Bedside Snapshot

Use It For
Type 2 diabetes; weight management; OSA with obesity (tirzepatide); noncirrhotic MASH (semaglutide); CKD in T2DM (Ozempic)
Adult Dose
  • Ozempic (semaglutide) weekly: 0.25 mg SC ×4 wk, then 0.5 mg; max 2 mg
  • Mounjaro (tirzepatide) weekly: 2.5 mg SC; max 15 mg
  • Victoza (liraglutide) daily: 0.6 mg SC ×1 wk, then 1.2 mg; max 1.8 mg
Pediatric Dose
Not established under 10 yr. Ages 10+ (diabetes) or 12+ (weight) only: tirzepatide max 10 mg weekly; dulaglutide max 1.5 mg weekly; liraglutide max 1.8 mg daily (diabetes) or 3 mg daily (weight, over 60 kg)
Onset / Duration
  • SC weekly products: peak 8 hr to 3 days
  • SC liraglutide (daily): peak 8 to 12 hr
Do Not Give / Hold If
Personal or family history of MTC or MEN 2; serious hypersensitivity; suspected pancreatitis; vomiting or dehydration with rising creatinine (reassess)
Watch For
Pancreatitis (persistent abdominal pain radiating to back); aspiration at anesthesia or sedation; acute kidney injury after GI losses; hypoglycemia with insulin or a sulfonylurea
Reversal / Rescue
No specific antidote: supportive care by signs. Hypoglycemia per protocol (dextrose, glucagon). Airway protection and RSI for vomiting or sedation per protocol
Must Remember
Weekly versus daily, and product strength: confirm the product, pen strength and dosing frequency. Compounded vials have caused 5 to 20 times the intended dose

Indications

Emergency & Prehospital

  • No acute emergency indication: these are chronic home medicines. EMS and ED teams meet them through the complications. Vomiting or dehydration. Low glucose on insulin or a sulfonylurea. Aspiration risk at airway management.

ED / ICU / Transport

  • Type 2 diabetes: adjunct to diet and exercise for glycemic control. Ages 10 and older for liraglutide (Victoza), dulaglutide (Trulicity) and tirzepatide (Mounjaro).
  • Cardiovascular risk reduction: adults with type 2 diabetes and established cardiovascular disease (semaglutide, liraglutide, dulaglutide, tirzepatide at high risk); adults with established cardiovascular disease and obesity or overweight (Wegovy).
  • Kidney disease (Ozempic): adults with type 2 diabetes and chronic kidney disease, to reduce sustained eGFR decline, end-stage kidney disease and cardiovascular death. Check the current label for the full indication list.
  • Chronic weight management: adults with obesity or overweight with a weight-related comorbidity (Wegovy, Zepbound, Saxenda); ages 12 and older with obesity (Wegovy; Saxenda only above 60 kg).
  • Obstructive sleep apnea with obesity: moderate to severe OSA in adults (Zepbound).
  • Noncirrhotic MASH: metabolic dysfunction-associated steatohepatitis (Wegovy injection).

Dosing & Administration

Doses vary by protocol; follow local protocols and medical direction. The doses below are the labeled regimens for each product. Pin down the exact product and pen strength first. Then read the dose.

