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Landiolol Uses, Dosage, Side Effects & Warnings | DrugsAtlas

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DRUG NAME: Landiolol

Therapeutic Class: Beta-adrenergic blocker
Subclass: Ultra-short-acting selective β1-blocker
Speciality: Critical Care Medicine
Schedule (India): Schedule H
Route(s): Intravenous
Formulations Available in India:
Formulation Strength Pack Size
Injection 20 mg 2 mL vial
Injection 50 mg 5 mL vial
Injection 300 mg 20 mL vial
Note: Limited availability in India; primarily through institutional/hospital procurement channels.

INDICATIONS + DOSING — FOR CLINICIAN USE ONLY

Primary Indications (Approved / Standard in India)

⮞ Supraventricular Tachyarrhythmias (Atrial Fibrillation/Flutter, Non-compensatory Sinus Tachycardia) — Short-term Rate Control in ICU/Perioperative Setting
Parameter Recommendation
Starting dose 10 µg/kg/min IV infusion (optional loading: 1 mg/kg bolus over 1 minute)
Titration Increase by 10 µg/kg/min every 10–15 minutes based on heart rate and haemodynamic response
Usual maintenance dose 10–40 µg/kg/min
Maximum dose 80 µg/kg/min (ICU-monitored, select patients only)
Clinical Notes:
  • Onset of action: within 5 minutes
  • Elimination half-life: approximately 4 minutes
  • Offset: haemodynamic recovery within 15–20 minutes of discontinuation
  • Requires continuous ECG and blood pressure monitoring throughout administration
  • Haemodynamically unstable patients: use with extreme caution; specialist-only and ICU setting mandatory
  • Reconstitution: dilute with normal saline or 5% dextrose as per manufacturer guidelines

Secondary Indications — Adults Only (Off-label, if any)

⮞ Perioperative Control of Tachycardia/Hypertension in Non-cardiac Surgery — OFF-LABEL
Parameter Details
Indication Intraoperative rate/BP control
Starting dose 5–10 µg/kg/min IV infusion
Titration Adjust based on haemodynamic targets
Duration Taper and discontinue postoperatively as targets achieved
Supervision Specialist only — anaesthesiologist or intensivist required
Evidence basis Small RCTs (predominantly Japanese/European); used in select Indian tertiary centres

PAEDIATRIC DOSING (Specialist Only)

Primary Indications (Approved / Standard in India)

NOT ROUTINELY APPROVED for paediatric use. Limited Indian data available.
⮞ Rate Control in Supraventricular Tachyarrhythmia — Critical Care Use Only
For Paediatric Cardiologist/Intensivist use only:
Weight Starting Dose Titration Maximum Dose
≥10 kg 1–5 µg/kg/min IV infusion Increase by 1–2 µg/kg/min every 10–20 minutes 40 µg/kg/min
Safety Monitoring:
  • Continuous ECG monitoring mandatory
  • Continuous arterial blood pressure monitoring
  • Heart rate target assessment every 5–10 minutes during titration
  • Watch for hypotension and bradycardia
Age Restrictions:
  • Avoid in neonates — safety not established
  • Use only in specialist paediatric cardiac/ICU units

Secondary Indications — Paediatric Doses (Off-label, if any)

NOT RECOMMENDED — No validated off-label indications in Indian paediatric practice.

Statement: Not recommended in children below 10 kg or neonates except under specialist supervision in tertiary care settings with full resuscitation facilities.

RENAL ADJUSTMENT

Renal Status Recommendation
All stages of CKD No dose adjustment required
Haemodialysis No supplemental dosing needed
Rationale: Landiolol undergoes rapid ester hydrolysis; minimal renal clearance of parent drug.

HEPATIC ADJUSTMENT

Severity Recommendation
Mild impairment No adjustment required
Moderate impairment Use with caution; initiate at lower infusion rate (5 µg/kg/min) and titrate slowly
Severe impairment Limited data; initiate only under specialist supervision with close haemodynamic monitoring

CONTRAINDICATIONS

  • Severe hypotension (systolic BP <90 mmHg)
  • Cardiogenic shock
  • Decompensated heart failure
  • Severe bradycardia (heart rate <50 bpm)
  • Second or third-degree atrioventricular block (without functional pacemaker)
  • Sick sinus syndrome (without functional pacemaker)
  • Known hypersensitivity to landiolol or other beta-blockers
  • Untreated phaeochromocytoma

CAUTIONS

  • Compensated heart failure — use only under close specialist supervision
  • Bronchial asthma or COPD — although β1-selective, may precipitate bronchospasm at higher doses
  • Diabetes mellitus — may mask adrenergic warning symptoms of hypoglycaemia
  • Peripheral arterial disease — may exacerbate claudication symptoms
  • Concurrent use of calcium channel blockers (verapamil/diltiazem) — risk of additive bradycardia and AV block
  • Hypokalaemia or hypomagnesaemia — correct electrolyte abnormalities before initiation
  • Abrupt discontinuation — may cause rebound tachycardia; taper when clinically feasible

PREGNANCY

Parameter Details
Safety category Limited human data; not well studied in pregnancy
Risk Potential fetal bradycardia, hypoglycaemia, growth restriction
Preferred alternatives Labetalol or metoprolol when beta-blockade indicated
When permissible Only in life-threatening maternal arrhythmia when benefit clearly outweighs risk; ICU setting only
Monitoring Maternal blood pressure, heart rate; fetal heart rate monitoring if used in second/third trimester

