Metaraminol Uses, Dosage, Side Effects & Warnings | DrugsAtlas
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DRUG NAME: Metaraminol
Therapeutic Class: Vasopressor
Subclass: Alpha-adrenergic agonist
Speciality: Anaesthesiology
Subclass: Alpha-adrenergic agonist
Speciality: Anaesthesiology
Schedule (India): Schedule H
Route(s): Intravenous (IV)
Formulations Available in India:
• Injection: 10 mg/mL in 1 mL ampoule (as metaraminol bitartrate)
Route(s): Intravenous (IV)
Formulations Available in India:
• Injection: 10 mg/mL in 1 mL ampoule (as metaraminol bitartrate)
INDICATIONS + DOSING — FOR CLINICIAN USE ONLY
Primary Indications (Approved / Standard in India)
▶ Treatment of Hypotension during Anaesthesia
| Parameter | Recommendation |
|
Starting dose
|
0.5–2.5 mg IV bolus |
|
Titration
|
Repeat bolus every 2–5 minutes as needed; single bolus not to exceed 5 mg |
|
Usual maintenance dose
|
Continuous IV infusion at 0.5–5 mg/hour, titrated to blood pressure response |
|
Maximum dose
|
Not formally defined; guided by blood pressure control and adverse effect profile |
Clinical Notes:
• Dilute prior to infusion: typically 10 mg in 500 mL of 5% dextrose or 0.9% sodium chloride
• Central venous access preferred for prolonged infusion
• Ensure adequate volume resuscitation before initiating vasopressor therapy
• Use with caution in patients with pre-existing cardiac disease or uncorrected hypovolaemia
• Dilute prior to infusion: typically 10 mg in 500 mL of 5% dextrose or 0.9% sodium chloride
• Central venous access preferred for prolonged infusion
• Ensure adequate volume resuscitation before initiating vasopressor therapy
• Use with caution in patients with pre-existing cardiac disease or uncorrected hypovolaemia
Secondary Indications — Adults (Off-label, if any)
▶ Vasopressor Support in Septic Shock (as adjunct to norepinephrine) — OFF-LABEL
| Parameter | Recommendation |
|
Starting dose
|
2–5 mg IV bolus |
|
Titration
|
Follow with infusion at 0.5–5 mg/hour, titrated to target MAP |
|
Usual maintenance dose
|
Based on haemodynamic response |
|
Maximum dose
|
Titrate to effect; no defined upper limit |
|
Duration
|
Short-term use during vasodilatory shock |
• Specialist only
• Evidence basis: Limited observational data; extrapolated from anaesthesia protocols; not first-line agent for septic shock
• Evidence basis: Limited observational data; extrapolated from anaesthesia protocols; not first-line agent for septic shock
PAEDIATRIC DOSING (Specialist Only)
Primary Indication
▶ Intraoperative Hypotension — OFF-LABEL USE
| Parameter | Recommendation |
|
Starting dose (IV bolus)
|
10–20 mcg/kg |
|
Titration
|
May repeat every 5–10 minutes based on blood pressure |
|
Usual maintenance dose (infusion)
|
Start at 1 mcg/kg/min; titrate to response |
|
Maximum dose
|
Up to 5 mcg/kg/min |
|
Minimum age
|
Use only under paediatric anaesthetist guidance; no established lower age limit |
Safety Monitoring:
• Confirm adequate intravascular volume prior to use
• Continuous blood pressure and heart rate monitoring mandatory
• Central line access preferred for infusion
• Confirm adequate intravascular volume prior to use
• Continuous blood pressure and heart rate monitoring mandatory
• Central line access preferred for infusion
Secondary Indications — Paediatric Doses (Off-label, if any)
• No well-established off-label indications in paediatric practice beyond anaesthesia settings in India
• Use restricted to operating theatre or paediatric intensive care under specialist supervision
• Use restricted to operating theatre or paediatric intensive care under specialist supervision
RENAL ADJUSTMENT
| Renal Function | Recommendation |
| Mild to moderate impairment | No dose adjustment required |