Available Forms

  • Semaglutide injection (Ozempic): single-patient pens of 0.68 mg/mL (2 mg/3 mL, delivers 0.25 or 0.5 mg), 1.34 mg/mL (4 mg/3 mL, delivers 1 mg) and 2.68 mg/mL (8 mg/3 mL, delivers 2 mg); single-dose prefilled syringes of 0.25, 0.5 and 1 mg per 0.5 mL.
  • Semaglutide tablet (Rybelsus): 3 mg, 7 mg and 14 mg tablets, taken once daily.
  • Semaglutide tablet (Ozempic tablets): 1.5 mg, 4 mg and 9 mg tablets, taken once daily. Not mg-for-mg interchangeable with Rybelsus.
  • Semaglutide tablet (Wegovy tablets): 1.5 mg, 4 mg, 9 mg and 25 mg tablets, taken once daily (adult cardiovascular risk reduction or weight reduction).
  • Tirzepatide (Mounjaro, Zepbound): single-dose pens and vials of 2.5 to 15 mg per 0.5 mL. Multi-dose vials and single-patient KwikPens contain 4 doses each, and each dose is drawn or dialed in 0.6 mL (4.17 to 25 mg/mL). Unlike the 0.5 mL single-dose products, check the syringe volume against the product.
  • Liraglutide (Victoza): 18 mg/3 mL (6 mg/mL) prefilled pen that delivers 0.6, 1.2 or 1.8 mg.
  • Liraglutide (Saxenda): 3 mL prefilled pen (6 mg/mL) that delivers 0.6, 1.2, 1.8, 2.4 or 3 mg.
  • Semaglutide injection (Wegovy): single-dose pens of 0.25, 0.5, 1, 1.7 and 2.4 mg per 0.5 or 0.75 mL; WEGOVY HD single-dose pen of 7.2 mg per 0.75 mL; single-patient FlexTouch pen with 4 doses of 2.4 mg; single-dose syringes of 0.25 to 2.4 mg.
  • Dulaglutide (Trulicity): single-dose pens of 0.75, 1.5, 3 and 4.5 mg per 0.5 mL.
  • EMS / transport: EMS and transport teams rarely stock these agents. Patients usually bring their own pens. Ask for the product name, pen strength, dose frequency and date of the last injection.

Adult Dosing

IndicationDose & RouteRepeat / MaxNotes
Type 2 diabetes: semaglutide (Ozempic)
0.25 mg SC weekly for 4 weeks, then 0.5 mg weekly; maintenance 0.5, 1 or 2 mg SC weekly
Max 2 mg SC weekly; step up only after at least 4 weeks
Missed dose: give within 5 days; otherwise skip. Rybelsus and Ozempic tablets are not mg-for-mg interchangeable (see the tablet rows).
Type 2 diabetes with CKD: semaglutide (Ozempic)
0.25 mg SC weekly for 4 weeks, then 0.5 mg weekly; increase to 1 mg weekly after at least 4 weeks on 0.5 mg
CKD maintenance 1 mg SC weekly; 2 mg is the general Ozempic maximum for glycemic control
Indication: reduce sustained eGFR decline, end-stage kidney disease and cardiovascular death. Same missed-dose rule as Ozempic.
Type 2 diabetes: tirzepatide (Mounjaro)
2.5 mg SC weekly; increase in 2.5 mg steps after at least 4 weeks
Max 15 mg SC weekly
Missed dose: give within 4 days (96 hours); otherwise skip and resume the usual day.
Type 2 diabetes: dulaglutide (Trulicity)
0.75 mg SC weekly; increase to 1.5 mg after at least 4 weeks, then in 1.5 mg steps
Max 4.5 mg SC weekly
Escalate only after at least 4 weeks on the current dose. Missed dose: give if at least 3 days (72 hours) remain before the next dose; otherwise skip.
Type 2 diabetes: liraglutide (Victoza)
0.6 mg SC daily for 1 week, then 1.2 mg daily; 1.8 mg daily if more control is needed
Max 1.8 mg SC daily; 0.6 mg step is for titration only
Missed dose: take the next scheduled dose; do not double. If more than 3 days have passed, restart at 0.6 mg.
Type 2 diabetes: oral semaglutide (Rybelsus)
3 mg PO once daily for days 1 to 30, then 7 mg daily from day 31; 14 mg daily from day 61 if needed
Max 14 mg PO daily
Take on an empty stomach with up to 4 oz of water; wait at least 30 minutes before food, drinks or other oral medicines. Missed dose: skip and take the next dose the following day.
Type 2 diabetes: semaglutide tablets (Ozempic tablets)
1.5 mg PO once daily for days 1 to 30 (not effective for glycemic control); 4 mg days 31 to 60; then 4 mg or 9 mg daily from day 61
Max 9 mg PO daily
Not mg-for-mg interchangeable with Rybelsus. Do not switch between the two tablet products during days 1 to 30. Missed dose: skip and take the next dose the following day.
Weight management: semaglutide (Wegovy)
0.25 mg SC weekly, then 0.5 mg, 1 mg and 1.7 mg at 4-week steps; maintenance 2.4 mg weekly (or 1.7 mg)
Max 7.2 mg SC weekly; adult weight reduction only, after at least 4 weeks on 2.4 mg
Missed dose: if the next dose is more than 2 days away, give as soon as possible; otherwise skip and resume the usual day. If 2 or more consecutive doses are missed, restart escalation at a lower dose. Stop at least 2 months before a planned pregnancy (see Special Populations).
Weight management: semaglutide tablets (Wegovy tablets)
1.5 mg PO once daily for days 1 to 30; 4 mg days 31 to 60; 9 mg days 61 to 90; then 25 mg daily from day 91
Max 25 mg PO daily
Adults only. Switching from the 2.4 mg injection: start 25 mg tablets one week after the last injection, per label. Missed dose: skip and take the next dose the following day.
Weight management: tirzepatide (Zepbound)
2.5 mg SC weekly for 4 weeks (initiation only), then 5 mg; increase in 2.5 mg steps after at least 4 weeks
Max 15 mg SC weekly
2.5 mg is not a maintenance dose. Missed dose: give within 4 days (96 hours).
Weight management: liraglutide (Saxenda)
0.6 mg SC daily for 1 week, then 1.2, 1.8 and 2.4 mg at weekly steps; 3 mg daily from week 5
Max 3 mg SC daily
Reassess at 16 weeks; stop if weight loss is under 4% of baseline.

