What are the medications used to treat hypotension?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 26, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Medications for Treating Hypotension

Norepinephrine is the first-line vasopressor for treating hypotension, initiated at 0.1-0.5 mcg/kg/min (or 0.2-1.0 μg/kg/min) via central line to maintain mean arterial pressure ≥65 mmHg. 1, 2

Initial Management Algorithm

Step 1: Rapid Volume Assessment and Fluid Resuscitation

  • Administer crystalloids immediately if the patient shows signs of hypovolemia or has a positive passive leg raise test 1, 2
  • Give an initial bolus of 30 mL/kg (approximately 1-2 L in adults) of crystalloids rapidly, preferably lactated Ringer's solution or normal saline 1, 2
  • Continue fluid administration as long as hemodynamic parameters (blood pressure, heart rate, peripheral perfusion) improve 2
  • Albumin may be added when patients require substantial amounts of crystalloids 1

Step 2: First-Line Vasopressor Therapy

  • Start norepinephrine as the primary vasopressor after rapid volume assessment 3, 1, 2
  • Target mean arterial pressure (MAP) ≥65 mmHg 1, 2
  • Central line administration is strongly preferred to minimize risk of tissue necrosis from extravasation 1, 4
  • Typical starting dose: 0.1-0.5 mcg/kg/min, titrated to effect 1

Step 3: Second-Line Vasopressor Options (If Norepinephrine Insufficient)

When norepinephrine alone fails to maintain adequate blood pressure:

  • Add vasopressin at 0.03 units/min (do not exceed this dose) to raise MAP or decrease norepinephrine requirements 1, 2
  • Alternatively, add epinephrine at 0.05-0.5 μg/kg/min as a second-line agent for refractory shock 3, 1, 2
  • Avoid dopamine due to risk of tachyarrhythmias, except in highly selected patients with relative bradycardia 2, 5

Step 4: Inotropic Support for Low Cardiac Output States

When hypotension is due to reduced cardiac output (cardiogenic shock):

  • Add dobutamine at 2-20 μg/kg/min (start at 2-5 mcg/kg/min) after blood pressure is stabilized with norepinephrine 3, 1, 2
  • Dobutamine is given without a bolus dose 1
  • Consider milrinone (25-75 μg/kg bolus over 10-20 min, then 0.375-0.75 μg/kg/min) if tachycardia is problematic with dobutamine 3
  • Levosimendan (0.1 μg/kg/min, adjustable to 0.05-0.2 μg/kg/min) may be used if counteracting beta-blocker effects is necessary 3

Specific Clinical Scenarios

Cardiogenic Shock with Severe Hypoperfusion

  • Norepinephrine first to maintain MAP ≥65 mmHg 6, 2
  • Then add dobutamine (2.5-10 μg/kg/min) if evidence of low cardiac output persists 6, 2
  • Reserve inotropes for patients with such severe reduction in cardiac output that vital organ perfusion is compromised 3

Refractory Shock Requiring High-Dose Vasopressors

  • Add hydrocortisone 50 mg IV every 6 hours (or 200-mg continuous infusion) for 7 days or until ICU discharge 1
  • Consider epinephrine as an additional agent or substitute for norepinephrine 2

Dopamine Dosing (When Used Despite Limitations)

  • Low dose (<3 μg/kg/min): Potential renal effect (uncertain benefit) 3, 5
  • Medium dose (3-5 μg/kg/min): Inotropic effect 3
  • High dose (>5 μg/kg/min): Inotropic plus vasopressor effect 3
  • Monitor arterial oxygen saturation as dopamine may cause hypoxemia; administer supplemental oxygen as needed 3

Critical Monitoring Requirements

  • Continuous monitoring of ECG, blood pressure, oxygen saturation, and urine output 6, 1, 2
  • Arterial blood gas and serum lactate levels to assess tissue perfusion 6, 2
  • Invasive hemodynamic monitoring (arterial and central venous catheter) may be needed for adequate assessment and titration 1
  • Echocardiography to evaluate volume status, cardiac function, and mechanical complications 1

Important Caveats and Pitfalls

Vasopressor-Related Risks

  • Norepinephrine can cause tissue necrosis if extravasation occurs; central line administration is mandatory 6, 1
  • Inotropes cause sinus tachycardia and may induce myocardial ischemia and arrhythmias; there is long-standing concern about increased mortality 3
  • Epinephrine overdosage may produce extremely elevated arterial pressure, cerebrovascular hemorrhage, pulmonary edema, and fatal cardiac arrhythmias 4

Drug Interactions

  • Tricyclic antidepressants potentiate cardiovascular effects of adrenergic agents 5
  • Beta-blockers antagonize cardiac effects of dopamine and dobutamine 5
  • Butyrophenones and phenothiazines can suppress dopaminergic renal vasodilation 5
  • Phenytoin administration to patients receiving dopamine may lead to hypotension and bradycardia; consider alternatives 5

Fluid Therapy Considerations

  • Avoid excessive fluid administration as hypotension is associated with higher mortality when blood pressure drops too low 3
  • Balanced crystalloids (lactated Ringer's) are preferred over normal saline 1, 2
  • Use fluid challenge technique: continue administration only as long as hemodynamic improvement occurs 1

References

Guideline

Management of Hypotension

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Hypotensive Emergency

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Cardiogenic Shock

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.