or pancreatic surgery. Dosing must account for meal fat content and individual enzyme activity.
Pancreatic enzymes must be taken with food and are best given as enteric-coated formulations to protect enzyme activity in the stomach. Acid-suppressive therapy (PPIs) may enhance absorption in selected patients. Labeled dosing is weight-based, so treat the fixed adult range as a starting point and individualize it to symptoms and stool fat.
GLP-1 receptor agonists: GI considerations for gastroenterology
GLP-1 receptor agonists (semaglutide, liraglutide) and the dual GIP/GLP-1 agonist tirzepatide are increasingly prescribed for weight loss and diabetes. Gastroenterologists need to recognize delayed gastric emptying and gastroparesis risk in patients presenting with nausea or vomiting. Many of these patients are prescribed by practices running software for weight-loss clinics, so ask for their titration history at referral.
- Common GI side effects: nausea, vomiting, diarrhea, constipation, abdominal pain (usually mild and transient)
- Serious risk: Gastroparesis and delayed gastric emptying have been reported in post-marketing surveillance. Distinguish them from other causes of GERD-like symptoms
- Monitoring: Screen patients for GI symptoms at follow-up visits; refer for upper endoscopy if gastroparesis is suspected
- Interaction with GI conditions: Use caution in patients with prior GI surgery, severe reflux, or known gastroparesis
Refer to FDA prescribing information and the latest FDA drug safety updates for current guidance on GLP-1 agonist adverse events. For brand-by-brand dosing, see our GLP-1 medication list.
How Pabau supports GI medication documentation and safety
A printed list by the nurses’ station works until someone updates the PDF and the laminated copy stays as it was. The fix is to keep the reference where clinicians already document.
Pabau’s patient records hold each patient’s medication history next to their consultation notes. Pabau Scribe, our AI medical scribe, drafts the note from the conversation, so the drug and dose discussed land in the record without retyping.

Store the GI medication list in Pabau as a linked resource in consultation forms. Clinicians can then check dosing during the appointment without switching systems.
Automated workflow reminders can flag the quarterly list review and each patient’s medication review date, so neither one slips.

Keep GI medication records accurate and current
Pabau links your medication reference to patient records and consultation notes, and automates review reminders. Your team documents GI prescribing faster, with fewer transcription errors.
Conclusion
A GI medication list only protects patients if the team trusts it, so ownership matters more than format. Name one clinician to own the quarterly review, and log every change with a date.
Trim the PDF to the drugs on your own formulary first. A list that matches local prescribing is quicker to scan mid-consultation, and stale entries stand out when they do creep in.
The next step is moving the list into the record your clinicians already write in. Book a demo to see how Pabau keeps GI medication histories and review reminders in one place.
Continue your research
Treating ulcerative colitis specifically? Ulcerative colitis medication list sorts aminosalicylates, steroids, and biologics by disease severity.
Managing acute diarrhea? Antidiarrheal medication list covers loperamide, bismuth, and the other agents that sit opposite the laxatives above.
Pairing PPIs with diet advice? 7-day GERD diet plan gives reflux patients a week of meals to follow alongside acid suppression.
Supporting patients after a GI flare? Gastrointestinal soft diet food list lists gentle foods for recovery after procedures or flares.
Working up IBS symptoms? FODMAP food list helps patients trial a low-FODMAP diet before you add antispasmodics.
Frequently asked questions
What is a GI medication list?
A GI medication list is a clinical reference that groups gastrointestinal drugs by class, such as PPIs, H2 blockers, antiemetics, laxatives, and immunosuppressants. For each drug it records generic and brand names, typical dosing, and indications.
What is the most common GI medication?
Proton pump inhibitors (PPIs) such as omeprazole are among the most frequently prescribed GI medications. They are first-line for GERD, peptic ulcer disease, and other acid-related disorders.
When should I use H2 blockers instead of PPIs?
H2 blockers like famotidine are preferred for mild reflux symptoms, patients intolerant to PPIs, or situations requiring less aggressive acid suppression. PPIs remain first-line for erosive GERD and peptic ulcers due to superior efficacy.
What antiemetics are safest for routine GI practice?
Ondansetron (5-HT3 antagonist) is widely considered safe and effective for post-procedure nausea. Metoclopramide provides prokinetic benefit but carries a black-box warning for long-term use. Reserve it for short-term acute indications.
How do I organize and maintain a GI medication list for my practice?
Download the template above and customize it for your prescribers’ formulary and local guidelines. Print copies for clinical areas, and link a digital version in your practice management system. Schedule quarterly reviews to check for withdrawn agents and update dosing guidance.