Pediatric Dosing

IndicationDose (per kg) & RouteMax Single / Max TotalNotes
Type 2 diabetes, ages 10+: liraglutide (Victoza)
Fixed dose, not per kg: 0.6 mg SC daily; increase in 0.6 mg steps after at least 1 week
Max 1.8 mg SC daily
Labeled for ages 10 and older only.
Type 2 diabetes, ages 10+: dulaglutide (Trulicity)
Fixed dose, not per kg: 0.75 mg SC weekly; increase to 1.5 mg after at least 4 weeks
Max 1.5 mg SC weekly
Pediatric maximum is lower than the adult maximum of 4.5 mg weekly.
Type 2 diabetes, ages 10+: tirzepatide (Mounjaro)
Fixed dose, not per kg: 2.5 mg SC weekly; increase in 2.5 mg steps after at least 4 weeks
Max 10 mg SC weekly
KwikPen is not recommended for self-administration by pediatric patients.
Obesity, ages 12+: semaglutide (Wegovy)
Fixed dose, not per kg: adult 4-week steps from 0.25 mg; maintenance 2.4 mg or 1.7 mg SC weekly
Maintenance 2.4 mg weekly (or 1.7 mg); no higher dose is labeled for ages 12 to 17
Weight management indication only.
Obesity, ages 12+ and over 60 kg: liraglutide (Saxenda)
Fixed dose, not per kg: 0.6 mg SC daily, escalated weekly to 3 mg daily
Max 3 mg SC daily
Body weight above 60 kg and initial BMI corresponding to 30 kg/m² or greater for adults by international cut-offs. May reduce to 2.4 mg daily if 3 mg is not tolerated. Stop if BMI has not fallen at least 1% after 12 weeks on maintenance.
Under 10 years, all products
Not established in children under 10
Not established
Ozempic, Zepbound and Rybelsus labels state safety and effectiveness are not established in pediatric patients.
Pediatric labels: the table lists the labeled age limits and maximum doses so you can recognize them. It does not guide starting these drugs in children. That call belongs to the prescriber.

