Mastodon

Pentamin (Solution) Instructions for Use

ATC Code

C02BC (Bis-quaternary ammonium compounds)

Active Substance

Azamethonium bromide (Rec.INN registered by WHO)

Clinical-Pharmacological Group

Ganglioblocking agent

Pharmacotherapeutic Group

Antihypertensive agents; antiadrenergic agents, ganglioblockers; bis-quaternary ammonium compounds.

Pharmacological Action

Ganglioblocker, a bis-quaternary ammonium compound. It has hypotensive, arterio- and venodilating effects. It blocks the n-cholinergic receptors of the autonomic ganglia and, in connection with this, inhibits the transmission of nerve impulses from preganglionic to postganglionic fibers of the autonomic nerves.

The autonomic ganglia also become less sensitive to the excitatory action of a number of cholinergic stimulants (including acetylcholine, nicotine, lobeline, cytisine). By interrupting the conduction of nerve impulses through the autonomic ganglia, ganglioblockers change the functions of organs supplied with autonomic innervation.

This results in a decrease in blood pressure, which is mainly associated with a reduction in the influx of vasoconstrictor impulses to the blood vessels and the expansion of the peripheral vascular bed (primarily arterioles).

Inhibition of impulse conduction along cholinergic nerve fibers leads to impaired accommodation, bronchial dilation, decreased motility of the gastrointestinal tract organs, inhibition of gland secretion, increased heart rate, and decreased bladder tone. Inhibition of n-cholinergic receptors in the chromaffin tissue of the adrenal glands leads to a decrease in the release of adrenergic substances and a weakening of reflex pressor reactions.

In high doses, it can block the n-cholinergic receptors of skeletal muscles and the central nervous system.

Azamethonium bromide is somewhat inferior to benzohexonium in terms of activity and duration of action.

Indications

Diseases and conditions caused by spasms of peripheral vessels (including endarteritis, intermittent claudication).

As part of combination therapy for hypertensive crisis, pulmonary edema, cerebral edema.

In anesthesiological practice – for controlled arterial hypotension.

In urological practice – during cystoscopy in men (to facilitate the passage of the cystoscope through the urethra).

ICD codes

ICD-10 code Indication
G93.6 Cerebral edema
I10 Essential [primary] hypertension
I73.0 Raynaud's syndrome
I73.1 Obliterative thromboangiitis [Buerger's disease]
I73.9 Peripheral vascular disease, unspecified (including intermittent claudication, arterial spasm)
J81 Pulmonary edema
Z51.4 Preparatory procedures for subsequent treatment or examination, not elsewhere classified
ICD-11 code Indication
4A44.8 Thromboangiitis obliterans
8D60.1 Cerebral edema
BA00.Z Essential hypertension, unspecified
BD42.0 Raynaud's disease
BD42.1 Raynaud's syndrome
BD42.Z Raynaud's phenomenon, unspecified
BD4Z Chronic obliterative arterial diseases, unspecified
CB01 Pulmonary edema
QB9A Preparatory procedures for subsequent treatment

Dosage Regimen

The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen.

Administer Pentamin solution intramuscularly or intravenously; the route depends on the clinical urgency and desired onset of action.

Set the dose individually for each patient, titrating against blood pressure response and therapeutic goal.

For hypertensive crisis, administer intravenously to achieve a rapid, controlled reduction in blood pressure.

For controlled arterial hypotension in surgery, use intravenous administration under continuous hemodynamic monitoring.

For peripheral vascular spasms, intramuscular injection is typically employed.

For cystoscopy in men, administer intramuscularly to facilitate instrument passage through the urethra.

Initiate therapy with a low test dose, approximately half the intended therapeutic dose, to assess individual tolerance.

Keep the patient in a supine position before injection and for 1-2 hours post-injection to mitigate the risk of orthostatic collapse.

Monitor blood pressure and pulse frequently during and after administration.

Do not exceed the maximum single dose of 150 mg for intramuscular administration.

Do not exceed the maximum daily dose of 450 mg for intramuscular administration.

Adjust dosage cautiously in elderly patients due to increased sensitivity to hypotensive effects.

Discontinue therapy if signs of severe intolerance or progressive hypotension occur.

Adverse Reactions

From the cardiovascular system: possible increased pulse, orthostatic collapse (due to inhibition of reflex mechanisms that maintain a constant level of blood pressure).

From the digestive system: dry mouth; with long-term use in high doses, intestinal atony (up to paralytic intestinal obstruction) is possible.

From the central nervous system: possible general weakness, dizziness.

From the organ of vision: mydriasis, accommodation paresis, injection of scleral vessels.

From the urinary system: with long-term use in high doses, bladder atony with anuria is possible.

Contraindications

Angle-closure glaucoma, acute phase of myocardial infarction, pronounced arterial hypotension, shock, impaired liver and/or kidney function, pheochromocytoma, degenerative diseases of the central nervous system, hypersensitivity to azamethonium bromide.

