Product image of Midodrine Hydrochloride Aspire (Midodrine Hydrochloride) supplied by GNH India

Midodrine Hydrochloride Aspire

Active Ingredient:
Midodrine Hydrochloride
Origin:
EU

Midodrine Hydrochloride Aspire (Midodrine Hydrochloride)

Midodrine, the active ingredient in Midodrine Hydrochloride Aspire, is a Alpha-1 adrenergic agonist presented as an oral tablet for systemic use. It is used to raise blood pressure in patients who experience orthostatic hypotension and related forms of low blood pressure. GNH India supplies Midodrine Hydrochloride Aspire as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aspire Pharma (Malta) Limited

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Indications & Clinical Uses

Midodrine acts as an antihypotensive agent by stimulating peripheral alpha‑1 receptors to increase vascular tone.

  • Orthostatic hypotension: improves standing blood pressure and reduces symptoms of dizziness or fainting when changing posture.

How It Works

  • Midodrine is a selective alpha‑1 adrenergic receptor agonist. After oral absorption, it is converted to the active metabolite desglymidodrine, which binds to peripheral alpha‑1 receptors on vascular smooth muscle, causing vasoconstriction and an increase in systemic vascular resistance, thereby elevating arterial blood pressure.

Side Effects

Midodrine may cause a range of adverse reactions, most of which are dose‑related and reversible upon discontinuation.

Common Side Effects

  • Piloerection: localized goose‑flesh skin reaction.
  • Itching: mild pruritus often on the torso.
  • Urinary retention: difficulty initiating or completing urination.
  • Headache: pressure‑type headache, especially when standing.
  • Gastrointestinal upset: nausea or abdominal discomfort.

Serious or Rare Side Effects

  • Supine hypertension: significant blood pressure rise when lying down.
  • Bradycardia: unusually slow heart rate requiring monitoring.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Ischemic events: chest pain or peripheral ischemia in susceptible patients.
  • Arrhythmia: irregular heart rhythm that may need cardiology evaluation.

Precautions & Warnings

Before prescribing Midodrine, clinicians should evaluate patient‑specific risk factors and monitor for adverse outcomes.

  • Monitor blood pressure: check supine and standing readings regularly.
  • Avoid supine position after dosing: keep patients upright for at least 4 hours.
  • Caution in cardiovascular disease: assess risk of hypertension‑related complications.
  • Adjust for renal impairment: consider dose reduction in severe kidney dysfunction.
  • Review concomitant antihypertensives: avoid additive blood‑pressure lowering effects.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Midodrine can interact with several drug classes, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Clonidine: opposing effects on blood pressure may cause instability.
  • Other vasoconstrictors (e.g., phenylephrine): excessive hypertension.

Moderate Interactions (Monitor Closely)

  • Diuretics: may amplify orthostatic changes in volume status.
  • Beta‑blockers: combined effect on heart rate and blood pressure.
  • ACE inhibitors or ARBs: additive hypotensive or hypertensive responses.
  • Other antihypertensive agents: require careful titration and monitoring.

Frequently Asked Questions

Midodrine Hydrochloride Aspire is prescribed to treat orthostatic hypotension, a condition where blood pressure falls upon standing, causing dizziness, light‑headedness, or fainting. By raising standing blood pressure, it helps patients maintain adequate cerebral perfusion during postural changes.

Midodrine is converted after ingestion to desglymidodrine, which selectively stimulates peripheral alpha‑1 adrenergic receptors. This activation causes blood vessels to constrict, increasing systemic vascular resistance and thereby elevating arterial blood pressure, especially when a patient stands up.

The specific dose and dosing schedule for Midodrine Hydrochloride Aspire are determined by the prescribing clinician based on the patient’s blood‑pressure response, severity of symptoms, and overall health status. Patients should follow the prescriber’s instructions precisely.

Safety data for Midodrine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Midodrine is a selective alpha‑1 agonist, whereas other antihypotensive agents such as fludrocortisone act by expanding plasma volume. Midodrine provides rapid, short‑acting blood‑pressure elevation, making it useful for patients who need prompt symptom relief, while other agents may be preferred for chronic volume‑expansion strategies.

Midodrine Hydrochloride Aspire should be stored at room temperature, below 25 °C, in its original packaging. Protect the tablets from moisture, heat and direct sunlight to maintain potency throughout its shelf life.

The medication is taken orally, usually with a full glass of water. It is commonly prescribed to be taken during the day, avoiding doses close to bedtime to reduce the risk of supine hypertension.

The most serious risks include supine hypertension, which can lead to cardiovascular complications, and rare severe allergic reactions. Patients should be monitored for elevated blood pressure while lying down and instructed to report any signs of rash, swelling, or difficulty breathing.

Midodrine is contraindicated in patients with severe organic heart disease, acute renal failure, or known hypersensitivity to the drug. It should also be avoided in individuals who cannot safely remain upright for several hours after dosing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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