Preparation & Administration

  • Route: subcutaneous injection in the abdomen, thigh or upper arm, rotating sites. Oral route only for the tablet. Inspect the solution before use. It should be clear and colorless.
  • Pen and needle: single-patient use. Never share a pen between patients. A new needle does not make it safe.
  • Oral semaglutide: swallow whole with up to 4 oz of water on an empty stomach in the morning.
  • Weekly dosing: you can move the weekday, as long as doses stay at least 2 days apart for semaglutide or 3 days apart for tirzepatide, per label.
  • Storage: unused Ozempic and Mounjaro pens are refrigerated at 2 to 8 °C (36 to 46 °F); do not freeze. In-use Ozempic pens last 56 days at room temperature or in the refrigerator. Ozempic prefilled syringes may be kept at 8 to 30 °C (46 to 86 °F) for up to 28 days.
Dosing Notes:
  • Doses are fixed milligram amounts. Adults on these products are not dosed by weight.
  • Weekly products: semaglutide injection, tirzepatide, dulaglutide. Daily products: liraglutide and oral semaglutide (Rybelsus, Ozempic tablets, Wegovy tablets).
  • Step up only at the labeled interval. That is at least 4 weeks for weekly products and 1 week between liraglutide steps. The slow climb limits GI effects.

Contraindications & Precautions

Contraindications

  • Personal or family history of medullary thyroid carcinoma (MTC): absolute (all labeled products on this page).
  • Multiple endocrine neoplasia syndrome type 2 (MEN 2): absolute.
  • Serious hypersensitivity to the product or its excipients, including anaphylaxis or angioedema.

Precautions

  • Pancreatitis: acute pancreatitis has occurred, including fatal and necrotizing cases. If you suspect it, stop the drug.
  • Gallbladder disease: acute gallbladder disease has been reported.
  • Severe GI disease: semaglutide is not recommended in severe gastroparesis. Post-marketing reports include ileus and intestinal obstruction.
  • Volume depletion: acute kidney injury has been reported, some needing dialysis. It mainly followed vomiting, diarrhea or poor intake.
  • Diabetic retinopathy (semaglutide): in a 2-year trial of patients with type 2 diabetes and high cardiovascular risk, complications ran higher than placebo: 3.0% vs 1.8%.

Hold / Reassess If

  • Suspected pancreatitis: discontinue promptly and start usual management (labels).
  • Vomiting, diarrhea or inability to keep fluids down: assess volume status and kidney function. The labels say to monitor renal function. They give no numeric hold threshold.
  • Low glucose on insulin or a sulfonylurea: the labels advise lowering the sulfonylurea or insulin dose.
  • Planned surgery or sedation: tell the anesthesia team (see the aspiration warning below).
FDA Boxed Warning: Risk of thyroid C-cell tumors. Rodent studies showed these tumors, and the effect depended on dose and duration. Human relevance is unknown. Contraindicated with a personal or family history of MTC or MEN 2. Counsel patients on the signs of thyroid tumors: a neck mass, dysphagia, dyspnea or persistent hoarseness.
Aspiration risk at anesthesia: these drugs slow gastric emptying. Rare postmarketing reports describe aspiration of residual gastric contents in patients who had fasted before surgery. Treat a patient with vomiting or GI symptoms on one of these drugs as a possible full stomach. Use airway protection per protocol.

Adverse Effects & Toxicity

Common

  • GI effects: nausea, vomiting, diarrhea, constipation and abdominal pain are the most frequent adverse reactions. They cluster during dose escalation.
  • Heart rate increase (semaglutide, Wegovy): mean increases of 1 to 4 beats per minute in trials.

Serious / Life-Threatening

EffectRecognitionManagement
Acute pancreatitis
Persistent severe abdominal pain, often radiating to the back, with or without vomiting
Stop the drug; check lipase; treat per protocol
Pulmonary aspiration
Vomiting or regurgitation at induction or sedation
Suction and airway protection; RSI when indicated (see rapid sequence intubation)
Acute kidney injury
Vomiting, diarrhea or poor intake; low urine output; rising creatinine
Treat volume depletion per protocol; check creatinine
Hypoglycemia (with insulin or sulfonylurea)
Confusion, sweating, tremor or altered mental status; low glucose
Glucose check; dextrose or glucagon per protocol
Anaphylaxis or angioedema
Urticaria, airway swelling, wheeze, hypotension
Epinephrine IM per protocol (see epinephrine IM)
Ileus or intestinal obstruction
Abdominal distension, no flatus, persistent vomiting or severe constipation
Hospital evaluation; imaging and surgical consult per local protocol

