Product image of Mayul (Terazosin Hydrochloride Dihydrate) supplied by GNH India

Mayul

Active Ingredient:
Terazosin Hydrochloride Dihydrate
Origin:
EU

Mayul (Terazosin Hydrochloride Dihydrate)

Terazosin, the active ingredient in Mayul, is a alpha-1 adrenergic blocker presented as an oral tablet for oral use. It is indicated for the management of hypertension and for relief of urinary symptoms associated with benign prostatic hyperplasia in adult patients.

GNH India supplies Mayul as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratorios Q Pharma S.L.

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Indications & Clinical Uses

Terazosin is an alpha‑1 adrenergic blocker that acts on vascular smooth muscle and prostatic tissue to improve blood pressure control and urinary flow.

  • Hypertension: lowers systemic blood pressure by causing vasodilation.
  • Benign prostatic hyperplasia (BPH): reduces prostate smooth‑muscle tone, improving urinary stream.
  • Urinary retention due to BPH: decreases bladder outlet resistance, facilitating bladder emptying.

How It Works

  • Terazosin selectively antagonizes alpha‑1 adrenergic receptors located on vascular smooth muscle and in the prostate and bladder neck. Blocking these receptors prevents norepinephrine‑mediated contraction, leading to vasodilation, reduced peripheral resistance, and relaxation of prostatic smooth muscle, which together lower blood pressure and improve urinary flow.

Side Effects

Terazosin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Dizziness: feeling light‑headed, especially after standing.
  • Headache: mild to moderate intensity.
  • Fatigue: general tiredness or lack of energy.
  • Nasal congestion: blocked or runny nose.
  • Peripheral edema: swelling of the lower limbs.
  • Nausea: upset stomach or urge to vomit.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure that can cause fainting.
  • Syncope: sudden loss of consciousness.
  • Priapism: prolonged, painful erection requiring urgent care.
  • Anaphylaxis: severe allergic reaction with breathing difficulty.
  • Liver injury: signs of hepatitis such as jaundice.
  • Cardiac arrhythmia: irregular heart rhythm.

Precautions & Warnings

Before initiating therapy with Mayul, several safety considerations should be reviewed.

  • Blood pressure monitoring: check baseline and periodic readings.
  • Hepatic impairment: use caution and consider dose adjustment.
  • Orthostatic hypotension: advise patients to rise slowly from sitting or lying positions.
  • Concomitant antihypertensives: assess risk of additive blood‑pressure lowering.
  • Elderly patients: start at lower dose and titrate slowly.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Terazosin can interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Other alpha‑1 blockers: may cause excessive vasodilation.
  • Potent CYP3A4 inhibitors (e.g., ketoconazole): increase terazosin plasma levels.
  • Strong antihypertensives (e.g., nitroprusside): risk of severe hypotension.

Moderate Interactions (Monitor Closely):\n- Diuretics: may enhance orthostatic blood‑pressure drop.

  • NSAIDs: can blunt antihypertensive effect.
  • Phosphodiesterase‑5 inhibitors (e.g., sildenafil): may lead to pronounced hypotension.

Frequently Asked Questions

Mayul contains the active ingredient terazosin, which is prescribed to lower high blood pressure and to relieve urinary symptoms caused by benign prostatic hyperplasia. It works by relaxing blood vessels and prostate smooth muscle, improving circulation and urinary flow.

Terazosin selectively blocks alpha‑1 adrenergic receptors on vascular smooth muscle and in the prostate. This inhibition prevents norepinephrine‑induced contraction, leading to vasodilation that reduces blood pressure and relaxation of prostatic tissue that eases urinary obstruction.

The exact dose of Mayul is determined by the prescribing clinician based on the individual’s medical condition, response, and tolerance. Physicians typically start with a low dose and adjust gradually to achieve the desired therapeutic effect while monitoring safety.

Safety of terazosin in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To request Mayul, 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.

Mayul (terazosin) shares the same class mechanism as drugs like prazosin and doxazosin. Compared with prazosin, terazosin generally has a longer half‑life, allowing once‑daily dosing. Doxazosin offers similar efficacy but may differ in side‑effect profiles; selection depends on patient tolerance and clinician preference.

Mayul tablets should be stored at ambient temperature below 25 °C, kept in the original container, and protected from moisture and direct sunlight. Do not store in a refrigerator or freezer, and keep out of reach of children.

Mayul is taken orally as a tablet. Patients should swallow the tablet whole with a glass of water, with or without food, as directed by their prescriber. Consistency in timing each day helps maintain stable blood levels.

The most serious adverse events include severe hypotension, syncope (fainting), priapism (prolonged erection), and rare cases of anaphylaxis or significant liver injury. Patients should seek immediate medical attention if they experience sudden dizziness, fainting, painful erection lasting more than four hours, or signs of an allergic reaction.

Mayul should be avoided in individuals with known hypersensitivity to terazosin or any component of the formulation, in patients with severe hepatic impairment, and in those experiencing uncontrolled orthostatic hypotension. Clinicians must evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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