LACTATION

Parameter Details
Compatibility Unknown — no human lactation data available
Drug levels in milk Likely very low due to ultra-short half-life and IV-only administration
Preferred alternatives Labetalol or metoprolol (oral) if beta-blockade required during lactation
Infant monitoring Feeding tolerance, signs of bradycardia, lethargy if exposure suspected

ELDERLY

Parameter Recommendation
Starting dose Lower initial rate: 5 µg/kg/min IV infusion
Titration Slower titration; increase by 5 µg/kg/min every 15–20 minutes
Special risks Increased sensitivity to hypotension, bradycardia; higher risk of falls if mobilised early post-procedure
Monitoring More frequent BP and HR checks; assess renal and cardiac reserve before initiation

MAJOR DRUG INTERACTIONS

Interacting Drug Effect Management
Verapamil, diltiazem (IV or oral) Severe additive bradycardia, AV block, hypotension Avoid concurrent use; if essential, intensive cardiac monitoring required
Amiodarone Profound bradycardia, AV block, hypotension Avoid combination; use alternative rate control if possible
Digoxin Additive negative chronotropic effect; risk of AV block Monitor heart rate closely; consider dose reduction of one agent
General anaesthetic agents (volatile anaesthetics) Synergistic myocardial depression, hypotension, bradycardia Coordinate with anaesthesiologist; reduce doses of both agents
Catecholamine-depleting drugs (reserpine, guanethidine) Enhanced beta-blockade; severe bradycardia/hypotension Avoid combination

MODERATE DRUG INTERACTIONS

Interacting Drug Effect Management
Other antihypertensives (ACE inhibitors, ARBs, diuretics) Additive hypotensive effect Monitor blood pressure; adjust doses as needed
Insulin, sulfonylureas Masking of hypoglycaemic symptoms (tachycardia, tremor) Frequent blood glucose monitoring in diabetic patients
Neuromuscular blocking agents Possible potentiation of neuromuscular blockade Monitor neuromuscular function during anaesthesia
Clonidine Risk of rebound hypertension if clonidine stopped abruptly Discontinue beta-blocker before tapering clonidine

COMMON ADVERSE EFFECTS

  • Hypotension
  • Bradycardia
  • Nausea
  • Dizziness
  • Injection site reactions (pain, erythema)

SERIOUS ADVERSE EFFECTS

Adverse Effect Clinical Action
Severe hypotension or shock Discontinue immediately; IV fluids, vasopressors as needed
High-degree AV block or asystole Stop infusion; atropine, temporary pacing if required
Severe bradycardia (<40 bpm) Discontinue; atropine, glucagon, or isoprenaline as indicated
Bronchospasm Discontinue; administer bronchodilators; avoid rechallenge
Acute heart failure exacerbation Discontinue; initiate appropriate heart failure management

MONITORING REQUIREMENTS

Phase Parameters
Baseline 12-lead ECG, blood pressure, heart rate, serum electrolytes (K⁺, Mg²⁺), LVEF (if cardiac function questionable)
During infusion Continuous ECG and invasive/non-invasive BP monitoring; heart rate every 5–10 minutes during titration phase
After discontinuation Monitor for rebound tachycardia for at least 30–60 minutes; reassess haemodynamic stability

BRANDS AVAILABLE IN INDIA

Brand Name Manufacturer Remarks
Rapibloc Nichi-Iko / Takeda (via institutional tie-ups) Available primarily through hospital-based procurement
Note: Limited commercial availability in India; primarily accessed through institutional import or specialty distributors.

PRICE RANGE (INR)

Formulation Approximate Price
20 mg/2 mL vial ₹800–1,000
50 mg/5 mL vial ₹1,800–2,200
300 mg/20 mL vial ₹8,000–9,500
  • Not included under NLEM
  • Available through institutional/hospital procurement primarily
  • Price may vary based on import and procurement channel

CLINICAL PEARLS

  • Ultra-short half-life advantage: Approximately 4-minute half-life allows rapid titration and quick offset; particularly useful in haemodynamically unstable patients requiring careful rate control
  • Comparison with esmolol: Higher β1-selectivity than esmolol; consider when esmolol is not tolerated or unavailable
  • ICU/OT setting only: Not suitable for chronic oral rate control; strictly IV and monitored-setting use
  • Elderly patients: Start at lower infusion rates (5 µg/kg/min) and titrate more gradually
  • Cost consideration: Significantly more expensive than esmolol; reserve for cases where alternative ultra-short-acting beta-blockers are insufficient or contraindicated
  • Continuous monitoring mandatory: Never administer without ECG and blood pressure monitoring in place

TAGS

landiolol; beta-blocker; ultra-short-acting; supraventricular tachycardia; ICU; perioperative; IV antiarrhythmic; rate control; atrial fibrillation; bradycardia-risk; critical-care

VERSION

RxIndia v0.1 — 19 Feb 2026

REFERENCES

  • CDSCO import registrations and product information
  • Indian hospital ICU protocols (AIIMS, select tertiary centres)
  • Goodman & Gilman’s The Pharmacological Basis of Therapeutics
  • API Textbook of Medicine
  • Indian cardiology and anaesthesiology specialist practice protocols
  • Published RCTs for off-label perioperative indications (Japan, EU data) — noted as off-label
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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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