Overdose & Toxicity Management

  • Labeled overdose effects: severe nausea, severe vomiting and severe hypoglycemia (liraglutide label).
  • Management: supportive care, guided by the clinical signs. The labels name no specific antidote. For advice, call Poison Help at 1-800-222-1222 or reach a medical toxicologist.
  • Observation: the labels call for prolonged observation because the half-life is long. Semaglutide's half-life is about 1 week, and tirzepatide's is about 5 days.
  • Hypoglycemia: treat per protocol with dextrose or glucagon, and recheck glucose during the observation period.

Monitoring

ParameterWhen / How OftenTarget / Act If
Clinical
—
—
Abdominal pain
Any GLP-1 receptor agonist patient with abdominal symptoms
Severe, persistent pain radiating to the back: stop the drug; check lipase; treat per protocol
Volume status
Vomiting, diarrhea or poor intake
Tachycardia, low BP, dry mucosa or low urine output: fluids per protocol; check creatinine
Mental status and glucose
Altered patients on insulin or a sulfonylurea
Any low glucose: treat per protocol (the label trial definition of hypoglycemia is below 54 mg/dL)
Airway and aspiration risk
Before sedation or anesthesia; GI symptoms in the prior 24 hours
Treat as full stomach; use RSI per protocol
Laboratory
—
—
Creatinine and BUN
Vomiting, diarrhea or dehydration
Rising creatinine above baseline: treat volume loss; reassess the drug (labels: monitor renal function)
Lipase
Compatible abdominal pain
Elevated lipase with compatible pain: pancreatitis work-up; stop the drug
Point-of-care glucose
Insulin or sulfonylurea co-therapy, or any altered patient
Low glucose: treat per protocol; repeat checks during observation

Interactions & Compatibility

Clinically Significant Interactions

Drug / ClassEffectWhat To Do
Insulin or sulfonylureas
Additive hypoglycemia, including severe hypoglycemia
Expect low glucose. Labels advise lowering the sulfonylurea or insulin dose. Check glucose on altered patients.
General anesthesia or deep sedation
Delayed gastric emptying; rare aspiration reports
Treat as full stomach; RSI per protocol (see Contraindications).
Oral medicines with narrow therapeutic index (e.g., warfarin, levothyroxine)
Delayed gastric emptying can change absorption; levothyroxine exposure rose 33% with semaglutide tablets
Labels advise monitoring patients on such drugs when the GLP-1 receptor agonist is started or changed.
Oral hormonal contraceptives (tirzepatide labels)
Possible reduced contraceptive effect
Switch to a non-oral method or add a barrier method for 4 weeks after starting and after each dose increase.
Other GLP-1 receptor agonists
Duplicate therapy; not recommended by label
Do not combine (includes other liraglutide-containing products).

No IV line, no compatibility question. Every product on this page goes in under the skin or by mouth.

Special Populations

  • Pediatrics: labeled for ages 10 and older (diabetes) or 12 and older (weight management), depending on the product. The Ozempic, Zepbound and Rybelsus labels say pediatric safety and efficacy are not established. Check the Pediatric Dosing table.
  • Pregnancy: semaglutide labels say to stop at least 2 months before a planned pregnancy, because the washout is long. Animal studies showed embryofetal harm with semaglutide and malformations with tirzepatide at high exposures. Human data are limited. Pregnancy does not change emergency care. Bring in the prescriber and obstetric team.
  • Lactation: there are no human milk data for semaglutide or liraglutide. Animal data show transfer into milk. In a single-dose study, tirzepatide was undetectable or low in breast milk. Weigh the benefits of breastfeeding against maternal need.
  • Older Adults: older trial patients on semaglutide or tirzepatide showed no overall difference in safety or efficacy. Greater sensitivity in some older patients cannot be ruled out.
  • Renal Impairment: none of these four needs a dose adjustment. The risk that matters is volume depletion. After GI losses, it can progress to acute kidney injury.
  • Hepatic Impairment: semaglutide and tirzepatide need no dose adjustment.
  • Obesity / Dosing Weight: every product on this page uses a fixed milligram dose. Dosing is not by weight.
  • Gastroparesis: semaglutide is not recommended in severe gastroparesis. Expect more GI symptoms and a higher aspiration concern.