| Severe impairment | Use with caution; potential for prolonged drug clearance |
Monitoring: Blood pressure and urine output should be closely monitored
HEPATIC ADJUSTMENT
| Severity | Recommendation |
| Mild impairment | No specific adjustment; monitor blood pressure and perfusion |
| Moderate impairment | No specific adjustment; monitor closely |
| Severe impairment | Use with caution; titrate slowly; no specific hepatotoxicity documented |
CONTRAINDICATIONS
• Known hypersensitivity to metaraminol or any formulation excipient
• Phaeochromocytoma
• Mesenteric or peripheral vascular thrombosis (risk of worsening ischaemia from vasoconstriction)
• Concurrent use of monoamine oxidase inhibitors (MAOIs) — risk of hypertensive crisis
• Phaeochromocytoma
• Mesenteric or peripheral vascular thrombosis (risk of worsening ischaemia from vasoconstriction)
• Concurrent use of monoamine oxidase inhibitors (MAOIs) — risk of hypertensive crisis
CAUTIONS
• Ischaemic heart disease, arrhythmias, or cardiomyopathy
• Uncorrected hypovolaemia — volume resuscitation must precede vasopressor use
• Elderly or frail patients — heightened risk of excessive hypertensive response
• Extravasation risk — may cause tissue necrosis; avoid peripheral infusion for prolonged use
• Use only under continuous blood pressure monitoring
• Uncorrected hypovolaemia — volume resuscitation must precede vasopressor use
• Elderly or frail patients — heightened risk of excessive hypertensive response
• Extravasation risk — may cause tissue necrosis; avoid peripheral infusion for prolonged use
• Use only under continuous blood pressure monitoring
PREGNANCY
| Consideration | Recommendation |
| Overall safety | Use with caution — limited human data available |
| When it may be used | May be considered for hypotension during spinal or epidural anaesthesia if benefit outweighs risk |
| Risk | Potential uterine vasoconstriction; may affect uteroplacental perfusion |
| Preferred alternatives | Phenylephrine is commonly used in obstetric anaesthesia; consult specialist |
| Monitoring | Uteroplacental perfusion, fetal heart rate if used antenatally |
• Specialist use only
LACTATION
| Consideration | Recommendation |
| Compatibility | Not well studied; compatibility with breastfeeding uncertain |
| Drug levels in milk | Likely present in low amounts; minimal oral bioavailability expected in infant |
| Preferred alternatives | Consider alternatives where possible |
| Infant monitoring | Feeding difficulty, irritability, behavioural changes |
ELDERLY
| Consideration | Recommendation |
| Starting dose | Use lower end of bolus range (e.g., 0.5–1 mg IV) |
| Titration | Slower titration preferred |
| Risks | Increased susceptibility to hypertensive response, reflex bradycardia, arrhythmias |
| Monitoring | Cardiac status, renal perfusion, blood pressure continuously |
MAJOR DRUG INTERACTIONS
| Interacting Drug | Effect / Mechanism | Recommendation |
| Monoamine oxidase inhibitors (MAOIs) | Hypertensive crisis risk due to inhibited catecholamine breakdown |
Avoid combination
|
| Tricyclic antidepressants | Potentiation of vasopressor effects |
Avoid or monitor closely
|
| Halothane | Risk of ventricular arrhythmias (sensitises myocardium to catecholamines) |
Use with extreme caution during anaesthesia
|
| Ergot alkaloids | Additive vasoconstriction; risk of severe peripheral ischaemia |
Avoid combination
|
MODERATE DRUG INTERACTIONS
| Interacting Drug | Effect / Mechanism | Recommendation |
| Beta-blockers | May enhance reflex bradycardia | Monitor heart rate |
| Diuretics | Hypovolaemia may blunt pressor response | Correct volume status before use |
| Corticosteroids | May enhance pressor response | Adjust dose if combined |