Use in Pregnancy and Lactation

Data on the safety of azamethonium bromide use during pregnancy and lactation (breastfeeding) are not available.

Use in Hepatic Impairment

Contraindication: impaired liver function.

Use in Renal Impairment

Contraindication: impaired kidney function.

Geriatric Use

Azamethonium bromide should be used with caution in elderly patients.

Special Precautions

Azamethonium bromide should be used with caution in bronchial asthma with difficult sputum discharge, intestinal and bladder atony of various etiologies, in thrombosis, thrombophlebitis, degenerative diseases of the central nervous system, bronchial asthma (with difficult sputum discharge), and in elderly patients.

Treatment with ganglioblockers should be carried out under close medical supervision.

To avoid the development of orthostatic collapse, it is recommended that the patient be in a lying position before the administration of azamethonium bromide and for 1-2 hours after the injection. It is recommended at the beginning of treatment to check the patient’s reaction to small doses of azamethonium bromide: administer 1/2 of the average dose and monitor the patient’s condition.

It should be borne in mind that with elevated blood pressure, the hypotensive effect is more pronounced.

In open-angle glaucoma, a decrease in intraocular pressure may be observed, which is due to a decrease in the production of aqueous humor under the influence of ganglioblockers.

Drug Interactions

With simultaneous use, ganglioblockers enhance the effect of adrenomimetics.

Anticholinesterase drugs are antagonists of ganglioblockers.

With simultaneous use with tricyclic antidepressants, the hypotensive effect of ganglioblockers is reduced.

Storage Conditions

Store at 15°C (59°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

Dispensing Status

Rx Only

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.

Medical Disclaimer

Brand (or Active Substance), Marketing Authorisation Holder, Dosage Form

Marketing Authorization Holder

Dalkhimpharm, JSC (Russia)

Dosage Form

Bottle Rx Icon Pentamin Solution for intravenous and intramuscular administration 50 mg/1 ml: amp. 10 pcs.

Dosage Form, Packaging, and Composition

Solution for intravenous and intramuscular administration 1 ml
Azamethonium bromide 50 mg

1 ml – ampoules (10) made of neutral glass – cardboard boxes.
1 ml – ampoules (5) made of neutral glass – contour cell packs (2) – cardboard packs.

Marketing Authorization Holder

Dalkhimpharm, JSC (Russia)

Dosage Form

Bottle Rx Icon Pentamin Solution for intravenous and intramuscular injection 5% (100 mg/2 ml): amp. 10 pcs.

Dosage Form, Packaging, and Composition

Solution for intravenous and intramuscular administration 1 ml 1 amp.
Azamethonium bromide 50 mg 100 mg

1 ml – ampoules (10) made of neutral glass – cardboard boxes.
1 ml – ampoules (5) made of neutral glass – contour cell packs (2) – cardboard packs.

Marketing Authorization Holder

Novosibkhimpharm, JSC (Russia)

Dosage Form

Bottle Rx Icon Pentamin Solution for intravenous and intramuscular injection 50 mg/1 ml: amp. 1 ml or 2 ml 5, 10, or 20 pcs.

Dosage Form, Packaging, and Composition

Solution for intravenous and intramuscular administration in the form of a colorless, transparent liquid.

1 ml
Azamethonium bromide (calculated as 100% substance) 50 mg

Excipients: water for injections – up to 1 ml.

1 ml – glass ampoules (10) – cardboard boxes.
1 ml – glass ampoules (5) – contour cell packs (1) – cardboard packs.
1 ml – glass ampoules (5) – contour cell packs (2) – cardboard packs.
1 ml – glass ampoules (10) – contour cell packs (1) – cardboard packs.
1 ml – glass ampoules (10) – contour cell packs (2) – cardboard packs.
2 ml – glass ampoules (10) – cardboard boxes.
2 ml – glass ampoules (5) – contour cell packs (1) – cardboard packs.
2 ml – glass ampoules (5) – contour cell packs (2) – cardboard packs.
2 ml – glass ampoules (10) – contour cell packs (1) – cardboard packs.
2 ml – glass ampoules (10) – contour cell packs (2) – cardboard packs.

Marketing Authorization Holder

Usolye-Sibirskiy Chemical and Pharmaceutical Plant, JSC (Russia)

Manufactured By

Armavir Biopharmaceutical Plant, FSE (Russia)

Dosage Form

Bottle Rx Icon Pentamin Solution for intravenous and intramuscular administration 50 mg/ml: 1 ml or 2 ml amp. 10 pcs.

Dosage Form, Packaging, and Composition

Solution for intravenous and intramuscular administration colorless, transparent.

1 ml
Azamethonium bromide 50 mg

Excipients: water for injections – up to 1 ml.

1 ml – ampoules made of neutral glass (10) – cardboard packs.
1 ml – ampoules made of neutral glass (5) – contour cell packs (2) – cardboard packs.
2 ml – ampoules made of neutral glass (10) – cardboard packs.
2 ml – ampoules made of neutral glass (5) – contour cell packs (2) – cardboard packs.

TABLE OF CONTENTS