Field & Transport Considerations

  • Scope: EMS and critical-care transport usually treat the complications, not the drug. How you manage hypoglycemia, dehydration, vomiting and airway risk varies by state and agency protocol.
  • Storage & Stability: unused Ozempic and Mounjaro pens are refrigerated at 2 to 8 °C; do not freeze. An in-use Ozempic pen is good for 56 days at room temperature. An Ozempic prefilled syringe may be kept at 8 to 30 °C for up to 28 days. A Mounjaro single-dose pen can stay unrefrigerated at up to 30 °C for a total of 21 days.
  • Carried Concentration: pen strengths differ by product. Ozempic comes at 0.68, 1.34 and 2.68 mg/mL. Compounded products may be labeled in units or milliliters, not milligrams. Confirm the dose in mg.
  • Infusions in Transport: not applicable. These go subcutaneous or by mouth only, so there is no drip to run.
  • Handoff Essentials: product and pen strength; weekly or daily; date and time of the last dose; GI symptoms and oral intake; glucose; insulin or sulfonylurea use; and whether the patient is planning pregnancy.

Clinical Pearls

Full stomach until proven otherwise: a 2026 systematic review linked GI symptoms in the 24 hours before a procedure to retained gastric contents. Perioperative guidance has changed. ASA (2023) said to hold weekly agents for 1 week before elective surgery. The 2024 multisociety guidance (Kindel et al.) swaps routine withholding for individual risk assessment. Patients at highest GI risk start with a liquid diet. Your facility's anesthesia policy sets the rule. Unplanned or emergency airways count as a full stomach either way.
Compounded-product dosing error: the FDA alert of July 2024 describes patients drawing up 5 to 20 times the intended dose from multi-dose vials. Some were told to use an insulin syringe, which reads in units. A 5-unit dose became 50 units. Confirm the dose in mg and the syringe volume.
Weekly or daily? Weekly: Ozempic or Wegovy injection, Mounjaro, Zepbound, Trulicity. Daily: Victoza, Saxenda, Rybelsus, Ozempic tablets, Wegovy tablets. Ozempic and Wegovy each come as a weekly injection and as a daily tablet. Confirm the formulation. One molecule can come as products with different maximum doses. Check the Adult Dosing table.
Low glucose has a usual cause: the labels tie hypoglycemia to insulin or a sulfonylurea taken alongside the drug. An altered patient on these agents gets a glucose check first.
Exam discriminator (CCRN, CFRN): the semaglutide maximum is 2 mg weekly for diabetes (Ozempic injection). It is 7.2 mg weekly for adult weight management only (Wegovy injection, after 2.4 mg). The tablets are daily and carry their own maximums: Ozempic tablets 9 mg, Rybelsus 14 mg, Wegovy tablets 25 mg. Before you name a maximum, ask which product and which indication.
Missed-dose rules differ: Ozempic injection allows a late dose within 5 days. Wegovy injection gives one only if more than 2 days remain. Trulicity needs at least 3 days (72 hours) left. Tirzepatide allows a late dose within 4 days (96 hours). The oral tablets skip to the next day. Liraglutide says to take the next scheduled dose, and never double.

Pharmacology

Mechanism of Action

  • GLP-1 receptor: activating it raises insulin secretion and lowers glucagon secretion. Both depend on glucose.
  • Delayed gastric emptying: the stomach empties more slowly. That blunts the rise in glucose after a meal, and it also explains the GI effects and the aspiration risk.
  • Tirzepatide: it activates two receptors: GIP and GLP-1.
  • Half-life extension: fatty-acid chains latch onto albumin. Semaglutide is more than 99% bound, and that binding allows weekly dosing.