| Other vasopressors (e.g., norepinephrine, phenylephrine) | Additive haemodynamic effects | Titrate cautiously |
COMMON ADVERSE EFFECTS
• Hypertension
• Reflex bradycardia
• Headache
• Palpitations
• Nausea
• Reflex bradycardia
• Headache
• Palpitations
• Nausea
SERIOUS ADVERSE EFFECTS
| Adverse Effect | Clinical Note |
| Ventricular arrhythmias | Risk increased with halogenated anaesthetics |
| Extravasation injury | Causes local tissue necrosis; requires immediate treatment with phentolamine infiltration |
| Myocardial ischaemia | Monitor for chest pain in at-risk patients |
| Peripheral or mesenteric ischaemia | Due to excessive vasoconstriction |
| Pulmonary oedema | Rare |
MONITORING REQUIREMENTS
| Phase | Parameters |
|
Baseline
|
Blood pressure, ECG, volume status assessment |
|
During treatment
|
Continuous BP and ECG monitoring, heart rate, urine output |
|
Infusion site
|
Monitor for extravasation; use central line for prolonged infusion |
|
Signs of ischaemia
|
Chest pain, peripheral pulses, signs of organ hypoperfusion |
BRANDS AVAILABLE IN INDIA
• Aramine Injection (Abbott)
• Metaramin Injection (Neon Laboratories)
• Metaramin Injection (Neon Laboratories)
Note: Availability may vary by region and institutional procurement
PRICE RANGE (INR)
• Approximately ₹120–₹200 per 1 mL ampoule (10 mg/mL)
• Not under NPPA price control
• Prices may differ between institutional procurement and retail pharmacies
• Not under NPPA price control
• Prices may differ between institutional procurement and retail pharmacies
CLINICAL PEARLS
• Reserve metaraminol as second-line vasopressor in shock; norepinephrine remains first-line in septic shock
• Ideal agent for managing hypotension during regional anaesthesia or anaesthesia-induced vasodilation
• Never initiate without prior volume resuscitation — may worsen organ perfusion in hypovolaemia
• Always dilute before IV infusion; prefer central venous access for prolonged administration
• Reflex bradycardia is common — reduce dose or discontinue if excessive
• Extravasation requires prompt treatment with local phentolamine infiltration to prevent tissue necrosis
• Ideal agent for managing hypotension during regional anaesthesia or anaesthesia-induced vasodilation
• Never initiate without prior volume resuscitation — may worsen organ perfusion in hypovolaemia
• Always dilute before IV infusion; prefer central venous access for prolonged administration
• Reflex bradycardia is common — reduce dose or discontinue if excessive
• Extravasation requires prompt treatment with local phentolamine infiltration to prevent tissue necrosis
TAGS
metaraminol; vasopressor; alpha-agonist; anaesthesia; hypotension; IV infusion; pregnancy-caution; bradycardia risk; specialist-only
VERSION
RxIndia v1.1 — 18 Feb 2026
REFERENCES
• CDSCO
• Indian Pharmacopoeia (IP)
• National Formulary of India (NFI)
• AIIMS Anaesthesia Protocols
• Goodman & Gilman’s The Pharmacological Basis of Therapeutics
• API Textbook of Medicine
• Indian tertiary care hospital protocols
• Indian Pharmacopoeia (IP)
• National Formulary of India (NFI)
• AIIMS Anaesthesia Protocols
• Goodman & Gilman’s The Pharmacological Basis of Therapeutics
• API Textbook of Medicine
• Indian tertiary care hospital protocols
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Clinical Responsibility
This platform is designed strictly for healthcare professionals. Data provided is synthesized from authoritative pharmacological sources and clinical registries. Do not use for consumer medical decisions. Always verify critical dosing and contraindications with official institutional protocols and peer-reviewed journals.
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