IV ↔ PO route conversion

Convert a dose between intravenous and oral routes for drugs where the ratio is not one to one.

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What is this for?

For drugs with incomplete or variable oral bioavailability, the intravenous and oral doses are not the same. Metoprolol requires two and a half times the oral dose because of extensive first-pass metabolism; levothyroxine requires only about three quarters of the oral dose intravenously because oral absorption is incomplete.

How to use it

  1. Select the drug. Only agents with a non-trivial route ratio are listed.
  2. Choose the direction of the switch.
  3. Enter the current dose in whatever unit the product uses; the ratio is dimensionless.

Worked example

A patient is receiving metoprolol 5 mg intravenously and is being switched to oral therapy. What is the equivalent oral dose?

Answer: 5 mg × 2.5 = 12.5 mg orally. In practice this would be rounded to an available strength, typically 12.5 mg using half of a 25 mg tablet.

Clinical pearls & pitfalls

  • Metoprolol undergoes extensive first-pass metabolism, so the oral dose is two and a half times the intravenous dose. Converting one to one substantially underdoses the patient.
  • Levothyroxine runs the other way: the intravenous dose is about 75% of the oral dose because oral absorption is only around 75% complete.
  • Many drugs genuinely are one to one — levofloxacin, linezolid, metronidazole, fluconazole. For those, IV to PO switching is a straightforward opportunity to reduce line days and cost.
  • IV to PO switch protocols are a core antimicrobial stewardship intervention. The criteria are usually clinical stability, a functioning gut, and an available oral formulation with adequate bioavailability.
  • Immediate-release and modified-release oral products are not interchangeable at the same total daily dose for every drug. Check the formulation, not just the dose.

Assumptions & limitations

  • Covers only the listed agents. Most drugs require their own product-specific guidance.
  • Ratios are population averages. Individual bioavailability varies, particularly where gut oedema, malabsorption, or short bowel is present.
  • Does not account for differences in dosing frequency between formulations, which frequently change alongside the route.
  • Does not evaluate whether the switch is clinically appropriate — that is a separate assessment.

References

  • Product labelling for metoprolol tartrate and levothyroxine sodium injection.
  • Cyriac JM, James E. Switch over from intravenous to oral therapy: a concise overview. J Pharmacol Pharmacother. 2014;5(2):83-87.
  • Barlam TF, et al. Implementing an antibiotic stewardship program: guidelines by IDSA and SHEA. Clin Infect Dis. 2016;62(10):e51-e77.

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