Pharmacokinetics

RouteOnsetPeakDuration
SC semaglutide (weekly)
Gradual; steady state at 4 to 5 weeks
1 to 3 days
Half-life about 1 week
SC tirzepatide (weekly)
Not defined in label
8 to 72 hours (median 24)
Half-life about 5 days
SC dulaglutide (weekly)
Not defined in label
24 to 72 hours (median 48)
Half-life about 5 days
SC liraglutide (daily)
Not defined in label
8 to 12 hours
Half-life 13 hours
  • Half-life: semaglutide about 1 week; tirzepatide about 5 days; dulaglutide about 5 days; liraglutide 13 hours.
  • Metabolism: two routes clear semaglutide and tirzepatide: proteolytic cleavage of the peptide backbone, and beta-oxidation.
  • Protein binding: semaglutide more than 99% and tirzepatide about 99%, both bound to albumin.

Names & Classification

Generic Name
Semaglutide; tirzepatide; liraglutide; dulaglutide (class page). Exenatide and lixisenatide are not covered here; they share class cautions and are not dosed on this page.
Brand Names
Ozempic (injection and tablets), Wegovy (injection and tablets), Rybelsus (oral semaglutide), Mounjaro, Zepbound, Victoza, Saxenda, Trulicity
Pharmacologic Class
GLP-1 receptor agonist (incretin mimetic); tirzepatide is a GIP and GLP-1 receptor agonist
Therapeutic Class
Antidiabetic (incretin-based); anti-obesity agent
Controlled Substance
Not controlled
ISMP High-Alert
No
Look-Alike / Sound-Alike
None confirmed for this class. The practical confusion is weekly versus daily dosing and product strength.
Error-Prone Abbreviations to Avoid
qd and qw (write "once daily" or "once weekly"); milligram doses written as units or milliliters on compounded products

References

  1. Novo Nordisk. (2026). Ozempic (semaglutide) injection, for subcutaneous use: Prescribing information (revised 6/2026). DailyMed, U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=adec4fd2-6858-4c99-91d4-531f5f2a2d79. Related labels: Novo Nordisk. (2026). Wegovy (semaglutide) injection and tablets (revised 6/2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ee06186f-2aa3-4990-a760-757579d8f77b; Novo Nordisk. (2026). Rybelsus and Ozempic (semaglutide) tablets (revised 8/2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=27f15fac-7d98-4114-a2ec-92494a91da98
  2. Eli Lilly and Company. (2026). Mounjaro (tirzepatide) injection: Prescribing information (revised 9/2026). DailyMed, U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d2d7da5d-ad07-4228-955f-cf7e355c8cc0. Related labels: Eli Lilly and Company. (2026). Zepbound (tirzepatide) injection (revised 9/2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=487cd7e7-434c-4925-99fa-aa80b1cc776b; Eli Lilly and Company. (2026). Trulicity (dulaglutide) injection (revised 8/2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=463050bd-2b1c-40f5-b3c3-0a04bb433309
  3. Novo Nordisk. (2025). Victoza (liraglutide) injection: Prescribing information (revised 11/2025). DailyMed, U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5a9ef4ea-c76a-4d34-a604-27c5b505f5a4. Related label: Novo Nordisk. (2026). Saxenda (liraglutide) injection (revised 6/2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3946d389-0926-4f77-a708-0acb8153b143
  4. Kindel TL, Wang AY, Wadhwa A, et al. (2024). Multisociety clinical practice guidance for the safe use of glucagon-like peptide-1 receptor agonists in the perioperative period. Surgery for Obesity and Related Diseases, 20(12), 1183–1186. https://doi.org/10.1016/j.soard.2024.08.033
  5. Merhavy ZI, Kowal Z, Spencer T, et al. (2026). Perioperative anesthesia management of GLP-1 receptor agonists: a systematic review of potential risks. Perioperative Medicine (London), 15(1). https://doi.org/10.1186/s13741-026-00662-9
  6. United States Food and Drug Administration. (2024). FDA alerts health care providers, compounders and patients of dosing errors associated with compounded injectable semaglutide products. https://www.fda.gov/drugs/human-drug-compounding/fda-alerts-health-care-providers-compounders-and-patients-dosing-errors-associated-compounded

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